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PLOS ONE logoLink to PLOS ONE
. 2022 Mar 17;17(3):e0264964. doi: 10.1371/journal.pone.0264964

Seroepidemiology of SARS-CoV-2 in healthcare personnel working at the largest tertiary COVID-19 referral hospitals in Mexico City

Vanessa Dávila-Conn 1,#, Maribel Soto-Nava 1,#, Yanink N Caro-Vega 2,#, Héctor E Paz-Juárez 1, Pedro García-Esparza 1, Daniela Tapia-Trejo 1, Marissa Pérez-García 1, Pablo F Belaunzarán-Zamudio 3, Gustavo Reyes-Terán 4, Juan G Sierra-Madero 2, Arturo Galindo-Fraga 2, Santiago Ávila-Ríos 1,*
Editor: Leeberk Raja Inbaraj5
PMCID: PMC8929624  PMID: 35298500

Abstract

Introduction

We performed a longitudinal SARS-CoV-2 seroepidemiological study in healthcare personnel of the two largest tertiary COVID-19 referral hospitals in Mexico City.

Methods

All healthcare personnel, including staff physicians, physicians in training, nurses, laboratory technicians, researchers, students, housekeeping, maintenance, security, and administrative staff were invited to voluntarily participate, after written informed consent. Participants answered a computer-assisted self-administered interview and donated blood samples for antibody testing every three weeks from October 2020 to June 2021.

Results

A total of 883 participants (out of 3639 registered employees) contributed with at least one blood sample. The median age was 36 years (interquartile range: 28–46) and 70% were women. The most common occupations were nurse (28%), physician (24%), and administrative staff (22%). Two hundred and ninety participants (32.8%) had a positive-test result in any of the visits, yielding an overall adjusted prevalence of 33.5% for the whole study-period. Two hundred and thirty-five positive tests were identified at the baseline visit (prevalent cases), the remaining 55 positive tests were incident cases. Prevalent cases showed associations with both occupational (institution 2 vs. 1: adjusted odds ratio [aOR] = 2.24, 95% confidence interval [CI]: 1.54–3.25; laboratory technician vs. physician: aOR = 4.38, 95% CI: 1.75–10.93) and community (municipality of residence Xochimilco vs. Tlalpan: aOR = 2.03, 95% CI: 1.09–3.79) risk-factors. The incidence rate was 3.0 cases per 100 person-months. Incident cases were associated with community-acquired risk, due to contact with suspect/confirmed COVID-19 cases (HR = 2.45, 95% CI: 1.21–5.00).

Conclusions

We observed that between October 2020 and June 2021, healthcare workers of the two largest tertiary COVID-19 referral centers in Mexico City had similar level of exposure to SARS-CoV-2 than the general population. Most variables associated with exposure in this setting pointed toward community rather than occupational risk. Our observations are consistent with successful occupational medicine programs for SARS-CoV-2 infection control in the participating institutions but suggest the need to strengthen mitigation strategies in the community.

Introduction

Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) disease (COVID-19) was first confirmed in Mexico in late February 2020, reaching over 2 million confirmed cases and 200,000 deaths one year later [1]. To face the COVID-19 epidemic, official contingency measures were established in Mexico on March 23rd 2020. These included a non-compulsory stay-at-home policy, protection of highly vulnerable groups, and designation and conditioning of tertiary level institutions as referral centers for COVID-19 care exclusively, to increase hospitalization capacity [2, 3]. These included the National Institute of Respiratory Diseases (INER) and National Institute of Medical Sciences and Nutrition (INCMNZS), two of the largest COVID-19 response centers in Mexico City, where more than a quarter of the total accumulated COVID-19 cases in Mexico have occurred [1]. These institutions are characterized by highly qualified personnel, well-equipped facilities, and better access to medical supplies; both are part of the tertiary healthcare institution network in Mexico, where highly specialized health care and basic, clinical and epidemiological research take place [4].

Before the arrival of the omicron variant, three epidemiological waves of COVID-19 were observed in Mexico, with peaks in July 2020, January 2021, August 2021, and the currently ongoing fourth wave caused by the omicron variant. We enrolled participants during the second wave, which in Mexico City reached an estimated cumulative incidence of 434 cases per 100,000-person, reaching a maximum of 7371 cases per day (and over 20,000 cases per day at the country level) [1, 5]. Preliminary and recently published results of nationally representative seroepidemiological surveys in Mexico estimated that over one third of the general population had been exposed to SARS-CoV-2 in Mexico by December 2020 [6, 7]. While prevalence depends on the moment of estimation, as well as on duration of immunity, it is expected to increase after each epidemiological wave.

Overall, health care workers are expected to have increased risk of exposure to SARS-CoV-2 associated with frequent contact with both asymptomatic and hospitalized COVID-19 patients or with handling biological specimens. While many studies around the world have reported higher prevalence of SARS-CoV-2 infection in healthcare personnel, compared to the general population [8, 9], others report similar prevalence in both groups [10]. The risk of exposure for healthcare personnel may be determined by occupational factors, such as availability of personal protective equipment (PPE), infrastructure, workplace setting, access to training; in addition to the baseline risk of community-acquired infection. Reported levels of exposure to SARS-CoV-2 in healthcare workers varies widely in different settings and around the world, with studies reporting from low seroprevalence [1128], to studies reporting seroprevalence over 10% [2940]. This variation may be additionally influenced by the prevention and mitigation measures established in different countries, the prevalence of chronic diseases in the population, individual risk behaviors, the local stage of the epidemic at the time of the survey, the frequency of screening, and the vaccination coverage in key populations.

As of June 2021, there were nearly 240,000 COVID-19 cases reported in healthcare workers in Mexico, from a total of over 2,240,000 cases nationwide. Among this group, Mexico City had the largest number of cases and deaths, with the highest case fatality rate at the beginning of the epidemic (nearly 6%) with reductions thereof (below 2% by June 2021 compared to 5% in the general population) [5]. This reduction can be attributed to the uptake of COVID-19 vaccines among healthcare workers of COVID-19 referral centers, which were prioritized to start vaccinations in late December 2020.

Seroepidemiological studies can contribute with knowledge on the level of exposure to SARS-CoV-2 and the burden of disease in different populations and epidemiological contexts, estimating the total number of exposure cases, independently of clinical presentation. They can also provide information on the spread and specific transmission risks associated with a pathogen. In the case of healthcare workers, this knowledge can help to better understand occupational hazards, assess the effectiveness of prevention measures, and inform prevention policies. The level of exposure to SARS-CoV-2 in healthcare personnel in Mexico has not been reported. This information could help to identify work-associated risks of infection, which in turn can be used to design more effective occupational medicine programs and optimize vaccination strategies.

Here, we present results of a longitudinal seroepidemiological study in healthcare personnel working at the two largest tertiary referral hospitals in Mexico City functioning as COVID-19-only facilities since the beginning of the pandemic. We aimed to assess the overall prevalence and incidence of SARS-CoV-2 infection in the local context for all occupational risk categories (from physicians and nurses to administrative staff), and analyze specific community- and work-associated exposure hazards.

Materials and methods

Study design and settings

This was an observational, prospective, longitudinal, cohort study among healthcare personnel working at the two largest, tertiary care, National Ministry of Health referral hospitals for COVID-19 in Mexico City: the National Institute of Respiratory Diseases (INER) and the National Institute of Medical Sciences and Nutrition Salvador Zubirán (INCMNSZ). These institutions were converted into COVID-19-only referral facilities for severely-ill patients at the beginning of the sanitary crisis in the city. Participants were enrolled between October 2020 and June 2021, and followed-up for up to five visits, separated at least 21 days one from each other. In each visit, we collected blood samples for SARS-CoV-2 antibody testing and applied structured questionnaires to collect information of sociodemographic characteristics, and occupational and community risk exposure.

Ethics statement

The study was reviewed and approved by the Institutional Review Boards of both participating institutions: The National Institute of Medical Sciences and Nutrition (registry: CONBIOÉTICA-09CEI-011-20160627), project code 3432, and the National Institute of Respiratory Diseases (registry: CONBIOÉTICA-09CEI-003-20160427), project code C35-20. Participants went through an informed consent process both at registration to the study in the electronic portal and in a written form when attending their first appointment for blood draw. Data was stored in a local server, assuring confidentiality of participants’ information. Results from antibody tests were uploaded to each participant’s account in the portal, for personal consultation. Only key research personnel and IT staff had access to the data and databases used for the analyses were previously de-identified. Each participant had access to a portal containing their individually scheduled appointments and the results from serological tests. Data privacy and access policies were explained to and accepted by the participants during the informed consent process and before answering the computer-assisted self-administered interview (CASI). The study was conducted according to the principles of the Declaration of Helsinki.

Study participants

We invited all healthcare personnel of the two institutions to voluntarily participate in the study. We included staff physicians and physicians in training (residents and fellows), nurses, laboratory technicians, researchers, graduate biomedical research students, and housekeeping, maintenance, laundry, security, kitchen, and administrative staff. All occupations were included, given the hypothesized overall increased risk of exposure in the work environment due to the concentration of severely ill persons in the participating institutions, as well as the possibility of frequent contact of co-workers with different risk of exposure to SARS-CoV-2 according to their activities.

