Skip to main content
Download PDF
  • Research article
  • Open access
  • Published:

Enteric pathogen infection and consequences for child growth in young Aboriginal Australian children: a cross-sectional study

BMC Infectious Diseases volume 21, Article number: 9 (2021) Cite this article

Abstract

Background

To determine the prevalence of enteric infections in Aboriginal children aged 0–2 years using conventional and molecular diagnostic techniques and to explore associations between the presence of pathogens and child growth.

Methods

Cross-sectional analysis of Aboriginal children (n = 62) residing in a remote community in Northern Australia, conducted from July 24th - October 30th 2017. Stool samples were analysed for organisms by microscopy (directly in the field and following fixation and storage in sodium-acetate formalin), and by qualitative PCR for viruses, bacteria and parasites and serology for Strongyloides-specific IgG. Child growth (height and weight) was measured and z scores calculated according to WHO growth standards.

Results

Nearly 60% of children had evidence for at least one enteric pathogen in their stool (37/62). The highest burden of infection was with adenovirus/sapovirus (22.9%), followed by astrovirus (9.8%) and Cryptosporidium hominis/parvum (8.2%). Non-pathogenic organisms were detected in 22.5% of children. Ten percent of children had diarrhea at the time of stool collection. Infection with two or more pathogens was negatively associated with height for age z scores (− 1.34, 95% CI − 2.61 to − 0.07), as was carriage of the non-pathogen Blastocystis hominis (− 2.05, 95% CI - 3.55 to − 0.54).

Conclusions

Infants and toddlers living in this remote Northern Australian Aboriginal community had a high burden of enteric pathogens and non-pathogens. The association between carriage of pathogens/non-pathogens with impaired child growth in the critical first 1000 days of life has implications for healthy child growth and development and warrants further investigation. These findings have relevance for many other First Nations Communities that face many of the same challenges with regard to poverty, infections, and malnutrition.

Peer Review reports

Background

Infections with enteric pathogens are common in disadvantaged populations with low socio-economic status due to inadequate sanitation and hygiene, overcrowded living conditions, and gaps in health literacy [1]. During the first two years of life, enteric infections have a particularly devastating effect on child health as a result of poor nutritional status, loss of appetite and diarrhea, disturbances in intestinal function that lead to impaired absorption of micronutrients and low grade inflammation [2]. More specifically, infection with Shigella sp.and Giardia lamblia have been associated with a significantly higher risk of stunting [2]; enterotoxigenic Escherichia coli with a higher risk of being underweight [3] Campylobacter jejuni has been shown to be associated with lower growth rates for both length and weight [4]; and hookworm and Trichuris trichiura have been associated with anaemia [5, 6]. As well as impaired growth and cognitive development, children may have anaemia and experience lethargy, which can result in reduced educational achievement and decreased opportunities in later life [7, 8]. Impaired child growth in the first 1000 days of life is also associated with long-lasting adverse consequences for adult health, including increased risk of chronic diseases [8,9,10].

A high prevalence of enteric infections has been previously reported in Australian Aboriginal communities, from a small number of surveys in older children and adults [11,12,13,14,15]. However there is a paucity of studies of enteric infections in very young children in these communities. This is mainly due to difficulties in collecting and transporting samples from isolated locations, the limitations of conventional methodology, [11, 12] and challenges in achieving an accurate diagnosis in a field setting. New technologies such as multiplex molecular assays now allow more rapid and sensitive and simultaneous diagnosis of multiple enteric organisms [16] and more reliable diagnosis in remote settings. Recent studies suggest that “silent” enteric infections, in the absence of overt diarrhea, may still result in significantly adverse clinical outcomes, such as growth faltering [17,18,19]. The goal of our study was to determine: i) the prevalence of enteric carriage in all Aboriginal children aged between 0 and 2 years living in a remote Northern Australian community using conventional and molecular techniques, and ii) the association between the presence of enteric pathogens/non-pathogens and child growth outcomes.

Methods

Study design

We conducted a cross-sectional study of children residing in a remote Aboriginal community in Northern Australia who were between 0 and 2 years of age. Primary outcomes were i) prevalence of enteric infections (bacterial, viral, parasitic) using microscopy, PCR and serology; ii) child growth outcomes (height for age, weight for age, and weight for height z scores).

Study setting and participants

The study was conducted in a remote tropical Northern Territory community between July 24th and October 30th 2017. All Aboriginal children aged between 0 and 2 years who were resident in the local community during this period (n ~ 100) and had primary carers who gave consent for participation in the study were eligible for enrolment in the study. Information relating to socio-demographic and food security data were collected via questionnaire, and anthropometric measurements were performed. Fresh stool samples were collected from the child’s nappy.

