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. 2019 Oct 7;14(10):e0221190. doi: 10.1371/journal.pone.0221190

Intestinal parasitic infection among household contacts of primary cases, a comparative cross-sectional study

Berhanu Elfu Feleke 1,*, Melkamu Bedimo Beyene 1, Teferi Elfu Feleke 2, Tadesse Hailu Jember 3, Bayeh Abera 4
Editor: Chia Kwung Fan5
PMCID: PMC6779256  PMID: 31589618

Abstract

Background

Intestinal parasitic infection affects 3.5 billion people in the world and mostly affecting the low socio-economic groups. The objectives of this research works were to estimate the prevalence and determinants of intestinal parasitic infection among family members of known intestinal parasite infected patients.

Methods and materials

A comparative cross-sectional study design was implemented in the urban and rural settings of Mecha district. The data were collected from August 2017toMarch 2019 from intestinal parasite infected patient household members. Epi-info software was used to calculate the sample size, 4531 household members were estimated to be included. Data were collected using interview technique, and collecting stool samples from each household contact of intestinal parasite patients. Descriptive statistics were used to estimate the prevalence of intestinal parasites among known contacts of intestinal parasite patients/family members. Binary logistic regression was used to identify the determinant factors of intestinal parasitic infection among family members.

Results

The prevalence of intestinal parasite among household contacts of intestinal parasite-infected family members was 86.14% [95% CI: 86.14% - 87.15%]. Hookworm infection was the predominant type of infection (18.8%). Intestinal parasitic infection was associated with sex, environmental sanitation, overcrowding, personal hygiene, residence, substandard house, role in the household, source of light for the house, trimmed fingernails, family size, regular handwashing practice. Protozoa infection was associated with habit of ingesting raw vegetable, playing with domestic animals, water source and the presence of household water filtering materials.

Conclusion

High prevalence of intestinal parasitic infection was observed among household contacts of primary cases.

Introduction

Intestinal parasites are groups of worm’s primary affecting the gastrointestinal tracts, they broadly contain flatworms (tapeworms and flukes) and roundworms (Ascariasis, Pinworm, and Hookworm infections) [1]. The mode of transmission includes ingestion of uncooked animal products, consuming infected water, absorption through the skin and feco-oral routes [2][3]. That means all family members living in intestinal parasite-infected patients are at higher risk of acquiring the infection.

Abdominal cramp, vomiting, excessive bowl sound, nausea, diarrhea, loss of appetite, malabsorption, skin itching are some of the manifestations of intestinal parasites [4].The diagnosis of intestinal parasitic infection usually performed by taking stool samples and applying different laboratory techniques, concentration technique is more valid than the other laboratory techniques [5].

Intestinal parasitic infection affects 3.5 billion people in the world and mostly affecting the low socio-economic groups [6]. Soil-transmitted helminths infection (Ascaris Lumbricoides, Trichuris trichiura, and Hookworm) alone affects 1.5 billion people worldwide [7]. Sub-Saharan Africa bears the highest-burden for both helminths infection and other intestinal parasitic infections [8].

Intestinal parasitic infection can be complicated with malnutrition, intestinal obstruction, growth retardation, immunodeficiency and affecting the socioeconomic development of the nations [9].

Gender, age, role in the household, socioeconomic characteristics, levels of education, poor sanitation, proximity to water sources, family size, environmental sanitation, handwashing practice, untrimmed fingernail, housing conditions, resident, barefoot are some of the predictors of intestinal parasitic infection [1018].

The management of intestinal parasitic infection was not complicated and most intestinal parasitic infection can be effectively treated with a single dose of anti-helminths. However, the intestinal parasitic intervention neglects the household contacts because there is no available evidence on the prevalence of intestinal parasites among household members; so, this study was conducted to give baseline evidence on the estimate of household secondary cases.

The objectives of this research works were to estimate the prevalence and determinants of intestinal parasitic infection among family members of known intestinal parasitic infected patients.

Methods and materials

The comparative cross-sectional study design was implemented in the urban and rural settings of mecha district. Mecha district is located in the north-west of Ethiopia. In the district; there are 10 health centers and 1 general hospital. The data were collected from August 2017 to March 2019. Data were collected from intestinal parasitic infected patient household members.

The sample size was calculated using Epi-info software version 7 using the assumption of 95% CI, power of 85, rural to an urban ratio of 2:1, the none response rate of 10% gives an estimated 1510 household members from the urban setting and 3021 household members from the rural settings.

Household members were selected using contact tracing. A patient diagnosed positive for the parasitic infection in the district health facility was used to trace for their family members intestinal parasitic infection status. Intestinal parasitic infection status was checked from all household contacts.

Interview technique and laboratory methods were used to collect the data. Clinical nurses were recruited for the interview and health officers were recruited for the supervision. The stool sample was collected from each family member of known intestinal parasitic infected patients and transported to the nearby health facility for the analysis. From each known contact, one gram stool sample was collected in 10 ml SAF (sodium acetate- acetic acid-formalin solution). Direct microscopic stool examination and concentration techniques were used. Formal ether concentration technique was used to identify the presence of intestinal parasites. The stool sample was well mixed and filtered using a funnel with gauze. Around 7 ML (Milliliter) normal saline and 3 ml of ether was added, mixed well and then centrifuged for 5 minutes at 2000 RPM. Finally, the supernatant was discarded and the sediment was examined for parasites under the microscope [19].

Data were entered to Epi-info software and transported to SPSS for the analysis. Descriptive statistics were used to estimate the prevalence of intestinal parasites. Binary logistic regression was used to identify the determinant factors of intestinal parasitic infection among family members. Handwashing practice was measured if the participants wash his/her hands after visiting the toilet, before cooking food and before feeding.

Ethical clearance was obtained from Bahir Dar university ethical review board of (ethical approval number የአ.ህ.ጤቴ/ሽ/ዳ/01/795). Permission letter was obtained from Amhara National Regional State Health Bureau ethical committee and Mecha district health office. Written informed consent was obtained from each study participant or guardians. Those study participants with intestinal parasites were referred to the nearby health facility for further management. The confidentiality of the data was kept at all stages.