Participants were invited to enroll through different institutional communication channels, including advertisements in institutional web pages, official social media accounts (Facebook, Twitter), email lists, conferences, posters, and flyers. Participants were asked to register in an electronic portal designed specifically for the project, answer a computer-assisted self-administered interview (CASI) on occupational and community exposure to SARS-CoV-2 infection, and schedule an appointment to donate a blood sample for antibody testing.

To minimize attrition, we sent email reminders to schedule follow-up appointments ideally every 21 days (plus/minus one week) until a maximum of five follow-up visits were completed.

Data collection

We collected general sociodemographic information, data on community and occupational exposure, as well as history of symptoms since the beginning of the epidemic upon registration for the study, using a baseline CASI. Data was stored in a local secured server. From the second visit onwards, we applied similar CASI for the occurrence of exposure variables and symptoms in the previous 15 days. General characteristics collected included sex, age, occupation, institution, place of residence, and contact information. For occupational and community exposure, we collected data on access to PPE, contact with COVID-19 patients, compliance with basic preventive measures. The latter included physical distancing, hand washing and use of face masks, which were recorded as categorical variables (always, generally, sometimes, and never). In addition, handling of biological samples, contact with any known or suspect COVID-19 case, and use of public transport to commute to work, were recorded as dichotomous variables (yes, no). The presence or absence of symptoms was also recorded in a dichotomous manner (see S1 Appendix).

Antibody tests

We measured total anti-SARS-CoV-2 nucleocapsid (N) protein antibodies using an electrochemiluminescence-based commercial assay from EDTA-anticoagulated plasma, as recommended by the manufacturer (Elecsys Anti-SARS-CoV-2, Roche, Basel, Switzerland), on a Cobas e411 instrument. Results were expressed as cut-off index (COI) values. A COI ≥1 was considered reactive. The reported test sensitivity is 97.92% and specificity 99.95% [41].

Statistical analyses

We classified participants in three groups based on the serology test results: prevalent cases (participants with positive antibody tests at the first visit), incident cases (participants with a positive test result after having at least the first negative test result) and non-cases (participants that remained seronegative during the study period). Seroprevalence was estimated as the percentage of individuals with a positive antibody test at any time during the study period of the total of enrolled participants. We adjusted prevalence to test performance with the formula:

AdjustedPrevalence=CrudePrevalence+Specificity1Sensitivity+Specificity1

We estimated the incidence rate excluding the prevalent cases. We counted the number of new positive cases and divided them over the sum of person-time in follow up. The person-time was calculated as follows: incident cases contributed with the time elapsed from the date of their first sample to the date of their first positive sample, and non-cases contributed with their complete follow-up time from their first to their last sample date. Participants with only one follow-up visit contributed with one person-day. We expressed the measure of incidence in cases per 100 person-months of observation. We additionally used a Kaplan-Meier curve to show incidence in the cohort. We report the total number of serological tests and the number of positive tests per week across the study period.

General characteristics, presence of symptoms, compliance with basic preventive measures and occupational hazard factors were analyzed using medians and interquartile ranges or absolute counts and percentages, as appropriate. We constructed univariate and multivariate logistic regression models to explore possible associations between these variables and SARS-CoV-2 exposure for prevalent cases, from answers provided at the baseline questionnaire. To study factors associated with incident cases we used a Cox regression model, stratified by institution, based on the data collected in the questionnaire applied at the visits of the first positive test. Multivariable adjustment included all variables showing significant bivariate associations, and occupational hazard variables, age, and sex, which were included in the model a priori.

All analyses were performed using STATA v16 and R version 1.2.5019.

Results

Study population

A total of 1,129 individuals registered as volunteers in the electronic database between October 2020 and June 2021. Of these, 883 (78%) turned up to at least one appointment for blood sample collection. The median age of participants was 36 years (interquartile range, IQR: 28–46) and the majority (70%) were women. The most common occupations were nurse (28%), physician (including staff, residents, and fellows) (24%) and administrative staff (22%). Regarding occupational hazards, 37% reported handling biological specimens from patients with COVID-19, and 42% reported frequent contact with patients with COVID-19. Compliance with preventive measures at work was high: 92% reported always or generally using PPE, 99% reported always or generally wearing face masks, and 100% reported frequent hand washing (Table 1). Interestingly, 54% reported having had recent contact with any person with COVID-19 either at work or in the community and 48% used public transport to commute to work.

Table 1. Baseline characteristics of healthcare personal of two of the largest COVID-19 referral hospitals in Mexico City by study group, October 2020-June 2021.

Total N = 883 Incident n = 55 Prevalent n = 235 Non-cases n = 593 P value a
Sex, n (%) b Female 620 (70) 37 (67) 158 (68) 425 (72) 0.44
Male 262 (30) 18 (33) 76 (32) 168 (28)
Age (Median, IQR) 36 (28–46) 34 (27–44) 36 (28–45) 36 (28–46) 0.57
Institution, n (%) INER 548 (62) 36 (65) 115 (49) 397 (67) <0.001
INCMNSZ 335 (38) 19 (35) 120 (51) 196 (33)
State of residency, n (%) Mexico City 752 (86) 49 (89) 187 (81) 516 (88) 0.08
State of Mexico 100 (11) 4 (7) 34 (15) 62 (10)
Other 23 (3) 2 (4) 10 (4) 11 (2)
Municipality, n (%) Tlalpan 283 (38) 17 (35) 65 (35) 201 (39) 0.16
Coyoacán 108 (14) 6 (12) 22 (12) 80 (15)
Xochimilco 71 (10) 4 (8) 26 (14) 41 (8)
Iztapalapa 63 (8) 7 (14) 11 (6) 45 (9)
Other c 223 (30) 15 (31) 61 (33) 147 (29)
Occupation, n (%) Physician 212 (24) 16 (29) 47 (20) 149 (25) 0.005
Nurse 244 (28) 16 (29) 76 (33) 152 (26)
Lab Technician 38 (4) 0 (0) 16 (7) 22 (4)
Administrative 195 (22) 19 (35) 44 (19) 132 (22)
Other 189 (22) 4 (7) 50 (21) 135 (23)
Previous COVID-19 Yes 187 (21) 5 (9) 163 (70) 19 (3) <0.001
diagnosis, n (%) No 694 (79) 50 (91) 71 (30) 573 (97)
Contact with any person Yes 480 (54) 35 (64) 129 (55) 316 (53) 0.34
with COVID-19, n (%) d No/Unknown 401 (46) 20 (36) 105 (45) 276 (47)
Handling of biological Yes 326 (37) 21 (38) 97 (41) 208 (35) 0.23
specimens, n (%) No/Unknown 555 (63) 34 (62) 137 (59) 384 (65)
Contact with COVID-19 Frequently 367 (42) 21 (38) 113 (48) 233 (39) 0.06
patients, n (%) Never/Ocassionally 514 (58) 34 (62) 121 (52) 359 (61)
Use of PPE, n (%) Always/Generally 812 (92) 52 (95) 208 (89) 552 (93) 0.09
Sometimes/Never 69 (8) 3 (5) 26 (11) 40 (7)
Use of face mask, n (%) Always/Generally 875 (99) 55 (100) 231 (99) 589 (99) 0.39
Sometimes/Never 6 (1) 0 (0) 3 (1) 3 (1)
Hand washing, n (%) Always/Generally 879 (100) 55 (100) 233 (100) 591 (100) 0.73
Sometimes/Never 2 (0) 0 (0) 1 (0) 1 (0)
Use of public transport, Yes 426 (48) 32 (58) 121 (52) 273 (46) 0.11
n %) No 455 (52) 23 (42) 113 (48) 319 (54)
Vaccinated, n (%) e Yes 597 (68) 40 (73) 171 (73) 386 (65) 0.07
No 286 (32) 15 (27) 64 (27) 207 (35)

INCMNSZ, National Institute of Medical Sciences and Nutrition; INER, National Institute of Respiratory Diseases; PPE, Personal Protection Equipment

a Chi-square test considering incident, prevalent and non-cases, two-sided P values are shown

b Column percentages are shown in all cases

c Includes the remaining municipalities in Mexico City and municipalities in other states.

d Suspected or confirmed cases during the last 15 days.

e Starting from late December 2020, as per national policy, until last follow up visit.

Antibody prevalence estimation

At the end of the study, 290 participants had a positive result in any of the antibody tests, yielding an overall prevalence in the study period, adjusted by sensitivity and specificity of the antibody test, of 33.5%. There were 235/290 positive tests (81.9%) at baseline (prevalent cases), and the remaining 55/290 (18.9%) seroconverted during the follow up period (incident cases). The median time between visits was 29 days (IQR: 23–40). The total observation time was 76,392 days (2,546.4 months) in 883 participants. There were 774 (88%) participants with at least two follow-up test results, 662 (70%) had at least three, and only a third completed the planned five visits (280/883, 32%) (S1 Table). Fig 1A shows variation of enrolment and seropositivity rate along the study period.

Fig 1. Variation of enrolment and SARS-CoV-2 seropositivity rate along the study period in healthcare workers of the two largest COVID-19 referral hospitals in Mexico City, October 2020-June 2021.

