Infectivity of a novel type of Cryptosporidium andersoni to laboratory mice
Previously, we reported ‘a novel type’ of Cryptosporidium andersoni detected from cattle in Japan, and showed that the isolate was infective to mice. In the present study, we examined the patterns of oocyst shedding in both immunocompromised and immunocompetent mice, as well as pathological lesions...
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Veröffentlicht in: | Veterinary parasitology 2005-04, Vol.129 (1), p.165-168 |
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creator | Matsubayashi, Makoto Kimata, Isao Iseki, Motohiro Hajiri, Tomoya Tani, Hiroyuki Sasai, Kazumi Baba, Eiichiroh |
description | Previously, we reported ‘a novel type’ of
Cryptosporidium andersoni detected from cattle in Japan, and showed that the isolate was infective to mice. In the present study, we examined the patterns of oocyst shedding in both immunocompromised and immunocompetent mice, as well as pathological lesions in the infected mice. After oral inoculation with 1
×
10
6 oocysts, all five severe combined immunodeficiency (SCID) mice began to shed endogenously produced oocysts on day 6 post-inoculation (p.i.). The number of oocysts per day (OPD) reached 1
×
10
6 on day 17 p.i., and an OPD level of 1
×
10
6 to 10
7 was maintained until 91 days p.i. when the mice were sacrificed. In the five immunocompetent mice inoculated with 1
×
10
6 oocysts, the pre-patent and patent periods were 6 and 19 days, respectively, and the maximal OPD level was 1.5
×
10
5 on average. On histological examinations of infected SCID mice, a large number of parasites were present on the surface of the gastric glands of the stomach, but not in other organs examined. In conclusion, the novel type of
C. andersoni, which genetically coincides with
C. andersoni reported in other countries, is infective to mice, but susceptibility was lower than that of
Cryptosporidium muris infecting rodents from the perspective of infectivity to immunocompetent mice. |
doi_str_mv | 10.1016/j.vetpar.2005.01.003 |
format | Article |
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Cryptosporidium andersoni detected from cattle in Japan, and showed that the isolate was infective to mice. In the present study, we examined the patterns of oocyst shedding in both immunocompromised and immunocompetent mice, as well as pathological lesions in the infected mice. After oral inoculation with 1
×
10
6 oocysts, all five severe combined immunodeficiency (SCID) mice began to shed endogenously produced oocysts on day 6 post-inoculation (p.i.). The number of oocysts per day (OPD) reached 1
×
10
6 on day 17 p.i., and an OPD level of 1
×
10
6 to 10
7 was maintained until 91 days p.i. when the mice were sacrificed. In the five immunocompetent mice inoculated with 1
×
10
6 oocysts, the pre-patent and patent periods were 6 and 19 days, respectively, and the maximal OPD level was 1.5
×
10
5 on average. On histological examinations of infected SCID mice, a large number of parasites were present on the surface of the gastric glands of the stomach, but not in other organs examined. In conclusion, the novel type of
C. andersoni, which genetically coincides with
C. andersoni reported in other countries, is infective to mice, but susceptibility was lower than that of
Cryptosporidium muris infecting rodents from the perspective of infectivity to immunocompetent mice.</description><identifier>ISSN: 0304-4017</identifier><identifier>EISSN: 1873-2550</identifier><identifier>DOI: 10.1016/j.vetpar.2005.01.003</identifier><identifier>PMID: 15817217</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Cattle ; Cattle Diseases - immunology ; Cattle Diseases - parasitology ; cryptosporidiosis ; Cryptosporidiosis - immunology ; Cryptosporidiosis - parasitology ; Cryptosporidium ; Cryptosporidium - growth & development ; Cryptosporidium - pathogenicity ; Cryptosporidium andersoni ; Cryptosporidium muris ; fecal oocyst shedding ; Feces - parasitology ; Female ; gastric mucosa ; Gastric Mucosa - parasitology ; Immunocompetence ; Immunocompromised Host ; immunocompromised mice ; Infectivity to mice ; lesions (animal) ; Mice ; Mice, SCID ; oocysts ; Oocysts - isolation & purification ; Oocysts - pathogenicity ; Parasite Egg Count - veterinary ; patent period ; pathogenicity ; Pattern of oocyst shedding ; prepatent period ; Random Allocation ; severe combined immunodeficiency ; strains</subject><ispartof>Veterinary parasitology, 2005-04, Vol.129 (1), p.165-168</ispartof><rights>2005 Elsevier B.V.