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. 2023 Jun 7;11(4):e00876-23. doi: 10.1128/spectrum.00876-23

Seroprevalence of COVID-19 in Oran: Cross-Sectional Study

Abdessamad Dali-Ali a,b,, Dalia Kheira Derkaoui c, Mohamed Zina d, Asmaa Oukebdane e
Editor: Rosemary C Shef
PMCID: PMC10433985  PMID: 37284756

ABSTRACT

The coronavirus disease 2019 (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was introduced in Algeria in March 2020. This study aimed to estimate the seroprevalence of SARS-CoV-2 infection in Oran, Algeria, and to identify factors associated with seropositivity. This was a cross-sectional seroprevalence study conducted between 7 and 20 January 2021 across all 26 municipalities in the province of Oran. The study employed a random cluster sampling technique stratified by age and sex to select participants from households, who were then administered a rapid serological test. The overall seroprevalence and specific seroprevalences by municipality were calculated, and the number of COVID-19 cases in Oran was estimated. The correlation between population density and seroprevalence was also examined. Among the participants, 422 (35.6%; 95% confidence interval [CI], 32.9 to 38.4) had a positive serological test for SARS-CoV-2, and eight municipalities had seroprevalence rates above 73%. We found a strong positive correlation between population density and seroprevalence (r = 0.795, P < 0.001), indicating that areas with higher population density had higher numbers of positive COVID-19 cases. Our study provides evidence of a high seroprevalence of SARS-CoV-2 infection in Oran, Algeria. The estimated number of cases based on seroprevalence is much higher than the number of cases confirmed by PCR. Our findings suggest that a large proportion of the population has been infected with SARS-CoV-2, highlighting the need for continued surveillance and control measures to prevent further spread of the virus.

IMPORTANCE This is the first and only seroprevalence study of COVID-19 conducted in the general population in Algeria prior to the national vaccination campaign against COVID-19. The significance of this study lies in its contribution to our understanding of the spread of the virus in the population before the implementation of the vaccination program.

KEYWORDS: cross-sectional study, Algeria, seroprevalence, COVID-19, SARS-CoV-2, Oran

INTRODUCTION

As of 5 July 2021, more than 183 million confirmed cases of coronavirus disease 2019 (COVID-19) had been reported to the World Health Organization (WHO), with 3,978,581 deaths, and 2,988,941,529 doses of vaccine administered (1). The United States ranked first with over 33,378,423 cases, followed by India (30,585,229 cases) and Brazil (18,742,259 cases) (1).

In Algeria, the first imported case was recorded on 25 February 2020 in the province of Ouargla in an Italian national. However, the first indigenous outbreak was reported in the province of Blida on 1 March 2020, marking the effective start of the epidemic (2). Between March 2020 and March 2021, Algeria experienced two waves of the COVID-19 epidemic caused by the Alpha variant of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The second wave began in October 2020 and continued until March 2021 (1).

As of 28 June 2021, there were 138,840 PCR-confirmed cases of COVID-19 in Algeria, with an incidence rate of 325.92 cases per 100,000 population (2). The central health region had the highest incidence rate (385.09 per 100,000 inhabitants), followed by the western, eastern, and southern health regions with incidence rates of 310.00, 308.58, and 230.59 per 100,000 inhabitants, respectively (2). However, it is the province of Oran that has always ranked first, with a cumulative incidence rate equal to 742.69 per 100,000 inhabitants (2).

The spread of the disease within the population is estimated based on confirmation of infection by PCR in symptomatic cases, which excludes asymptomatic individuals or those with mild symptoms who contribute to the spread of the virus. In fact, some studies suggest that the number of asymptomatic cases exceeds that of symptomatic cases (3, 4), highlighting the importance of conducting seroprevalence surveys based on the detection of anti-SARS-CoV-2 antibodies (5). To do so, the random selection of a representative sample of the general population, as well as the use of an accurate screening test, allows the estimation of the real extent of the epidemic within a given region (6).

In the absence of a seroprevalence survey conducted to date in Algeria and based on a working hypothesis stating a high prevalence of COVID-19, the objective of our study was to determine the seroprevalence of SARS-CoV-2 infection within the population of Oran, as well as the factors associated with a positive seroprevalence.

RESULTS

Steps of study participation.

