Skip to main content
PLOS One logoLink to PLOS One
. 2020 Sep 28;15(9):e0239680. doi: 10.1371/journal.pone.0239680

Prevalence and risk factors of geohelminthiasis among the rural village children in Kota Marudu, Sabah, Malaysia

A Lim-Leroy 1, Tock H Chua 1,*
Editor: Arun K Yadav2
PMCID: PMC7521721  PMID: 32986746

Abstract

Geohelminthiasis is a worldwide problem, especially in low-income countries. Children from rural areas and those living in poverty, lacking basic health amenities and having poor environmental sanitation are likely to be affected. Adverse effects such as anemia, protein malnutrition, colitis are common which can affect both the children’s physical and mental growing development. A cross-sectional study on geohelminthiasis was conducted among children from 238 households in 13 villages in Kota Marudu of northern Sabah, East Malaysia. The study involved interviewing villagers using questionnaires to collect demographic and socio-economic data, getting faecal samples from the children, collecting soil samples and identifying parasite eggs with microscopy and molecular methods. A total of 407 children (6 months-17 years old) enrolled in the study. Geohelminthiasis was detected in the faecal samples of children from 54% (7/13) of the villages with mean prevalence of infection per village of 9.0% (0%-34.9%). On a household basis, 18% (43/238) of the households sampled had infected children, with mean prevalence rate per household of 11% (0%-43%). The prevalence was for Ascaris lumbricoides: 9.6% (39/407), Trichuris trichiura: 2.7% (11/407) and hookworms (Necator americanus and Ancylostoma sp.): 2.7% (11/407). The overall mean infection rate of the children examined was 14.3%. Significantly higher prevalence was recorded for the children of mothers who did not have any formal education (p = 0.003); household income of less than USD119 (RM500) (p<0.001); children from homes without proper sanitation facilities (p<0.001); children who usually go about barefoot (p<0.001) and not washing feet before entering the house (p = 0.017). Soil samples were found to have geohelminth eggs or larvae which could be due to unhygienic sanitation practices. This study shows the geohelminthiasis is prevalent in the villages, and the risk factors are lack of maternal education, low income, poor sanitation facilities and irregular deworming practice. Expanding deworming coverage in the study region may help reduce the worm infections in these communities, so that the mental and physical development of the children would not be affected by geohelminthiasis. The data on the prevalence of geohelminthiasis in this study would contribute to better public health monitoring and operation to reduce the infection in rural areas.

Introduction

The term soil-transmitted helminths (STH) or geohelminths refers to Ascaris lumbricoides, hookworms or Trichuris trichiura, and infection by these helminths is collectively known as geohelminthiasis. It is a worldwide problem, especially in low-income countries.

In 2010, it was estimated that globally 438.9 million people were infected with hookworm, 819.0 million with A. lumbricoides and 464.6 million with T. trichiura [1]. Chronic infections of Ascaris, Trichuris, and hookworm in children have adverse effects on their physical and mental development, and the severity of these effects are dependent on the intensity of the infection [2].

Children, especially from rural areas, living in poverty, lacking basic amenities and having poor environmental sanitation and hygiene, are often infected with geohelminths. Infection by Ascaris lumbricoides rarely causes death, but it can cause anemia affecting children’s physical and mental growing development [3, 4]. Heavy hookworm infection in children could lead to “hookworm disease” [5] with characteristic iron deficiency anemia and protein malnutrition resulting from intestinal blood loss. More importantly, anemia during pregnancy can result in prematurity, low birthweight, and impaired lactation [6]. Infection by Trichuris trichiura is comparatively less harmful and without symptoms although medium to heavy infections can lead to colitis, with associated chronic abdominal pain and diarrhoea, and Trichuris dysentery syndrome [7]. In Malaysia, geohelminthiasis is considered endemic, with the most common STH being Ascaris lumbricoides, Trichuris trichiura and hookworm [8]. Although the living standards of the Malaysian rural communities and indigenous people have been upgraded with better facilities through the government’s efforts, high incidences of geohelminthiasis are still being reported [9, 10].

Several studies of geohelminth infection have been conducted in West Malaysia among the children of various communities, backgrounds and settings. High prevalence of A. lumbricoides (59.9%) and T. trichiura (47.1%) were detected in the children of the indigenous communities (Orang Asli) [11]. Sinniah et al. [12] reviewed 101 studies covering 42 years of research on intestinal parasitic infections among communities living in different habitats and recorded high incidence of STH infection among the indigenous children. Globally, it appears that Malaysia had the highest prevalence of T. trichiura infections (49.9%) [1].

Comparatively fewer studies had been conducted in the rural areas of both states of Sabah and Sarawak of East Malaysia [13, 14] which have provided some basic information on the prevalence of STH infection. This study was conducted at 13 rural communities in the district of Kota Marudu, Sabah, to determine the prevalence of geohelminthiasis, particularly ascariasis among the indigenous children of these villages between the age of 6-month-old to 17-years as well as to identify the potential associated risk factors.

Materials and methods

This study was approved by the Malaysian National Medical Research Register (NMRR, Ref. 25014_20161014_070033_067). Signed consent was obtained from the village heads of all villages, and the parents of the children before data collection commenced.

Study area and population

The study, lasting from April 2015 to September 2017, was carried out at Kota Marudu district, located in the northern region and which is one of the districts in Sabah currently undergoing rapid urbanization (Fig 1).

Fig 1. Map of Kota Marudu district, Sabah where the study was conducted, indicating the location of the villages.

Fig 1

The figure was modified using a map available from http://www.supercoloring.com/coloring-pages/malaysia-map, and the village location plotted with Google earth software.

Thirteen villages in Kota Marudu district (out of 138) were selected as study sites, based on the following criteria: they must be rural, more than 5 km away from Kota Marudu town, accessible by road, and had >20 houses with a population of >100 villagers. Ninety three villages fulfilled the criteria. The distance of the village from the Kota Marudu town and the elevation were further considered in the selection to examine if the geohelminthiasis prevalence was associated with these factors (Table 1). Permission to carry out study was sought from the heads of the final list of 30 villages who were briefed on the purpose of the study. Due to time and fund constraints, the first 13 villages with given permission were chosen as the combined population provided a large sampling pool.

Table 1. Details of the villages in Kota Marudu selected for the study.

Elevation of the villages is given as metres above sea level (masl). Total participants in the study were 407.

Villages Population Distance from Kota Marudu Town (km) GPS Coordinates Eleva-tion (m asl) Total participants
Kg. Bintasan Darat 214 23 6.5878 N 116.6909 E 43 46
Kg. Bintasan Tengah 288 20 6.5844 N 116.7031 E 43 30
Kg. Minansad 265 25 6.5692 N 116.7021 E 48 13
Kg. Boluot 115 25 6.5704 N 116.704 E 31 17
Kg. Mangin 1 299 14 6.5543 N 116.6912 E 55 35
Kg. Mangin 2 318 17 6.5589 N 116.6817 E 118 23
Kg. Korongkom 650 5 6.50765 N 116.7767 E 13 25
Kg. Liabas 618 20 6.56921 N 116.8698 E 168 35
Kg. Bombong 1 443 30 6.5163 N 116.9716 E 49 11
Kg. Gana 361 38 6.3391 N 116.9044 E 715 71
Kg. Kinangkaban 410 28 6.5441 N 116.9025 E 279 63
Kg. Patiu 231 10 6.4419 N 116.7374 E 260 23
Kg. Sorinsim 158 30 6.2943 N 116.7111 E 180 15

Although these villages are accessible by road, they are rather traditional and have very basic social facilities and infrastructure. Despite the current development taking place in Kota Marudu district, some of the villagers were found during the study, to live in poor environmental sanitation conditions with no proper toilet facilities which resulted in some villagers defecating in the bushes. Many households still rely on untreated rainwater for bathing and washing, while some use gravity-feed or dug-well water. Only two villages have piped treated water.

The population of the district in 2017 was 77,100, of which 27,240 were 17 years old and below, consisting mainly Kadazan-Dusun (62%), Bajau (15%) and other native sub-ethnic groups (17%) (Dept of Statistics, 2017). Within each village, all the children of age 6 months– 17 years old who were residing there were invited to participate in the study.

Sampling size

The required sampling size for the study was estimated by the formula:

n=z2p(1-p)/d2=384;

where z = 1.96; p = proportion of the population infected = 0.5 [10]; d = level of significance = 0.05. Assuming a non-response rate of 5%, the targeted sampling size was 384/0.05 = 404.

Collection of demographic data

Household data was collected through interviewing the children’s parents or guardians in the respondent’s house using structured questionnaires (S1 Questionnaire). The questionnaire was administered verbally in the Malaysian language and the answers recorded on paper.