Data collection and analysis

The field team consisted of two Aboriginal Health Practitioners, five Aboriginal Community Based Researchers, two parasitologists and three research scientists (including a paediatrician). According to information from the health services, it was estimated that 100 eligible children aged between 0 and 2 years of age were currently resident in the community.

Prior to commencement of the study, the local research team received a one week training course which included information on the study protocol; recruitment of participants and consent; telling of the research story in the local languages; data collection techniques (including the use of mobile devices for data collection and use of Research Electronic Data Capture - RedCap); faecal parasites and microscope literacy; anthropometric measurements; and assistance with blood collection (venous and Haemacue® machine). Eligible children were identified through a number of sources including the local health clinics, day care centre, local play group, community child nutrition programs, local Aboriginal researcher contacts and by visiting individual houses.

Maternal characteristics

Trained research staff collected maternal socio-demographic, nutritional, environmental, wealth index, breast feeding patterns and food security information via RedCap using a structured questionnaire (Supplementary 1). The questionnaire was initially tested in a focus group session among community members and local staff during the training course, and refined according to local community feedback. An information sheet including pictorial information was prepared by the research team, refined according to community feedback and then translated into local language by Aboriginal researchers.

Anthropometric measurements

Child anthropometric measurements (height/length and weight) were measured on enrolment using a portable infantometer (Shorr Board®) for length and standard anthropometer for height. A digital infant weighing scale/ or mother-infant scale (Secca 876) with precision to the nearest 10 g was used to measure weight. A mother-Infant scale (Secca 876) was used to determine maternal weights. Height was measured to the nearest 0.5 cm using a standard anthropometer. Maternal body mass index was calculated using maternal height and weight (kg/m2) Child weight for age, weight for length and length for age z scores were calculated using WHO Anthro (version 3.2.2, January 2011) [20]. Stunting was defined as height or length-for-age z scores less than two standard deviations below WHO Child Growth Standards [20].

Wealth Index

To construct a wealth index for the infant’s household, principal component analysis was used from the items belonging to the following three component indices: i) housing quality (three items: average number of persons per room [number], floor [five responses], wall [four responses]), ii) consumer durables (four items [yes/no]: fridge, television, car, phone), and iii) cooking energy [three responses]. The wealth index score was grouped into tertiles from tertile 1 (poorest) to tertile 3 (richest) [21].

Clinical examination

Following enrolment into the study each child received a general health check by a paediatrician. This included clinical history of diarrhea at presentation (defined as maternal report of three or more loose stools in 24 h), and clinical examination for signs of infection (respiratory, skin, ears) [22]. If signs of infection were detected on clinical examination, the child was referred to the local clinic for further management. Children with infection were included in the analysis.

Stool collection and analysis

Primary carers were instructed to deliver soiled nappies to the study field laboratory or telephone the research team who collected them within two hours. Fresh stool was examined as soon as possible by direct microscopy and Kato-Katz, and participants with enteric infections were referred to the health clinic for further management. Of the remaining sample, an aliquot was stored in 10 ml of sodium acetate formalin (SAF) solution (Bioline), and another frozen at − 20 °C for PCR analysis. Stool samples collected into SAF were sent to the Victorian Infectious Diseases Reference Laboratory, The Peter Doherty Institute for Infection and Immunity, Melbourne, Australia for testing using the formalin ethyl acetate (FEA) concentration method [23]. Stained fixed smear and modified acid-fast staining methods were also applied.

PCR detection of stool pathogens and non-pathogens

DNA was extracted from stool samples using the MolBio Powersoil® kit (QIAgen, Melbourne, Australia) for faecal pathogens and soil-transmitted helminths. DNA concentration was measured using Quant-iT™ dsDNA HS assay kit (Life Technologies, Australia) and normalized to 1 ng/μl in UltraPure DNase/RNase-free distilled water (Invitrogen). DNA samples (10 μl) were tested using the Tandem- Plex™ Fecal Pathogens M kit (Ausdiagnostics, Sydney, Australia) as described by the manufacturer Bacteria and viruses tested for are listed in Supplementary 2. An aliquot of the DNA extracted using the MolBio Powersoil Kit® was tested using the Tandem Plex™ Soil Transmitted Helminths kit (Ausdiagnostics) for the following soil-transmitted helminths: Ascaris lumbricoides, Necator americanus, Ancylostoma ceylanicum, Ancylostoma duodenale (“pan-hookworm”), Trichuris trichiura and Strongyloides stercoralis. In addition, DNA was extracted from 0.2 g of fresh stool sample on the Freedom Evo 100® (Tecan. Swithzerland) robotics system using the NucleoMagR Virus Kit (Macherey Nagel, Germany) as per manufacturer’s instructions. Prior to DNA extraction on the Freedom Evo 100®, a processing step of mechanical lysis as described by Mu, et al [24] was performed with the following modification: Lysis Matrix E (MP Biomedicals) 2 ml tubes were used. DNA extracts were also tested in the Allplex™ GI-Helminth(I) Assay® (Seegene Inc., Seoul, Korea) as per manufacturer’s instructions. The panel of targets tested was as follows: Hymenolepis species (re-classified as Rodentolepis species), Enterocytozoon/Encephalitozoon species, Taenia species, Strongyloides species, Ascaris species, Trichuris trichiura, Ancylostoma species and Necator americanus. The limits of detection of the assay for the selected targets is reported to range between 17 and 93 copies/10uL by the manufacturer, [25] but is likely higher in our study due to modifications to the recommended DNA extraction procedures described above. Non-pathogens are defined as enteric parasites which do not cause disease. Included in this list were Blastocystis hominis, Entamoeba coli, Iodamoeba butschlii, Chilomastix mesnili.

