Molecular characterisation and risk factor analysis of Cryptosporidium spp. in calves from Italy
To provide up-to-date information on the occurrence of Cryptosporidium in pre-weaned calves from Sardinia (Italy), the species implicated and their zoonotic potential, 147 faecal samples from 22 cattle herds were microscopically examined for Cryptosporidium oocysts; positive isolates were molecularl...
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creator | Díaz, P. Varcasia, A. Pipia, A. P. Tamponi, C. Sanna, G. Prieto, A. Ruiu, A. Spissu, P. Díez-Baños, P. Morrondo, P. Scala, A. |
description | To provide up-to-date information on the occurrence of
Cryptosporidium
in pre-weaned calves from Sardinia (Italy), the species implicated and their zoonotic potential, 147 faecal samples from 22 cattle herds were microscopically examined for
Cryptosporidium
oocysts; positive isolates were molecularly characterised. A questionnaire was developed to identify risk factors for
Cryptosporidium
infection. Overall, the percentage of positive calves and farms was 38.8 and 68.2%, respectively. The SSU rRNA-based PCR identified two
Cryptosporidium
species,
Cryptosporidium parvum
(95.8%) and
C. bovis
(4.2%). Sequence analyses of the glycoprotein (
gp60
) gene revealed that all
C. parvum
isolates belonged to the subtype family IIa (IIaA15G2R1 and IIaA16G3R1), with the exception of three isolates that belonged to the subtype family IId (IIdA20G1b and IIdA20). Mixed logistic regression results indicated that calves aged 15–21 days were more likely to be
Cryptosporidium
-positive. The risk of being positive was also significantly higher in herds from Central Sardinia and in farms using non-slatted flooring. In addition, the application of disinfectants and milk replacers was significantly associated with higher
Cryptosporidium
prevalence. In contrast, the risk of being positive was significantly reduced in halofuginone-treated calves. Our results reveal that a significant percentage of suckling calves are carriers of zoonotic subtypes of
C. parvum
. Thus, both healthy and diarrhoeic calves younger than 1 month may represent a risk for the transmission of cryptosporidiosis in humans and animals. |
doi_str_mv | 10.1007/s00436-018-6000-x |
format | Article |
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Cryptosporidium
in pre-weaned calves from Sardinia (Italy), the species implicated and their zoonotic potential, 147 faecal samples from 22 cattle herds were microscopically examined for
Cryptosporidium
oocysts; positive isolates were molecularly characterised. A questionnaire was developed to identify risk factors for
Cryptosporidium
infection. Overall, the percentage of positive calves and farms was 38.8 and 68.2%, respectively. The SSU rRNA-based PCR identified two
Cryptosporidium
species,
Cryptosporidium parvum
(95.8%) and
C. bovis
(4.2%). Sequence analyses of the glycoprotein (
gp60
) gene revealed that all
C. parvum
isolates belonged to the subtype family IIa (IIaA15G2R1 and IIaA16G3R1), with the exception of three isolates that belonged to the subtype family IId (IIdA20G1b and IIdA20). Mixed logistic regression results indicated that calves aged 15–21 days were more likely to be
Cryptosporidium
-positive. The risk of being positive was also significantly higher in herds from Central Sardinia and in farms using non-slatted flooring. In addition, the application of disinfectants and milk replacers was significantly associated with higher
Cryptosporidium
prevalence. In contrast, the risk of being positive was significantly reduced in halofuginone-treated calves. Our results reveal that a significant percentage of suckling calves are carriers of zoonotic subtypes of
C. parvum