The questions included parents’ education background, occupation, source of drinking water, standard of hygiene practice (eg whether washing hands before meals, or after going to the toilet), consumption of raw meat, or aquatic vegetables, keeping pets in the house, allowing domestic animals (including pigs and goats) into the house, whether the children go barefoot, geophagy among the children, household waste disposal method etc. The quality of water supply, sanitation facilities, type and structure of house, and general cleanliness of the house environment were also recorded.

Collection of faecal samples

All the households in each selected village were given a participant information sheet and then briefed on the objectives of the study. In addition, each household was provided with pre-labelled, clean, dry, leak-proof plastic, screw-capped stool containers, one bottle per child. The parents and older children were briefed on the procedure of stool collection, to ensure they adhere to the correct procedure for collecting the faecal samples. The parents/guardians of each respondent also signed an informed consent form in the Malaysian language. Confidentiality of participants was ensured throughout the study. To ensure a sufficient final sample size, a total of 500 bottles were given out.

Examination of faecal samples

A direct wet mount of each faecal sample was made and examined by microscopy for the presence of geohelminth eggs in the laboratory of the district hospital within the same day. Egg count for positive samples was however not performed. After microscopy, all samples were then fixed with 10% formalin for further analysis at the laboratory of Pathobiology and Diagnostic Department, Universiti Malaysia Sabah. In the university laboratory, the negative samples were reexamined using formalin-ether concentration method (FEC) [15].

The geohelminths were initially identified based on the morphology of the eggs. Subsequent confirmation of A. lumbricoides and speciation of hookworm was done using polymercase chain reaction with the following primers. For A. lumbricoides the primer pair was EU582499 Fw: 5’-GGAGGTTTTTGGGTCTTTGG-3’ and Rw: 5’-CCAAACAAGGTAGCCAACCA-3’ [16]. For Necator americanus, the primers were AJ001680 Fw: 5’ ATGCTTGGCAAGAGTCGTTT 3’ and Rw: 5’TGTTGGCGTCCACACATATT 3’ [16] and for Ancylostoma species, the primers were Ad125F: 5’ GAATGACAGCAAACTCGTTGTTG 3’ and Ad195R: 5’ATACTAGCCACTGCCGAAACGT 3’ [17].

Collection of soil and water samples

If the microscopy examination of the faecal samples indicated worm infection in the children, soil samples were taken for examination within four weeks after checking the faecal samples. Soil samples were taken from 40 households which had sandy or loamy house compounds. Within the compound where the children frequently played, two samples each about 200 g of soil were randomly collected with an ethanol-treated hand shovel at 5 cm beneath the surface of the soil which was not exposed to direct sunlight, placed in a new Quart Zipper Storage polyethylene bag and labelled accordingly.

The soil samples were processed in the laboratory using modified flotation method [18] with zinc sulphate (ZnSO4) solution of specific gravity 1.18–1.20. About 100 mL of distilled water was first added to 10 g of soil which was then homogenized with a glass rod before straining it through gauze and net mesh to remove large particles/stones. The strained mixture was then poured into two 50 mL conical tubes and centrifuged at 2500 rpm for one minute (Kubota 4000 Laboratory Centrifuge). The supernatant fluid was discarded, saline was added to the sediment and centrifuged. This process was repeated 2–3 times until the supernatant was clear. Approximately 5 mL of zinc sulphate (ZnSO4) was then added into the sediment and the mixture vortexed at 2200 rpm to loosen the pellet/sediment before being transferred into a 15 mL centrifuge tube. More ZnSO4 solution was added to the tube to make up to 15 mL, which was centrifuged again for five minutes at 1500 rpm (Hettich, Universal 320 laboratory 75 centrifuge). A coverslip was later placed on the top of the tube for 10–15 minutes to provide enough time for the STH eggs / larvae (if any) to float up and attach to the coverslip. The cover slip with eggs stuck to it was removed and examined under the microscope.

In each village which had children with geohelminth infection, two water samples were also collected from the river at the areas where the children reportedly always played or bathed or washed clothes. In the laboratory, the water sample was transferred to 15 mL screw-lid centrifuge tubes and centrifuged at 1500–2000 rpm for 5–10 minutes. The supernatant fluid was carefully decanted till 0.5 mL was left. The sediment was resuspended in the remaining supernatant before emptying it onto a glass slide and examined under the microscope for presence of geohelminth eggs.

Statistical analyses

The relationship between various variables related to socio-economic factors and geohelminthiasis was examined with Pearson’s χ2 test (SPSS version 22, Chicago, IL, USA) to identify the potential risk factors. This was followed by logistic regression to determine the odds ratios (OR) and 95% confidence interval (CI) (z = 1.96).

The geohelminthiasis infection data was further analyzed for clustering effect with the R package “Cluster Bootstrap” (https://github.com/mathijsdeen/ClusterBootstrap) [19] using R version 3.5.2 [20]. This package fits a generalized linear model (GLM) with cluster bootstrapping for analysis of clustered data. This was done separately for the number of children infected with (a) geohelminthiasis, and (b) ascariasis as a function of the various measured variables. Each village was considered as a cluster, while income, mother’s education, availability of proper sanitation facility, household income, general hygiene etc, were treated as fixed factors. In each run, 5,000 bootstrap replicates were used. Clustering effect of infection within families was also similarly investigated by considering each family as a cluster and running GLM with 5,000 cluster bootstrap replicates.

Results

Demographic data

Fresh stool samples were collected from a total of 407 children (201 f and 206 m) aged between 6 months -17 years of age from 238 households. The response rate was 81% (407/500) and non-response reasons included constipation, having gone to the toilet the previous night or having lost the collection bottle.

There were 15 participants who were less than one year old, while the 4–6 and 7–12 year-olds formed the largest groups (26.5 and 41.3% respectively) (Table 2). The sex-ratio was about equal. About 83.8% of the respondent’s mothers were housewives with no education (27.8%), primary (32.7%) or secondary education (36.6%), while only 8 had attended college/university. More than half (57%, 232/407) had monthly household income of less than US$119 (RM500, $1 = RM4.20) and 65.1% (265/407) stayed in one-storey stilted wooden house. Only 15% (45/407) had treated water where as the rest used untreated water from sources such as gravity-feed, dug well, river or rainwater. Most of the respondents (74.9%) still used pour flush toilets. Overall only about half of the children (49.9%) were reported to habitually wash their hands with soap. More children claimed they did not go barefoot (59.4%), did not wash their feet (77.2%), and did not trim their nails regularly (77.6%). However, more children had taken deworming medicine at least once (62.7%).

Table 2. Socio-demographic data of participants in this study.

Total respondents = 407.

Parameter classes N (%)
Age 6–11 months 15 (3.7)
1–3 years old 83 (20.4)
4–6 years old 108 (26.5)
7–12 years old 168 (41.3)
13–17 years old 33 (8.1)
Gender Female 201 (49.4)
Male 206 (50.6)
Mother’s Level of Education None 113 (27.8)
Pre-school 4 (1.0)
Primary 133 (32.7)
Secondary 149 (36.6)
College/University 8 (1.9)
Monthly Household Income Less than USD 119 232 (57.0)
More than USD 119 175 (43)
People per household Less than 5 people 82 (20.1)
More than 5 people 325 (79.9)
Type of House One-storey house with stilt 265 (65.1)
One-storey house on the ground 104 (25.6)
Long house 3 (0.7)
Double-storey house 35 (8.6)
Source of water Untreated water 362 (88.9)
Treated water 45 (11.1)
Types of Toilet No toilet 39 (9.6)
Flush toilets 41 (10.1)
Pour flush toilets 305 (74.9)
Pit Latrine 22 (5.4)
Wash hands with Soap before eating No 204 (50.1)
Yes 203 (49.9)
Barefooted Yes 158 (40.6)
No 231 (59.4)
Washing of Feet No 312 (77.2)
Yes 92 (22.8)
Trimming of Nails Yes 90 (22.4)
No 311 (77.6)
Deworming No or not sure 152 (37.3)
Yes 255 (62.7)
With domestic animals Dogs 262 (64.6%)
Cats 222 (54.5%)
Poultry 187 (45.9%)
Pigs 16 (3.9%)
Cattles 14 (3.4%)
Goats 12 (2.9%)

Prevalence of geohelminthiasis

The FEC method gave a higher estimate of geohelminthiasis than direct wet faecal mount (14.3% compared to 10.6%) (Table 3). Overall, 9.6% of the sampled children had ascariasis, while 2.7% had either hookworm or Trichuris infection. Ascaris lumbricoides was the most common geohelminth detected in the infected children at 67.2% (or 62.1% for single-species infection), followed by hookworm (18.9%) and Trichuris trichiura (18.9%).

Table 3. Prevalence of geohelminthiasis among the children in Kota Marudu.