Serodiagnosis of strongyloidiasis

Strongyloides infections were diagnosed serologically using a commercially available ELISA that detects IgG antibodies against NIE, a recombinant protein from S. stercoralis, following kit manufacturer’s instructions (InBios, Inc., Seattle, USA). Positive and negative controls were tested in duplicate and patient serum samples tested singly. Control sera and sera from each subject were diluted to 1/100 using sample diluent buffer. It should be noted the kit manufacturer does not provide a cut- off value. As stated by the manufacturer the ‘cut-off value will vary depending on the test population and geographical location where the kit is being used.’ We calculated a cut-off value using ROC analysis of 98 sera collected in Australia. The results are reported qualitatively [26].

Statistical analysis

Data was analyzed using StataIC, version 14 (StataCorp, College Station, TX, USA). Categorical data are presented as percentages with frequency, and continuous data are presented as mean and standard deviation (SD). Multivariate linear (height for age z scores) and logistic regression (stunting) was performed to examine the association between prevalence of enteric infection and child growth outcomes. Unadjusted and adjusted estimates of mean differences or odds ratios, and their 95% confidence intervals (CI) are presented. Potential confounding factors were selected a priori. All variables were included and adjusted for in the final model.

Results

We enrolled 70 of the ~ 100 children aged between 0 and 2 years resident in the community. Stool samples were collected from 62 (88.5%) children. In the sample of children who had stool samples collected, more than half of mothers/carers (51.6%) were educated to year 11 level. The prevalence of maternal underweight was 23%, overweight 19.4%, and obesity 8.1%. A smoker resided in 87.1% of households, and the average number of residents per household was six. Traditional medicine was used by 70.9% of families. The majority of children (87.1%) were currently breastfed. Food insecurity was common with 58.1% of households reporting running out of food in the previous two weeks. Almost all women (98.4%) received government benefits. Baseline characteristics are shown in Table 1.

Table 1 Baseline characteristic of mothers and children in a remote Aboriginal community (n = 62)
Full size table

Prevalence of enteric infections

The prevalence of enteric infections is presented in Table 2. Overall prevalence of pathogen carriage was 59.7% (37/62) (i.e 37 out of 62 children had at least one pathogen detected), and three children were infected with three or more pathogens. More parasites were detected by microscopy of SAF samples (15 isolates from 62 samples) than direct stool microcopy (6/62). . Twenty- five children had no pathogens detected by any method.

Table 2 Prevalence of pathogenic versus non-pathogenic enteric carriage in young Aboriginal children residing in a remote community
Full size table

Of the 24 children who had an enteric viral infection, eleven (47.8%) were co -infected with another pathogen, including Cryptosporidium, Shigella, Salmonella, Giardia and Enterobius vermicularis. The most commonly detected pathogen was adenovirus/sapovirus (14/61 samples tested; the two virus species are not distinguishable by the primers used in this kit), followed by astrovirus (6/61) and Cryptosporidium hominis/parvum (5/61). No cases of strongyloidiasis infection were detected by stool testing or serology (53 serology samples tested). No cases of hookworm were detected. Non-pathogens were detected in 14/62 (22.5%) of children, and in 10 cases coexisted with a pathogen. Ninety two percent of pathogen carriage was asymptomatic, with no reports of diarrhea or fever on clinical history or examination. Of the seven children who presented with diarrhea at the time of stool collection, pathogens were identified in four stool samples and included adenovirus, Giardia lamblia, Rodentolepsis nana (R.nana), Trichuris trichiura, and Dientamoeba fragilis and Blastocystis hominis.

