10 research outputs found

    Epidemiology of intestinal helminthiases in a rural community of Ethiopia: Is it time to expand control programs to include Strongyloides stercoralis and the entire community?

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    Soil transmitted helminths are highly prevalent worldwide. Globally, approximately 1.5 billion people are infected with Ascaris lumbricoides, Trichuris trichiura or hookworm. Endemic countries carry out periodic mass treatment of at-risk populations with albendazole or mebendazole as a control measure. Most prevalence studies have focused on school aged children and therefore control programs are implemented at school level, not at community level. In this study, the prevalence of intestinal helminths, including Strongyloides stercoralis, was examined using a comprehensive laboratory approach in a community in north-western Ethiopia. A cross-sectional survey was conducted on 792 individuals ≥5 years old in randomly selected houses in a rural district. Stools were examined using three techniques: a formol-ether concentration, the Baermann technique and a real time polymerase chain reaction test (these last two specific for S. stercoralis). Statistical analyses were performed between two large age groups, children (≤14 years old) and adults (≥15 years old). The prevalence of helminths was 91.3%; (95% CI: 89.3-93.3%). Hookworm was the most prevalent, 78.7% (95% CI 75.6-81.4%), followed by S. stercoralis 55.7% (95% CI 52.2-59.1%). Co-infection with both was detected in 45.4% (95% CI 42.0-49.0%) of the participants. The mean age of hookworm-infected individuals was significantly higher than non-infected ones (p = 0.003). Also, S. stercoralis infection was significantly associated with age, being more prevalent in adults (p = 0.002). This is the highest prevalence of S. stercoralis detected in Ethiopia so far. Our results highlight the need of searching specifically for infection by this parasite since it usually goes unnoticed if helminth studies rely only on conventional diagnostic techniques, i.e. Kato-Katz. Moreover, the focus of these programs on children undermines the actual prevalence of hookworm. The adult population acts as a reservoir for both hookworm and S. stercoralis and this fact may negatively impact the current control programs in Ethiopia which only target treatment of school aged children. This reservoir, together with a lack of adequate water, sanitation and hygiene, increases the probability of re-infection in children. Finally, the high prevalence of S. stercoralis found calls for a comprehensive diagnostic approach in endemic areas in addition to a revision of control measures that is, adding ivermectin to current albendazole/mebendazole, since it is the drug of choice for S. stercoralis.This study was funded by the Mundo Sano Foundation and the Spanish Network on Tropical Diseases Research (Red de Investigación cooperativa de Enfermedades Tropicales-RICET RD12/0018/0001. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.S

    Prevalence and Genetic Diversity of <i>Giardia duodenalis</i> and <i>Cryptosporidium</i> spp. among School Children in a Rural Area of the Amhara Region, North-West Ethiopia

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    <div><p>Backgroud</p><p><i>Giardia duodenalis</i> and <i>Cryptosporidium</i> spp. are enteric protozoan causing gastrointestinal illness in humans and animals. Giardiasis and cryptosporidiosis are not formally considered as neglected tropical diseases, but belong to the group of poverty-related infectious diseases that impair the development and socio-economic potential of infected individuals in developing countries.</p><p>Methods</p><p>We report here the prevalence and genetic diversity of <i>G</i>. <i>duodenalis</i> and <i>Cryptosporidium</i> spp. in children attending rural primary schools in the Bahir Dar district of the Amhara Region, Ethiopia. Stool samples were collected from 393 children and analysed by molecular methods. <i>G</i>. <i>duodenalis</i> was detected by real-time PCR, and the assemblages and sub-assemblages were determined by multilocus sequence-based genotyping of the glutamate dehydrogenase and β-giardin genes of the parasite. Detection and identification of <i>Cryptosporidium</i> species was carried out by sequencing of a partial fragment of the small-subunit ribosomal RNA gene.</p><p>Principal Findings</p><p>The PCR-based prevalences of <i>G</i>. <i>duodenalis</i> and <i>Cryptosporidium</i> spp. were 55.0% (216/393) and 4.6% (18/393), respectively. A total of 78 <i>G</i>. <i>duodenalis</i> isolates were successfully characterized, revealing the presence of sub-assemblages AII (10.3%), BIII (28.2%), and BIV (32.0%). Discordant typing results AII/AIII and BIII/BIV were identified in 7.7% and 15.4% of the isolates, respectively. An additional five (6.4%) isolates were assigned to assemblage B. No mixed infections of assemblages A+B were found. Extensive genetic variation at the nucleotide level was observed within assemblage B (but no within assemblage A), resulting in the identification of a large number of sub-types. <i>Cryptosporidium</i> diversity was demonstrated by the occurrence of <i>C</i>. <i>hominis</i>, <i>C</i>. <i>parvum</i>, and <i>C</i>. <i>viatorum</i> in the population under study.</p><p>Conclusions</p><p>Our data suggest an epidemiological scenario with an elevated transmission intensity of a wide range of <i>G</i>. <i>duodenalis</i> genetic variants. Importantly, the elevated degree of genetic diversity observed within assemblage B is consistent with the occurrence of intra-assemblage recombination in <i>G</i>. <i>duodenalis</i>.</p></div

    Evolutionary relationships among assemblages of <i>G</i>. <i>duodenalis</i> at the <i>BG</i> locus inferred by a Neighbor-Joining analysis of the nucleotide sequence covering a 487-bp region (positions 108 to 573 of GenBank accession number AY072727) of the gene.

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    <p>The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (500 iterations) is indicated next to the branches. Bootstrap values lower than 50% were not displayed. The evolutionary distances were computed using the Kimura 2-parameter method. The rate variation among sites was modelled with a gamma distribution (shape parameter = 2). Filled circles represent B sequences from this study, whereas open circles indicate B sequences previously reported in human isolates from Ethiopia (see ref. [<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0159992#pone.0159992.ref022" target="_blank">22</a>]).No outgroup taxa was used as beta-giardin is a <i>Giardia</i>-specific structural protein.</p

    Evolutionary relationships among assemblages of <i>G</i>. <i>duodenalis</i> at the <i>GDH</i> locus inferred by a Neighbor-Joining analysis of the nucleotide sequence covering a 403-bp region (positions 80 to 467 of GenBank accession number L40508) of the gene.

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    <p>The percentage of replicate trees in which the associated taxa clustered together in the bootstrap test (1,000 iterations) is indicated next to the branches. Bootstrap values lower than 50% were not displayed. The evolutionary distances were computed using the Kimura 2-parameter method. The rate variation among sites was modelled with a gamma distribution (shape parameter = 2). Filled circles and squares represent BIII and BIV sequences, respectively, from this study. Open squares indicate BIV sequences previously reported in human isolates from Ethiopia [see ref. <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0159992#pone.0159992.ref022" target="_blank">22</a>]. <i>Spironucleus vortens</i> was used as outgroup taxa.</p
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