Fig 1

A. Sampling distribution along the study period (October 2020-June 2021). New seropositive participants correspond to those having a positive serological test result in the first visit; seropositive follow-up corresponds to those having a positive serological test from the second visit onwards; seronegatives include both new and follow-up. B. Kaplan-Meier curve showing the unadjusted probability of being seronegative along time.

Risk factors in prevalent cases

Among the 235 cases with positive antibody test at their first visit, 163 (70%) reported having previously been diagnosed with SARS-CoV-2 infection (either by RT-PCR or rapid antigen test) (Table 1), with a median time between diagnosis and sample donation of 103 days (IQR: 45–314). As expected, having previous diagnosis of SARS-CoV-2 infection was strongly associated with having a positive antibody test (odds ratio [OR] = 63.3, 95% confidence interval [CI]: 38.5, 104.1); thus, we excluded this variable from the multivariable model due to collinearity (Table 2). The observed seroprevalence at baseline in physicians was 22%, 31% in nurses, 42% in laboratory technicians, and 23% in administrative staff (Table 2). When considering prevalent cases exclusively, physicians and nurses had a higher frequency of contact with COVID-19 patients, and handled biological specimens more often than administrative staff (P<0.001 in both cases) (S3 Table). The most frequent symptoms in prevalent cases were fatigue (65%), headache (65%), and myalgia (63%) (S2 Table). Nearly all symptoms assessed were more frequent in prevalent cases than in non-cases (P<0.01 in all cases) (S2 Table).

Table 2. Characteristics of prevalent cases and associated risks of having a positive serological test at baseline in healthcare workers of the two largest COVID-19 referral hospitals in Mexico City, October 2020-June 2021.

    n (%) a OR 95% CI aOR 95% CI
Sex Male 76/262 (29) Reference
  Female 158/620 (25) 0.84 0.61–1.16 0.86 0.58–1.29
Age  N/A N/A 1.00 0.98–1.01 1.00 0.98–1.02
Municipality Tlalpan 65/283 (23) Reference
  Coyoacán 22/108 (20) 0.86 0.50–1.48 0.93 0.52–1.66
  Xochimilco 26/71 (37) 1.94 1.11–3.38 2.03 1.09–3.79
  Iztapalapa 11/63 (17) 0.71 0.35–1.44 0.69 0.32–1.51
  Other b 61/223 (27) 1.26 0.84–1.89 1.31 0.85–2.02
Institution INER 115/548 (21) Reference
  INCMNSZ 120/335 (36) 2.10 1.55–2.85 2.24 1.54–3.25
Occupation Physician 47/212 (22) Reference
Nurse 76/244 (31) 1.59 1.04–2.42 1.02 0.57–1.81
Lab Technician 16/38 (42) 2.55 1.24–5.25 4.38 1.75–10.93
Administrative 44/195 (23) 1.02 0.64–1.63 1.18 0.64–2.17
Other 50/189 (26) 1.26 0.80–2.00 1.40 0.79–2.50
Contact with any person with COVID-19 129/480 (27) 1.04 0.77–1.40 0.78 0.52–1.19
Handling of biological specimens 97/326 (30) 1.29 0.95–1.75 1.09 0.67–1.77
Contact with COVID-19 patients 113/367 (31) 1.44 1.07–1.95 1.61 0.99–2.61
Use of PPE 208/812 (26) 0.57 0.34–0.95 0.60 0.32–1.13
Use of face mask 231/875 (26) 0.36 0.07–1.79 0.44 0.05–3.91
Use of public transport 121/426 (28) 1.20 0.89–1.62 1.27 0.87–1.85

aOR, adjusted odds ratio; OR, crude odds ratio; CI, confidence interval; INCMNSZ, National Institute of Medical Sciences and Nutrition; INER, National Institute of Respiratory Diseases; N/A, not applicable; PPE, Personal Protection Equipment.

a Row percentages are shown.

b Includes the remaining municipalities in Mexico City and municipalities in other states. Only the variables shown in the table were included in the multivariable model.

Persons working at INCMNSZ vs. INER (adjusted odds ratio [aOR] = 2.2, 95% CI: 1.5, 3.3), living in the municipality of Xochimilco vs. Tlalpan in Mexico City (aOR: 2.0, 95% CI: 1.1, 3.8), and working as laboratory technician in comparison to physicians (aOR: 4.4, 95% CI: 1.8, 10.9) had increased odds of having a positive test in the first visit. Associations were adjusted by sex, age, recent contact with persons with COVID-19, handling biological specimens of patients with COVID-19, contact with COVID-19 patients, appropriate use of PPE, and using public transportation for commuting to work (Table 2).

Risk factors in incident cases

After excluding the 235 participants with positive tests in the first visit (prevalent cases), the remaining 55 with positive tests seroconverted during the 55,008 days (1,833.6 months) of follow-up, resulting in an overall incidence of 3.0 cases per 100 persons-month. Of the 55 incident cases, 30 were identified at the second visit, 15 at the third, seven at the fourth, and three at the fifth (Fig 1B; S1 Table). Using a Cox regression model stratified by institution, contact with any suspected or confirmed COVID-19 case in the previous 15 days increased the hazard of becoming an incident case (HR = 2.5, 95% CI: 1.2, 5.0), while having a different occupation to physician, nurse or administrative staff, decreased this hazard (HR = 0.23, 95% CI: 0.06, 0.83) (Table 3). No additional hazard associations were observed including use of PPE, contact with COVID-19 patients, or use of public transport.

Table 3. Cox model on risks associated with being an incident case in healthcare workers of the two largest COVID-19 referral hospitals in Mexico City, October 2020-June 2021.

Variable Categories n a HR 95% CI
Sex Female 37 Reference
Male 18 0.65 0.34–1.24
Age 0.80 0.58–1.10
Occupation Physician 16 Reference
Nurse 16 0.94 0.40–2.19
Administrative 19 1.55 0.68–3.52
Other 4 0.23 0.06–0.83
Contact with any person with COVID-19 b No/Unknown 7 Reference
Yes 48 2.45 1.21–5.00
Contact with patients with COVID-19 Never/Occasionally 17 Reference
Frequently 38 1.18 0.55–2.50
Use of PPE No 2
Yes 53 0.38 0.14–1.01
Use of public transport No 30 Reference
Yes 25 1.30 0.68–2.50

HR, Hazard ratio; CI, confidence interval; PPE, Personal Protection Equipment

a Total incident cases = 55

b Suspected or confirmed during the last 15 days. Only the variables shown in the table were included in the multivariable model.

The most frequently observed symptoms among incident cases were fatigue (60%) and headache (51%) (S2 Table). Fever, myalgia, diarrhea, anosmia, and ageusia were significantly less frequent in incident cases, compared to prevalent cases (P<0.05 in all cases) (S2 Table). Contact with COVID-19 patients was significantly less frequent in incident cases among administrative staff, compared to physicians and nurses (p<0.05), while contact with any person with COVID-19, both at work and in the community, was frequent in all occupations: physicians (50%), nurses (88%), administrative staff (42%) (S4 Table).

Discussion

To our knowledge, this is the first report on seroprevalence of SARS-CoV-2 infection in healthcare workers in a Mexican setting. The participating institutions are the largest tertiary care, referral centers in Mexico City, transformed into COVID-19-only facilities to care for severely ill patients. Our results show a notably high seroprevalence to SARS-CoV-2 in healthcare workers at these institutions with nearly a third of the participants showing exposure to SARS-CoV-2 at any time during the study period, most of them at their first visit. Prevalent cases (those positive at the first visit) appeared to be associated with both occupational and community exposure to SARS-CoV-2 infection, including institution, occupation, and place of residence; while incident cases were strongly associated with community exposure, mainly contact with persons with COVID-19 outside of the hospital.

The institutions selected for the study were amongst the ones with better access to resources to respond to the sanitary crisis, which could decrease occupational hazard in the study population and makes it difficult to extrapolate the results to other institutions in the country and even in Mexico City, with generally poorer infrastructure and access to medical supplies, and training. Indeed, in our study, access to PPE and personnel training were good in general, as suggested by most participants reporting high frequency of PPE use and compliance with contingency sanitary measures. Despite this, the observed overall seroprevalence (33.5%) is amongst the highest reported in the literature [32, 36, 39]. This observation could be explained by several factors. First, the study period (October 2020-June 2021) comprised the second epidemiological wave observed in Mexico during the winter season, with the highest peak of daily cases, both nationwide and in Mexico City [1]. This study was conducted later during the pandemic than other studies with similar and lower prevalence [810, 33]; thus, the observed high prevalence may be explained by higher accumulation of cases. Second, our results are consistent with those of two large, national, seroepidemiological surveys, that observed that approximately one third of the general population had been exposed to SARS-CoV-2 by December 2020 [3, 6, 7]. This could be especially true in large urban centers such as Mexico City, which has contributed with a large proportion of the total national cases [1, 3]. It is also consistent with the predominantly community-associated risk observed in this study, especially in incident cases.