Out of 1,200 subjects randomly selected, 1,187 subjects agreed to participate in the study (13 refusals), resulting in a participation rate of 98.9%. After checking the survey forms, we found that two forms had a significant amount of missing data, leading to their exclusion from the analysis. In total, the survey included 1,185 subjects (Fig. 1).

FIG 1.

FIG 1

COVID-19 seroprevalence survey: flowchart.

Descriptive data.

The study enrolled 1,185 participants with a mean age of 39.3 ± 21.6 years (mean ± standard deviation). The age group with the highest representation was individuals aged 10 to 19 years. Comparison of age means between males (39.6 ± 22.3 years) and females (39.0 ± 20.9 years) showed no statistically significant difference (P = 0.62).

The most frequent symptoms were represented by headaches (19.2%), cough (16.0%), and fatigue (15.4%). Anosmia and ageusia accounted for 7.8% and 7.0% respectively (Table 1).

TABLE 1.

Characteristics of the study population

Variable No. of participants (n = 1,185) %
Sex
 Female 598 50.5
 Male 587 49.5
Age (yrs)
 <10 86 7.3
 10–19 217 18.3
 20–29 119 10.0
 33–39 162 13.7
 40–49 189 15.9
 50–59 183 15.4
 60–69 129 10.9
 70–79 65 5.5
 ≥80 35 3.0
Exposure to SARS-CoV-2
 Yes 197 16.6
 No 988 83.4
Type of contact (n = 197)
 Family 107 54.3
 Professional 40 20.3
 Friends 9 4.6
 Neighborhood 5 2.5
 Other 36 18.3
Presence of symptoms suggestive of COVID-19 in 2020
 Yes 376 31.7
 No 809 68.3
Symptoms suggestive of COVID-19 (n = 376)
 Headache 227 19.2
 Cough 190 16.0
 Fatigue 182 15.4
 Fever 163 13.8
 Shortness of breath 106 8.9
 Anosmia 92 7.8
 Ageusia 83 7.0
 Diarrhea 68 5.7
 Nausea/Vomiting 52 4.4
 Muscle pain 8 0.7
 Chills 5 0.4
Presence of comorbidities
 Yes 251 21.2
 No 934 78.8
Types of comorbidities
 Hypertension 154 13.0
 Diabetes 99 8.4
 Cardiovascular diseases 28 2.4
 Allergies 17 1.4
 Respiratory diseases 12 1.0
 Pregnancy 7 0.6
 Anemia 4 0.3
 Rheumatic diseases 4 0.3

Of the participants, 197 individuals reported exposure to SARS-CoV-2, with family exposure being the most common (54.3%), followed by occupational exposure (20.3%) (Table 1).

A relatively high prevalence of underlying health conditions was observed in the study sample, with comorbidities present in 251 individuals, accounting for 21.2% of the study population. The most common comorbidities identified in the study population were arterial hypertension (13.8%), diabetes mellitus (8.4%), and cardiovascular diseases (2.4%) (Table 1).

Seroprevalence results.

According to the data, 8.9% (106 individuals) of the sample reported undergoing a COVID-19 screening or diagnostic test in 2020. Among those who were tested, the most common type of test was serology (5.4%), followed by PCR (3.2%), CT scan (1.7%), and antigen test (0.6%), as shown in Table 2. Of the survey participants who underwent serological testing, 422 tested positive for COVID-19 antibodies. This corresponds to a seroprevalence rate of 35.6% (95% confidence interval [CI], 32.9 to 38.4), indicating that over a third of individuals who underwent serological testing had been infected with COVID-19 at some point prior to the test (Table 2).

TABLE 2.

Results of the seroprevalence study

Variable No. of participants (n = 1,185) %
Underwent a screening and/or diagnostic test for COVID-19 in 2020
 Yes 106 8.9
 No 1,079 91.1
Types of screening and/or diagnostic tests for COVID-19 in 2020 (n = 106)
 Serology 64 5.4
 PCR 38 3.2
 CT scan 20 1.7
 Antigen test 7 0.6
Results of rapid serological test of the prevalence survey (n = 1,185)
 Positive 422 35.6
 Negative 763 64.4
Detailed antibody results (n = 422)
 IgM+ IgG+ 139 11.7
 IgM+ IgG 40 3.4
 IgM IgG+ 243 20.5
 IgM IgG 763 64.4

It should be noted that eight communes had seroprevalence rates higher than 73%, namely, Marsat El Hadjaj, Bethioua, Benfreha, Sidi Ben Yabka, Hassi Bounif, Boufatis, Hassi Mefsoukh, and Gdyel (Fig. 2).