Association between enteric infection and child growth outcomes

Univariate and multivariate regression analyses to determine associations between pathogen and non-pathogen carriage and growth outcomes are presented in Table 3. Infection with two or more pathogens was found to negatively influence height for age z scores in young children (− 1.34, 95% CI − 2.61 to − 0.07), but not weight for age or weight for height z scores. No association was seen with risk of stunting. Infection separately with a bacterial, viral or parasitic infection was not associated with child growth outcomes. Infection with Blastocystis alone was also associated with reduced height for age z scores (− 2.05, 95% CI − 3.55 to − 0.54).

Table 3 Association between enteric carriage and child growth outcomes in a remote Indigenous community
Full size table

Discussion

To our knowledge, this is the largest survey of young children aged 0–2 years in a remote Aboriginal community to document the prevalence of enteric infections and impact on child growth outcomes, and the first to compare different methodologies for identification of pathogens in this remote setting. We found that almost 60% of young children were infected with at least one enteric pathogen, most commonly adenovirus/sapovirus and Cryptosporidium, and infections with two or more pathogens was associated with impaired linear growth.

There is a paucity of data on the prevalence of enteric pathogen infections in infants and toddlers living in remote Aboriginal communities. We found only two studies in a remote Aboriginal community in the Northern Territory which documented the presence of intestinal parasites in 0–2 year old children [12]. One study in 1994–1996 at the same location identified the presence of Ancylostoma. duodenale (A.duodenale) (9%), T.trichiura (36%), R.nana (9%) and Entamoeba spp (9%). in < 24 months old children (n = 11), and S. stercoralis (27%), R. nana (17%), Giardia duodenalis (13%), Entamoeba spp. (10%), A. duodenale (13%), and T.trichiura (87%) in children aged 2–4 years 11 months (n = 30) between July 1994 to October 1996 [12]. Another study in the same location between 2010 and 2011 in children aged < 24 months demonstrated a prevalence of S.stercoralis (3% on microscopy (n = 29), 9% on agar plate culture (n = 23), 8% on PCR [11] (personal communication Dr. Deborah Holt Sept 2019), 28% on serology (n = 38) [27] (personal communication Dr. Kate Mounsey Sept 2019), T.trichiura (14% on microscopy) and R.nana (7% on microscopy) (n = 29) [11] These findings are in contrast to those of our study, in which no cases of strongyloidiasis or hookworm were observed and the percentage of T. trichiura and R. nana positive were reduced. This reflects the implementation of public health measures (preventive chemotherapy, test and treat strategies) in this area that were introduced for soil transmitted helminths (albendazole from 1995, and an ivermectin mass drug administration in 2010 and 2011), leading to a reduction in S. stercoralis and hookworm prevalence [11, 15]. Another study examined long-term cryptosporidiosis patterns across Western Australia between 2002 and 2012, using data obtained from the Western Australian Notifiable Infectious Disease Database, and demonstrated a high burden of cryptosporidiosis in Aboriginal children aged 0–4 years of age (33.3%) [28]. Specific practices and environmental factors (e.g. hygiene and socioeconomic factors, presence of livestock and other animals, previous de-worming programs, weather patterns) may account for the different rate in our study, in which there were only five (8.2%) isolates of cryptosporidium.

There is growing evidence of the importance of pathogens in a child’s gut, even when asymptomatic. This “pathobiome” is thought to be causal in the development of ‘environmental enteropathy’, with associated chronic intestinal inflammation, villous blunting and intestinal leakage and malabsorption, leading to a cycle of malnutrition, micronutrient deficiencies, and growth impairment [29]. Childhood diarrhoea has been conceptualized as a syndrome of enteropathogen excess, rather than a single infection, with diarrhoea more likely to occur when a quantitative threshold of pathogen burden is exceeded [30]. Indeed in our study, the majority of children did not present with diarrhoea, and pathogen burden was likely to be low (as most isolates were only identified by PCR and diarrhoea was uncommon); however carriage of two or more enteric pathogens or Blastocystis hominis was associated with impaired linear growth (lower height for age z scores). This confirms that pathogens not causing diarrhoea may still cause significant morbidity in resource- constrained settings, and efforts towards improving environmental conditions including improvements in clean drinking water, housing standards and hygiene and sanitation are critical.

B.hominis is usually considered a non-pathogen but in some instances has been reported as a pathogen [31]. We observed a significant association between carriage of B. hominis and lower height for age z scores. This has been documented previously, with infection with B. hominis shown to be associated with lower anthropometric indexes in young children in Turkey [32]. These findings suggest that organisms characterised as ‘non-pathogenic’ may in fact carry some pathogenic potential, possibly through disturbance of the gut microbiome and/or damage to the intestinal mucosa resulting in increased intestinal permeability and impaired nutrient absorption [28]. Poor nutritional status may also have preceded infection by B.hominis [33].. The finding of B. hominis in stool may also represent exposure to organisms spread by the faecal-oral route [34].

