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Genomic <jats:styled-content style=\"fixed-case\">DNA<\/jats:styled-content>s from fecal samples were subjected to <jats:styled-content style=\"fixed-case\">PCR<\/jats:styled-content>\u2010amplification of regions in the glycoprotein (<jats:italic>gp60<\/jats:italic>) or triose phosphate isomerase (<jats:italic>tpi<\/jats:italic>) gene, or the second internal transcribed spacer of nuclear ribosomal <jats:styled-content style=\"fixed-case\">DNA<\/jats:styled-content> (<jats:styled-content style=\"fixed-case\">ITS<\/jats:styled-content>\u20102). <jats:italic>Cryptosporidium<\/jats:italic>, <jats:italic><jats:styled-content style=\"fixed-case\">G<\/jats:styled-content>iardia<\/jats:italic>, and strongylid nematodes were detected in 94, 132 and 12 samples. <jats:italic>Cryptosporidium hominis<\/jats:italic> subgenotypes <jats:styled-content style=\"fixed-case\">I<\/jats:styled-content>b<jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>10<jats:styled-content style=\"fixed-case\">G<\/jats:styled-content>2, <jats:styled-content style=\"fixed-case\">I<\/jats:styled-content>d<jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>15<jats:styled-content style=\"fixed-case\">G<\/jats:styled-content>1, <jats:styled-content style=\"fixed-case\">I<\/jats:styled-content>g<jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>17, <jats:styled-content style=\"fixed-case\">I<\/jats:styled-content>g<jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>18, and <jats:styled-content style=\"fixed-case\">I<\/jats:styled-content>f<jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>13<jats:styled-content style=\"fixed-case\">G<\/jats:styled-content>1 were identified in 74.6, 16.9, 5.6, 1.4, and 1.4% of 71 samples, respectively. For <jats:italic>Cryptosporidium parvum<\/jats:italic>, subgenotypes <jats:styled-content style=\"fixed-case\">II<\/jats:styled-content>a<jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>17<jats:styled-content style=\"fixed-case\">G<\/jats:styled-content>2<jats:styled-content style=\"fixed-case\">R<\/jats:styled-content>1 (47.6%) and <jats:styled-content style=\"fixed-case\">II<\/jats:styled-content>a<jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>18<jats:styled-content style=\"fixed-case\">G<\/jats:styled-content>3<jats:styled-content style=\"fixed-case\">R<\/jats:styled-content>1 (23.8%) were identified in 23 samples. <jats:italic>Giardia duodenalis<\/jats:italic> assemblage <jats:styled-content style=\"fixed-case\">B<\/jats:styled-content> (78%) was more common than assemblage A (22%). In addition, <jats:styled-content style=\"fixed-case\">DNA<\/jats:styled-content> of the nematodes <jats:italic><jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>ncylostoma ceylanicum<\/jats:italic> (<jats:italic>n<\/jats:italic>\u00a0= 2), <jats:italic><jats:styled-content style=\"fixed-case\">A<\/jats:styled-content>ncylostoma duodenale<\/jats:italic> (4), <jats:italic><jats:styled-content style=\"fixed-case\">N<\/jats:styled-content>ecator americanus<\/jats:italic> (5), and <jats:italic>Haemonchus contortus<\/jats:italic> (1) was specifically detected. This is the first report of <jats:italic>A. ceylanicum<\/jats:italic> in two persons in Australia and, we provide molecular evidence of <jats:italic>H. contortus<\/jats:italic> in a child. This <jats:styled-content style=\"fixed-case\">SSCP<\/jats:styled-content>\u2010based approach should provide a useful diagnostic and analytical tool for a wide range of pathogens.<\/jats:p>","DOI":"10.1002\/elps.201300100","type":"journal-article","created":{"date-parts":[[2013,4,16]],"date-time":"2013-04-16T15:01:09Z","timestamp":1366124469000},"page":"1720-1728","source":"Crossref","is-referenced-by-count":46,"title":["Genetic characterization of selected parasites from people with histories of gastrointestinal disorders using a mutation scanning\u2010coupled approach"],"prefix":"10.1002","volume":"34","author":[{"given":"Anson V.","family":"Koehler","sequence":"first","affiliation":[{"name":"Faculty of Veterinary Science University of Melbourne  Victoria Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Richard S.","family":"Bradbury","sequence":"additional","affiliation":[{"name":"Medical Research Council International Nutrition Group  Keneba The Gambia"},{"name":"School of Medicine University of Tasmania  Hobart Tasmania Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Melita A.","family":"Stevens","sequence":"additional","affiliation":[{"name":"Melbourne Water Corporation  Victoria Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Shane R.","family":"Haydon","sequence":"additional","affiliation":[{"name":"Melbourne Water Corporation  Victoria Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Aaron R.","family":"Jex","sequence":"additional","affiliation":[{"name":"Faculty of Veterinary Science University of Melbourne  Victoria Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Robin B.","family":"Gasser","sequence":"additional","affiliation":[{"name":"Faculty of Veterinary Science University of Melbourne  Victoria Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2013,5,26]]},"reference":[{"key":"e_1_2_7_2_1","doi-asserted-by":"publisher","DOI":"10.1128\/CMR.05038-11"},{"key":"e_1_2_7_3_1","first-page":"197","volume":"81","author":"Kosek M.","year":"2003","journal-title":"Bull. 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