FIG 2.

FIG 2

Seroprevalence of COVID-19 in the province of Oran by municipality.

However, the study of the correlation between population density and the number of positive COVID-19 rapid tests showed a highly significant relationship between the two variables, with a Spearman’s rank correlation coefficient of 0.795 (P < 0.001) (Table 3).

TABLE 3.

Prevalence of COVID-19 in Oran Province by municipality

Municipality Area (km2) Population Population density (inhabitants/km2) Sample size No. of positive tests Prevalence (%) 95% CI
Oran 64.00 674,273 10,535.52 308 104 33.8 28.71–39.22
Bir El Djir 32.46 171,883 5,295.22 257 27 10.5 7.32–14.85
Sidi Chahmi 69.50 114,050 1,641.01 118 39 33.1 25.22–41.95
Es Senia 48.51 97,500 2,009.89 77 19 24.7 16.4–35.35
Arzew 71.90 85,658 1,191.35 64 43 67.2 55.0–77,43
Hassi Bounif 31.77 63,581 2,001.29 53 41 77.4 64.47–86.54
Gdyel 93.82 39,129 417.06 30 22 73.3 55.55–85.82
Ain El Turk 39.14 35,687 911.78 29 13 44.8 28.41–62.45
El Kerma 63.55 25,636 403.40 26 0 0 0–12.87
Ain El Bia 36.15 32,611 902.10 24 17 70.8 50.83–85.08
Misserghin 428.28 26,554 62.00 23 4 17.4 6.98–37.14
Benfreha 69.29 23,254 335.60 21 18 85.7 65.37–95.02
Boutlelis 135.97 23,920 175.92 19 5 26.3 11.81–48.79
Bousfer 46.20 18,361 397.42 17 6 35.3 17.31–58.7
Oued Tlelat 84.11 19,384 230.46 15 5 33.3 15,18–58.29
Hassi Mefsoukh 25.67 12,836 500.04 12 9 75.0 46.77–91.11
Mers El Hedjaj 52.29 13,153 251.54 12 11 91.7 64.61–98.51
Mers El Kebir 10.98 17,957 1,635.43 12 6 50.0 25.38–74.62
Hassi Ben Okba 37.47 13,905 371.10 12 6 50.0 25.38–74.62
Bethioua 108.57 18,215 167.77 11 10 90.9 62.27–98.38
Tafraoui 182.00 12,089 66.42 10 1 10.0 1.79–40.41
El Onçor 66.44 11,469 172.62 10 3 30.0 10.78–60.32
Boufatis 99.06 11,872 119.85 8 6 75.0 40.93–92.85
El Braya 57.26 6,292 109.88 6 2 33.3 9.68–70.0
Sidi Benyebkra 51.69 7,825 151.38 6 5 83.3 43.65–96.99
Ain El Kerma 107.92 7,513 69.62 5 0 0 0.0–43.45
Total 2,114 1,584,607 30,125.69 1,185 422 35.6 32.94–38.38

Of the 197 individuals exposed to SARS-CoV-2, only 23 had undergone a PCR test, with 11 of them testing positive, resulting in a positivity rate of 47.8%. Additionally, among these 197 individuals, 98 individuals tested positive on the rapid serological test, representing 49.7% (Table 4).

TABLE 4.

Factors associated with a positive result on rapid SARS-CoV-2 screening test in univariate and multivariate analysis

