{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,10,2]],"date-time":"2023-10-02T05:11:28Z","timestamp":1696223488968},"reference-count":47,"publisher":"Wiley","issue":"5","license":[{"start":{"date-parts":[[2013,8,17]],"date-time":"2013-08-17T00:00:00Z","timestamp":1376697600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Zoonoses and Public Health"],"published-print":{"date-parts":[[2014,8]]},"abstract":"<jats:title>Summary<\/jats:title><jats:p><jats:italic><jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>ryptosporidium<\/jats:italic> are ubiquitous and significant enteropathogens of all classes of vertebrates and a major cause of human morbidity and mortality worldwide. Of the 24 recognized species, the zoonotic <jats:italic><jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>ryptosporidium parvum<\/jats:italic> and the host\u2010specific <jats:italic><jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>ryptosporidium hominis<\/jats:italic> cause the majority of cases of human cryptosporidiosis. Here, we report on structural and transcriptional variability between <jats:italic><jats:styled-content style=\"fixed-case\">C<\/jats:styled-content><\/jats:italic>.\u00a0<jats:italic>parvum<\/jats:italic> and <jats:italic><jats:styled-content style=\"fixed-case\">C<\/jats:styled-content><\/jats:italic>.\u00a0<jats:italic>hominis<\/jats:italic> at the <jats:styled-content style=\"fixed-case\">MIC<\/jats:styled-content>1 locus, which encodes a microneme localized thrombospondin\u2010like domain containing protein previously demonstrated to be critical for host cell infection by <jats:italic><jats:styled-content style=\"fixed-case\">C<\/jats:styled-content><\/jats:italic>.\u00a0<jats:italic>parvum<\/jats:italic>. We demonstrate, using reverse transcription quantitative <jats:styled-content style=\"fixed-case\">PCR<\/jats:styled-content> with the aid of genomic data from the <jats:styled-content style=\"fixed-case\">E<\/jats:styled-content>u<jats:styled-content style=\"fixed-case\">P<\/jats:styled-content>ath<jats:styled-content style=\"fixed-case\">DB<\/jats:styled-content> site, that the transcribed product in <jats:italic><jats:styled-content style=\"fixed-case\">C<\/jats:styled-content><\/jats:italic>.\u00a0<jats:italic>hominis<\/jats:italic> is both truncated and significantly down\u2010regulated in the sporozoite. We hypothesize that <jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>p<jats:styled-content style=\"fixed-case\">MIC<\/jats:styled-content>1 may be a genetic factor involved in facilitating the wider host range of <jats:italic><jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>.\u00a0parvum<\/jats:italic> in comparison with the specific host range of <jats:italic><jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>.\u00a0hominis<\/jats:italic>. Furthermore, we show that the presence of a microsatellite (<jats:styled-content style=\"fixed-case\">ML<\/jats:styled-content>\u20102) within the <jats:italic><jats:styled-content style=\"fixed-case\">C<\/jats:styled-content><\/jats:italic>.\u00a0<jats:italic>parvum <\/jats:italic><jats:styled-content style=\"fixed-case\">MIC<\/jats:styled-content>\u20101 locus enables the development of a <jats:styled-content style=\"fixed-case\">PCR<\/jats:styled-content> marker that can rapidly distinguish the zoonotic <jats:italic><jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>.\u00a0parvum<\/jats:italic> from <jats:italic><jats:styled-content style=\"fixed-case\">C<\/jats:styled-content><\/jats:italic>.\u00a0<jats:italic>hominis<\/jats:italic> and other significant human infectious <jats:italic><jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>ryptosporidium<\/jats:italic> species due to reproducible <jats:styled-content style=\"fixed-case\">PCR<\/jats:styled-content> slippage across the <jats:styled-content style=\"fixed-case\">ML<\/jats:styled-content>\u20102 microsatellite. Additionally, we demonstrate that this locus is tightly linked to the <jats:styled-content style=\"fixed-case\">GP<\/jats:styled-content>60 locus, a locus commonly used in the genetic characterization of <jats:italic><jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>.\u00a0parvum<\/jats:italic> and <jats:italic><jats:styled-content style=\"fixed-case\">C<\/jats:styled-content><\/jats:italic>.\u00a0<jats:italic>hominis<\/jats:italic> isolates. This marker should provide a robust and additional tool to aid in the rapid identification of <jats:italic><jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>.\u00a0parvum<\/jats:italic> from other <jats:italic><jats:styled-content style=\"fixed-case\">C<\/jats:styled-content>ryptosporidium<\/jats:italic> species.<\/jats:p>","DOI":"10.1111\/zph.12074","type":"journal-article","created":{"date-parts":[[2013,8,17]],"date-time":"2013-08-17T05:38:47Z","timestamp":1376717927000},"page":"324-337","source":"Crossref","is-referenced-by-count":3,"title":["<scp>PCR<\/scp> Slippage Across the <scp>ML<\/scp>\u20102 Microsatellite of the <i><scp>C<\/scp>ryptosporidium <\/i><scp>MIC<\/scp>1 Locus Enables Development of a <scp>PCR<\/scp> Assay Capable of Distinguishing the Zoonotic <i><scp>C<\/scp>ryptosporidium parvum<\/i> From Other Human Infectious <i><scp>C<\/scp>ryptosporidium<\/i> Species"],"prefix":"10.1111","volume":"61","author":[{"given":"M. A.","family":"Webber","sequence":"first","affiliation":[{"name":"Department of Medical Biotechnology School of Medicine Flinders University Bedford Park SA Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"I.","family":"Sari","sequence":"additional","affiliation":[{"name":"School of Pharmacy and Medical Sciences University of South Australia Adelaide SA Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"D.","family":"Hoefel","sequence":"additional","affiliation":[{"name":"Australian Water Quality Centre South Australian Water Corporation Adelaide SA Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P. T.","family":"Monis","sequence":"additional","affiliation":[{"name":"Department of Medical Biotechnology School of Medicine Flinders University Bedford Park SA Australia"},{"name":"School of Pharmacy and Medical Sciences University of South Australia Adelaide SA Australia"},{"name":"Australian Water Quality Centre South Australian Water Corporation Adelaide SA Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"B. J.","family":"King","sequence":"additional","affiliation":[{"name":"Department of Medical Biotechnology School of Medicine Flinders University Bedford Park SA Australia"},{"name":"Australian Water Quality Centre South Australian Water Corporation Adelaide SA Australia"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2013,8,17]]},"reference":[{"key":"e_1_2_7_2_1","doi-asserted-by":"publisher","DOI":"10.1128\/JCM.41.6.2744-2747.2003"},{"key":"e_1_2_7_3_1","doi-asserted-by":"publisher","DOI":"10.1016\/S0020-7519(01)00233-8"},{"key":"e_1_2_7_4_1","doi-asserted-by":"publisher","DOI":"10.1086\/519842"},{"key":"e_1_2_7_5_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1365-2672.2010.04764.x"},{"key":"e_1_2_7_6_1","doi-asserted-by":"crossref","first-page":"1","DOI":"10.2807\/ese.14.02.19086-en","article-title":"Long\u2010term Cryptosporidium typing reveals the aetiology and species\u2010specific epidemiology of human cryptosporidiosis in England and Wales, 2000 to 2003","volume":"14","author":"Chalmers R. 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