We observed that in prevalent cases, place of residence was associated with exposure, with Xochimilco municipality associated with higher seropositivity at the first visit. Regarding occupational hazards for prevalent cases, working at INCMNSZ and being a laboratory technician were associated with higher odds of exposure. The fact that this association was only observed with prevalent cases but not incident cases, could imply that mitigation measures in general and training for healthcare personnel, improved over time in both institutions, but especially at INCMNSZ. The higher risk observed in laboratory technicians cannot be explained by work-associated activities such as frequency of biological specimen handling and contact with COVID-19 patients, which were similar to those reported by physicians and nurses (S3 Table), and could reflect selection bias in this occupational group. Indeed, laboratory technicians showed a higher frequency of previous COVID-19 diagnosis (36.8%), compared to physicians (18.0%), nurses (23.5%) or administrative staff (19%), suggesting a higher enrollment of participants interested in the results of the antibody tests for this occupational group. A recent study reported low nosocomial acquisition of SARS-CoV-2 infection at INER, one of the two participating institutions here, with the implementation of a successful occupational medicine program [42]. This program included intensive training on adequate use of PPE, and follow-up of workers with readily available molecular and antigen testing for SARS-CoV-2. Although we did observe occupational risks of exposure, our results are consistent with this report with an observed predominance of community-associated risk as the study progressed.

We cannot rule out that the high prevalence observed in our study could also reflect selection bias, as participants could have been led to participation by interest in the result of the serological test, having had a high suspicion of previous disease or exposure. Moreover, participation in the study was much lower than expected, with only 45% (548/1,211) of INER and 14% (335/2,428) of the registered personnel of INCMNSZ enrolled. This could be attributable to lack of interest in participating, little time due to high-work burden, competing research protocols, problems accessing the electronic portal because of poor computational skills or lack of information on the current work (even after multiple communication efforts to promote the study). Indeed, we observed some differences between persons who did not attend (n = 246) versus those who attended (n = 883) their appointment for blood collection after registering in the study portal, including lower age, higher percentage of workers from INCMNSZ, higher proportion of nurses, higher proportion of persons that reported handling biological specimens, having frequent contact with patients with COVID-19, and using public transport (P<0.05 in all cases; S5 Table).

Our study has several limitations worth mentioning. First, the enrolment method was susceptible to selection bias, as mentioned above. Second, although the study was performed in the two largest COVID-19 facilities in Mexico City, the fact that only two centers were included could affect representativeness of the study. Also, the participating institutions were among the ones with better access to medical supplies, PPE and training, and the results may not be representative of other COVID-19 centers in Mexico or even in Mexico City. Third, regarding possible risk factors and symptoms associated with prevalent cases, information bias could exist, as participants were asked to recall information of events that could have happened since March 2020, during the enrolment period starting in October 2020. For incident cases, this memory bias is expected to be reduced, with the questionnaire referring to events happening in the previous 15 days to sample collection. Fourth, the high rate of follow-up loses, with only a third of the participants completing the total of follow up visits planed could affect incidence estimations. Finally, as discussed in a recently published study [43], using anti-N antibody tests for population-based seroprevalence studies may result in the underestimation of prevalence due to waning of these antibodies over time in comparison with anti-S antibodies. This is a limitation of our study, although the impact of this observation in our setting would need to be assessed given that the first cases of SARS-CoV-2 infection in Mexico were reported in March 2020 and enrollment in our study began in October 2020, coinciding with the onset of the second wave that significantly increased infection incidence [1]. Thus, we would expect a high proportion of the detected infections at baseline to be relatively recent. On the other hand, measuring anti-N antibodies allows to distinguish previously infected individuals from vaccinated individuals (for most approved vaccines). This is important given that vaccination efforts for healthcare personnel in Mexico started by the end of 2020. Nevertheless, even considering a possible underestimation, the prevalence rate was notably high in the examined population.

Conclusion

We observed a high rate of exposure to SARS-CoV-2 in healthcare workers in Mexico City, with overall seroprevalence in the study period of 33.5% from October 2020 to June 2021. The incidence rate was 3.0 cases/100 person-months. Our study suggests that the highest risk of exposure in healthcare workers in this setting occurred in the community, although occupational risk was also observed, especially in prevalent cases. Prevalent cases were associated with institution, occupation, and place of residence, while incident cases with recent contact with persons with COVID-19. No associations of a positive antibody test and contact with COVID-19 patients or handling of biological specimens were observed. Moreover, a high proportion of the participants reported good compliance with contingency measures and good access to PPE. Our observations are consistent with successful occupational medicine programs for SARS-CoV-2 infection control in the participating institutions but suggest the need to strengthen mitigation strategies in the community.

Supporting information

S1 Appendix. Computer-assisted self-administered interview questions.

(DOCX)

S2 Appendix. De-identified database.

(DTA)

S1 Table. Variation in the number of participants at baseline and follow-up along the study period.

(DOCX)

S2 Table. Symptoms reported by exposure group in healthcare workers of the two largest COVID-19 referral hospitals in Mexico City, October 2020-June 2021.

(DOCX)

S3 Table. Risk factors by occupation in prevalent cases, October 2020-June 2021.

(DOCX)

S4 Table. Risk factors by occupation in incident cases, October 2020-June 2021.

(DOCX)

S5 Table. Differences between persons who did and did not attend at least one visit for blood sample donation for antibody testing that registered in the study database of healthcare workers of the two largest COVID-19 referral hospitals in Mexico City, October 2020-June 2021.

(DOCX)

Acknowledgments

We thank all participants for their time and generosity. We acknowledge Edna Rodríguez-Aguirre, Martha Huertas, and the sample collection staff at INER and INCMNSZ for their contribution to this work.

Data Availability

The de-identified dataset used for analysis is available as part of the supporting information.

Funding Statement

This work was supported by Consejo Nacional de Ciencia y Tecnología (CONACyT) (Fondo FORDECYT-PRONACES) and the Mexican Government (Programa Presupuestal P016; Anexo 13 del Decreto del Presupuesto de Egresos de la Federación) to SAR. Funders had no role in study design, data collection, analysis or interpretation, writing of the report and decision to submit for publication.