Variable SARS-CoV-2 antibody result
Value froma:
Positive (n = 422)
Negative (n = 763)
Univariate analysis
Multivariate analysis
No. % No. % OR 95% CI P value aOR 95% CI P value
Sex
 Female 234 39.1 364 60.9 1.36 1.07–1.73 0.01 1.30 1.01–1.68 0.04
 Male 188 32.0 399 68.0 Ref Ref
Age (yrs)
 <10 30 34.9 56 65.1 Ref Ref
 10–19 60 27.6 157 72.4 0.71 0.42–1.22 0.21 0.75 0.43–1.30 0.30
 20–29 40 33.6 79 66.4 0.94 0.53–1.69 0.85 0.76 0.41–1.39 0.37
 30–39 62 38.3 100 61.7 1.16 0.67–2.00 0.56 1.06 0.60–1.87 0.85
 40–49 72 38.1 117 61.9 1.15 0.67–1.95 0.61 0.90 0.52–1.58 0.72
 50–59 70 38.3 113 61.7 1.16 0.68–1.97 0.59 1.00 0.57–1.75 1.00
 60–69 51 39.5 78 60.5 1.22 0.69–2.15 0.49 1.01 0.55–1.87 0.97
 70–79 26 40.0 39 60.0 1.24 0.64–2.42 0.52 0.99 0.48–2.04 0.98
 ≥80 11 31.4 24 68.6 0.86 0.37–1.98 0.72 0.69 0.28–1.68 0.41
Exposure to SARS-CoV-2 in 2020
 Yes 98 49.7 99 50.3 2.03 1.49–2.76 <0.001 1.34 0.95–1.90 0.09
 No 324 32.8 664 67.2 Ref Ref
COVID-19 symptoms in 2020
 Yes 207 55.1 169 44.9 3.38 2.62–4.37 <0.001 2.9 2.22–3.80 <0.001
 No 215 26.6 594 73.4 Ref Ref
Comorbidities
 Yes 111 44.2 140 55.8 1.59 1.20–2.11 0.01 1.32 0.94–1.85 0.10
 No 311 33.3 623 66.7 Ref Ref
COVID-19 screening and/or diagnostic test in 2020
 Yes 61 57.5 45 42.5 2.7 1.80–4.04 <0.001 1.83 1.18–2.85 0.008
 No 361 33.5 718 66.5 Ref Ref
PCR
 Positive 15 93.8 1 6.2 12.5 1.4–111.84 0.012b
 Negative 12 54.5 10 45.5 Ref
Serology
 Positive 12 66.7 6 33.3 2.84 0.91–8.9 0.10b
 Negative 19 41.3 27 58.7 Ref
CT scan
 Positive 13 92.9 1 7.1 13.0 0.98–172.9 0.06b
 Negative 3 50.0 3 50.0 Ref
Antigen test
 Positive 1 100.0 0 0.0 0.29b
 Negative 1 16.7 5 83.3
a

OR, crude odds ratio; aOR, adjusted odds ratio; Ref, reference category.

b

Fisher test.

The rapid diagnostic test was also positive in 207 of 376 individuals (55.1%) who reported having symptoms suggestive of COVID-19 in the previous year. Finally, only 38 people (3.2%) underwent a PCR test, 16 of whom tested positive, with 15 of them also testing positive on the rapid diagnostic test, resulting in a concordance rate of 93.8% (Table 4).

Factors associated with seropositivity.

The results of the univariate analysis revealed several factors that were significantly associated with a positive result on the rapid SARS-CoV-2 screening test. These factors included being female (odds ratio [OR] = 1.36; 95% CI, 1.07 to 1.73; P = 0.01), previous exposure to SARS-CoV-2 (OR = 2.03; 95% CI, 1.49 to 2.76; P < 0.001), presence of COVID-19 symptoms (OR = 3.38; 95% CI, 2.62 to 4.37; P < 0.001), presence of comorbidities (OR = 1.59; 95% CI, 1.20 to 2.11; P = 0.01), undergoing COVID-19 screening and/or diagnostic testing (OR = 2.7; 95% CI, 1.80 to 4.04; P < 0.001), and a history of positive PCR (OR = 12.5; 95% CI, 1.4 to 111.84; P = 0.012) (Table 4). In multivariate analysis, female gender (adjusted odds ratio [aOR] = 1.30; 95% CI, 1.01 to 1.68; P = 0.04), presence of COVID-19 symptoms (aOR = 2.9; 95% CI, 2.22 to 3.80; P < 0.001), and undergoing COVID-19 screening and/or diagnostic test (aOR = 1.83; 95% CI, 1.18 to 2.85; P = 0.008) were significant predictors of a positive rapid SARS-CoV-2 screening test (Table 4).

