Abstract

(1) Background: soil-transmitted helminths are a problem worldwide, largely affecting disadvantaged populations. The little data available indicates high rates of infection in some remote Aboriginal communities in Australia. Studies of helminths were carried out in the same remote community in the Northern Territory in 1994–1996 and 2010–2011; (2) Methods: fecal samples were collected from children aged <10 years and examined for helminths by direct smear microscopy. In the 2010–2011 study, some fecal samples were also analyzed by agar plate culture and PCR for Strongyloides stercoralis DNA. Serological analysis of fingerprick dried blood spots using a S. stercoralis NIE antigen was also conducted; (3) Results and Conclusions: a reduction in fecal samples positive for S. stercoralis, hookworm and Trichuris trichiura was seen between the studies in 1994–1996 and 2010–2011, likely reflecting public health measures undertaken in the region to reduce intestinal helminths. Comparison of methods to detect S. stercoralis showed that PCR of fecal samples and serological testing of dried blood spots was at least as sensitive as direct smear microscopy and agar plate culture. These methods have advantages for use in remote field studies.

Highlights

  • Soil-transmitted helminths are a worldwide problem generally affecting poor and vulnerable populations [1]

  • More recent surveys of S. stercoralis prevalence indicate that it is endemic in many northern Australian Aboriginal communities [4,5,6]

  • The mean number of intestinal parasites identified per fecal sample was 1.5 in 1994–1996 and 2 in 2010–2011

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Summary

Introduction

Soil-transmitted helminths are a worldwide problem generally affecting poor and vulnerable populations [1]. In Australia, there is a paucity of studies documenting the prevalence of soil-transmitted helminths due to the difficulties in diagnosing infection in communities, and timely transport to the nearest diagnostic laboratory. Routine direct smear microscopy of single stool specimens has a low sensitivity in chronic cases and can fail to detect larvae in up to 70% of chronic infections [7,10]. The use of the agar culture plate technique has improved detection in chronic S. stercoralis, with a sensitivity of 96% when compared with direct fecal smear, formalin-ethyl acetate concentration and Harada-Mori filter paper culture [7]. Serological examination for S. stercoralis antibodies improves detection in those with chronic infection. It may not readily detect those with acute infection as the prepatent period can be up to 28 days [8,11]

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