References

  • 1.Gobierno de México. [COVID-19 in Mexico. General Information]. 2021 [July 2021]. Available from: https://datos.covid-19.conacyt.mx/
  • 2.Instituto Nacional de Salud Pública. [Reflections on the COVID-19 response in Mexico and suggestions to face future challenges]. 2020 [July 2021]. Available from: https://www.insp.mx/avisos/recomendaciones-pandemia
  • 3.UCSF Institute for Global Health Sciences. Mexico’s Response to COVID-19: A Case Study. 2021 [July 2021]. Available from: https://globalhealthsciences.ucsf.edu/news/mexicos-response-covid-19-case-study
  • 4.Gobierno de México. [National Institutes of Health: Actions and programmes] [updated July 2021]. Available from: https://www.gob.mx/insalud/acciones-y-programas/institutos-nacionales-de-salud-27376
  • 5.Gobieno de México. [Reports on COVID-19 in Healthcare personnel in Mexico 2021] [July 2021]. Available from: https://www.gob.mx/salud/documentos/informes-sobre-el-personal-de-salud-covid19-en-mexico-2021
  • 6.Instituto Nacional de Salud Pública. [Preliminary results of the COVID-19 National Health and Nutrition Survey]. 2020 [July 2021]. Available from: https://www.insp.mx/avisos/resultados-preliminares-de-la-encuesta-nacional-de-salud-y-nutricion-covid-19
  • 7.Muñoz-Medina JE, Grajales-Muñiz C, Salas-Lais AG, Fernandes-Matano L, López-Macías C, Monroy-Muñoz IE, et al. SARS-CoV-2 IgG Antibodies Seroprevalence and Sera Neutralizing Activity in MEXICO: A National Cross-Sectional Study during 2020. Microorganisms. 2021;9(850). Epub 2021 April 15. doi: 10.3390/microorganisms9040850 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Galanis P, Vraka I, Fragkou D, Bilali A, Kaitelidou D. High Seroprevalence of SARS-CoV-2 among Healthcare Workers in a North Italy Hospital. J Hosp Infect. 2021;108:120–34. Epub 2020 Nov 16. doi: 10.1016/j.jhin.2020.11.008 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Gómez-Ochoa SA, Franco OH, Rojas LZ, Raguindin PF, Roa-Díaz ZM, Wyssmann BM, et al. COVID-19 in Health-Care Workers: A Living Systematic Review and Meta-Analysis of Prevalence, Risk Factors, Clinical Characteristics, and Outcomes. Am J Epidemiol. 2021;190(1):161–75. doi: 10.1093/aje/kwaa191 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Lai CC, Wang JH, Hsueh PR. Population-based seroprevalence surveys of anti-SARS-CoV-2 antibody: An up-to-date review. Int J Infect Dis. 2020;101:314–22. Epub 2020 Oct 9. doi: 10.1016/j.ijid.2020.10.011 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Akinbami LJ, Vuong N, Petersen LR, Sami S, Patel A, Lukacs SL, et al. SARS-CoV-2 Seroprevalence among Healthcare, First Response, and Public Safety Personnel, Detroit Metropolitan Area, Michigan, USA, May-June 2020. Emerg Infect Dis. 2020;26(12):2863–71. Epub 2020 Sep 21. doi: 10.3201/eid2612.203764 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Alserehi HA, Alqunaibet AM, Al-Tawfiq JA, Alharbi NK, Alshukairi AN, Alanazi KH, et al. Seroprevalence of SARS-CoV-2 (COVID-19) among healthcare workers in Saudi Arabia: comparing case and control hospitals. Diagn Microbiol Infect Dis. 2021;99(3):115273. Epub 2020 Nov 20. doi: 10.1016/j.diagmicrobio.2020.115273 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Brant-Zawadzki M, Fridman D, Robinson PA, Zahn M, Chau C, German R, et al. SARS-CoV-2 antibody prevalence in health care workers: Preliminary report of a single center study. PLoS One. 2020;15(11):e0240006. doi: 10.1371/journal.pone.0240006 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Della Valle P, Fabbri M, Madotto F, Ferrara P, Cozzolino P, Calabretto E, et al. Occupational Exposure in the Lombardy Region (Italy) to SARS-CoV-2 Infection: Results from the MUSTANG-OCCUPATION-COVID-19 Study. Int J Environ Res Public Health. 2021;18(5):2567. doi: 10.3390/ijerph18052567 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Dimeglio C, Herin F, Miedougé M, Cambus JP, Abravanel F, Mansuy JM, et al. Screening for SARS-CoV-2 antibodies among healthcare workers in a university hospital in southern France. J Infect. 2021;82(1):e29–e32. Epub 2020 Sep 30. doi: 10.1016/j.jinf.2020.09.035 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Dubiela ALF, Dalla Lana DF, Aerts APK, Marques CG, Cassol R, Dalarosa MG, et al. Prevalence of COVID-19 in healthcare professionals working in hospital emergencies during first wave peak in 2020, Porto Alegre—Brazil. Infect Control Hosp Epidemiol. 2021:1–8. Epub Online ahead of print. doi: 10.1017/ice.2021.139 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Ebinger JE, Botwin GJ, Albert CM, Alotaibi M, Arditi M, Berg AH, et al. Seroprevalence of antibodies to SARS-CoV-2 in healthcare workers: a cross-sectional study. BMJ Open. 2021;11(2):e043584. doi: 10.1136/bmjopen-2020-043584 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Egger M, Bundschuh C, Wiesinger K, Bräutigam E, Berger T, Clodi M, et al. Prevalence of SARS-CoV-2 antibodies in health care personnel of two acute care hospitals in Linz, Austria. Clin Chem Lab Med. 2021. Epub Online ahead of print. doi: 10.1515/cclm-2020-1681 [DOI] [PubMed] [Google Scholar]
  • 19.Iversen K, Bundgaard H, Hasselbalch RB, Kristensen JH, Nielsen PB, Pries-Heje M, et al. Risk of COVID-19 in health-care workers in Denmark: an observational cohort study. Lancet Infect Dis. 2020;20(12):1401–8. Epub 2020 Aug 3. doi: 10.1016/S1473-3099(20)30589-2 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Jespersen S, Mikkelsen S, Greve T, Kaspersen KA, Tolstrup M, Boldsen JK, et al. SARS-CoV-2 seroprevalence survey among 17,971 healthcare and administrative personnel at hospitals, pre-hospital services, and specialist practitioners in the Central Denmark Region. Clin Infect Dis. 2020;2020:ciaa1471. Epub Online ahead of print. doi: 10.1093/cid/ciaa1471 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Jones CR, Hamilton FW, Thompson A, Morris TT, Moran E. SARS-CoV-2 IgG seroprevalence in healthcare workers and other staff at North Bristol NHS Trust: A sociodemographic analysis. J Infect. 2021;82(3). Epub 2020 Dec 1. doi: 10.1016/j.jinf.2020.11.036 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Kantele A, Lääveri T, Kareinen L, Pakkanen SH, Blomgren K, Mero S, et al. SARS-CoV-2 infections among healthcare workers at Helsinki University Hospital, Finland, spring 2020: Serosurvey, symptoms and risk factors. Travel Med Infect Dis. 2021;39:101949. Epub 2020 Dec 13. doi: 10.1016/j.tmaid.2020.101949 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Kasztelewicz B, Janiszewska K, Burzyńska J, Szydłowska E, Migdał M, Dzierżanowska-Fangrat K. Prevalence of IgG antibodies against SARS-CoV-2 among healthcare workers in a tertiary pediatric hospital in Poland. PLoS One. 2021;16(4):e0249550. doi: 10.1371/journal.pone.0249550 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Lidström AK, Sund F, Albinsson B, Lindbäck J, Westman G. Work at inpatient care units is associated with an increased risk of SARS-CoV-2 infection; a cross-sectional study of 8679 healthcare workers in Sweden. Ups J Med Sci. 2020;125(4):305–10. Epub 2020 Jul 20. doi: 10.1080/03009734.2020.1793039 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Plebani M, Padoan A, Fedeli U, Schievano E, Vecchiato E, Lippi G, et al. SARS-CoV-2 serosurvey in health care workers of the Veneto Region. Clin Chem Lab Med. 2020;58(12):2107–11. doi: 10.1515/cclm-2020-1236 [DOI] [PubMed] [Google Scholar]
  • 26.Psichogiou M, Karabinis A, Pavlopoulou ID, Basoulis D, Petsios K, Roussos S, et al. Antibodies against SARS-CoV-2 among health care workers in a country with low burden of COVID-19. PLoS One. 2020;15(12):e0243025. doi: 10.1371/journal.pone.0243025 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Self WH, Tenforde MW, Stubblefield WB, Feldstein LR, Steingrub JS, Shapiro NI, et al. Seroprevalence of SARS-CoV-2 Among Frontline Health Care Personnel in a Multistate Hospital Network—13 Academic Medical Centers, April-June 2020. MMWR Morb Mortal Wkly Rep. 2020;69(35):1221–6. doi: 10.15585/mmwr.mm6935e2 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Steensels D, Oris E, Coninx L, Nuyens D, Delforge ML, Vermeersch P, et al. Hospital-Wide SARS-CoV-2 Antibody Screening in 3056 Staff in a Tertiary Center in Belgium. JAMA. 2020;324(2):195–7. doi: 10.1001/jama.2020.11160 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Airoldi C, Patrucco F, Milano F, Alessi D, Sarro A, Rossi MA, et al. High Seroprevalence of SARS-CoV-2 among Healthcare Workers in a North Italy Hospital. Int J Environ Res Public Health. 2021;18(7):3343. doi: 10.3390/ijerph18073343 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Comelli A, Focà E, Sansone E, Tomasi C, Albini E, Quiros-Roldan E, et al. Serological Response to SARS-CoV-2 in Health Care Workers Employed in a Large Tertiary Hospital in Lombardy, Northern Italy. Microorganisms. 2021;9(3):488. doi: 10.3390/microorganisms9030488 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Goenka M, Afzalpurkar S, Goenka U, Das SS, Mukherjee M, Jajodia S, et al. Seroprevalence of COVID-19 Amongst Health Care Workers in a Tertiary Care Hospital of a Metropolitan City from India. J Assoc Physicians India. 2020;68(11):14–9. [PubMed] [Google Scholar]
  • 32.Grant JJ, Wilmore SMS, McCann NS, Donnelly O, Lai RWL, Kinsella MJ, et al. Seroprevalence of SARS-CoV-2 antibodies in healthcare workers at a London NHS Trust. Infect Control Hosp Epidemiol. 2021;42(2):212–4. Epub 2020 Aug 4. doi: 10.1017/ice.2020.402 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Hossain A, Nasrullah SM, Tasnim Z, Hasan MK, Hasan MM. Seroprevalence of SARS-CoV-2 IgG antibodies among health care workers prior to vaccine administration in Europe, the USA and East Asia: A systematic review and meta-analysis. EClinicalMedicine. 2021;33:100770. Epub 2021 Mar 8. doi: 10.1016/j.eclinm.2021.100770 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Lumley SF O’Donnell D, Stoesser NE, Matthews PC, Howarth A, Hatch SB, et al. Antibody Status and Incidence of SARS-CoV-2 Infection in Health Care Workers. N Engl J Med. 2021;384(6):533–40. Epub 2020 Dec 23. doi: 10.1056/NEJMoa2034545 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Moscola J, Sembajwe G, Jarrett M, Farber B, Chang T, McGinn T, et al. Prevalence of SARS-CoV-2 Antibodies in Health Care Personnel in the New York City Area. JAMA. 2020;324(9):893–5. doi: 10.1001/jama.2020.14765 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Noor M, Haq M, Ul Haq N, Amin S, Rahim F, Bahadur S, et al. Does Working in a COVID-19 Receiving Health Facility Influence Seroprevalence to SARS-CoV-2? Cureus. 2020;12(11):e11389. doi: 10.7759/cureus.11389 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Rudberg AS, Havervall S, Månberg A, Jernbom FA, Aguilera K, Ng H, et al. SARS-CoV-2 exposure, symptoms and seroprevalence in healthcare workers in Sweden. Nat Commun. 2020;11(1):5064. doi: 10.1038/s41467-020-18848-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Shorten RJ, Haslam S, Hurley MA, Rowbottom A, Myers M, Wilkinson P, et al. Seroprevalence of SARS-CoV-2 infection in healthcare workers in a large teaching hospital in the North West of England: a period prevalence survey. BMJ Open. 2021;11(3):e045384. doi: 10.1136/bmjopen-2020-045384 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Shrotri M, Harris RJ, Rodger A, Planche T, Sanderson F, Mahungu T, et al. Persistence of SARS-CoV-2 N-Antibody Response in Healthcare Workers, London, UK. Emerg Infect Dis. 2021;27(4):1155–8. Epub 2021 Mar 18. doi: 10.3201/eid2704.204554 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Sydney ER, Kishore P, Laniado I, Rucker LM, Bajaj K, Zinaman MJ. Antibody evidence of SARS-CoV-2 infection in healthcare workers in the Bronx. Infect Control Hosp Epidemiol. 2020;41(11):1348–9. Epub 2020 Aug 26. doi: 10.1017/ice.2020.437 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Riester E, Findeisen P, Hegel K, Kabesch M, Ambrosch A, Rank CM, et al. Performance evaluation of the Roche Elecsys Anti-SARS-CoV-2 S immunoassay. medRxiv. 2021. doi: 10.1016/j.jviromet.2021.114271 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Salazar MA, Chavez-Galan L, Castorena-Maldonado A, Mateo-Alonso M, Diaz-Vazquez NO, Vega-Martínez AM, et al. Low Incidence and Mortality by SARS-CoV-2 Infection Among Healthcare Workers in a Health National Center in Mexico: Successful Establishment of an Occupational Medicine Program. Front Public Health. 2021;9:651144. Epub 2021 April 13. doi: 10.3389/fpubh.2021.651144 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Fenwick C, Croxatto A, Coste AT, Pojer F, André C, Pellaton C, et al. Changes in SARS-CoV-2 Spike versus Nucleoprotein Antibody Responses Impact the Estimates of Infections in Population-Based Seroprevalence Studies. J Virol. 2021;95(3):e01828–20. doi: 10.1128/JVI.01828-20 [DOI] [PMC free article] [PubMed] [Google Scholar]