Presence of geohelminths was detected by direct wet mount and formalin-ether concentration methods. Sample size = 407.

Method % of sampled children
Direct Wet Mount Formalin-Ether Concentration
Negative samples 364 (89.4%) 349 (85.7%)
Positive samples 43 (10.6%) 58 (14.3%)
Among the positive samples
Ascaris lumbricoides 31(72.1%) 36(62.1%)
Hookworm 7(16.3%) 10(17.2%)
Trichuris trichiura 4(9.3%) 9(15.5%)
Ascaris + hookworm 1(2.3%) 1(1.7%)
Ascaris + Trichuris 0 2(3.4%)
Total infected with*
Ascaris 32 (74.4%) 39 (67.2%) 9.6%
hookworm 8 (18.6%) 11(18.9%) 2.7%
Trichuris 4 (9.3%) 11(18.9%) 2.7%

* including multispecies infection

The mean infection rate among the children per village was 9.0% (0%-34.9%) or 16.8% (n = 7) considering only the villages with infected children. High prevalence of geohelminthiasis was detected in three villages, namely Kg. Kinangkaban (34.9%), Kg. Gana (25.4%) and Kg. Bintasan Darat (17.4%) (Table 4). However, geohelminthiasis was not detected in six villages. A total of 54% (7/13) of villages had children infected with worm infection. Overall, the mean rate of infection of the children per village was 38.5% for Ascaris, 38.5% for hookworms and 30.8% for Trichuris. In Kg. Kinangkaban, 21/22 infections were ascariasis. Out of 238 households sampled, 43 (18%) had children with geohelminthiasis. The mean percentage of households with infected children in a village was 10.9±8.6%. (Table 5).

Table 4. Prevalence of geohelminthiasis in each village in Kota Marudu.

Villages Popula-tion No. samples No. Samples with eggs of total (%)
Ascaris Hookworm Trichuris
Kg. Bintasan Darat 214 46 4 3 1 8 (17.4%)
Kg. Bintasan Tengah 288 30 - - - 0
Kg. Minansad 265 13 - - - 0
Kg. Boluot 115 17 - 3 - 3 (17.6%)
Kg. Mangin 1 299 35 1 3 - 3* (8.6%)
Kg. Mangin 2 318 23 - - - 0
Kg. Korongkom 650 25 2 - - 2 (8.0%)
Kg. Liabas 618 35 - - 2 2 (5.7%)
Kg. Bombong 1 443 11 - - - 0
Kg. Gana 361 71 11 1 7 18* (25.4%)
Kg. Kinangkaban 410 63 21 1 1 22* (34.9%)
Kg. Patiu 231 23 - - - 0
Kg. Sorinsim 158 15 - - - 0
% village with geohelminth detected 38.5% 38.5% 30.8% Mean/village9.0% (n = 13)
16.8% (n = 7)

* denotes multiple infection by more than one species of geohelminth

Table 5. Geohelminthiasis prevalence among the children within each household.

Village total households sampled Households with 1 child Households with ≥2 children Total households with Infected children % of households with infected children
number Infected number 1 child infected ≥2 infected Total infected
Kg Bombong 1 10 9 0 1 0 0 0 0 0.0
Kg Bintasan Darat 25 8 1 17 4 1 5 6 24.0
Kg Boluot 7 1 0 6 1 0 1 1 14.3
Bintasan Tengah 16 7 0 9 0 0 0 0 0.0
Kg Gana 37 13 3 24 11 2 3 16 43.2
Kg Korongkom 14 6 0 8 0 1 1 1 7.1
Kg Kinangkaban 41 21 4* 20 6* 6* 12 16 39.0
Kg Liabas 19 11 0 8 1 0 1 1 5.3
Kg Mangin 1 23 14 0 9 1 1 2 2 8.7
Kg Mangin 2 16 10 0 6 0 0 0 0 0.0
Kg Minansad 6 1 0 5 0 0 0 0 0.0
Kg Sorinsim 9 4 0 5 0 0 0 0 0.0
Kg Patiu 15 7 0 8 0 0 0 0 0.0
total 238 112 8 126 14 11 25 43 10.9±8.6

* all children were infected with Ascaris

Of the 126 households which had ≥2 children per household, infection of ≥2 children in the same household was observed only in Kg Kanangaban which had six households (6/12) with more than one child infected with Ascaris (Table 5).

Association analysis for risk factors

Using univariate analysis, the following factors: age (odds ratio, OR = 0.586) gender (OR = 0.745), the number of people in the household (OR = 1.812), type of house (OR = 1.316), burning of household waste (OR = 1.115), not trimming nails (OR = 1.281), keeping domestic animals in the house, and deworming (OR = 1.121) were not risk factors of geohelminthiasis (Table 6).

Table 6. Association analysis of factors with geohelminthiasis (univariate analysis).

Data based on 407 children in 13 rural villages in Kota Marudu). Missing data were omitted from the analysis.

Factors N (%) Positive samples Prevalence (%) X2 value (p-value) Odds ratio (95% CI)
Age group
12 years and below 374 (91.9%) 51 13.6 1.424 0.586
13 years and above 33 (8.1%) 7 21.2 (0.233) (0.242–1.421)
Gender
Male 206 (50.6%) 33 16.0 1.068 0.745
Female 201 (49.4%) 25 12.4 (0.301) (0.425–1.304)
Mother’s Education
None 113 (27.8%) 45 22.1 8.546 2.317
Yes 294 (72.2%) 13 11.2 (0.003)* (1.315–4.113)
Monthly household income
< RM500 (<USD119) 232 (57.0%) 50 21.6 23.537 5.735
> RM500 175 (43.0%) 8 4.6 (<0.001)* (2.641–12.452)
People per household
< 5 people 82 (20.1%) 17 20.7 3.530 1.812
> 5 people 325 (79.9) 41 12.6 (0.06) (0.968–3.389)
Type of House
One-storey house with stilt 372 (91.4%) 54 14.5 0.250 1.316
Others 35 (8.6%) 4 11.4 (0.617) (0.447–3.877)
Source of Water
Untreated water 362 (88.9%) 56 15.5 3.981 3.935
Treated water 45 (11.1%) 2 4.4 (0.046)* (0.927–16.709)
Proper sanitation facility
None 39 (9.6%) 18 46.2 35.927 7.029
Yes 368 (82%) 40 10.8 (<0.001)* (3.456–14.296)
Household Waste
Burning 309 (75.9%) 45 14.6 0.103 1.115
Not burning 98 (24.1%) 13 13.3 (0.749) (0.574–2.165)
Wash hands with Soap before meals
No 204 (50.1%) 36 17.6 3.861 1.763
Yes 203 (49.9%) 22 10.8 (0.049)* (0.997–3.119)
Barefooted
Yes 158 (40.6%) 35 22.2 11.964 2.703
No 231 (59.4%) 22 9.5 (0.001)* (1.517–4.818)
Washing of Feet
No 312 (77.2%) 51 16.3 5.659 2.801
Yes 92 (22.8%) 6 6.5 (0.017)* (1.161–6.754)
Trimming of Nails
Yes 90 (22.4%) 15 16.7 0.572 1.281
No 311 (77.6%) 42 13.5 (0.449) (0.674–2.436)
Deworming status
No or Not sure 152 (37.3%) 23 15.1 0.154 1.121
Yes 255 (62.7%) 35 13.7 (0.695) (0.634–1.980)

* p-value < 0.05

The following factors were found significantly associated with geohelminth infections: mother’s lack of education (22.1% vs 11.2% infection for mothers with at least kindergarten education, p = 0.003) (Table 6), monthly household income of <USD119 (<RM500) (21.5% vs 4.6% infection for >USD119, <0.001), using untreated water (15.5% vs 4.4%, p = 0.046), lack of proper sanitation facilities (46.2% vs 10.9%, p = <0.001), not washing hands with soap before meals (17.6% vs 10.8%, p = 0.049), going barefoot outside the house (22.2% vs 9.5%, p = 0.001), and not washing feet before entering the house (16.3% vs 6.5%, p = 0.017). Additionally, children walking barefooted was a significant factor of hookworm infection (X2 = 4.84, df = 1, p = 0.028).

Similarly logistic regression analysis indicated the following risk factors of geohelminthiasis: mothers lacking education (OR = 0.445, p = 0.006); household income of less than USD119 (OR = 0.174, p<0.0001); lack of proper sanitation facilities (OR = 0.142, p<0.0001); children who go barefoot (OR = 0.370, p = 0.001) and children not washing the feet (OR = 0.357, p = 0.022) (Table 7).

Table 7. Logistic regression analysis of risk factors associated with geohelminth infections among the children of 13 villages in Kota Marudu.