Results

A total of 4436 study participants were included giving for the response rate of 98%, 64 study participants were unwilling to participate in the study and 31 study participants were excluded due to poor quality of stool sample. Female constitute 50% of the study participants, and 67% of the study participants were from the rural area. (Table 1)

Table 1. Population profile of the study participants (n = 4436).

Serial number Population profile Frequency Percentage
1. Sex Female 2206 49.7
Male 2230 50.3
2. Environmental sanitation Clean 1323 29.8
Dirty 3113 70.2
3. Source of light for the house Modern 1073 24.2
Traditional 3363 75.8
4. Floor materials of the house Mud 3190 71.8
Others 1246 28.2
5. Household water filtering mechanisms Present 861 19.4
Absent 3575 80.6
6. Fingernails of the respondents Trimmed 927 20.9
Not trimmed 3509 79.1
7. Family size ≤4 661 14.9
>4 3775 85.1
8. Educational status Illiterate 1744 39.3
Formal education 2557 57.6
Informal education 135 3
9. Resident Rural 2960 66.7
Urban 1476 33.3
10. Marital status Single 3320 74.8
Married 1056 23.8
Divorced 42 0.9
Widowed 18 0.4
11. Age in years 0–10 1744 39.3
11–20 2035 45.9
21–30 215 4.8
31–40 303 6.8
41–50 12 0.3
>50 127 2.9

The prevalence of intestinal parasitic infection among family members was 86.14% [95% CI: 86.14% - 87.15%]. Hookworm infection (18.8%) was the predominant parasitic infection followed by Enatmeba histolytic/dispar (11.4%), 36.2% of family members had heavy intensity of infection (Table 2).

Table 2. The type of parasitic infection among household members (n = 4436).

Intestinal parasitic species Frequency Percent
Not infected 615 13.9
Hookworm 834 18.8
Ascaris lumbricoides 375 8.5
S. mansoni 198 4.5
Trichuris trichiura 332 7.5
E. histolytica/dispar 505 11.4
Balantidium coli 411 9.3
G. lamblia 302 6.8
Hymenolepis nana 29 .7
Mixed infections 835 18.8

Intestinal parasitic infection among children

The prevalence of intestinal parasitic infection among children family members was 82.77% [95% CI: 81.08% -84.47%]. After adjusting for sex, environmental sanitation, source of light for the house, size of the fingernails, family size, overcrowding, personal hygiene, the presence of chicken in the house, and substandard house: Intestinal parasitic infection among household members was associated with sex, environmental sanitation, the presence of chicken in the house, overcrowding, personal hygiene, residence, and substandard house (Table 3)

Table 3. The determinants of intestinal parasitic infection among children household members (n = 1904).

Variable IP COR [95% CI] AOR [95% CI] p-value
Infected Not infected
Sex Male 717 168 0.79 [0.62–1.02] 0.76[0.58–0.99] 0.04
Female 859 160
Environmental sanitation Clean 168 10 3.79 [1.92–7.71] 0.04 [0.01–0.14] <0.01
Dirty 1408 318
Chicken in the household Present 1069 256 0.59 [0.44–0.79] 4.42 [2.81–6.95] <0.01
Absent 507 72
Overcrowding Present 956 152 1.79 [1.40–2.28] 2.14 [1.6–2.88] 0.01
Absent 620 176
Personal hygiene Clean 1395 312 0.4 [0.22–0.68] 0.26 [0.07–0.93] 0.04
Not clean 181 16
Resident Urban 576 92 1.48 [1.13–1.94] 2.68 [1.86–3.89] <0.01
Rural 1000 236

Substandard house
Yes 237 42 1.21 [0.84–1.74] 1.92 [1.03–3.6] 0.04
no 1339 286

Intestinal parasitic infection in adult household members

The prevalence of intestinal parasitic infection among household members whose age greater than 16 years was 88.67% [95% CI: 87.43% -89.90%]. After adjusting for sex, role in the household, environmental sanitation, source of light, trimmed fingernails, substandard house, family size, the presence of chicken in the house, handwashing behavior, overcrowding, personal hygiene, residence and chronic illness: intestinal parasitic infection among household members were associated with sex, role in the household, environmental sanitation, source of light, trimmed fingernails, substandard house, family size, the presence of chicken in the house, regular handwashing practice, personal hygiene, and resident (Table 4).

Table 4. The determinants of intestinal parasitic infection among adult household members (n = 2532).

Variable IP COR [95% CI] AOR [95% CI] p-value
Positive Negative
Sex Male 1079 266 0.07 [0.05–0.12] 0.04 [0.02–0.09] <0.01
Female 1166 21
Environmental sanitation Clean 1280 107 2.23 [1.72–2.90] 0.18 [0.12–0.27] 0.01
Dirty 965 180
Chicken Present 1454 63 6.54 [4.83–8.85] 3.59 [2.38–5.41] <0.01
Absent 791 224
Role in the household Children or mothers 1277 39 8.39 [5.85–12.07] 2.75 [1.51–4.99] 0.01
Others 968 248
Personal hygiene Clean 2113 270 1.01 [0.58–1.74] 0.04 [0.01–0.12] <0.01
Not clean 132 17
Resident Urban 719 89 1.05 [0.8–1.38] 2.32 [1.5–3.55] <0.01
Rural 1526 198
Substandard house Yes 946 108 1.21 [0.93–1.57] 4.09[2.44–6.87] <0.01
no 1299 179
Source of light for the house Traditional 1692 247 0.5 [0.34–0.71] 2.28 [1.19–4.37] <0.01
Modern 553 40
Family size >4 1946 158 5.31 [4.05–6.97] 7.18 [3.89–13.37] <0.01
≤4 299 129
Regular handwashing practice Present 208 2037 0.6 [0.41–0.87] 0.4 [0.2–0.79] <0.01
Absent 42 245

The odds of soil transmitted helminths among barefooted individuals were 1.51 folds higher. Habit of ingesting raw vegetables increases the odds of protozoa infection by 2.96 folds. Habit of playing with domestic animals increases the odds of protozoa infection by 3.82 folds. (Table 5)

Table 5. Specific predictors for soil transmitted helminths and protozoa infections.