DISCUSSION

In our study, the seroprevalence rate of COVID-19 in Oran Province was 35.6% (95% CI, 32.9 to 38.4). Thus, taking into account the population of Oran, the estimated number of COVID-19 cases in the province would be 564,121 cases, which is 44.5 times higher than the number of PCR-confirmed cases, which was 12,665 cases as of 20 January 2021, according to the Health and Population Directorate of the province (7).

Regarding the COVID-19 pandemic worldwide, a literature review (6) conducted between 1 January and 12 August 2020 showed that the proportion of COVID-19 cases detected by seroprevalence surveys was significantly higher than the proportion of cases diagnosed by PCR. Thus, the estimated seroprevalence was 0.56 to 717 times higher than the cumulative number of reported cases. In half of the studies, the prevalence was 10 times higher (6).

For example, in Iran, a study conducted in the province of Guilan (8) from 11 to 19 April 2020 found an adjusted prevalence rate of 22.2% (95% CI, 16.4 to 28.5). This rate was 2.8%, nearly 10 times lower, in a study conducted in Santa Clara County, USA, from 3 to 4 April 2020, with an estimated number of cases 50 to 85 times higher than the number of cases confirmed by PCR (4). It should be noted that this study has received several criticisms related to the small sample size and low statistical power (9).

Furthermore, a study conducted in the city of Kobe, Japan, from 31 March to 7 April 2020 found an age and sex-adjusted seroprevalence rate of 2.7% (95% CI, 1.8 to 3.9), which is 396 to 858 times higher than the number of PCR-confirmed COVID-19 cases in the same city (10).

The situation in Italy was not far from the rates recorded in Japan. Indeed, a study conducted from 24 February to 8 April 2020 among blood donors showed a clear increase in the adjusted seroprevalence, which increased from 2.7% (95% CI, 0.3 to 6.0) to 5.2% (95% CI, 2.4 to 9.0) (11).

It should be noted, however, that few seroprevalence studies had been conducted in Africa, according to Rostami’s literature review (12). The review showed that seroprevalence varied from 4.62% (95% CI, 1.71 to 9.78) in Libya to 5.62% (95% CI, 4.83 to 6.49) in Kenya (12).

In contrast, a study conducted in the Democratic Republic of Congo from May to August 2020 found an estimated anti-SARS-CoV-2 seroprevalence of 40.8% among travelers and workers requiring a medical certificate, which represents a high rate compared to the previously cited studies (13), Several factors can account for variations in COVID-19 seroprevalence rates observed across different countries.

In the Middle East and North Africa (MENA) region, discrepancies in COVID-19 seroprevalence rates between studies can be attributed to variations in testing protocols and methods. A recent population-based study conducted in Tunisia between March and April 2021 found a seroprevalence rate of 38.0%, which is similar to the rate observed in our study, where two enzyme-linked immunosorbent assays (ELISAs) developed at the Pasteur Institute of Tunis were used to detect SARS-CoV-2 antibodies (14).

Similarly, a cross-sectional, community-based study conducted in November and December 2020 in Aden, located in southern Yemen, using Healgen COVID-19 rapid diagnostic test cassettes and ELISA for confirmation, revealed a COVID-19 prevalence rate of 27.4% (15).

Furthermore, the duration of a study can also affect seroprevalence rates, as seen in the El-Ghitani study conducted in Egypt over 6 months between January and June 2021, which coincided with the second and third waves of the COVID-19 pandemic and reported a seroprevalence rate of 53.6% (16).

Moreover, the evolution of the epidemic over time can explain differences in seroprevalence rates. For example, a study in Jordan by Bellizzi et al. (17) showed that the seroprevalence rate increased from 0.3% in August to 7% in October and reached 34.2% by the end of 2020.

Finally, variations in seroprevalence rates can also be attributed to the sampling strategy. A study conducted in Riyadh, Saudi Arabia, in June 2020 reported a seroprevalence rate of 7.8% for COVID-19, but the study sample only included hospitalized patients and healthy blood donors and did not represent the general population (18).

In our study, eight municipalities had recorded seroprevalence rates higher than 73%. However, the study of the relationship between population density and COVID-19 seroprevalence revealed a highly significant positive linear correlation between these two variables (P < 0.001). This strong correlation indicates that population density has a significant influence on the number of positive rapid COVID-19 tests and suggests that densely populated areas may be more susceptible to the risk of disease spread. The study conducted by Wong and Li (19) confirms this finding, showing that population density at the county level is a reliable predictor of total infection cases.