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c481t-f75414c4fec3894afa60c74beceeb31f53f73bee464e2071ea90390c3d1aadfa3</citedby><cites>FETCH-LOGICAL-c481t-f75414c4fec3894afa60c74beceeb31f53f73bee464e2071ea90390c3d1aadfa3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.vetpar.2005.01.003$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15817217$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Matsubayashi, Makoto</creatorcontrib><creatorcontrib>Kimata, Isao</creatorcontrib><creatorcontrib>Iseki, Motohiro</creatorcontrib><creatorcontrib>Hajiri, Tomoya</creatorcontrib><creatorcontrib>Tani, Hiroyuki</creatorcontrib><creatorcontrib>Sasai, Kazumi</creatorcontrib><creatorcontrib>Baba, Eiichiroh</creatorcontrib><title>Infectivity of a novel type of Cryptosporidium andersoni to laboratory mice</title><title>Veterinary parasitology</title><addtitle>Vet Parasitol</addtitle><description>Previously, we reported ‘a novel type’ of
Cryptosporidium andersoni detected from cattle in Japan, and showed that the isolate was infective to mice. In the present study, we examined the patterns of oocyst shedding in both immunocompromised and immunocompetent mice, as well as pathological lesions in the infected mice. After oral inoculation with 1
×
10
6 oocysts, all five severe combined immunodeficiency (SCID) mice began to shed endogenously produced oocysts on day 6 post-inoculation (p.i.). The number of oocysts per day (OPD) reached 1
×
10
6 on day 17 p.i., and an OPD level of 1
×
10
6 to 10
7 was maintained until 91 days p.i. when the mice were sacrificed. In the five immunocompetent mice inoculated with 1
×
10
6 oocysts, the pre-patent and patent periods were 6 and 19 days, respectively, and the maximal OPD level was 1.5
×
10
5 on average. On histological examinations of infected SCID mice, a large number of parasites were present on the surface of the gastric glands of the stomach, but not in other organs examined. In conclusion, the novel type of
C. andersoni, which genetically coincides with
C. andersoni reported in other countries, is infective to mice, but susceptibility was lower than that of
Cryptosporidium muris infecting rodents from the perspective of infectivity to immunocompetent mice.</description><subject>Animals</subject><subject>Cattle</subject><subject>Cattle Diseases - immunology</subject><subject>Cattle Diseases - parasitology</subject><subject>cryptosporidiosis</subject><subject>Cryptosporidiosis - immunology</subject><subject>Cryptosporidiosis - parasitology</subject><subject>Cryptosporidium</subject><subject>Cryptosporidium - growth & development</subject><subject>Cryptosporidium - pathogenicity</subject><subject>Cryptosporidium andersoni</subject><subject>Cryptosporidium muris</subject><subject>fecal oocyst shedding</subject><subject>Feces - parasitology</subject><subject>Female</subject><subject>gastric mucosa</subject><subject>Gastric Mucosa - parasitology</subject><subject>Immunocompetence</subject><subject>Immunocompromised Host</subject><subject>immunocompromised mice</subject><subject>Infectivity to mice</subject><subject>lesions (animal)</subject><subject>Mice</subject><subject>Mice, SCID</subject><subject>oocysts</subject><subject>Oocysts - isolation & purification</subject><subject>Oocysts - pathogenicity</subject><subject>Parasite Egg Count - veterinary</subject><subject>patent period</subject><subject>pathogenicity</subject><subject>Pattern of oocyst shedding</subject><subject>prepatent period</subject><subject>Random Allocation</subject><subject>severe combined immunodeficiency</subject><subject>strains</subject><issn>0304-4017</issn><issn>1873-2550</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFq3DAQhkVpaDZp36C0PvVmd8aSLftSKEubhgZySHMWsjwqWmzLlbQLfvt48UJv7WkY-Oaf4RvG3iMUCFh_PhQnSrMORQlQFYAFAH_FdthInpdVBa_ZDjiIXADKa3YT4wEABNTyDbvGqkFZotyxn_eTJZPcyaUl8zbT2eRPNGRpmenc78MyJx9nH1zvjmOmp55C9JPLks8G3fmgkw9LNjpDb9mV1UOkd5d6y56_f_u1_5E_PN7d778-5EY0mHIrK4HCiHUvb1qhra7BSNGRIeo42opbyTsiUQsqQSLpFngLhveodW81v2Wfttw5-D9HikmNLhoaBj2RP0ZVS1lCWcv_gijrCkR7BsUGmuBjDGTVHNyow6IQ1Nm2OqjNtjrbVoBqtb2OfbjkH7uR-r9DF70r8HEDrPZK_w4uquenEpADtE3DsVmJLxtBq7CTo6CicTQZ6l1Y_6J67_59wwts9Zz0</recordid><startdate>20050420</startdate><enddate>20050420</enddate><creator>Matsubayashi, Makoto</creator><creator>Kimata, Isao</creator><creator>Iseki, Motohiro</creator><creator>Hajiri, Tomoya</creator><creator>Tani, Hiroyuki</creator><creator>Sasai, Kazumi</creator><creator>Baba, Eiichiroh</creator><general>Elsevier B.V</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>M7N</scope><scope>7X8</scope></search><sort><creationdate>20050420</creationdate><title>Infectivity of a novel type of Cryptosporidium andersoni to laboratory mice</title><author>Matsubayashi, Makoto ; Kimata, Isao ; Iseki, Motohiro ; Hajiri, Tomoya ; Tani, Hiroyuki ; Sasai, Kazumi ; Baba, Eiichiroh</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c481t-f75414c4fec3894afa60c74beceeb31f53f73bee464e2071ea90390c3d1aadfa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Animals</topic><topic>Cattle</topic><topic>Cattle