Risk factors for
Soil transmitted helminths Protozoa infections
Variables AOR [95% CI] P-value Variables AOR [95% CI] P-value
Barefoot 1.51 [1.28–1.78] <0.01 Habit of ingesting raw vegetable 2.96 [2.33–3.75] <0.01
Floor 2.1 [1.81–2.44] <0.01 Habit of playing with domestic animals 3.82 [3.17–4.61] <0.01
Water source 0.8 [0.68–0.95] <0.01
Water filter 0.65 [0.55–0.76] <0.01

Discussion

The prevalence of intestinal parasitic infection among family members of known intestinal parasitic case was 86.14% [95% CI: 85.12% - 87.15%]. The prevalence of intestinal parasitic infection among children family members was 82.77% [95% CI: 81.08% -84.47%]. The prevalence of intestinal parasitic infection among household members whose age greater than 16 years was 88.67% [95% CI: 87.43% -89.90%]. This result was in line with finding from Sudan and Central African Republic (95% CI for prevalence 78.69% -88.23%) [20, 21]. However, these results were higher than finding from Uganda (Prevalence of 55.04%) [22], and England (Prevalence of 30%) [23]. This might be due to the difference in living conditions. Our study area contains numerous contacts which increase the risk of acquiring intestinal parasitic infections.

The odds of intestinal parasitic infections among female household members were 24% higher during childhood and 96% higher during adulthood. This finding agrees with other scholar works [24]. This is due to the fact that women in the household are responsible to care for the child and disposal of the waste of the child which increases their risk of acquiring infection easily [25].

Environmental sanitation decreases the odds of intestinal parasitic infection by 96% during childhood, and by 82% during adulthood. This finding agrees with finding from other parts of Ethiopia [26]. This is because environmental sanitation eliminates the reservoir for intestinal parasitic infection which finally blocks the infectious cycle of the parasites [27].

The odds of intestinal parasitic infection were 2.75 higher in children and mothers as compared to the other household members. This finding agrees with findings from Accra [28]. This is because of the proximity of mothers and children to the household wastes, which contains numerous intestinal parasites [29].

The odds of intestinal parasitic infections were 2.68 folds higher among urban children, and 2.32 folds higher in urban adults. This finding agrees with findings from India [30]. This might be due to poor environmental sanitation conditions with the overcrowding situation in the urban area [31].

Personal hygiene decreases the odds of intestinal parasitic infection by 74% among children, and by 96% lower in adults. This finding agrees with systematic review report [32]. This is because personal hygiene breaks the chain of intestinal parasitic transmission cycle [33].

Living in the substandard housing condition increases the odds of intestinal parasitic infection by 1.92 folds higher in children, and by 4 folds higher in adults. This finding agrees with finding from Brazil [34]. This is because of better sanitary facility access of the group [35].

The odds of intestinal parasitic infection were 2.28 folds higher among household members using traditional light for their house. This finding agrees with clinical trial results [36]. This is because if the household was supplied with electricity, the household members can become aware of a health- related condition thought radio, television mass education which finally increases their awareness of a health- related condition.

Regular handwashing practice decreases the odds of intestinal parasitic infection by 60%. This finding was in line with 2018 finding from Ethiopia [37]. This is because the feco-oral route of transmission will be blocked by applying regular handwashing practice [38].

Higher family size increases the odds of intestinal parasitic infection by 7.18 folds. This finding agrees with the previous finding from the same study area [39]. This is because high family size decreases the access to the basic sanitary facility due to sharing of the limited resources.

The presence of chicken in the house increases the odds of intestinal parasitic infection by 4.42 folds higher in children, and by 3.39 folds higher in adults. This finding agrees with findings from China [40]. This is because chickens act as a reservoir to numerous intestinal parasite species [41].

The presence of household water filtering materials decreases the odds of protozoa infection by 35%. This finding agrees with systematic review pools across the globe [42]. This is because of water treatment at the households levels eliminates the eggs or cysts of protozoa from the water [43].

Habit of playing with a domestic animal increases the odds of protozoa infection by 3.82 folds. This finding agrees with finding from Canada [44]. This is because most protozoa infections are transmitted from animals to humans (zoonotic) [45].

Using pipe water decreases the odds of protozoa infection by 20%. This finding agrees with finding from Brazil [46]. This indicated that untreated water is a potential source of protozoa infection [47].

Barefoot behavior increases the odds of soil-transmitted helminths infection by 4.5 folds. This finding was in line with 2018 results from Nigeria [48]. This is because barefoot allows the entry of soil transmitted helminths like hookworm at its infective stage [49].

The odds of soil-transmitted helminths were 2 folds higher in individuals living in a house made from the mud floor. This finding agrees with finding from Kenya [50]. This is because most people prefer barefoot in the house which increases the risk of soil-transmitted helminths.

The main limitation of this study was a failure to identify the incident and prevalent cases, but the overall aim of this study was to estimate the prevalence of intestinal parasitic infection among household members mixing of new or pre-existing cases will not create a huge problem.

Conclusion

The prevalence of intestinal parasites was high among household contacts of intestinal parasite-infected family members. Intestinal parasitic infection among household members was determined by family size, environmental sanitation, substandard housing, gender, household water treatment, habit of playing with domestic animals, The presence of chicken in the house, source of water, role in the household, resident, source of light, handwashing practice, and barefoot.

Recommendation

Clinicians must trace and care for all household contacts of intestinal parasite patients to make the interventions effective at the community level.

Supporting information

S1 Questionnaire. The data collection tool (questionnaire for the study).

(DOCX)

S1 Data. The SPSS data file of the research.

(SAV)

Acknowledgments

Our heartfelt acknowledgment goes to household members for good cooperation during the fieldwork. We would also like to acknowledge Mecha district health office for their unreserved efforts. At last but not least we would also like to acknowledge all organization and individuals that contributed to this research work.

Data Availability

All relevant data are within the manuscript and its Supporting Information files.