Factor Odds ratio (OR) 95% CI P-value
Mother’s lack of education 0.445 0.251–0.789 0.006**
Household income of less than RM500 0.174 0.080–0.379 0.000***
Using of untreated water as water source 0.254 0.060–1.079 0.0063
Do no wash hands with soap before meals 0.567 0.321–1.003 0.051
Availability of sanitation facilities 0.142 0.070–0.289 0.000***
Children who were barefooted 0.370 0.208–0.659 0.001**
Not washing the feet 0.357 0.148–0.861 0.022*

* p-value < 0.05;

**p-value < 0.01;

*** p-value < 0.001

Analysis of clustering of infection

Analysis using generalized linear model with cluster bootstrapping was done to see if there was clustering effect at the village level, since only Kg Gana and Kg Kinangkaban had high infection rate. However, bootstrapping was not possible with two variables, viz. treated water source (ie piped water) versus untreated (rainfall, well, river) for both drinking and for other uses. This is because only two children from the two villages with treated water supply (all households in Kg Korongkom and 6/14 in Kg Bintasan Tengah) had geohelminth infection. This results in a lack of variation in the outcome variable and no contrast was possible in the GLM run. Similarly, bootstrapping with sanitation facility was not possible as only 2/4 villages (Kg Bintasan Darat and Kg Kinangkaban) without sanitation facility had recorded geohelminth infection among the children (S1 Table).

Adjusting for the effect of infection clusters in the villages, only household income (≥USD119) had almost a significant impact on reducing total geohelminth infection (three species combined) (Table 8). The other factors (eg mother’s education level, deworming, proper sanitation facility) had some positive but non-significant effect only. Adjusting for family clustering, GLM analysis bootstrapping indicated proper sanitation facility has a significant positive effect on reducing Ascaris infection (P<0.05), but not for total worm infection (Table 9).

Table 8. Analysis using generalized linear model with villages considered as clusters of geohelminthiasis.

Bootstrapping with 5000 replicates was performed. The parameter “proper sanitation” had been omitted since it has only one level in some villages.

Parameter Estimate SE z
Infection with Ascaris
Intercept -1.5428 1.1578
Mother’s education level (none vs at least kindergarten) -0.4160 0.3043 -1.3672
Household income (<RM 500/USD119 vs more) -3.2462 4.4375 -0.7315
Use of soap in washing hands -0.0841 0.6547 -0.1285
Washing feet before entering house (not washing vs washing) -1.6849 4.0613 -0.4149
Deworming vs none 0.1062 0.8632 0.1230
Infection with all species
Intercept -0.9129 0.6613
Mother’s education level (none vs at least kindergarten) -0.1964 0.4390 -0.4473
Household income (<RM 500/USD119 vs more) -1.7810 0.9105 -1.9561
Use of soap in washing hands -0.5044 0.3467 -1.4552
Washing feet before entering house (not washing vs washing) -1.2990 2.4698 -0.5260
Keeping of domestic animals vs none 0.0278 0.5678 0.0489
Deworming vs none -0.1964 0.4390 -0.4473

Table 9. Analysis of factors of ascariasis using generalized linear model with families considered as clusters of geohelminthiasis.

Bootstrapping with 5000 replicates was performed.

Parameter Estimate SE z
Infection with Ascaris
Intercept 2.6369 1.6622
Mother’s education level (none vs at least kindergarten) -1.0310 1.1693 -0.8817
Household income (<RM 500/USD119 vs more) -7.5320 7.8494 -0.9595
Use of soap in washing hands -1.2254 1.2488 -0.9813
Washing feet before entering house (not washing vs washing) -0.6683 2.7825 -0.2402
Deworming vs none -0.7647 0.6812 -1.1226
Proper sanitation facility vs none -3.5419 1.7360 -2.0403*

* p < 0.05

Analysis of soil and water samples

Almost all the soil samples collected (36/40) from the house compounds had loamy texture (definition of Zenner et al. [21]). Geohelminths were detected in the soil samples of 14 houses (35%), 12 of which had hookworm eggs, one sample had Ascaris eggs, and another had both hookworm and Trichuris eggs (Table 10). Ascaris eggs were found in the soil sample of a household in Kg. Kinangkaban whose child was also infected with A. lumbricoides (KK09). Similarly, Trichuris eggs were found in the soil sample taken from the house (GN47) which had the child infected with Trichuris in Kg. Gana. All the soil samples positive with STH eggs were of loamy texture.

Table 10. Detection of geohelminth stages from soil samples.

Samples were taken from the compound of 40 households whose children’s faecal samples had tested positive for worms.

Village Houses Ascaris eggs Hookworm eggs Trichuris eggs
Kg. Bintasan Darat 5 0 2 0
Kg. Boluot 1 0 0 0
Kg. Gana 14 0 7* 1
Kg. Korongkom 1 0 0 0
Kg. Kinangkaban 15 1 2 0
Kg. Liabas 2 0 2 0
Kg. Mangin 1 2 0 0 0
Total 40 1 13 1

* indicates a soil sample from one household (GN47) had both hookworm and Trichuris eggs

In the analysis of water samples taken from the villages where worm-infected children were recorded, none of the samples was positive with any of the helminth eggs although unidentified larvae and algae were observed under the microscope.

Analysis of geohelminth infection with altitude and distance of village from the main town

The percentage geohelminth infection increased, but not significantly, with both the distance from the main town (Kota Marudu), and the altitude of the village (see S1 Fig).

Discussion

This is the first study on the prevalence rate of geohelminthiasis available in Kota Marudu, a fast-developing town. Our results show that geohelminth infections are still prevalent at 54% of the villages studied, 18% of the households sampled and 14.3% of the children examined. Proportion of ascariasis among the infected children was 67.2%, hookworm 18.9% and Trichuris trichiura 18.9%.

The risk factors are maternal lack of education, low household income (<USD119), lack of proper sanitation facility, not wearing footwear, washing feet, and washing hands before meals. The factors which were found not affecting geohelminthiasis are age, gender, the number of people in the household, type of house, burning of household waste, untrimmed nails and deworming.

The geohelminthiasis prevalence recorded (14.3%) was almost similar to a previous study in 2003 among the communities in the fringes of the Crocker Range Park, Sabah at 14.7% [14] which is about 144 km away by road. This seems to indicate that the prevalence has not changed much over the years. Our research recorded prevalence rates among the children for Ascaris, Trichuris and hookworm of 9.6%, 2.7% and 2.7% compared to 8.7%, 10% and 3.3% for all age groups (up to >31 years old) [14]. In West Malaysia, the prevalence reported for aboriginal children of Pos Sungai Rual, Kelantan was much higher at 40.5%, 65.8% and 25.8% respectively [22]. The Sabah prevalence rates are comparable to those recorded in neighbouring Sarawak in two studies on children with the respective rates of 7–12.8%, 28.4% and 7.2% [23, 24] The prevalence of Trichuris in Kota Marudu villages appears to be lower compared to the other Malaysian study sites, but we are unable to ascertain why.

Taking clustering effect at the village level, GLM analysis indicated low income of ≤RM500 (USD119) is an important factor of Ascaris infection, whereas at the family level, lack of sanitation facilities is a significant risk factor.

Some maternal formal education was shown to be a positive factor. This is in concordance with the findings by other workers. In Sri Lanka, poor maternal education was identified as a risk factor for infection [25], and in Bihar, India the mother’s literacy was found significantly associated with geohelminth infections [26]. Low literacy has somehow affected the level of hygiene practiced in a household and has also resulted in low household income and related health problems. Furthermore, we showed that, considering the clustering effect at the village level, receiving some education does have some positive effect. Among the households where mothers had no formal education, washing hands with soap appears to be more important: 18/66 (38%) of children who did not wash their hands with soap were infected compared to 7/47 (18%) of those who used soap.

Higher income (>USD 119) has a positive effect on reducing geohelminthiasis, and has clustering effect at the village level. Low household income was found to be negatively associated with geohelminthiasis in another study among the indigenous children (Orang Asli) in Lipis, Pahang, West Malaysia [27]. Low income may result in reluctance to build proper sanitation facilities, and defecation in the open space, bushes, field or jungle is commonly practiced in poor villages, which could cause many environmental and health problems. This could partly explain the prevalence of STH in these villages where hygiene is poor, lacking sanitation facilities and treated water.