Our study also provides important evidence on the application of molecular diagnostics to identify enteric pathogen burden. Use of PCR has previously been shown to substantially alter previous estimates of pathogen prevalence. Re-analysis of specimens from the MAL-ED cohort study using quantitative PCR demonstrated a predominance of viral causes of diarrhea (including sapovirus, rotavirus and adenovirus) with only two pathogens (rotavirus and enterotoxigenic E. coli) remaining in the top five causes of diarrhea identified by the original microbiological work up [35]. In our study, the majority of pathogens in stool samples from children were detected by PCR (qualitative), allowing increased detection rates and correlation with clinical outcomes.

Strengths of this study are that we worked closely with the local primary health care providers and trained Aboriginal Community Based Researchers to carry out the research, resulting in a high representative sample of young children in this remote Aboriginal community. We were also able to collect comprehensive information on possible nutritional, environmental and socio-demographic influences on clinical outcomes. Limitations are the relatively small sample size (even though it represented 68% of the target population), stool samples were not collected from mothers or carers of the child and hygiene practices being assessed only by questionnaire and not by direct observation (which may have introduced some recall bias); and we only asked about diarrheal infections in the last 24 h.

Conclusions

We found a high prevalence of enteric pathogen and non-pathogen carriage in Australian Aboriginal infants and toddlers and a significant association between infection with multiple pathogens and child growth (impaired height for age z scores). These findings suggest that environmental contamination in remote Northern communities where extreme heat and humidity is common, may contribute to the high rates of childhood growth impairment and stunting reported, [36] with health implications extending into adulthood. The findings highlight the urgent need for sustainable strategies to improve housing, hygiene and sanitation in remote Aboriginal communities. Our findings also have relevance for many other First Nations Communities around the world that face similar challenges with regard to poverty, infections, and malnutrition.

Availability of data and materials

Study data and materials may be made available from the corresponding author on request with appropriate human research ethics committee approval and with the consent of the participating community as required by Australian criteria for research with Indigenous communities.

Abbreviations

A. duodenale :

Ancylostoma duodenale

B.hominis :

Blastocystis hominis

BMI:

Body Mass Index

cm:

centimetre

FEA:

formalin ethyl acetate

kg:

kilogram

R. nana :

Rodentolepis nana

SAF:

sodium acetate formalin

SD:

standard deviation

S.stercoralis :

Strongyloides stercoralis

T.trichiura :

Trichuris trichiura

WHO:

World Health Organization

References

  1. Kotloff KL, Nataro JP, Blackwelder WC, Nasrin D, Farag TH, Panchalingam S, et al. Burden and aetiology of diarrhoeal disease in infants and young children in developing countries (the global enteric multicenter study, GEMS): a prospective, case-control study. Lancet. 2013;382(9888):209–22.

    Article  PubMed  Google Scholar 

  2. George CM, Burrowes V, Perin J, Oldja L, Biswas S, Sack D, et al. Enteric infections in young children are associated with environmental Enteropathy and impaired growth. Tropical Med Int Health. 2018;23(1):26–33.

    Article  CAS  Google Scholar 

  3. Bagamian KH, Anderson JD, Muhib F, Cumming O, Laytner LA, Wierzba TF, et al. Heterogeneity in enterotoxigenic Escherichia coli and shigella infections in children under 5 years of age from 11 African countries: a subnational approach quantifying risk, mortality, morbidity, and stunting. Lancet Glob Health. 2020;8(1):e101–e12.

    Article  PubMed  Google Scholar 

  4. Lee G, Pan W, Penataro Yori P, Paredes Olortegui M, Tilley D, Gregory M, et al. Symptomatic and asymptomatic campylobacter infections associated with reduced growth in Peruvian children. PLoS Negl Trop Dis. 2013;7(1):e2036.

    Article  PubMed  PubMed Central  Google Scholar 

  5. Quihui-Cota L, Morales-Figueroa GG, Esparza-Romero J, Valencia ME, Astiazaran-Garcia H, Mendez RO, et al. Trichuriasis and low-iron status in schoolchildren from Northwest Mexico. Eur J Clin Nutr. 2010;64(10):1108–15.

    Article  CAS  PubMed  Google Scholar 

  6. Molla E, Mamo H. Soil-transmitted helminth infections, anemia and undernutrition among schoolchildren in Yirgacheffee, South Ethiopia. BMC Res Notes. 2018;11(1):585.