Funding Statement

This research work was financially sponsored by Bahir Dar University and the funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

References

  • 1.Kaushik J, Baishya K, Sharma S, Sharma R. A REVIEW ON KRIMI ROGA IN CHILDREN WSR TO WORM INFESTATIONS. International Journal of Engineering Science and Generic Research. 2018;4(4). [Google Scholar]
  • 2.Bhunia AK. Foodborne microbial pathogens: mechanisms and pathogenesis: Springer; 2018. [Google Scholar]
  • 3.Bharti B, Bharti S, Khurana S. Worm infestation: Diagnosis, treatment and prevention. The Indian Journal of Pediatrics. 2018;85(11):1017–24. 10.1007/s12098-017-2505-z [DOI] [PubMed] [Google Scholar]
  • 4.Botero JH, Castaño A, Montoya MN, Ocampo NE, Hurtado MI, Lopera MM. A preliminary study of the prevalence of intestinal parasites in immunocompromised patients with and without gastrointestinal manifestations. Revista do Instituto de Medicina Tropical de São Paulo. 2003;45(4):197–200. 10.1590/s0036-46652003000400004 [DOI] [PubMed] [Google Scholar]
  • 5.Truant AL, Elliott SH, Kelly MT, Smith JH. Comparison of formalin-ethyl ether sedimentation, formalin-ethyl acetate sedimentation, and zinc sulfate flotation techniques for detection of intestinal parasites. Journal of clinical microbiology. 1981;13(5):882–4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Saki J, Khademvatan S, Foroutan-Rad M, Gharibzadeh M. Prevalence of Intestinal Parasitic Infections in Haftkel County, Southwest of Iran. Int J Infect. 2017;4(4):e15593 Epub 2016-06-01. 10.5812/iji.15593 [DOI] [Google Scholar]
  • 7.Farrell SH, Coffeng LE, Truscott JE, Werkman M, Toor J, de Vlas SJ, et al. Investigating the effectiveness of current and modified world health organization guidelines for the control of soil-transmitted helminth infections. Clinical Infectious Diseases. 2018;66(suppl_4):S253–S9. 10.1093/cid/ciy002 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Dejon-Agobé JC, Zinsou JF, Honkpehedji YJ, Ateba-Ngoa U, Edoa J-R, Adegbite BR, et al. Schistosoma haematobium effects on Plasmodium falciparum infection modified by soil-transmitted helminths in school-age children living in rural areas of Gabon. PLoS neglected tropical diseases. 2018;12(8):e0006663 10.1371/journal.pntd.0006663 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Chifunda K, Kelly P. Parasitic infections of the gut in children. Paediatrics and international child health. 2018:1–8. [DOI] [PubMed] [Google Scholar]
  • 10.Kimani VN, Mitoko G, McDermott B, Grace D, Ambia J, Kiragu MW, et al. Social and gender determinants of risk of cryptosporidiosis, an emerging zoonosis, in Dagoretti, Nairobi, Kenya. Tropical animal health and production. 2012;44 Suppl 1:S17–23. Epub 2012/08/07. 10.1007/s11250-012-0203-4 . [DOI] [PubMed] [Google Scholar]
  • 11.Fernandez-Nino JA, Astudillo-Garcia CI, Segura LM, Gomez N, Salazar AS, Tabares JH, et al. [Profiles of intestinal polyparasitism in a community of the Colombian Amazon region]. Biomedica: revista del Instituto Nacional de Salud. 2017;37(3):368–77. Epub 2017/10/03. 10.7705/biomedica.v37i3.3395 . [DOI] [PubMed] [Google Scholar]
  • 12.Faria CP, Zanini GM, Dias GS, da Silva S, de Freitas MB, Almendra R, et al. Geospatial distribution of intestinal parasitic infections in Rio de Janeiro (Brazil) and its association with social determinants. PLoS Negl Trop Dis. 2017;11(3):e0005445 Epub 2017/03/09. 10.1371/journal.pntd.0005445 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Ross AG, Olveda RM, McManus DP, Harn DA, Chy D, Li Y, et al. Risk factors for human helminthiases in rural Philippines. International journal of infectious diseases: IJID: official publication of the International Society for Infectious Diseases. 2017;54:150–5. Epub 2016/10/27. 10.1016/j.ijid.2016.09.025 . [DOI] [PubMed] [Google Scholar]
  • 14.W AL-K, H AL-T, Al-khateeb A, Shanshal MM. Intestinal parasitic diarrhea among children in Baghdad—Iraq. Trop Biomed. 2014;31(3):499–506. Epub 2014/11/11. . [PubMed] [Google Scholar]
  • 15.Tefera T, Mebrie G. Prevalence and predictors of intestinal parasites among food handlers in Yebu Town, southwest Ethiopia. PLoS One. 2014;9(10):e110621 Epub 2014/10/21. 10.1371/journal.pone.0110621 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Schule SA, Clowes P, Kroidl I, Kowuor DO, Nsojo A, Mangu C, et al. Ascaris lumbricoides infection and its relation to environmental factors in the Mbeya region of Tanzania, a cross-sectional, population-based study. PLoS One. 2014;9(3):e92032 Epub 2014/03/20. 10.1371/journal.pone.0092032 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Abera B, Alem G, Yimer M, Herrador Z. Epidemiology of soil-transmitted helminths, Schistosoma mansoni, and haematocrit values among schoolchildren in Ethiopia. J Infect Dev Ctries. 2013;7(3):253–60. Epub 2013/03/16. 10.3855/jidc.2539 . [DOI] [PubMed] [Google Scholar]
  • 18.Wumba R, Longo-Mbenza B, Menotti J, Mandina M, Kintoki F, Situakibanza NH, et al. Epidemiology, clinical, immune, and molecular profiles of microsporidiosis and cryptosporidiosis among HIV/AIDS patients. International journal of general medicine. 2012;5:603–11. Epub 2012/08/28. 10.2147/IJGM.S32344 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Institute S. Methods in Parasitology. Sodium acetate-acetic acid-formalin solution method for stool specimen. Basel: Swiss TPH: Swiss Tropical Institute; 2005. p. 1–18. [Google Scholar]
  • 20.Tékpa G, Fikouma V, Gbangba-Ngaï E, Bogning Mejiozem BO, Ningatouloum Nazita S, Koffi B. Epidemiological and clinical profile of intestinal parasitosis of children in rural areas in Central African Republic. Archives de Pédiatrie. 2019;26(1):34–7. 10.1016/j.arcped.2018.11.006 [DOI] [PubMed] [Google Scholar]
  • 21.Hamad M, Mokhtar A, Alameldin M. Prevalence of intestinal parasitic infections among school aged children in Berber locality, River Nile State, Sudan 2017. J Microbiol Exp. 2019;7(2):85–6. [Google Scholar]
  • 22.Oboth P, Gavamukulya Y, Barugahare BJ. Prevalence and clinical outcomes of Plasmodium falciparum and intestinal parasitic infections among children in Kiryandongo refugee camp, mid-Western Uganda: a cross sectional study. BMC infectious diseases. 2019;19(1):295 10.1186/s12879-019-3939-x [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Waldram A, Vivancos R, Hartley C, Lamden K. Prevalence of Giardia infection in households of Giardia cases and risk factors for household transmission. BMC Infect Dis. 2017;17(1):486 Epub 2017/07/12. 10.1186/s12879-017-2586-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Elfu Feleke B. Epidemiology of Hookworm Infection in the School-age Children: A Comparative Cross-sectional Study. Iranian journal of parasitology. 2018;13(4):560–6. Epub 2019/01/31. [PMC free article] [PubMed] [Google Scholar]
  • 25.Oyemade A, Omokhodion FO, Olawuyi JF, Sridhar MK, Olaseha IO. Environmental and personal hygiene practices: risk factors for diarrhoea among children of Nigerian market women. Journal of Diarrhoeal Diseases Research. 1998:241–7. [PubMed] [Google Scholar]