Geohelminthiasis is mostly transmitted when faeces containing eggs are deposited into the environment especially through open defecation, and ingested (eg. Ascaris) or transmitted across the skin boundary (eg hookworm) [2830]. Our results indicate 35% of the soil samples taken from the houses with infected children had geohelminth eggs, especially hookworm. Higher percentages were recorded in an indigenous village in west Malaysia, namely 90% of 40 soil samples tested positive for A. lumbricoides and 15% were positive for T. trichiura [31]. Contaminated soil in these villages is a risk factor in geohelminthiasis, as evident from our results that the children going barefoot outside the house and not washing feet before entering the house were both significantly associated with geohelminth infections, especially hookworm infection (p = 0.028). Similarly, villagers in Thailand, including children walking barefoot was also a significant factor of hookworm infection [32]. Regular deworming with benzimidazole anthelmintic drugs in school-age children has been shown to reduce and maintain the worm burden below the threshold associated with disease [33]. However, we are not able to establish deworming as a positive risk factor in our study (OR = 1.121, p>0.05), probably because the deworming was inconsistent and not all the children were taking deworming medicine. Although the Ministry of Health offers free deworming services, only 68% of the villagers confirmed their children had taken the deworming medicine at least once, sometime in the past, while some parents could not recall if their child had taken any. The questionnaire results also revealed that only l219/407 (54%) of the children took deworming medicine on the advice of the doctor. Nevertheless, the importance of deworming cannot be discounted.

The geohelminthiasis prevalence is a public health concern among the indigenous children of Kota Marudu. Studies have shown that in children with geohelminth infections psychological and physical development were delayed, and adversely affecting their ability to participate in life at school and at home. Such delays limit their ability to take full advantage of what is often their only opportunity for formal education and may limit their social functioning later in life [4].

In conclusion, this study clearly shows that geohelminthiasis still occurs with an overall prevalence of 14.3% among children of rural communities of Kota Marudu in Sabah. Infection by Ascaris had the highest rate at 67% compared to hookworm or T. trichiura. The most practical means of controlling geohelminthiasis in these communities would be expanding mass deworming programmes for school-age children, improving sanitation and water supplies, upgrading the socio-economic status and continually conducting health education programmes. The data on the prevalence of geohelminthiasis in this study would contribute to better public health monitoring and operation to reduce the infection in rural areas.

Supporting information

S1 Questinnaire. Sample pages of the questionnaire used in the study.

(PDF)

S1 Table. Distribution of geohelminth-infected children in the villages among the households with or without basic sanitation facilities.

(PDF)

S1 Fig. Regression of percentage geohelminthiasis among the children against (a) distance (km) of village from the main town (Kota Marudu), and (b) altitude of village (metres above sea level).

(TIF)

Acknowledgments

The authors wish to acknowledge the cooperation and support from the village heads and communities of Kota Marudu for assisting in conducting this research successfully. The authors would also like to thank Universiti Malaysia Sabah for the research facilities, and the Director, Science Officer, Senior Medical Laboratory Technologists and Medical Laboratory Technologists and staff of Kota Marudu Hospital for granting access to their laboratory and facilities.

Data Availability

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

Funding Statement

ALL was partly supported by United States Agency for International Development (USAID) Infectious Disease Emergence and Economics of Altered Landscapes: (IDEEAL) project, (Cooperative Agreement number AID-486-A-13-00005), and partly supported by Malaysian Ministry of Education research grant GSP001 awarded to THC. There was no additional external funding received for this study.

References

  • 1.Pullan RL, Smith JL, Jasrasaria R, Brooker SJ (2014) Global numbers of infection and disease burden of soil transmitted helminth infections in 2010. Parasites & Vectors 7: 37 10.1186/1756-3305-7-37 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Stephenson LS, Latham MC, Ottesen EA (2000) Malnutrition and parasitic helminth infections. Parasitology 121: S23–S38. 10.1017/s0031182000006491 [DOI] [PubMed] [Google Scholar]
  • 3.Hotez PJ, Bundy DAP, Beegle K, Brooker S, Drake L, et al. (2006) Helminth Infections: Soil-transmitted Helminth Infections and Schistosomiasis In: Jamison DT, Breman JG, Measham AR, Alleyne G, Claeson M et al. , editors. Disease Control Priorities in Developing Countries. Washington (DC): World Bank, The International Bank for Reconstruction and Development/The World Bank Group. [Google Scholar]
  • 4.Drake LJ, Jukes MCH, Sternberg RJ, Bundy DAP (2000) Geohelminth infections (ascariasis, trichuriasis, and hookworm): Cognitive and developmental impacts. Seminars in Pediatric Infectious Diseases 11: 245–251. 10.1053/spid.2000.9638 [DOI] [Google Scholar]
  • 5.Hotez PJ, Brooker S, Bethony JM, Bottazzi ME, Loukas A, et al. (2004) Hookworm Infection. New England Journal of Medicine 351: 799–807. 10.1056/NEJMra032492 [DOI] [PubMed] [Google Scholar]
  • 6.WHO Expert Committee on the Control of Schistosomiasis (2001: Geneva SWHO (2002) Prevention and control of schistosomiasis and soil-transmitted helminthiasis: report of a WHO expert committee.
  • 7.Bethony J, Brooker S, Albonico M, Geiger SM, Loukas A, et al. (2006) Soil-transmitted helminth infections: ascariasis, trichuriasis, and hookworm. [DOI] [PubMed] [Google Scholar]
  • 8.Norhayati M, Fatmah MS, Yusof S, Edariah AB (2003) Intestinal parasitic infections in man: a review. Med J Malaysia 58: 296–305. [PubMed] [Google Scholar]
  • 9.Nisha M, Kumarasamy V, Ambu S, Davamani F, Mak JW (2016) Factors Associated with Intestinal Parasite Infections in a Resettled Indigenous Community in Malaysia. 1–7 p. 10.9734/IJTDH/2016/21902 [DOI] [Google Scholar]
  • 10.Wong WK, Foo PC, Roze MN, Pim CD, Subramaniam P, et al. (2016) Helminthic Infection and Nutritional Studies among Orang Asli Children in Sekolah Kebangsaan Pos Legap, Perak. Can J Infect Dis Med Microbiol 2016: 1326085 10.1155/2016/1326085 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Rahmah N, Ariff RH, Abdullah B, Shariman MS, Nazli MZ, et al. (1997) Parasitic infections among aborigine children at Post Brooke, Kelantan, Malaysia. Med J Malaysia 52: 412–415. [PubMed] [Google Scholar]
  • 12.Sinniah B, Hassan AK, Sabaridah I, Soe MM, Ibrahim Z, et al. (2014) Prevalence of intestinal parasitic infections among communities living in different habitats and its comparison with one hundred and one studies conducted over the past 42 years (1970 to 2013) in Malaysia. Trop Biomed 31: 190–206. [PubMed] [Google Scholar]
  • 13.Kan SP, Yap SB, Yap PL (1987) Intestinal parasitism among Penan children of the Upper Baram, Sarawak. Asia Pacific Journal of Public Health / Asia-Pacific Academic Consortium for Public Health 1: 38–41. [DOI] [PubMed] [Google Scholar]
  • 14.Nor Aza A, Ashley S, Albert J (2003) Parasitic Infection in Human Communities living on the fringes of the Crocker Range Park Sabah, Malaysia. ASEAN Review of Biodiversity and Environmental Conservation (ARBEC). [Google Scholar]
  • 15.World Health Organization (2003) Manual of basic techniques for a health laboratory. 2nd ed Geneva: World Health Organization; 384 p. [Google Scholar]
  • 16.Phuphisut O, Yoonuan T, Sanguankiat S, Chaisiri K, Maipanich W, et al. (2014) Triplex polymerase chain reaction assay for detection of major soil-transmitted helminths, Ascaris lumbricoides, Trichuris trichiura, Necator americanus, in fecal samples. 267–275 p. [PubMed] [Google Scholar]
  • 17.Basuni M, Muhi J, Othman N, Verweij JJ, Ahmad M, et al. (2011) A pentaplex real-time polymerase chain reaction assay for detection of four species of soil-transmitted helminths. The American journal of tropical medicine and hygiene 84: 338–343. 10.4269/ajtmh.2011.10-0499 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Zenner l, Gounel JM, Chauve CM (2002) A standardized method for detecting parasite eggs and oocysts in soils. Revue Méd Vét 153: 729–734. [Google Scholar]
  • 19.Deen M, de Rooij M (2019) ClusterBootstrap: An R package for the analysis of hierarchical data using generalized linear models with the cluster bootstrap. Behavior Research Methods. 10.3758/s13428-019-01252-y [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.R Core Team (2003) R: A language and environment for statistical computing. Vienna: R Foundation for Statistical Computing. [Google Scholar]
  • 21.Lesikar B (2005) On-Site Wastewater Treatment Systems: Soil Particle Analysis Procedure. [Google Scholar]
  • 22.Hartini Y, Geishamimi G, Mariam AZ, Mohamed-Kamel AG, Hidayatul FO, et al. (2013) Distribution of intestinal parasitic infections amongst aborigine children at Post Sungai Rual, Kelantan, Malaysia. Tropical Biomedicine 30(4): 596–601. [PubMed] [Google Scholar]
  • 23.Sagin DD, Mohamed M, Ismail G, Jok JJ, Lim LH, et al. (2002) Intestinal parasitic infection among five interior communities at upper Rejang River, Sarawak, Malaysia. The Southeast Asian Journal of Tropical Medicine and Public Health 33: 18–22. [PubMed] [Google Scholar]
  • 24.Lee DL, Lee S, Chang MS, Paon AJ, Katip JT (1999) Intestinal helminth infections amongst school children in the Serian District of Sarawak. 96–101 p. [PubMed] [Google Scholar]
  • 25.Gunawardena K, Kumarendran B, Ebenezer R, Gunasingha MS, Pathmeswaran A, et al. (2011) Soil-Transmitted Helminth Infections among Plantation Sector Schoolchildren in Sri Lanka: Prevalence after Ten Years of Preventive Chemotherapy. PLoS Negl Trop Dis 5: e1341 10.1371/journal.pntd.0001341 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Greenland K, Dixon R, Khan SA, Gunawardena K, Kihara JH, et al. (2015) The Epidemiology of Soil-Transmitted Helminths in Bihar State, India. PLOS Neglected Tropical Diseases 9: e0003790 10.1371/journal.pntd.0003790 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Nasr N, Al-Mekhlafi H, Ahmed A, Roslan M, Bulgiba A (2013) Towards an effective control programme of soil-transmitted helminth infections among Orang Asli in rural Malaysia. Part 2: Knowledge, attitude, and practices. 28 p. 10.1186/1756-3305-6-28 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.de Silva NR, Brooker S, Hotez PJ, Montresor A, Engels D, et al. (2003) Soil-transmitted helminth infections: updating the global picture. Trends in Parasitology 19: 547–551. 10.1016/j.pt.2003.10.002 [DOI] [PubMed] [Google Scholar]
  • 29.Ogbaini-Emovon E, Eigbedion A, Chiedozie O, Kalu E (2014) Prevalence and impact of socio-economic/environmental factors on soil-transmitted helminths infection in children attending clinic in a tertiary hospital in Benin City, Nigeria. 65–70 p. [Google Scholar]
  • 30.Majorin F, Freeman MC, Barnard S, Routray P, Boisson S, et al. (2014) Child Feces Disposal Practices in Rural Orissa: A Cross Sectional Study. PLOS ONE 9: e89551 10.1371/journal.pone.0089551 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Nisha M, Amira NA, Nadiah N, Davamani F (2019) Detection of Ascaris lumbricoides and Trichuris trichiura in various soil types from from an indigenous village in Malaysia. Tropical Biomedicine 36: 201–208 [PubMed] [Google Scholar]
  • 32.Jiraanankul V, Aphijirawat W, Mungthin M, Khositnithikul R, Rangsin R, et al. (2011) Incidence and Risk Factors of Hookworm Infection in a Rural Community of Central Thailand. The American Journal of Tropical Medicine and Hygiene 84: 594–598. 10.4269/ajtmh.2011.10-0189 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Savioli L, Stansfield S, Bundy DAP, Mitchell A, Bhatia R, et al. (2002) Schistosomiasis and soil-transmitted helminth infections: forging control efforts. Trans R Soc Trop Med Hyg 96: 577–579. 10.1016/s0035-9203(02)90316-0 [DOI] [PMC free article] [PubMed] [Google Scholar]