Diseases - immunology</topic><topic>Cattle Diseases - parasitology</topic><topic>cryptosporidiosis</topic><topic>Cryptosporidiosis - immunology</topic><topic>Cryptosporidiosis - parasitology</topic><topic>Cryptosporidium</topic><topic>Cryptosporidium - growth & development</topic><topic>Cryptosporidium - pathogenicity</topic><topic>Cryptosporidium andersoni</topic><topic>Cryptosporidium muris</topic><topic>fecal oocyst shedding</topic><topic>Feces - parasitology</topic><topic>Female</topic><topic>gastric mucosa</topic><topic>Gastric Mucosa - parasitology</topic><topic>Immunocompetence</topic><topic>Immunocompromised Host</topic><topic>immunocompromised mice</topic><topic>Infectivity to mice</topic><topic>lesions (animal)</topic><topic>Mice</topic><topic>Mice, SCID</topic><topic>oocysts</topic><topic>Oocysts - isolation & purification</topic><topic>Oocysts - pathogenicity</topic><topic>Parasite Egg Count - veterinary</topic><topic>patent period</topic><topic>pathogenicity</topic><topic>Pattern of oocyst shedding</topic><topic>prepatent period</topic><topic>Random Allocation</topic><topic>severe combined immunodeficiency</topic><topic>strains</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Matsubayashi, Makoto</creatorcontrib><creatorcontrib>Kimata, Isao</creatorcontrib><creatorcontrib>Iseki, Motohiro</creatorcontrib><creatorcontrib>Hajiri, Tomoya</creatorcontrib><creatorcontrib>Tani, Hiroyuki</creatorcontrib><creatorcontrib>Sasai, Kazumi</creatorcontrib><creatorcontrib>Baba, Eiichiroh</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><jtitle>Veterinary parasitology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Matsubayashi, Makoto</au><au>Kimata, Isao</au><au>Iseki, Motohiro</au><au>Hajiri, Tomoya</au><au>Tani, Hiroyuki</au><au>Sasai, Kazumi</au><au>Baba, Eiichiroh</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Infectivity of a novel type of Cryptosporidium andersoni to laboratory mice</atitle><jtitle>Veterinary parasitology</jtitle><addtitle>Vet Parasitol</addtitle><date>2005-04-20</date><risdate>2005</risdate><volume>129</volume><issue>1</issue><spage>165</spage><epage>168</epage><pages>165-168</pages><issn>0304-4017</issn><eissn>1873-2550</eissn><abstract>Previously, we reported ‘a novel type’ of
Cryptosporidium andersoni detected from cattle in Japan, and showed that the isolate was infective to mice. In the present study, we examined the patterns of oocyst shedding in both immunocompromised and immunocompetent mice, as well as pathological lesions in the infected mice. After oral inoculation with 1
×
10
6 oocysts, all five severe combined immunodeficiency (SCID) mice began to shed endogenously produced oocysts on day 6 post-inoculation (p.i.). The number of oocysts per day (OPD) reached 1
×
10
6 on day 17 p.i., and an OPD level of 1
×
10
6 to 10
7 was maintained until 91 days p.i. when the mice were sacrificed. In the five immunocompetent mice inoculated with 1
×
10
6 oocysts, the pre-patent and patent periods were 6 and 19 days, respectively, and the maximal OPD level was 1.5
×
10
5 on average. On histological examinations of infected SCID mice, a large number of parasites were present on the surface of the gastric glands of the stomach, but not in other organs examined. In conclusion, the novel type of
C. andersoni, which genetically coincides with
C. andersoni reported in other countries, is infective to mice, but susceptibility was lower than that of
Cryptosporidium muris infecting rodents from the perspective of infectivity to immunocompetent mice.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>15817217</pmid><doi>10.1016/j.vetpar.2005.01.003</doi><tpages>4</tpages></addata></record> |
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source | MEDLINE; ScienceDirect Journals (5 years ago - present) |
subjects | Animals Cattle Cattle Diseases - immunology Cattle Diseases - parasitology cryptosporidiosis Cryptosporidiosis - immunology Cryptosporidiosis - parasitology Cryptosporidium Cryptosporidium - growth & development Cryptosporidium - pathogenicity Cryptosporidium andersoni Cryptosporidium muris fecal oocyst shedding Feces - parasitology Female gastric mucosa Gastric Mucosa - parasitology Immunocompetence Immunocompromised Host immunocompromised mice Infectivity to mice lesions (animal) Mice Mice, SCID oocysts Oocysts - isolation & purification Oocysts - pathogenicity Parasite Egg Count - veterinary patent period pathogenicity Pattern of oocyst shedding prepatent period Random Allocation severe combined immunodeficiency strains |
title | Infectivity of a novel type of Cryptosporidium andersoni to laboratory mice |
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