  • 26.Gizaw Z, Adane T, Azanaw J, Addisu A, Haile D. Childhood intestinal parasitic infection and sanitation predictors in rural Dembiya, northwest Ethiopia. Environmental health and preventive medicine. 2018;23(1):26 Epub 2018/06/24. 10.1186/s12199-018-0714-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.McKenna ML, McAtee S, Bryan PE, Jeun R, Ward T, Kraus J, et al. Human Intestinal Parasite Burden and Poor Sanitation in Rural Alabama. Am J Trop Med Hyg. 2017;97(5):1623–8. Epub 2017/10/11. 10.4269/ajtmh.17-0396 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Forson AO, Arthur I, Ayeh-Kumi PF. The role of family size, employment and education of parents in the prevalence of intestinal parasitic infections in school children in Accra. PloS one. 2018;13(2):e0192303 10.1371/journal.pone.0192303 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Zavala GA, García OP, Camacho M, Ronquillo D, Campos‐Ponce M, Doak C, et al. Intestinal parasites: Associations with intestinal and systemic inflammation. Parasite immunology. 2018;40(4):e12518 10.1111/pim.12518 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Sarkar R, Kattula D, Francis MR, Ajjampur SS, Prabakaran AD, Jayavelu N, et al. Risk factors for cryptosporidiosis among children in a semi urban slum in southern India: a nested case-control study. Am J Trop Med Hyg. 2014;91(6):1128–37. Epub 2014/10/22. 10.4269/ajtmh.14-0304 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Coker AO. Negative impacts of waste on human health and environment in Nigeria’s urban areas: innovative solutions to the rescue. Global Health Innovation. 2018;1(2). 10.15641/ghi.v1i2.585 [DOI] [Google Scholar]
  • 32.Cholapranee A, Ananthakrishnan AN. Environmental Hygiene and Risk of Inflammatory Bowel Diseases: A Systematic Review and Meta-analysis. Inflammatory bowel diseases. 2016;22(9):2191–9. Epub 2016/08/03. 10.1097/MIB.0000000000000852 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Leibler JH, Nguyen DD, Leon C, Gaeta JM, Perez D. Personal Hygiene Practices among Urban Homeless Persons in Boston, MA. Int J Environ Res Public Health. 2017;14(8). Epub 2017/08/19. 10.3390/ijerph14080928 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Da Silva JB, Bossolani GD, Piva C, Dias GB, Gomes Ferreira J, Rossoni DF, et al. Spatial distribution of intestinal parasitic infections in a Kaingang indigenous village from Southern Brazil. International journal of environmental health research. 2016;26(5–6):578–88. Epub 2016/08/20. 10.1080/09603123.2016.1217312 . [DOI] [PubMed] [Google Scholar]
  • 35.Crighton E, Gordon H, Barakat-Haddad C. Environmental health inequities: from global to local contexts Routledge Handbook of Health Geography: Routledge; 2018. p. 59–66. [Google Scholar]
  • 36.Steinbaum L, Mboya J, Mahoney R, Njenga SM, Null C, Pickering AJ. Effect of a sanitation intervention on soil-transmitted helminth prevalence and concentration in household soil: A cluster-randomized controlled trial and risk factor analysis. PLOS Neglected Tropical Diseases. 2019;13(2):e0007180 10.1371/journal.pntd.0007180 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Feleke BE, Jember TH. Prevalence of helminthic infections and determinant factors among pregnant women in Mecha district, Northwest Ethiopia: a cross sectional study. BMC Infect Dis. 2018;18(1):373 Epub 2018/08/08. 10.1186/s12879-018-3291-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Means AR, van Lieshout L, Brienen E, Yuhas K, Hughes JP, Ndungu P, et al. Combined effectiveness of anthelmintic chemotherapy and WASH among HIV-infected adults. PLoS neglected tropical diseases. 2018;12(1):e0005955 10.1371/journal.pntd.0005955 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Feleke BE. Nutritional Status and Intestinal Parasite in School Age Children: A Comparative Cross-Sectional Study. International journal of pediatrics. 2016;2016:1962128 Epub 2016/09/23. 10.1155/2016/1962128 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Zheng H, He J, Wang L, Zhang R, Ding Z, Hu W. Risk Factors and Spatial Clusters of Cryptosporidium Infection among School-Age Children in a Rural Region of Eastern China. International journal of environmental research and public health. 2018;15(5):924. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Ybañez RHD, Resuelo KJG, Kintanar APM, Ybañez AP. Detection of gastrointestinal parasites in small-scale poultry layer farms in Leyte, Philippines. Veterinary world. 2018;11(11):1587 10.14202/vetworld.2018.1587-1591 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Strunz EC, Addiss DG, Stocks ME, Ogden S, Utzinger J, Freeman MC. Water, sanitation, hygiene, and soil-transmitted helminth infection: a systematic review and meta-analysis. PLoS medicine. 2014;11(3):e1001620 10.1371/journal.pmed.1001620 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Amoah ID, Reddy P, Seidu R, Stenström TA. Removal of helminth eggs by centralized and decentralized wastewater treatment plants in South Africa and Lesotho: health implications for direct and indirect exposure to the effluents. Environmental Science and Pollution Research. 2018:1–13. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Luong L, Chambers J, Moizis A, Stock T, Clair CS. Helminth parasites and zoonotic risk associated with urban coyotes (Canis latrans) in Alberta, Canada. Journal of helminthology. 2018:1–5. [DOI] [PubMed] [Google Scholar]
  • 45.Sarvi S, Daryani A, Sharif M, Rahimi MT, Kohansal MH, Mirshafiee S, et al. Zoonotic intestinal parasites of carnivores: A systematic review in Iran. Veterinary world. 2018;11(1):58 10.14202/vetworld.2018.58-65 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Ignacio CF, Silva M, Handam NB, Alencar MFL, Sotero-Martins A, Barata MML, et al. Socioenvironmental conditions and intestinal parasitic infections in Brazilian urban slums: a cross-sectional study. Rev Inst Med Trop Sao Paulo. 2017;59:e56 Epub 2017/08/10. 10.1590/S1678-9946201759056 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Abd Ellatif N, Mohamed M, El-Taweel H, Hamam M, Saudi M. Intestinal protozoa in diarrheic children in an Egyptian rural area: Role of water contamination and other possible risk factors. Parasitologists United Journal. 2018;11(2):82–9. [Google Scholar]
  • 48.Ugbomeh A, Goodhead D, Green A, Onwuteaka J. Prevalence of Human Intestinal Nematode Parasites in Three Rural Communities of the Niger Delta, Nigeria. 2018. [Google Scholar]
  • 49.Mohanty A, Gupta P, Gupta P, Prasad RS. Diagnostic Dilemma in Hookworm Infection: An Unusual Presentation. Int J Curr Microbiol App Sci. 2018;7(3):3769–71. [Google Scholar]
  • 50.Worrell CM, Wiegand RE, Davis SM, Odero KO, Blackstock A, Cuéllar VM, et al. A cross-sectional study of water, sanitation, and hygiene-related risk factors for soil-transmitted helminth infection in urban school-and preschool-aged children in Kibera, Nairobi. PloS one. 2016;11(3):e0150744 10.1371/journal.pone.0150744 [DOI] [PMC free article] [PubMed] [Google Scholar]