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PONE-D-21-27465Seroepidemiology of SARS-CoV-2 in healthcare personnel working at the largest tertiary COVID-19 referral hospitals in Mexico City.PLOS ONE

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Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: This is an important study done during difficult times, among healthcare personnel and the work done is appreciated.

The study brings out the main point that the exposure in this healthcare setting pointed toward community rather than occupational risk. Some comments are:

1. Since the study reports a prevalence value among healthcare staff, it may be important to mention that since the Nucleocapsid antigen was used, there could be underestimation of the prevalence as compared to the assays using the Spike protein as per some reports (eg: Changes in SARS-CoV-2 Spike versus Nucleoprotein Antibody Responses Impact the Estimates of Infections in Population-Based Seroprevalence Studies | Journal of Virology (asm.org)).

2. Although lab technicians are stated to be associated with higher risk at the first visit, and this is mentioned as a significant result in the abstract, no details are available about the specific type of work done related to exposure (sample collection or testing etc), use and availability of PPE etc for this group and on the possible reasons for the same especially when compared to doctors and nurses. Or was it a selection bias alone?

3. Line 181: In the models, participants

“182 were censored at the time of their last test, when they did not complete the originally planned 183 five tests and had negative results in all their samples.”

This statement is not clear. Were they removed completely?

4. Line 321 – The use of the word “posterior “is confusing. Does it mean “behind/before” or after?

Reviewer #2: Abstract

• Details regarding the study participants can be added

• consent for participation and regular blood testing can be added

• Study duration and frequency of the blood tests done can be added

• What is the target sample size?

Introduction

• Information on the reported burden (how many cases were reported during the first wave) and rationale of seroprevalence can be linked

• More content needs to be added on the need and process of conducting seroprevalence studies.

• Need a clear description on what is the knowledge/ research gap and how current study tries to address it.

Methods

• The rationale for conducting this study is not clearly mentioned anywhere, especially What is the rationale of including all types of health workers, did the authors assume that the risk was same for all the workers. If it is different risk, how did they analyze the sample size for each risk level?

• Who had access to CASI data? How was the data security maintained?

• Line no. 146: please add reference number of approval from ethical committee

Results:

• Line number 233 to 235

• It is not clear as to whether it is a Figure title or started with explanation?

• What do you mean by prevalent cases as written in line number 250? The description of prevalent cases is given only in line number 275. It would be better to add it in line number 250 for better clarity

• Line No (255-262): Too lengthy sentence and not clear

• Table 2: What are the factors adjusted for Table 2? Please mention adjusted variables in the footnote of the table

Discussion

• Line No 343.:What are the reasons for lower participation rate in both the study centers?

• How the data privacy of the health care staff was maintained across the study centers? This might be one of the reasons for non-participation too. How does the study overcome this issue? Please describe.

• Line number 233 to 235: It is not clear as to whether it is a Figure title or started with explanation?

**********

6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

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Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

Reviewer #2: No

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

PLoS One. 2022 Mar 17;17(3):e0264964. doi: 10.1371/journal.pone.0264964.r002

Author response to Decision Letter 0


17 Jan 2022

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2. Please include additional information regarding the survey or questionnaire used in the study and ensure that you have provided sufficient details that others could replicate the analyses. For instance, if you developed a questionnaire as part of this study and it is not under a copyright more restrictive than CC-BY, please include a copy, in both the original language and English, as Supporting Information.

A: The questionnaire has been added as a supplementary file.

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“This work was supported by Consejo Nacional de Ciencia y Tecnología (CONACyT) (Fondo FORDECYT-PRONACES) and the Mexican Government (Programa Presupuestal P016; Anexo 13 del Decreto del Presupuesto de Egresos de la Federación) to SAR. Funders had no role in study design, data collection, analysis or interpretation, writing of the report and decision to submit for publication.”

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“This work was supported by Consejo Nacional de Ciencia y Tecnología (CONACyT) (Fondo FORDECYT-PRONACES) and the Mexican Government (Programa Presupuestal P016; Anexo 13 del Decreto del Presupuesto de Egresos de la Federación) to SAR. Funders had no role in study design, data collection, analysis or interpretation, writing of the report and decision to submit for publication.”

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A: The full ethics statement is now included in the Methods, including data on the IRB who approved the study.

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A: The ethics statement has been moved to the Methods and removed from other sections of the manuscript.



Reviewers' comments:

Reviewer's Responses to Questions


1. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented. 

Reviewer #1: Yes

Reviewer #2: Yes

2. Has the statistical analysis been performed appropriately and rigorously? 

Reviewer #1: Yes

Reviewer #2: Yes

3. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

4. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

5. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Comments to the Author

Reviewer #1: 

This is an important study done during difficult times, among healthcare personnel and the work done is appreciated.


The study brings out the main point that the exposure in this healthcare setting pointed toward community rather than occupational risk. Some comments are:

1. Since the study reports a prevalence value among healthcare staff, it may be important to mention that since the Nucleocapsid antigen was used, there could be underestimation of the prevalence as compared to the assays using the Spike protein as per some reports (eg: Changes in SARS-CoV-2 Spike versus Nucleoprotein Antibody Responses Impact the Estimates of Infections in Population-Based Seroprevalence Studies | Journal of Virology (asm.org)).

A: We thank the Reviewer for this observation. We have included an additional paragraph in the Discussion to mention this point as a limitation of the study: “Finally, as discussed in a recently published study [43], using anti-N antibody tests for population-based seroprevalence studies may result in the underestimation of prevalence due to waning of these antibodies over time in comparison with anti-S antibodies. This is a limitation of our study, although the impact of this observation in our setting would need to be assessed given that the first cases of SARS-CoV-2 infection in Mexico were reported in March 2020 and enrollment in our study began in October 2020, coinciding with the onset of the second wave that significantly increased infection incidence [1, 5]. Thus, we would expect a high proportion of the detected infections at baseline to be relatively recent. On the other hand, measuring anti-N antibodies allows to distinguish previously infected individuals from vaccinated individuals (for most approved vaccines). This is important given that vaccination efforts for healthcare personnel in Mexico started by the end of 2020. Nevertheless, even considering a possible underestimation, the prevalence rate was notably high in the examined population.”


2. Although lab technicians are stated to be associated with higher risk at the first visit, and this is mentioned as a significant result in the abstract, no details are available about the specific type of work done related to exposure (sample collection or testing etc), use and availability of PPE etc for this group and on the possible reasons for the same especially when compared to doctors and nurses. Or was it a selection bias alone?

A: The specific type of work of laboratory technicians was not collected as part of the metadata. However, we do have information on access to PPE, contact with COVID-19 patients and handling of biological specimens from COVID-19 patients (S3 Table). The self-reported frequency of biological specimen handling and contact with COVID-19 patients among laboratory technicians was not significantly different to that reported by nurses and physicians and thus, we would expect a higher significance of community-associated risk. However, this observation could also reflect selection bias in this group. Indeed, the frequency of previous COVI-19 diagnosis in laboratory technicians was higher than in physicians, nurses and administrative staff, suggesting a higher enrollment of persons interested in the results of the antibody tests for participants of this occupational group. This has been added to the Discussion.