    Article  PubMed  PubMed Central  Google Scholar 

  7. Ngure FM, Reid BM, Humphrey JH, Mbuya MN, Pelto G, Stoltzfus RJ. Water, sanitation, and hygiene (WASH), environmental enteropathy, nutrition, and early child development: making the links. Ann N Y Acad Sci. 2014;1308:118–28.

    Article  PubMed  Google Scholar 

  8. Hsu CN, Tain YL. The Good, the Bad, and the Ugly of Pregnancy Nutrients and Developmental Programming of Adult Disease. Nutrients. 2019;11(4)4):894. https://doi.org/10.3390/nu11040894.

  9. Prendergast AJ, Humphrey JH. The stunting syndrome in developing countries. Paediatr Int Child Health. 2014;34(4):250–65.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Black RE, Victora CG, Walker SP, Bhutta ZA, Christian P, de Onis M, et al. Maternal and child undernutrition and overweight in low-income and middle-income countries. Lancet. 2013;382(9890):427–51.

    Article  PubMed  Google Scholar 

  11. Holt DC, Shield J, Harris TM, Mounsey KE, Aland K, McCarthy JS, et al. Soil-Transmitted Helminths in Children in a Remote Aboriginal Community in the Northern Territory: Hookworm is Rare but Strongyloides stercoralis and Trichuris trichiura Persist. Trop Med Infect Dis. 2017;2(4):51. https://doi.org/10.3390/tropicalmed2040051.

  12. Shield J, Aland K, Kearns T, Gongdjalk G, Holt D, Currie B, et al. Intestinal parasites of children and adults in a remote Aboriginal community of the Northern Territory, Australia, 1994-1996. Western Pac Surveill Response J. 2015;6(1):44–51.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Hopkins RM, Gracey MS, Hobbs RP, Spargo RM, Yates M, Thompson RC. The prevalence of hookworm infection, iron deficiency and anaemia in an Aboriginal community in north-West Australia. Med J Aust. 1997;166(5):241–4.

    Article  CAS  PubMed  Google Scholar 

  14. Thompson RC, Reynoldson JA, Garrow SC, McCarthy JS, Behnke JM. Towards the eradication of hookworm in an isolated Australian community. Lancet. 2001;357(9258):770–1.

    Article  CAS  PubMed  Google Scholar 

  15. Kearns TM, Currie BJ, Cheng AC, McCarthy J, Carapetis JR, Holt DC, et al. Strongyloides seroprevalence before and after an ivermectin mass drug administration in a remote Australian Aboriginal community. PLoS Negl Trop Dis. 2017;11(5):e0005607.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  16. Binnicker MJ. Multiplex molecular panels for diagnosis of gastrointestinal infection: performance, result interpretation, and cost-effectiveness. J Clin Microbiol. 2015;53(12):3723–8.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Troeger C, Colombara DV, Rao PC, Khalil IA, Brown A, Brewer TG, et al. Global disability-adjusted life-year estimates of long-term health burden and undernutrition attributable to diarrhoeal diseases in children younger than 5 years. Lancet Glob Health. 2018;6(3):e255–e69.

    Article  PubMed  PubMed Central  Google Scholar 

  18. Kotloff KL, Nasrin D, Blackwelder WC, Wu Y, Farag T, Panchalingham S, et al. The incidence, aetiology, and adverse clinical consequences of less severe diarrhoeal episodes among infants and children residing in low-income and middle-income countries: a 12-month case-control study as a follow-on to the global enteric multicenter study (GEMS). Lancet Glob Health. 2019;7(5):e568–e84.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Collaborators GL. Estimates of the global, regional, and national morbidity, mortality, and aetiologies of lower respiratory tract infections in 195 countries: a systematic analysis for the global burden of disease study 2015. Lancet Infect Dis. 2017;17(11):1133–61.

    Article  Google Scholar 

  20. World Health Organisation. The WHO Child Growth Standards: WHO; 2018 [Available from: https://www.who.int/childgrowth/en/. Accessed Feb 2018.

  21. O'donnell O, Van Doorslaer E, Wagstaff A, Lindelow M. Measurement of living standards analyzing health equity using household survey data: a guide to techniques and their implementation. Washington. DC: World Bank; 2008.

    Google Scholar 

  22. World Health Organisation. Diarrhaoeal disease 2017 [Available from: https://www.who.int/news-room/fact-sheets/detail/diarrhoeal-disease. Accessed Feb 2018.