Decision Letter 0

Chia Kwung Fan

29 Aug 2019

[EXSCINDED]

PONE-D-19-20993

Intestinal parasitic infection among household contacts of primary cases, a comparative cross-sectional study

PLOS ONE

Dear Mr, Feleke,

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.

==============================

ACADEMIC EDITOR:In this manuscript, the authors tried to estimate the prevalence and determinants of intestinal parasitic infection among family members of known intestinal parasitic infected patients in Mecha district of Ethiopia. The manuscript has merit because the information is helpful to develop possible strategy for parasite prevention in Ethiopia. Although the study design is straightforward, but the content somewhat is too simple and not in-depth enough. Therefore, this article cannot be accepted for publication in current form d except some serious concerns have been clarified.

==============================

We would appreciate receiving your revised manuscript by Oct 13 2019 11:59PM. When you are 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.

If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter.

To enhance the reproducibility of your results, we recommend that if applicable you deposit your laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. For instructions see: http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols

Please include the following items when submitting your revised manuscript:

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Please note while forming your response, if your article is accepted, you may have the opportunity to make the peer review history publicly available. The record will include editor decision letters (with reviews) and your responses to reviewer comments. If eligible, we will contact you to opt in or out.

We look forward to receiving your revised manuscript.

Kind regards,

Chia Kwung Fan, LL.M, PhD

Academic Editor

PLOS ONE

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Please ensure that your manuscript meets PLOS ONE's style requirements, including those for file naming. The PLOS ONE style templates can be found at

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Reviewers' comments:

Reviewer's Responses to Questions

Comments to the Author

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: No

Reviewer #2: Partly

**********

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)

Reviewer #1: The study of intestinal parasitic infection among household contacts of primary cases, a comparative cross-sectional study is interesting; however, some major concerns should be clarified before its suitable publication in PLOS ONE.

1.Result: How do you make a confirmative diagnosis of Enatmeba histolytic (11.4%)? By what kind of criteria?

2.Discussion: line 167-Would you please compare the similarity or difference between your study and the other African countries, instead England only?

3.Line 174: Authors indicated that “environmental sanitation decreases the odds of intestinal parasitic infection by 96% during childhood, and by 82% during adulthood”, how can you get such an estimation? The other similar calculation should be indicated also.

Reviewer #2: In this manuscript, the authors tried to estimate the prevalence and determinants of intestinal parasitic infection among family members of known intestinal parasitic infected patients in Mecha district of Ethiopia. The manuscript has merit because the information is helpful to develop possible strategy for parasite prevention in Ethiopia. Although the study design is straightforward, but the content somewhat is too simple and not in-depth enough. Therefore, this article cannot be published except some serious problems have been addressed. These issues are discussed below.

1. Major problem is that the authors put all the intestinal parasite infection in together for survey without discussing the differences between all these distinct species, especially their infection routes. For example, hookworm and S. mansoni are infected by invading through skin; so the considered determinant parameters that should be different with the parasites of fecal-oral infection. However, authors here combine all these parasitic infection as a topic and compare to the same determinants. It would be also wrong to put protozoa and helminth as a simple field to discuss, because the inspection level and infection way are very different, such as soil- or water-transmission, reservoir host or not; it should be given more detailed division for considering their determinants. The influence of each parameter on different parasites cannot be the same.