Factors associated with SARS-CoV-2 seropositivity.

In our study, factors associated with SARS-CoV-2 seropositivity in multivariate analysis were female gender, presence of COVID-19 symptoms, and undergoing COVID-19 screening and/or diagnostic test in 2020.

Several studies have identified multiple factors associated with seropositivity, such as sex (20, 21), age (20, 21), obesity (20), exposure to more than one case among nonhousehold contacts (22), presence of multiple comorbidities (20), and previous performance of a PCR test (23).

Thus, the results of our study suggest that anti-SARS-CoV-2 seroprevalence is important compared to the incidence figures of the disease in Oran. Therefore, conducting other prevalence surveys allows tracking the evolution of seroprevalence over time and detecting the establishment of herd immunity, which, once achieved, can indirectly protect vulnerable individuals (24). However, if immunity is distributed heterogeneously within the population, clusters may appear among certain vulnerable individuals (24). Thus, the vaccination strategy could be directed toward the least immunized areas.

Strengths of the study.

It should be noted that prevalence surveys provide a better estimate of the extent of an epidemic than a surveillance system based on cumulative incidence (4).

In our study, the sample is representative of the population of Oran, given that the cross-sectional survey was based on a four-stage cluster random sampling, which eliminates any selection bias.

In our study, antibody detection was performed using the prick test, similar to some countries, such as the United States (4), that have used this test widely in SARS-CoV-2 screening surveys in the general population. Prick tests are easier to perform and less costly than serological tests (ELISAs), which require taking blood samples and transporting them to the laboratory for analysis, representing a major drawback in terms of feasibility, acceptability, and time (25).

Weaknesses of the study.

One potential weakness of our study is that we relied on measuring the presence of antibodies in the blood as a marker of immunity to the infection. As it is known that the level of IgG reaches its peak between the 4th and 6th month after infection (26, 27) and then gradually decreases over time (24), it is possible that our study did not capture the full extent of immunity in our study participants. Additionally, the rate of decrease in antibody levels over time may vary depending on individual factors like age and overall health, which could have impacted our results. Therefore, our study may have underestimated the true level of immunity to the infection in our study population.

In some studies, household sampling surveys as a sampling unit may lead to an overestimation of COVID-19 prevalence, as one infected person in the household can transmit the virus to all family members (8).

On the other hand, recruiting nonhospitalized patients, the majority of whom were asymptomatic at the time of the survey, could result in low or undetectable antibody titers, especially if the time elapsed between infection and testing is long (28). Additionally, the accuracy and reliability of rapid serological tests may vary depending on the type of test and other factors.

Ultimately, it should be noted that the results of our study are only representative of Oran Province and cannot be generalized to the rest of the country. Therefore, it is important to conduct a national prevalence survey to estimate the true extent of the COVID-19 epidemic in Algeria.

Finally, our study indicates that the actual number of SARS-CoV-2 infections in Oran is significantly higher than the number of PCR-confirmed cases, which only represents the tip of the iceberg. Moreover, the study shows that prevalence varies between different municipalities, suggesting that specific preventive strategies should be adopted according to the regions. Therefore, to achieve optimal herd immunity against COVID-19, it is advisable to target regions with lower disease prevalence for mass vaccination campaigns. Vaccination against COVID-19 remains the best way to protect against the disease, as the available vaccines are effective in preventing severe forms of the illness, hospitalizations, and COVID-19-related deaths. Further seroprevalence studies in other regions of the country would provide a more comprehensive estimate of the problem and help tailor the response to the epidemic at the national level.

MATERIALS AND METHODS

Study type, location, and period.

This was a cross-sectional study of anti-SARS-CoV-2 seroprevalence that included all 26 municipalities of Oran Province. The study specifically targeted household members and was conducted from 7 January to 20 January 2021, during the second wave of the epidemic when the Alpha variant was circulating in Algeria. It was carried out prior to the start of the national anti-COVID-19 vaccination campaign, which began on 30 January 2021 (1).

The Orient Gene kit was used to detect the presence of antibodies directed against the spike protein of the SARS-CoV-2 virus. These antibodies can be detected in the blood of people who have been infected with the virus and have developed an immune response.

