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
Hauptverfasser: Matsubayashi, Makoto, Kimata, Isao, Iseki, Motohiro, Hajiri, Tomoya, Tani, Hiroyuki, Sasai, Kazumi, Baba, Eiichiroh
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container_issue 1
container_start_page 165
container_title Veterinary parasitology
container_volume 129
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
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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 ; 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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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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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