  23. Khanna V, Sagar S, Khanna R, Chawla K. A comparative study of formalin-ethyl acetate sedimentation technique and mini Parasep((R)) solvent-free method in the rapid diagnosis of intestinal parasites. Trop Parasitol. 2018;8(1):29–32.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Mu A, Kwong JC, Isles NS, Goncalves da Silva A, Schultz MB, Ballard SA, et al. Reconstruction of the Genomes of Drug-Resistant Pathogens for Outbreak Investigation through Metagenomic Sequencing. mSphere.4:e00529–18. https://doi.org/10.1128/mSphere.00529-18.

  25. AusDiagnostics. FAECAL PATHOGENS B (16-WELL) REF 25033 PANEL OF ASSAYS 2019.

    Google Scholar 

  26. Krolewiecki AJ, Ramanathan R, Fink V, McAuliffe I, Cajal SP, Won K, et al. Improved diagnosis of Strongyloides stercoralis using recombinant antigen-based serologies in a community-wide study in northern Argentina. Clin Vaccine Immunol. 2010;17(10):1624–30.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  27. Mounsey K, Kearns T, Rampton M, Llewellyn S, King M, Holt D, et al. Use of dried blood spots to define antibody response to the Strongyloides stercoralis recombinant antigen NIE. Acta Trop. 2014;138:78–82.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. Ng-Hublin JSY, Combs B, Reid S, Ryan U. Differences in the occurrence and epidemiology of cryptosporidiosis in Aboriginal and non-Aboriginal people in Western Australia (2002-2012). Infect Genet Evol. 2017;53:100–6.

    Article  PubMed  Google Scholar 

  29. Ryan ET. The intestinal pathobiome: its reality and consequences among infants and young children in resource-limited settings. J Infect Dis. 2013;208(11):1732–3.

    Article  PubMed  Google Scholar 

  30. Taniuchi M, Sobuz SU, Begum S, Platts-Mills JA, Liu J, Yang Z, et al. Etiology of diarrhea in Bangladeshi infants in the first year of life analyzed using molecular methods. J Infect Dis. 2013;208(11):1794–802.

    Article  PubMed  PubMed Central  Google Scholar 

  31. Tan KS. New insights on classification, identification, and clinical relevance of Blastocystis spp. Clin Microbiol Rev. 2008;21(4):639–65.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  32. Ertug S, Karakas S, Okyay P, Ergin F, Oncu S. The effect of Blastocystis hominis on the growth status of children. Med Sci Monit. 2007;13(1):CR40–3.

    PubMed  Google Scholar 

  33. Lepczynska M, Bialkowska J, Dzika E, Piskorz-Ogorek K, Korycinska J. Blastocystis: how do specific diets and human gut microbiota affect its development and pathogenicity? Eur J Clin Microbiol Infect Dis. 2017;36(9):1531–40.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  34. Wawrzyniak I, Poirier P, Viscogliosi E, Dionigia M, Texier C, Delbac F, et al. Blastocystis, an unrecognized parasite: an overview of pathogenesis and diagnosis. Ther Adv Infect Dis. 2013;1(5):167–78.

    PubMed  PubMed Central  Google Scholar 

  35. Platts-Mills JA, Liu J, Rogawski ET, Kabir F, Lertsethtakarn P, Siguas M, et al. Use of quantitative molecular diagnostic methods to assess the aetiology, burden, and clinical characteristics of diarrhoea in children in low-resource settings: a reanalysis of the MAL-ED cohort study. Lancet Glob Health. 2018;6(12):e1309–e18.

    Article  PubMed  PubMed Central  Google Scholar 

  36. Northern Territory Government. NT Health Nutrition and Physical Activity Strategy 2015–2020. 2015.

    Google Scholar 

Download references

Acknowledgements

Membership of Child Health and Nutrition Study team- Yalurr Dhamarandji, David Djilimara, Elizabeth Bungawara, Lloyd Dhamarandji, Janice Djiliri, Jess Gatti, Jannie Kraayenhof, Noella Goveas. We thank the participants, their families and health workers in this community; Miwatj Health Aboriginal Corporation; Ana Malupo; Eddie Mulholland; Lucas de Toca and the Miwatj Health Aboriginal Corporation Board for their support; Marthakal Homelands Health Service; Families as First Teachers; Beth Hilton-Thorpe; and Christalla Hajisava.

Funding

This work was supported through a grant from the Hallmark Indigenous Research Initiative at the University of Melbourne. The funder had no role in study design, data collection and analysis, decision to publish or preparation of the manuscript.