Decision Letter 0

Arun K Yadav

23 Jul 2020

PONE-D-20-17984

Prevalence and risk factors of geohelminthiasis among the rural village children in Kota Marudu, Sabah, Malaysia

PLOS ONE

Dear Dr. Chua,

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

Please submit your revised manuscript by Sep 06 2020 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

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). You should upload this letter as a separate file labeled 'Response to Reviewers'.

  • A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'.

  • An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'.

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

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

We look forward to receiving your revised manuscript.

Kind regards,

Arun K Yadav, Ph.D.

Academic Editor

PLOS ONE

Journal Requirements:

When submitting your revision, we need you to address these additional requirements.

1. 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

https://journals.plos.org/plosone/s/file?id=wjVg/PLOSOne_formatting_sample_main_body.pdf and

https://journals.plos.org/plosone/s/file?id=ba62/PLOSOne_formatting_sample_title_authors_affiliations.pdf

Additional Editor Comments (if provided):

Thank you for submission of your manuscript. I have seriously gone through the reviewed article and could see that the reviewers have given a number of useful suggestions on your article. Kindly consider the raised points, which I think are truly worthy of consideration and can remarkably improve your manuscript. In particular, please look into the following suggestions very carefully:

- Please see that the criterion for selection of study area and sample size is very clear and is also appropriately justified in the light of reviewers' comments.

- Also please ensure that the introduction and discussion section of draft is not much generalized, instead focused, with proper highlights of major innovative findings of study.

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

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: Yes

Reviewer #2: Yes

**********

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

Reviewer #1: Yes

Reviewer #2: Yes

**********

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

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

Reviewer #1: Yes

Reviewer #2: Yes

**********

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

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

Reviewer #1: Yes

Reviewer #2: Yes

**********

5. Review Comments to the Author

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

Reviewer #1: General observations:

The authors present a cross section of data on the prevalence and risk factors for STH in children from 13 rural villages of a district in Sabah, Malaysia. This information will be useful for implementing strategies for the control and prevention of STH in this population.

Specific comments:

1. Abstract, Author Summary and text:

‘Mean infection rate’ should be changed to ‘mean prevalence of infection’ - this study has determined only point prevalence of STH infection; infection rate refers to new infections over a period of time.

Lines 27 – 30 in Abstract: include P values for the significant variables.

2. Introduction: provide references for the poor outcomes mentioned with hookworm disease and pregnancy (lines 68-70).

Line 71: Trichuris trichiura (or T. trichiura) – better to provide the entire scientific name when referring to the worms.

3. Materials and Methods: Line 99 refers to the 13 villages selected for the study out of 138 based on certain criteria. Were these 13 villages the only ones which fulfilled these criteria? Or were there others and only these 13 were selected? If so, how was the selection done?

Examination of faecal samples (lines 150-151) – what was the time duration between sample collection and examination of the direct wet mount done at the district hospital?

What was the reason for doing molecular testing for the positive samples? Shouldn’t the negative ones have been tested instead? That would have provided more accurate data on the prevalence of infection as PCR is more sensitive than the other two methods used. Furthermore, formalin preservation is known to fragment DNA with time and not usually used if PCR is being considered. So how can the authors ensure that the extracted DNA was of good quality? In addition, no information regarding the PCR test results have been mentioned in the text. My suggestion is to either entirely omit the mention of molecular testing as it doesn’t appear to add value to this manuscript in its current state or include the relevant data obtained through PCR testing and discuss their limitations.

Line 196 mentions collection of soil samples from 40 households which were selected randomly from among the positive children. Table 5 shows the total number of infected households as 25. Please state clearly the basis for collection of the soil samples.

4. Results: Lines 243-245 have discrepancies in either (or both) the percentages and/or the numbers mentioned which need to be corrected – Eg. 57%, 118/507 – according to Table 2 it should be 232/407; similarly, 265/507 should be 265/407; and 15% (161/507) should be 11.1% (45/407).

Line 248 – states that more children go barefooted (59.4%) but Table 2 states differently.

Line 316 – X2 value has to be included

Line 358 – Table 10 heading should read as Hookworm eggs (unless larvae were also found)

5. Discussion:

Under introduction it is stated that globally Malaysia records one of the highest prevalence rates for Trichuris. It is also apparent from other studies done in the area. Do the authors have any explanations as to why the prevalence rate seen in this study is lower? Especially since both Ascaris and Trichuris have similar transmission routes and are known to be co-extensive.

Line 407 mentions that 35% of households sampled had geohelminth eggs or other stages in the soil – please state the other stages that were found as they are not mentioned in Table 10.