3. Line 181: In the models, participants
“182 were censored at the time of their last test, when they did not complete the originally planned 183 five tests and had negative results in all their samples.”
This statement is not clear. Were they removed completely?

A: All the participants were included in the prevalence analysis. Participants with a positive result in their first sample were excluded from the incidence analysis and were considered prevalent cases. Participants who did not complete the five follow-up visits contributed person-time from all the available tests with negative results, until the first positive result or until their last available negative result. We have included the following sentence in the text to improve clarity: “In the models, participants with negative results in all their follow-up samples were censored at the time of their last available test.”


4. Line 321 – The use of the word “posterior “is confusing. Does it mean “behind/before” or after?

A: We have reworded the sentence in order to make it clearer: “This study comprises a later time period to that reported in other studies with similar and lower prevalence [8-10, 33].”

Reviewer #2: 

Abstract
• Details regarding the study participants can be added
• consent for participation and regular blood testing can be added
• Study duration and frequency of the blood tests done can be added
• What is the target sample size?

A: Considering word limit, the abstract has been modified to include the details requested by the Reviewer. Study duration and frequency of blood tests were already included in the original version.

Introduction
• Information on the reported burden (how many cases were reported during the first wave) and rationale of seroprevalence can be linked
• More content needs to be added on the need and process of conducting seroprevalence studies.
• Need a clear description on what is the knowledge/ research gap and how current study tries to address it.


A: We believe that the original version of the manuscript already includes several of the points raised by the Reviewer to explain the rationale of the study as well as the knowledge gap being addressed:

1. Higher risk of exposure among health workers than the general population: Lines 77-79

2. Association of exposure with activities at work and working conditions: Lines 81-84

3. Wide variation in reported seroprevalence in healthcare workers across studies worldwide: Lines 84-86.

4. Unknown seroprevalence for SARS-CoV-2 in healthcare workers in the Mexican setting: Lines 102-103.

5. Advantages of conducting seroprevalence studies in healthcare workers to better understand occupational hazards and improve prevention measures: Lines 97-102

In order to improve this justification, we have added some additional content to the Introduction, as suggested, including an update of the epidemiological background (lines 67-71) and rationale of the study (lines 104-106; lines 110-112).


Methods
• The rationale for conducting this study is not clearly mentioned anywhere, especially What is the rationale of including all types of health workers, did the authors assume that the risk was same for all the workers. If it is different risk, how did they analyze the sample size for each risk level?

A: We believe that the original version of the manuscript includes several points to explain the rationale of the study, as detailed above.

In order to improve this justification, and following the Reviewer’s suggestion, we have added additional text in the Methods, explaining the rationale for including all types of healthcare workers: “We invited all healthcare workers of the participating institutions to enroll, regardless of occupation (staff physicians, physicians in training, nurses, laboratory technicians, researchers, students, housekeeping, maintenance, security and administrative staff). We included all occupations, given the hypothesized overall increased risk of exposure in the working environment due to the concentration of severely ill persons in the participating institutions, as well as the possibility of frequent contact of co-workers with different risk of exposure to SARS-CoV-2 according to their activities. Participants were enrolled between October 2020 and June 2021 and followed-up for up to five visits, separated at least 21 days one from each other. We collected blood samples for antibody testing and applied structured questionnaires for sociodemographic and occupational and community risk exposure information at each visit. We evaluated the risk of exposure to SARS-CoV-2 using multivariable models including the type of occupation and potential community and work risk variables.”

Sample size for different risk levels according to occupation were not calculated. Instead, we analyzed the independent and potential association of each work and community risk variable (including occupation) with SARS-CoV-2 exposure using multivariable logistic models. Stratifying by occupation was not possible, given the low number of participants in some categories.


• Who had access to CASI data? How was the data security maintained?

A: We have added the following information to the “Data collection” section of the Methods: “Data was stored in a local secured server. Only key research personnel and IT staff had access to the data and databases used for the analyses were previously de-identified. Each participant had access to a portal containing their individually scheduled appointments and the results from serological tests. Data privacy and access policies were explained to and accepted by the participants during the informed consent process and before answering the CASI”.


• Line no. 146: please add reference number of approval from ethical committee


A: An Ethics Statement section has been added, including registry numbers of the Institutional Review Boards, as well as reference numbers of the approved protocol.

Results:
• Line number 233 to 235
• It is not clear as to whether it is a Figure title or started with explanation?

A: We apologize for the confusion. The Journal requires Figure Legends to be inserted across the manuscript. This paragraph includes the title and legend for Figure 1. We have corrected formatting issues in order to make it more understandable.


• What do you mean by prevalent cases as written in line number 250? The description of prevalent cases is given only in line number 275. It would be better to add it in line number 250 for better clarity

A: We define prevalent, incident and non-cases in the Methods (Statistical analyses section). For better clarity, we have added the definition in the suggested line: “Considering only prevalent cases (persons with a positive antibody test result in their first visit; see Methods)”


• Line No (255-262): Too lengthy sentence and not clear
• Table 2: What are the factors adjusted for Table 2? Please mention adjusted variables in the footnote of the table

A: We have reworded the paragraph, separating sentences to improve clarity. We have added a footnote in Tables 2 and 3, explaining that only variables shown in the table were included in the multivariable models. This information is also included in the Statistical Analysis section of the Methods.


Discussion
• Line No 343.: What are the reasons for lower participation rate in both the study centers?

A: The reasons for low participation rate and its impact as a possible bias in the study are discussed in the original manuscript (lines 362-373 of the revised version). This section of the text was kept as originally written in the revised version: “Participation in the study was much lower than expected, with only 45% (548/1,211) and 14% (335/2,428) of the registered personnel of INER and INCMNSZ enrolled. This could be attributable to lack of interest in participating, little time due to high work burden, competing research protocols, problems accessing the electronic portal because of poor computational skills or lack of information on the current work (even after multiple communication efforts to promote the study). Indeed, we observed some differences between persons who did not attend (n=246) versus those who attended (n=883) their appointment for blood collection after registering in the study portal, including lower age, higher percentage of workers from INCMNSZ, higher proportion of nurses, higher proportion of persons that reported handling biological specimens, having frequent contact with patients with COVID-19, and using public transport (P<0.05 in all cases; S5 Table).“


• How the data privacy of the health care staff was maintained across the study centers? This might be one of the reasons for non-participation too. How does the study overcome this issue? Please describe.


A: We do not believe that data privacy could be a reason for non-participation. The databases compiling information about the participating healthcare personnel were only available for key research personnel and IT staff and databases for the analyses were previously de-identified. Data privacy and access policy were stated in the informed consent and before providing access to the CASI in the portal. All participants agreed with data privacy policies before providing answers. These points have been added to the “Data collection” section of the Methods.

• Line number 233 to 235: It is not clear as to whether it is a Figure title or started with explanation?

A: We apologize for the confusion. As explained above, the Journal requires Figure Legends to be inserted across the manuscript. This paragraph includes the title and legend for Figure 1. We have corrected formatting issues in order to make it more understandable.

6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

Reviewer #2: No

Attachment

Submitted filename: Response to Reviewers.docx

Decision Letter 1

Leeberk Raja Inbaraj

7 Feb 2022

PONE-D-21-27465R1Seroepidemiology of SARS-CoV-2 in healthcare personnel working at the largest tertiary COVID-19 referral hospitals in Mexico City.PLOS ONE

Dear Dr. Avila-Rios,

Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process.

Please submit your revised manuscript by Mar 24 2022 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

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If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. Guidelines for resubmitting your figure files are available below the reviewer comments at the end of this letter.

If applicable, we recommend that you deposit your laboratory protocols in protocols.io to enhance the reproducibility of your results. Protocols.io assigns your protocol its own identifier (DOI) so that it can be cited independently in the future. For instructions see: https://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols. Additionally, PLOS ONE offers an option for publishing peer-reviewed Lab Protocol articles, which describe protocols hosted on protocols.io. Read more information on sharing protocols at https://plos.org/protocols?utm_medium=editorial-email&utm_source=authorletters&utm_campaign=protocols.

We look forward to receiving your revised manuscript.

Kind regards,

Leeberk Raja Inbaraj, MD

Academic Editor

PLOS ONE

Journal Requirements:

Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice.

[Note: HTML markup is below. Please do not edit.]

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: (No Response)

Reviewer #2: All comments have been addressed

**********

2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

Reviewer #2: Yes

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

Reviewer #2: Yes

**********

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: All comments except 3 are fully addressed.

Regarding the earlier comment 3.

Line 181: In the models, participants“182 were censored at the time of their last test, when they did not complete the originally planned 183 five tests and had negative results in all their samples.” This statement is not clear. Were they removed completely?

A: All the participants were included in the prevalence analysis. Participants with a positive result in their first sample were excluded from the incidence analysis and were considered prevalent cases. Participants who did not complete the five follow-up visits contributed person-time from all the available tests with negative results, until the first positive result or until their last available negative result. We have included the following sentence in the text to improve clarity: “In the models, participants with negative results in all their follow-up samples were censored at the time of their last available test.”