2. A lot of the parameters of tables are unclear and not accurate enough, e.g. "Environmental sanitation" only presents as clean or dirty, it should be shown with different levels for distinguishing. Additionally, the lack of in-death enough discussion about their data make the author’s descriptions in results or discussion section are too general and fuzzy, like a hodgepodge. It cannot show the relevance of their results as the hypothesis of this manuscript, even worse to arrive at the stated conclusions. The significance of these determinants for intestinal parasitic infection is not hand out.

3. In table 2, what kinds of parasite are included in the mixed infection? The patient is infected with two or three parasites? These data may be important to ascertain the source of dissemination and influenced determinants.

4. Authors should attach the Ethical approval number or the document by ethical committee for reference.

5. The authors analyzed the determinants of intestinal parasite infections in adult and child household members, but do not make any further explain between their difference and the reasons? Some determinants described in discussion section are unreasonable, e.g. the source of light is not relevant to the awareness of a health- related condition.

6. The author's recommendation is not specific enough and lacks order. Which determinant is the most important?

**********

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

[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 to be viewed.]

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 us at figures@plos.org. Please note that Supporting Information files do not need this step.

PLoS One. 2019 Oct 7;14(10):e0221190. doi: 10.1371/journal.pone.0221190.r002

Author response to Decision Letter 0


5 Sep 2019

Response to the reviewers

Manuscript title: Intestinal parasitic infection among household contacts of primary cases, a comparative cross-sectional study

Manuscript ID: PONE-D-19-20993

Reviewer #1: The study of intestinal parasitic infection among household contacts of primary cases, a comparative cross-sectional study is interesting; however, some major concerns should be clarified before its suitable publication in PLOS ONE.

1. Result: How do you make a confirmative diagnosis of Enatmeba histolytic (11.4%)? By what kind of criteria?

Response: Sorry it was the type error, Enatmeba histolytic was revised with Enatmeba histolytica/ dispar since we used microscopic stool examination. Result section, line number 122 -126 and table 2, page 8

• 2.Discussion: line 167-Would you please compare the similarity or difference between your study and the other African countries, instead England only?

• Response: revised, the finding was compared from African countries (Sudan, central African republic and Uganda ), discussion section page 16, line number 167-168

3.Line 174: Authors indicated that “environmental sanitation decreases the odds of intestinal parasitic infection by 96% during childhood, and by 82% during adulthood”, how can you get such an estimation? The other similar calculation should be indicated also.

• Response: when the odds ratio is less than 1, the protective fraction will be calculated by subtracting from 1. Result section page 10, table 3 shows that the association between environmental sanitation and IP infection was protective, i.e. AOR is less than 1(0.04), the preventive fraction was calculated by subtracting from (1 - 0.04=0.96, meaning environmental sanitation is 96 % protective). Table 4, page 13 presents the association between environmental sanitation and IP infection in adults was 0.18, the preventive fraction (1-0.18) = 82% protective.

Reviewer #2: In this manuscript, the authors tried to estimate the prevalence and determinants of intestinal parasitic infection among family members of known intestinal parasitic infected patients in Mecha district of Ethiopia. The manuscript has merit because the information is helpful to develop possible strategy for parasite prevention in Ethiopia. Although the study design is straightforward, but the content somewhat is too simple and not in-depth enough. Therefore, this article cannot be published except some serious problems have been addressed. These issues are discussed below.

1. Major problem is that the authors put all the intestinal parasite infection in together for survey without discussing the differences between all these distinct species, especially their infection routes. For example, hookworm and S. mansoni are infected by invading through skin; so the considered determinant parameters that should be different with the parasites of fecal-oral infection. However, authors here combine all these parasitic infection as a topic and compare to the same determinants. It would be also wrong to put protozoa and helminth as a simple field to discuss, because the inspection level and infection way are very different, such as soil- or water-transmission, reservoir host or not; it should be given more detailed division for considering their determinants. The influence of each parameter on different parasites cannot be the same.

• Response: the common predictors for all intestinal parasites like sex, environmental sanitation, role in the household, residence, personal hygiene, age, living in substandard house, regular handwashing practice and family size was presented together. These predictors are common for soil-transmitted helminths and protozoa infections. The specific predictors for protozoa(habit of ingesting raw vegetable, playing with domestic animals, water source, the presence of water filtering materials) and soil transmitted helminths(barefoot, floor materials) were presented in result section page 15, table 5 and well discussed in discussion section page 18, line number 208-223.

• 2. A lot of the parameters of tables are unclear and not accurate enough, e.g. "Environmental sanitation" only presents as clean or dirty, it should be shown with different levels for distinguishing. Additionally, the lack of in-death enough discussion about their data make the author’s descriptions in results or discussion section are too general and fuzzy, like a hodgepodge. It cannot show the relevance of their results as the hypothesis of this manuscript, even worse to arrive at the stated conclusions. The significance of these determinants for intestinal parasitic infection is not hand out.

• Response: the specific predictors for soil-transmitted helminths and protozoa were presented in table 5(result section, page 15) and discussed in discussion section page 18. But there are common risk factors for intestinal parasites like environmental sanitation, residence, sex, age, living in substandard housing conditions, role in the household and family size. These factors are common for all protozoa and soil transmitted helminths.

• 3. In table 2, what kinds of parasite are included in the mixed infection? The patient is infected with two or three parasites? These data may be important to ascertain the source of dissemination and influenced determinants.

• Response: mixed infection includes study participants infected by two or more parasites.

4. Authors should attach the Ethical approval number or the document by ethical committee for reference.

• Response: Attached, the ethical approval number for this research was “የአ.ህ.ጤቴ/ሽ/ዳ/01/795” methods section page 7, line number 109.

5. The authors analyzed the determinants of intestinal parasite infections in adult and child household members, but do not make any further explain between their difference and the reasons? Some determinants described in discussion section are unreasonable, e.g. the source of light is not relevant to the awareness of a health- related condition.