This test was chosen due to its ease of use and availability at the health department of our province.

Eligibility criteria.

Subjects participating in the study were selected using a four-stage cluster random sampling technique after random selection in each municipality of districts, neighborhoods, households, and individuals within each household. Stratification by age and sex categories was performed to increase the chances of obtaining a representative sample of the population of Oran Province. The selected household members were invited to undergo a blood test using a rapid COVID-19 IgG/IgM test cassette from Orient Gene Biotech (sensitivity, 90.5%; specificity, 100.0%) (29) and to complete a preestablished standardized questionnaire.

Ethical aspects.

The study was conducted after approval from the Health Directorate of Oran Province. The collection of information and screening tests were performed after obtaining informed consent from the subjects included in the study in accordance with the principles of the Helsinki Declaration with regard to confidentiality of personal information, anonymity, and protection of privacy.

Technique for conducting a screening test.

The COVID-19 IgG/IgM cassette (whole blood/serum/plasma) is a lateral flow immunochromatographic test. The test uses a human anti-IgM antibody, anti-human IgG, and rabbit IgG, mobilized on a nitrocellulose strip. The technique consists of taking a sample of whole blood, transferring the collected whole blood to the sample well of the test device, and adding 2 drops of sample buffer to the buffer well. After the appearance of colored lines, the result is read within 10 min.

In order to avoid potential measurement biases, the investigators received a training session on the conduct and interpretation of the screening test just before the start of the survey.

Study variables.

Before conducting the serological test, the following variables were collected through direct interview: gender, age, address, locality, history of exposure to SARS-CoV-2, type of contact (family, professional, neighborhood, or other), presence or absence of suggestive clinical signs of COVID-19 in the previous year, different clinical signs in favor of possible previous infection (headaches, cough, asthenia, fever, shortness of breath, anosmia, ageusia, nausea, diarrhea, chills), presence of comorbidities (hypertension, diabetes, cardiovascular diseases, and others), and history of screening or diagnostic testing for COVID-19 in the previous year. The result of the rapid serological test of the prevalence survey (positive or negative) was also recorded, and if positive, the type of antibody (IgM or IgG) was further detailed.

Sample size calculation.

Based on the population of Oran Province, estimated at 1,584,607 inhabitants, the sample size n was calculated using the following formula:

n = Deff × Np(1 − p)d21.962(N − 1) + p(1 − p)

Thus, assuming an anticipated disease frequency p of 50%, a calculation factor Deff of 1, a precision d of 3%, and a corresponding alpha error risk of 5% (E = 1.96), the calculated required number of subjects was 1,067. To mitigate the risk of refusal to participate in the study, the research team opted for a larger sample size of 1,200 subjects.

Statistical analysis.

The overall seroprevalence, as well as specific seroprevalences by commune, were calculated and presented with their 95% confidence intervals (CIs) based on Wilson’s score, provided by the OpenEpi program (30).

Quantitative variables were compared using Student’s t test, and the relationship between qualitative variables was examined using the chi-square test in our study. Both univariate and multivariate analyses were conducted for statistical analysis. Univariate analysis involved calculating odds ratios (ORs) to assess the strength of association between each independent variable and the outcome variable. In the multivariate analysis based on binary logistic regression, adjusted ORs (aORs) were calculated while controlling for potential confounding variables. All statistical analyses were performed using SPSS version 20. A P value of less than 0.05 was considered statistically significant for a relationship.

Data availability.

The data for this study can be accessed at the following link: https://zenodo.org/record/7991424.

ACKNOWLEDGMENTS

We extend our sincere gratitude to the Director of Health and Population of Oran province, as well as all the individuals who contributed to the successful completion of this study, including epidemiologists, general practitioners, and technicians. Special thanks are also due to Youcef Boukhari, the physician in charge of prevention, for his invaluable support and guidance throughout the project.

We declare no conflicts of interest.

Contributor Information

Abdessamad Dali-Ali, Email: abdessamad.daliali@gmail.com.

Rosemary C. She, Keck School of Medicine of the University of Southern California

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Associated Data

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

Data Availability Statement

The data for this study can be accessed at the following link: https://zenodo.org/record/7991424.


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