From the response to the earlier comment above, it appears that the person time included the time till their last available negative visit if they did not complete five visits.

"Participants who did not complete the five follow-up visits contributed person-time from all the available tests with negative results, until the first positive result or until their last available negative result."

“In the models, participants with negative results in all their follow-up samples were censored at the time of their last available test.”

But does “censored” mean that they were removed? It is confusing if they were removed, whether only the last test was removed and also why they were removed. Or were they removed for calculation of the incident cases ?

Additional comment 1:

At the end of the study, 290 participants had a positive result in any of the antibody tests, yielding 241 an overall prevalence in the study period, adjusted by sensitivity and specificity of the antibody

Line 242 test, of 33.5%. 235 positive cases (81.9%) were identified at baseline (prevalent cases), while the 243 remaining 55 (6.2%) seroconverted during the follow up period (incident cases).

Among the positive cases (290) – the prevalent cases were 235/290 = 81.9%, while the incident cases would be 55/290 which is 18.9 % and not 6.2% as mentioned – is that correct ?

Additional comment 2: Line 68 - spelling error "waive" caused by the omicron variant.

Reviewer #2: Thanks for addressing the earlier comments.

I encourage the authors to please check the manuscript for grammar and sentence structuring before final proof is sent.

**********

7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

If you choose “no”, your identity will remain anonymous but your review may still be made public.

Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

Reviewer #2: Yes: Giridhara R Babu

[NOTE: If reviewer comments were submitted as an attachment file, they will be attached to this email and accessible via the submission site. Please log into your account, locate the manuscript record, and check for the action link "View Attachments". If this link does not appear, there are no attachment files.]

While revising your submission, please upload your figure files to the Preflight Analysis and Conversion Engine (PACE) digital diagnostic tool, https://pacev2.apexcovantage.com/. PACE helps ensure that figures meet PLOS requirements. To use PACE, you must first register as a user. Registration is free. Then, login and navigate to the UPLOAD tab, where you will find detailed instructions on how to use the tool. If you encounter any issues or have any questions when using PACE, please email PLOS at figures@plos.org. Please note that Supporting Information files do not need this step.

PLoS One. 2022 Mar 17;17(3):e0264964. doi: 10.1371/journal.pone.0264964.r004

Author response to Decision Letter 1


11 Feb 2022

Journal Requirements:

Please review your reference list to ensure that it is complete and correct. If you have cited papers that have been retracted, please include the rationale for doing so in the manuscript text, or remove these references and replace them with relevant current references. Any changes to the reference list should be mentioned in the rebuttal letter that accompanies your revised manuscript. If you need to cite a retracted article, indicate the article’s retracted status in the References list and also include a citation and full reference for the retraction notice.

[Note: HTML markup is below. Please do not edit.]


A: References have been reviewed.

Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: (No Response)

Reviewer #2: All comments have been addressed

2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented. 

Reviewer #1: Yes

Reviewer #2: Yes

3. Has the statistical analysis been performed appropriately and rigorously? 

Reviewer #1: Yes

Reviewer #2: Yes

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

Reviewer #2: Yes

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

Reviewer #2: Yes

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: All comments except 3 are fully addressed.
Regarding the earlier comment 3.
Line 181: In the models, participants “182 were censored at the time of their last test, when they did not complete the originally planned 183 five tests and had negative results in all their samples.” This statement is not clear. Were they removed completely?


"All the participants were included in the prevalence analysis. Participants with a positive result in their first sample were excluded from the incidence analysis and were considered prevalent cases. Participants who did not complete the five follow-up visits contributed person-time from all the available tests with negative results, until the first positive result or until their last available negative result. We have included the following sentence in the text to improve clarity: “In the models, participants with negative results in all their follow-up samples were censored at the time of their last available test.”

 From the response to the earlier comment above, it appears that the person time included the time till their last available negative visit if they did not complete five visits.
"Participants who did not complete the five follow-up visits contributed person-time from all the available tests with negative results, until the first positive result or until their last available negative result."

“In the models, participants with negative results in all their follow-up samples were censored at the time of their last available test.”
But does “censored” mean that they were removed? It is confusing if they were removed, whether only the last test was removed and also why they were removed. Or were they removed for calculation of the incident cases?

A: In this version, we eliminated the term “censored”, which is different to “removed” to avoid any confusion. Instead, we simply describe how we made the calculations. We planned five follow-up visits for blood sample donation for every participant, but only a fraction of the participants complied with the five visits. The test result of the first visit for every participant was used to define prevalent cases. Participants that resulted positive were included in the seroprevalence calculation.

Prevalent cases were excluded from incidence estimations. All participants included in the incidence calculation contributed with follow-up time from the date of the first sample until the date of the first sample with a positive result (incident cases), or until the last date of follow up (non-cases). Please see the definition of the prevalent, incident and non-case groups, in lines 185-188. We have included the following text in the Statistical analyses section: “The person-time was calculated as follows: incident cases contributed with the time elapsed from the date of their first sample to the date of their first positive sample, and non-cases contributed with their complete follow-up time from their first to their last sample date.”

Additional comment 1:
At the end of the study, 290 participants had a positive result in any of the antibody tests, yielding 241 an overall prevalence in the study period, adjusted by sensitivity and specificity of the antibody
Line 242 test, of 33.5%. 235 positive cases (81.9%) were identified at baseline (prevalent cases), while the 243 remaining 55 (6.2%) seroconverted during the follow up period (incident cases).
Among the positive cases (290) – the prevalent cases were 235/290 = 81.9%, while the incident cases would be 55/290 which is 18.9 % and not 6.2% as mentioned – is that correct?

A: Thank you for pointing out this error. We have changed the text to 18.9%, to show the percentage relative to the total positive cases.

Additional comment 2: Line 68 - spelling error "waive" caused by the omicron variant.

A: The mistake has been corrected.

Reviewer #2: Thanks for addressing the earlier comments.
 I encourage the authors to please check the manuscript for grammar and sentence structuring before final proof is sent.

A: We thank the Reviewer for the comments. The manuscript has been checked for grammar and structure with the appropriate corrections.

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Reviewer #1: No

Reviewer #2: Yes: Giridhara R Babu

Attachment

Submitted filename: Response to Reviewers.docx

Decision Letter 2

Leeberk Raja Inbaraj

21 Feb 2022

Seroepidemiology of SARS-CoV-2 in healthcare personnel working at the largest tertiary COVID-19 referral hospitals in Mexico City.

PONE-D-21-27465R2

Dear Dr. Avila-Rios,

We’re pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it meets all outstanding technical requirements.

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Leeberk Raja Inbaraj, MD

Academic Editor

PLOS ONE

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Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation.

Reviewer #1: All comments have been addressed

**********

2. Is the manuscript technically sound, and do the data support the conclusions?

The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented.

Reviewer #1: Yes

**********

3. Has the statistical analysis been performed appropriately and rigorously?

Reviewer #1: Yes

**********

4. Have the authors made all data underlying the findings in their manuscript fully available?

The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified.

Reviewer #1: Yes

**********

5. Is the manuscript presented in an intelligible fashion and written in standard English?

PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here.

Reviewer #1: Yes

**********

6. Review Comments to the Author

Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters)

Reviewer #1: The authors detailed responses to the comments is appreciated. Please do check for further transcription errors and grammatical errors.

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7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files.

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Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy.

Reviewer #1: No

Acceptance letter

Leeberk Raja Inbaraj

4 Mar 2022

PONE-D-21-27465R2

Seroepidemiology of SARS-CoV-2 in healthcare personnel working at the largest tertiary COVID-19 referral hospitals in Mexico City.

Dear Dr. Ávila-Ríos:

I'm pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department.

If your institution or institutions have a press office, please let them know about your upcoming paper now to help maximize its impact. If they'll be preparing press materials, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org.

If we can help with anything else, please email us at plosone@plos.org.

Thank you for submitting your work to PLOS ONE and supporting open access.

Kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Dr. Leeberk Raja Inbaraj

Academic Editor

PLOS ONE

Associated Data

    This section collects any data citations, data availability statements, or supplementary materials included in this article.

    Supplementary Materials

    S1 Appendix. Computer-assisted self-administered interview questions.

    (DOCX)

    S2 Appendix. De-identified database.

    (DTA)

    S1 Table. Variation in the number of participants at baseline and follow-up along the study period.

    (DOCX)

    S2 Table. Symptoms reported by exposure group in healthcare workers of the two largest COVID-19 referral hospitals in Mexico City, October 2020-June 2021.

    (DOCX)

    S3 Table. Risk factors by occupation in prevalent cases, October 2020-June 2021.

    (DOCX)

    S4 Table. Risk factors by occupation in incident cases, October 2020-June 2021.

    (DOCX)

    S5 Table. Differences between persons who did and did not attend at least one visit for blood sample donation for antibody testing that registered in the study database of healthcare workers of the two largest COVID-19 referral hospitals in Mexico City, October 2020-June 2021.

    (DOCX)

    Attachment

    Submitted filename: Response to Reviewers.docx

    Attachment

    Submitted filename: Response to Reviewers.docx

    Data Availability Statement

    The de-identified dataset used for analysis is available as part of the supporting information.


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