• Response: it is commonly observed that if the house contains electricity, the probability of having Television and radio is very high which increases their awareness towards health related conditions because of mass health education given from the broadcast.

6. The author's recommendation is not specific enough and lacks order. Which determinant is the most important?

• Response: the prevalence of intestinal parasitic infection among children household members was 82% and the prevalence of intestinal parasite infection among adult household members was 86%. The intestinal parasitic infection intervention currently did not touch the contact tracing, the main message of this work is that clinicians was missing more than 80% of intestinal parasitic infection cases. So they should incorporate contact tracing.

Decision Letter 1

Chia Kwung Fan

19 Sep 2019

PONE-D-19-20993R1

Intestinal parasitic infection among household contacts of primary cases, a comparative cross-sectional study

PLOS ONE

Dear Mr, Feleke,

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.

==============================

ACADEMIC EDITOR: Although the authors have answered the reviewer's questions appropriately, however, minor errors should be amended before its suitable publication.

1.Table 2: intestinal parasites—the parasite name should be e.g., Ascaris lumbricoides instead Ascaris Lumbricoides. The first letter of the species should be lowercase. This indication

2.line 167: This results was in line with finding from Sudan 168 and central African republic [20, 21], higher than finding from Uganda [22], and England [23].

Please show their prevalence, respectively. Also, please check the grammar and spellings.

==============================

We would appreciate receiving your revised manuscript by Nov 03 2019 11:59PM. When you are 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.

If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter.

To enhance the reproducibility of your results, we recommend that if applicable you deposit your laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. For instructions see: http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols

Please include the following items when submitting your revised manuscript:

  • A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). This letter should be uploaded as separate file and labeled 'Response to Reviewers'.

  • A marked-up copy of your manuscript that highlights changes made to the original version. This file should be uploaded as separate file and labeled 'Revised Manuscript with Track Changes'.

  • An unmarked version of your revised paper without tracked changes. This file should be uploaded as separate file and labeled 'Manuscript'.

Please note while forming your response, if your article is accepted, you may have the opportunity to make the peer review history publicly available. The record will include editor decision letters (with reviews) and your responses to reviewer comments. If eligible, we will contact you to opt in or out.

We look forward to receiving your revised manuscript.

Kind regards,

Chia Kwung Fan, LL.M, PhD

Academic Editor

PLOS ONE

Additional Editor Comments (if provided):

Although the authors have answered the reviewer's questions appropriately, however, minor errors should be amended before its suitable publication.

1.Table 2: intestinal parasites—the parasite name should be e.g., Ascaris lumbricoides instead Ascaris Lumbricoides. The first letter of the species should be lowercase. This indication

2.line 167: This results was in line with finding from Sudan 168 and central African republic [20, 21], higher than finding from Uganda [22], and England [23].

Please show their prevalence, respectively. Also, please check the grammar and spellings.

[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: Although the authors have answered the reviewer's questions appropriately, however, minor errors should be amended before its suitable publication.

1.Table 2: intestinal parasites—the parasite name should be e.g., Ascaris lumbricoides instead Ascaris Lumbricoides. The first letter of the species should be lowercase. This indication

2.line 167: This results was in line with finding from Sudan 168 and central African republic [20, 21], higher than finding from Uganda [22], and England [23].

Please show their prevalence, respectively. Also, please check the grammar and spellings.

Reviewer #2: In this manuscript, the authors tried to estimate the prevalence and determinants of intestinal parasitic infection among family members of known intestinal parasitic infected patients in Mecha district of Ethiopia. The manuscript has merit because the information is helpful to develop possible strategy for parasite prevention in Ethiopia. All the comments have been addressed.

**********

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: 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 to be viewed.]

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 us at figures@plos.org. Please note that Supporting Information files do not need this step.

PLoS One. 2019 Oct 7;14(10):e0221190. doi: 10.1371/journal.pone.0221190.r004

Author response to Decision Letter 1


19 Sep 2019

Response to the reviewers

Although the authors have answered the reviewer's questions appropriately, however, minor errors should be amended before its suitable publication.

1.Table 2: intestinal parasites—the parasite name should be e.g., Ascaris lumbricoides instead Ascaris Lumbricoides. The first letter of the species should be lowercase.

• Response: revised based on the comment

This results was in line with finding from Sudan and central African republic [20, 21], higher than finding from Uganda [22], and England [23].

Please show their prevalence, respectively. Also, please check the grammar and spellings.

• Response: revised based on the comments.

Attachment

Submitted filename: Response to the reviewers.docx

Decision Letter 2

Chia Kwung Fan

25 Sep 2019

Intestinal parasitic infection among household contacts of primary cases, a comparative cross-sectional study

PONE-D-19-20993R2

Dear Dr. Feleke,

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

Within one week, you will receive an e-mail containing information on the amendments required prior to publication. When all required modifications have been addressed, you will receive a formal acceptance letter and your manuscript will proceed to our production department and be scheduled for publication.

Shortly after the formal acceptance letter is sent, an invoice for payment will follow. To ensure an efficient production and billing process, please log into Editorial Manager at https://www.editorialmanager.com/pone/, click the "Update My Information" link at the top of the page, and update your user information. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org.

If your institution or institutions have a press office, please notify them about your upcoming paper to enable them to help maximize its impact. If they will be preparing press materials for this manuscript, you must inform our press team as soon as possible and no later than 48 hours after receiving the formal acceptance. 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.

With kind regards,

Chia Kwung Fan, LL.M, PhD

Academic Editor

PLOS ONE

Additional Editor Comments (optional):

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

**********

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Acceptance letter

Chia Kwung Fan

30 Sep 2019

PONE-D-19-20993R2

Intestinal parasitic infection among household contacts of primary cases, a comparative cross-sectional study

Dear Dr. Feleke:

I am 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.

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With kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Dr. Chia Kwung Fan

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 Questionnaire. The data collection tool (questionnaire for the study).

    (DOCX)

    S1 Data. The SPSS data file of the research.

    (SAV)

    Attachment

    Submitted filename: Response to the reviewers.docx

    Data Availability Statement

    All relevant data are within the manuscript and its Supporting Information files.


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