6. Grammar and typing errors:

Abstract:

Lines 19 & 31: delete ‘the’; Line 29: should be USD 119

Author Summary:

Line 41: delete ‘old’; Line 42: delete the second ‘the’ (children); Line 47: change to - USD, facilities. Line 48: replace ‘had’ with ‘were’, delete ‘been’; Line 50: programs; Line 51: sanitation facilities

Introduction: Line 57: delete ‘the’; Line 76: replace ‘has’ with ‘have’; Line 78: replace ‘had’ with ‘have’; Line 79; backgrounds; Line 89: change to ‘between the ages of 6-months to 17 years’ and delete ‘old’

Materials and Methods: Line 93: ‘carried out’; Line 94: replace ‘of’ with ‘and’; Line 97: modified ‘using’ a map; Line 102: geohelminthiasis; Line 136: ‘washing’ hands, ‘the toilet’; Line 162: ‘microtube’; Line 179: Kuala ‘Lumpur’; Line 182: DNA ‘sequence’ results; Line 183: ‘databases’; Line 187: ‘amplify’; Line 222: ‘Pearson’s’

Results: Line 243: 8 had ‘attended’ college/university; Line 258: ‘Socio-demographic’; Line 265: remove ‘only’; Line 275: should read as ‘villages had children infected with’ worm infection, also delete ‘children per’ and change village to ‘villages’; Line 276: ‘infections were’; Line 315: 6.5%’,’ and delete ‘villagers including’ and change to ‘barefooted’; Line 317: logistic regression ‘analysis’; Line 319: ‘facilities’; Line 351: Ascaris ‘eggs’; Line 352: Trichuris ‘eggs’, Ascaris ‘eggs were’; Lines 353 -354: should read as ‘Similarly, Trichuris eggs were’; Line 359: (GN47) ‘which’ had, Trichuris ‘eggs’; Line 364: replace ‘was’ with ‘were’

Discussion: Line 372: ‘show’; Line 376: facility,; Line 382: should read as ‘Our research recorded prevalence rates’; Line 386: delete first ‘the’ (children); Line 391: ‘concordance’; Line 397: ‘hands’; Line 398: ‘wash their hands’; Line 400: ‘geohelminthiasis’; Line 403: sanitation ‘facilities’; Line 408: delete ‘were’; Line 409: 15% were positive ‘for’ T. trichura; Line 419: delete ‘periodically’; Line 431: delete ‘”’; Line 432: ‘practiced by the villagers’; Line 433: delete first ‘the’; Line 439: replace ‘of’ with ‘to their’; Lines 439-440: ‘trained at a very young age on the use of the toilet and wearing footwear outside the house’

Acknowledgements: Line 449: replace ‘which’ with ‘wish’; Line 450: for assisting in ‘conducting’ this research successfully. delete ‘conducted’.

Reviewer #2: The authors have discussed the Prevalence and risk factors of geohelminthiasis among the rural village children in Kota Marudu, Sabah, Malaysia. Of the 13 villages surveyed, geohelminthiasis was found prevalent only in 7, while there was no infection reported among the subjects of 6 villages. Though the authors have carried out extensive statistical analyses of data, the sample size in the study seems rather small. The results obtained through this study appear to be a corroboration of earlier studies carried out elsewhere across the globe.

[Eg., Prevalence and risk factors of soil-transmitted helminthiasis ...

bmcpublichealth.biomedcentral.com › articles;

Prevalence & risk factors for soil transmitted helminth infection ...

www.ncbi.nlm.nih.gov › pmc › articles › PMC3994744;

Prevalence and risk factors associated with the presence of ...

www.ncbi.nlm.nih.gov › pmc › articles › PMC4554591;

Prevalence & risk factors for soil transmitted helminth ...

www.researchgate.net › publication › 260610263_Prevalence_risk_fact.;

Prevalence and risk factors associated with worm infestation ...

www.researchgate.net › publication › 4181077_Prevalence_and_risk_f...;

Geohelminth Infections and Nutritional Status of Preschool ...

www.hindawi.com › journals › scientifica;

Prevalence, Intensity of Soil-Transmitted Helminths, and ...

www.hindawi.com › journals › jtm;

The prevalence, intensities and risk factors associated with ...

onlinelibrary.wiley.com › doi › full;

prevalence and risk factors associated with worm infestation in ...

www.bioline.org.br › pdf- to name a few].

I wish the authors had highlighted the novel findings emerging from their study and avoided a lengthy textbook account in ‘Introduction’ and generalizations in ‘Discussion’.

**********

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.]

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

PLoS One. 2020 Sep 28;15(9):e0239680. doi: 10.1371/journal.pone.0239680.r002

Author response to Decision Letter 0


21 Aug 2020

Reviewer #1: General observations:

The authors present a cross section of data on the prevalence and risk factors for STH in children from 13 rural villages of a district in Sabah, Malaysia. This information will be useful for implementing strategies for the control and prevention of STH in this population.

Specific comments:

1. Abstract, Author Summary and text:

‘Mean infection rate’ should be changed to ‘mean prevalence of infection’ - this study has determined only point prevalence of STH infection; infection rate refers to new infections over a period of time.

This has been done

Lines 27 – 30 in Abstract: include P values for the significant variables.

Done

2. Introduction: provide references for the poor outcomes mentioned with hookworm disease and pregnancy (lines 68-70).

Done

Line 71: Trichuris trichiura (or T. trichiura) – better to provide the entire scientific name when referring to the worms.

done

3. Materials and Methods: Line 99 refers to the 13 villages selected for the study out of 138 based on certain criteria. Were these 13 villages the only ones which fulfilled these criteria? Or were there others and only these 13 were selected? If so, how was the selection done?

How many fit criteria?

This has been explained more clearly in the revised version (see lines 99-106 revised copy)

Examination of faecal samples (lines 150-151) – what was the time duration between sample collection and examination of the direct wet mount done at the district hospital?

Within same day.

What was the reason for doing molecular testing for the positive samples? Shouldn’t the negative ones have been tested instead? That would have provided more accurate data on the prevalence of infection as PCR is more sensitive than the other two methods used. Furthermore, formalin preservation is known to fragment DNA with time and not usually used if PCR is being considered. So how can the authors ensure that the extracted DNA was of good quality? In addition, no information regarding the PCR test results have been mentioned in the text. My suggestion is to either entirely omit the mention of molecular testing as it doesn’t appear to add value to this manuscript in its current state or include the relevant data obtained through PCR testing and discuss their limitations.

Thank you for pointing this out. You are right, the molecular results have not been fully shown here. I agree with you that it’s better to omit it. However I include the primers used in the id of eggs as information to interested readers.

Line 196 mentions collection of soil samples from 40 households which were selected randomly from among the positive children. Table 5 shows the total number of infected households as 25. Please state clearly the basis for collection of the soil samples.

Thank you for highlighting this. Table 5 has been relabelled and the error corrected. The number of infected children in households with >2 children should be “11” and not “1”. The total households with infected children was 43, while samples were taken from 40 houses. 3 houses were not suitable for sampling.

4. Results: Lines 243-245 have discrepancies in either (or both) the percentages and/or the numbers mentioned which need to be corrected – Eg. 57%, 118/507 – according to Table 2 it should be 232/407; similarly, 265/507 should be 265/407; and 15% (161/507) should be 11.1% (45/407).

Thank you for pointing out this. The errors have been corrected, along with other errors as well.

Line 248 – states that more children go barefooted (59.4%) but Table 2 states differently.

The error has been corrected.

Line 316 – X2 value has to be included

Done

Line 358 – Table 10 heading should read as Hookworm eggs (unless larvae were also found)

done

5. Discussion:

Under introduction it is stated that globally Malaysia records one of the highest prevalence rates for Trichuris. It is also apparent from other studies done in the area. Do the authors have any explanations as to why the prevalence rate seen in this study is lower? Especially since both Ascaris and Trichuris have similar transmission routes and are known to be co-extensive.

This is a very good point, but we don’t know the answer. A sentence has been added to state this.

Line 407 mentions that 35% of households sampled had geohelminth eggs or other stages in the soil – please state the other stages that were found as they are not mentioned in Table 10.

Only eggs were detected. This has been corrected

6. Grammar and typing errors:

All grammatical errors pointed out in the following sections have been corrected .