Author information

Authors and Affiliations

  1. Department of Medicine at the Peter Doherty Institute for Infection and Immunity, University of Melbourne, Melbourne, Victoria, Australia

    Sarah Hanieh, Siddhartha Mahanty & Jenny Shield

  2. The Victorian Infectious Diseases Service, Royal Melbourne Hospital, Parkville, Victoria, 3052, Australia

    Siddhartha Mahanty, Katherine Gibney & Beverley-Ann Biggs

  3. Menzies School of Health Research, Darwin, Northern Territory, 0810, Australia

    George Gurruwiwi, Therese Kearns, Roslyn Dhurrkay & Veronica Gondarra

  4. Victorian Infectious Diseases Reference Laboratory, Peter Doherty Institute, Melbourne, Victoria, Australia

    Norbert Ryan, Francesca Azzato & Sullen Nicholson

  5. Microbiological Diagnostic Unit Public Health Laboratory at the University of Melbourne, The Peter Doherty Institute for Infection and Immunity, Melbourne, Australia

    Susan A. Ballard & Nicole Orlando

  6. Department of Nutrition, Dietetics and Food, Monash University, Clayton, Victoria, Australia

    Julie Brimblecombe

  7. Miwatj Health Aboriginal Corporation, Nhulunbuy, NT, 0881, Australia

    Wendy Page

  8. Public Health and Tropical Medicine, James Cook University, Cairns, QLD, 4870, Australia

    Wendy Page

  9. Walter and Eliza Hall Institute of Medical Research, Parkville, VIC, Australia

    Leonard C. Harrison

Authors
  1. Sarah Hanieh
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Siddhartha Mahanty
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. George Gurruwiwi
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Therese Kearns
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Roslyn Dhurrkay
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Veronica Gondarra
    View author publications

    You can also search for this author in PubMed Google Scholar

  7. Jenny Shield
    View author publications

    You can also search for this author in PubMed Google Scholar

  8. Norbert Ryan
    View author publications

    You can also search for this author in PubMed Google Scholar

  9. Francesca Azzato
    View author publications

    You can also search for this author in PubMed Google Scholar

  10. Susan A. Ballard
    View author publications

    You can also search for this author in PubMed Google Scholar

  11. Nicole Orlando
    View author publications

    You can also search for this author in PubMed Google Scholar

  12. Sullen Nicholson
    View author publications

    You can also search for this author in PubMed Google Scholar

  13. Katherine Gibney
    View author publications

    You can also search for this author in PubMed Google Scholar

  14. Julie Brimblecombe
    View author publications

    You can also search for this author in PubMed Google Scholar

  15. Wendy Page
    View author publications

    You can also search for this author in PubMed Google Scholar

  16. Leonard C. Harrison
    View author publications

    You can also search for this author in PubMed Google Scholar

  17. Beverley-Ann Biggs
    View author publications

    You can also search for this author in PubMed Google Scholar

Consortia

on behalf of the Child Health and Nutrition Study team

  • Yalurr Dhamarandji
  • , David Djilimara
  • , Elizabeth Bungawara
  • , Lloyd Dhamarandji
  • , Janice Djiliri
  • , Jess Gatti
  • , Jannie Kraayenhof
  •  & Noella Goveas

Contributions

SH conceptualized the study, analysed the data, managed the study, had primary responsibility for recruitment and data collection and lead the production of the manuscript. SM contributed to study design, contributed to the manuscript, and interpretation of laboratory data. TK contributed to study design, supervision of the study team and contributed to the manuscript. GG, RD and VG contributed to study design, development of the questionnaires and supervision of the study team. JS and NR contributed to study design, and were responsible for the laboratory components of the study in and outside of the field, interpretation of laboratory data. and contributed to the manuscript. FA, SAB, NO, SN and LH were responsible for the laboratory components of the study outside of the field, and contributed to the manuscript.KG, JB and WP contributed to study design, study implementation, supervision of the study team and contributed to the manuscript. BAB contributed to study design, provided significant input into the drafting of the manuscript, and assisted with interpretation of laboratory data. All authors have read and approved the final paper.

Corresponding author

Correspondence to Sarah Hanieh.

Ethics declarations

Ethics approval and consent to participate

The study protocol was approved by the Human Research Ethics Committee of the Northern Territory Department of Health and Menzies School of Health Research and the Melbourne Health Human Research Ethics Committee, Miwatj Health Aboriginal Corporation Board and the Local Shire Authority. Written informed consent was obtained from all parents/guardians on behalf of all child participants prior to enrolment.

Consent for publication

Not applicable.

Competing interests

None declared.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Hanieh, S., Mahanty, S., Gurruwiwi, G. et al. Enteric pathogen infection and consequences for child growth in young Aboriginal Australian children: a cross-sectional study. BMC Infect Dis 21, 9 (2021). https://doi.org/10.1186/s12879-020-05685-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12879-020-05685-1

Keywords

BMC Infectious Diseases

ISSN: 1471-2334

Contact us