Abstract:

Lines 19 & 31: delete ‘the’; Line 29: should be USD 119

Author Summary:

Line 41: delete ‘old’; Line 42: delete the second ‘the’ (children); Line 47: change to - USD, facilities. Line 48: replace ‘had’ with ‘were’, delete ‘been’; Line 50: programs; Line 51: sanitation facilities

Introduction: Line 57: delete ‘the’; Line 76: replace ‘has’ with ‘have’; Line 78: replace ‘had’ with ‘have’; Line 79; backgrounds; Line 89: change to ‘between the ages of 6-months to 17 years’ and delete ‘old’

Materials and Methods: Line 93: ‘carried out’; Line 94: replace ‘of’ with ‘and’; Line 97: modified ‘using’ a map; Line 102: geohelminthiasis; Line 136: ‘washing’ hands, ‘the toilet’; Line 162: ‘microtube’; Line 179: Kuala ‘Lumpur’; Line 182: DNA ‘sequence’ results; Line 183: ‘databases’; Line 187: ‘amplify’; Line 222: ‘Pearson’s’

Results: Line 243: 8 had ‘attended’ college/university; Line 258: ‘Socio-demographic’; Line 265: remove ‘only’; Line 275: should read as ‘villages had children infected with’ worm infection, also delete ‘children per’ and change village to ‘villages’; Line 276: ‘infections were’; Line 315: 6.5%’,’ and delete ‘villagers including’ and change to ‘barefooted’; Line 317: logistic regression ‘analysis’; Line 319: ‘facilities’; Line 351: Ascaris ‘eggs’; Line 352: Trichuris ‘eggs’, Ascaris ‘eggs were’; Lines 353 -354: should read as ‘Similarly, Trichuris eggs were’; Line 359: (GN47) ‘which’ had, Trichuris ‘eggs’; Line 364: replace ‘was’ with ‘were’

Discussion: Line 372: ‘show’; Line 376: facility,; Line 382: should read as ‘Our research recorded prevalence rates’; Line 386: delete first ‘the’ (children); Line 391: ‘concordance’; Line 397: ‘hands’; Line 398: ‘wash their hands’; Line 400: ‘geohelminthiasis’; Line 403: sanitation ‘facilities’; Line 408: delete ‘were’; Line 409: 15% were positive ‘for’ T. trichura; Line 419: delete ‘periodically’; Line 431: delete ‘”’; Line 432: ‘practiced by the villagers’; Line 433: delete first ‘the’; Line 439: replace ‘of’ with ‘to their’; Lines 439-440: ‘trained at a very young age on the use of the toilet and wearing footwear outside the house’

Acknowledgements: Line 449: replace ‘which’ with ‘wish’; Line 450: for assisting in ‘conducting’ this research successfully. delete ‘conducted’.

Reviewer #2: The authors have discussed the Prevalence and risk factors of geohelminthiasis among the rural village children in Kota Marudu, Sabah, Malaysia. Of the 13 villages surveyed, geohelminthiasis was found prevalent only in 7, while there was no infection reported among the subjects of 6 villages. Though the authors have carried out extensive statistical analyses of data, the sample size in the study seems rather small. The results obtained through this study appear to be a corroboration of earlier studies carried out elsewhere across the globe.

The introductory section on geohelminthiasis has been reduced from 3 to 1 paragraph.

Parts of the discussion have been revised.

[Eg., Prevalence and risk factors of soil-transmitted helminthiasis ...

bmcpublichealth.biomedcentral.com › articles;

Prevalence & risk factors for soil transmitted helminth infection ...

www.ncbi.nlm.nih.gov › pmc › articles › PMC3994744;

Prevalence and risk factors associated with the presence of ...

www.ncbi.nlm.nih.gov › pmc › articles › PMC4554591;

Prevalence & risk factors for soil transmitted helminth ...

www.researchgate.net › publication › 260610263_Prevalence_risk_fact.;

Prevalence and risk factors associated with worm infestation ...

www.researchgate.net › publication › 4181077_Prevalence_and_risk_f...;

Geohelminth Infections and Nutritional Status of Preschool ...

www.hindawi.com › journals › scientifica;

Prevalence, Intensity of Soil-Transmitted Helminths, and ...

www.hindawi.com › journals › jtm;

The prevalence, intensities and risk factors associated with ...

onlinelibrary.wiley.com › doi › full;

prevalence and risk factors associated with worm infestation in ...

www.bioline.org.br › pdf- to name a few].

I wish the authors had highlighted the novel findings emerging from their study and avoided a lengthy textbook account in ‘Introduction’ and generalizations in ‘Discussion’.

________________________________________

Attachment

Submitted filename: reply to Reviewers comments.docx

Decision Letter 1

Arun K Yadav

7 Sep 2020

PONE-D-20-17984R1

Prevalence and risk factors of geohelminthiasis among the rural village children in Kota Marudu, Sabah, Malaysia

PLOS ONE

Dear Dr. Chua,

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.

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

Thank you very much for revising your article, which looks much improved than before. Please find a minor suggestion from one of the reviewers, which I would again like to put for your kind consideration.

- The last two paras of conclusion may be reworked. 

Herein, I feel you may consider highlights of main findings/recommendations, may be in a single para. The last para of abstract may give you some idea about highlights/recommendations of study.

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

Please submit your revised manuscript by Oct 22 2020 11:59PM. If you will need more time than this to complete your revisions, please reply to this message or contact the journal office at plosone@plos.org. When you're ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file.

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). You should upload this letter as a separate file labeled 'Response to Reviewers'.

  • A marked-up copy of your manuscript that highlights changes made to the original version. You should upload this as a separate file labeled 'Revised Manuscript with Track Changes'.

  • An unmarked version of your revised paper without tracked changes. You should upload this as a separate file labeled 'Manuscript'.

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

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

We look forward to receiving your revised manuscript.

Kind regards,

Arun K Yadav, Ph.D.

Academic Editor

PLOS ONE

Additional Editor Comments (if provided):

Thank you very much for revising your article, which looks much improved than before. Please find a minor suggestion from one of the reviewers, which I would again like to put for your kind consideration.

- The last two paras of conclusion may be reworked.

Herein, I feel you may consider highlights of main findings/recommendations, may be in a single para. The last para of abstract may give you some idea about highlights/recommendations of study.

[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: All comments have been addressed

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: (No Response)

Reviewer #2: Yes

**********

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

Reviewer #1: (No Response)

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: (No Response)

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: (No Response)

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: (No Response)

Reviewer #2: My concerns raised in the earlier review have been addressed in the revised manuscript . However, a minor revision is still required. In Discussion' section- the last two paragraphs are actually 'conclusion' and/ or recommendations meant for policy makers and social/administrative bodies. These paras may be reworked so as to avoid generalized statements and give crisp/ abridged recommendations in a couple of sentences.

**********

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.]

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

PLoS One. 2020 Sep 28;15(9):e0239680. doi: 10.1371/journal.pone.0239680.r004

Author response to Decision Letter 1


9 Sep 2020

Reviewer #2: My concerns raised in the earlier review have been addressed in the revised manuscript . However, a minor revision is still required. In Discussion' section- the last two paragraphs are actually 'conclusion' and/ or recommendations meant for policy makers and social/administrative bodies. These paras may be reworked so as to avoid generalized statements and give crisp/ abridged recommendations in a couple of sentences.

The 2 paragraphs have now to been reduced to one shown below:

In conclusion, this study clearly shows that geohelminthiasis still occurs with an overall prevalence of 14.3% among children of rural communities of Kota Marudu in Sabah. Infection by Ascaris had the highest rate at 67% compared to hookworm or T. trichiura. The most practical means of controlling geohelminthiasis in these communities would be expanding mass deworming programmes for school-age children, improving sanitation and water supplies, upgrading the socio-economic status and continually conducting health education programmes. The data on the prevalence of geohelminthiasis in this study would contribute to better public health monitoring and operation to reduce the infection in rural areas.

Attachment

Submitted filename: Response to reviewer 8sept20.docx

Decision Letter 2

Arun K Yadav

11 Sep 2020

Prevalence and risk factors of geohelminthiasis among the rural village children in Kota Marudu, Sabah, Malaysia

PONE-D-20-17984R2

Dear Dr. Chua,

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

Within one week, you’ll receive an e-mail detailing the required amendments. When these have been addressed, you’ll receive a formal acceptance letter and your manuscript will be scheduled for publication.

An invoice for payment will follow shortly after the formal acceptance. To ensure an efficient process, please log into Editorial Manager at http://www.editorialmanager.com/pone/, click the 'Update My Information' link at the top of the page, and double check that your user information is up-to-date. 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 help maximize its impact. If they’ll be preparing press materials, please inform our press team as soon as possible -- 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.

Kind regards,

Arun K Yadav, Ph.D.

Academic Editor

PLOS ONE

Additional Editor Comments (optional):

Thank you very much for your sincere revision. The manuscript now appears suitable for publication.

Reviewers' comments:

Acceptance letter

Arun K Yadav

16 Sep 2020

PONE-D-20-17984R2

Prevalence and risk factors of geohelminthiasis among the rural village children in Kota Marudu, Sabah, Malaysia

Dear Dr. Chua:

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

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

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

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

Kind regards,

PLOS ONE Editorial Office Staff

on behalf of

Dr. Arun K Yadav

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 Questinnaire. Sample pages of the questionnaire used in the study.

    (PDF)

    S1 Table. Distribution of geohelminth-infected children in the villages among the households with or without basic sanitation facilities.

    (PDF)

    S1 Fig. Regression of percentage geohelminthiasis among the children against (a) distance (km) of village from the main town (Kota Marudu), and (b) altitude of village (metres above sea level).

    (TIF)

    Attachment

    Submitted filename: reply to Reviewers comments.docx

    Attachment

    Submitted filename: Response to reviewer 8sept20.docx

    Data Availability Statement

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


    Articles from PLoS ONE are provided here courtesy of PLOS

    RESOURCES