. Thus, both healthy and diarrhoeic calves younger than 1 month may represent a risk for the transmission of cryptosporidiosis in humans and animals.</description><identifier>ISSN: 0932-0113</identifier><identifier>EISSN: 1432-1955</identifier><identifier>DOI: 10.1007/s00436-018-6000-x</identifier><identifier>PMID: 30008134</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Animals ; Biomedical and Life Sciences ; Biomedicine ; calves ; Cattle ; Cattle Diseases - epidemiology ; Cattle Diseases - parasitology ; Cryptosporidiosis ; Cryptosporidiosis - epidemiology ; Cryptosporidiosis - parasitology ; Cryptosporidium ; Cryptosporidium - classification ; Cryptosporidium - genetics ; Cryptosporidium - isolation & purification ; Cryptosporidium parvum ; Disinfectants ; DNA, Protozoan - genetics ; Factor analysis ; Farms ; feces ; Feces - parasitology ; Female ; floors ; genes ; glycoproteins ; herds ; humans ; Immunology ; Infection ; Italy ; Italy - epidemiology ; Male ; Medical Microbiology ; Microbiology ; milk replacer ; Oocysts ; Oocysts - classification ; Oocysts - genetics ; Oocysts - isolation & purification ; Original Paper ; polymerase chain reaction ; Prevalence ; Protozoa ; questionnaires ; regression analysis ; Risk Factors ; RNA ; RNA, Ribosomal - genetics ; rRNA ; Sardinia ; sequence analysis ; suckling ; Suckling behavior ; Surveys ; Weaning ; Zoonoses</subject><ispartof>Parasitology research (1987), 2018-10, Vol.117 (10), p.3081-3090</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2018</rights><rights>COPYRIGHT 2018 Springer</rights><rights>2018© Springer-Verlag GmbH Germany, part of Springer Nature 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c570t-d1eea88638d8e2fa68f277e488e10541b29568a8564fb1ff28ccbfabd6eaddcf3</citedby><cites>FETCH-LOGICAL-c570t-d1eea88638d8e2fa68f277e488e10541b29568a8564fb1ff28ccbfabd6eaddcf3</cites><orcidid>0000-0003-2445-1095</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00436-018-6000-x$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00436-018-6000-x$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30008134$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Díaz, P.</creatorcontrib><creatorcontrib>Varcasia, A.</creatorcontrib><creatorcontrib>Pipia, A. P.</creatorcontrib><creatorcontrib>Tamponi, C.</creatorcontrib><creatorcontrib>Sanna, G.</creatorcontrib><creatorcontrib>Prieto, A.</creatorcontrib><creatorcontrib>Ruiu, A.</creatorcontrib><creatorcontrib>Spissu, P.</creatorcontrib><creatorcontrib>Díez-Baños, P.</creatorcontrib><creatorcontrib>Morrondo, P.</creatorcontrib><creatorcontrib>Scala, A.</creatorcontrib><title>Molecular characterisation and risk factor analysis of Cryptosporidium spp. in calves from Italy</title><title>Parasitology research (1987)</title><addtitle>Parasitol Res</addtitle><addtitle>Parasitol Res</addtitle><description>To provide up-to-date information on the occurrence of
Cryptosporidium
in pre-weaned calves from Sardinia (Italy), the species implicated and their zoonotic potential, 147 faecal samples from 22 cattle herds were microscopically examined for
Cryptosporidium
oocysts; positive isolates were molecularly characterised. A questionnaire was developed to identify risk factors for
Cryptosporidium
infection. Overall, the percentage of positive calves and farms was 38.8 and 68.2%, respectively. The SSU rRNA-based PCR identified two
Cryptosporidium
species,
Cryptosporidium parvum
(95.8%) and
C. bovis
(4.2%). Sequence analyses of the glycoprotein (
gp60
) gene revealed that all
C. parvum
isolates belonged to the subtype family IIa (IIaA15G2R1 and IIaA16G3R1), with the exception of three isolates that belonged to the subtype family IId (IIdA20G1b and IIdA20). Mixed logistic regression results indicated that calves aged 15–21 days were more likely to be
Cryptosporidium
-positive. The risk of being positive was also significantly higher in herds from Central Sardinia and in farms using non-slatted flooring. In addition, the application of disinfectants and milk replacers was significantly associated with higher
Cryptosporidium
prevalence. In contrast, the risk of being positive was significantly reduced in halofuginone-treated calves. Our results reveal that a significant percentage of suckling calves are carriers of zoonotic subtypes of
C. parvum
. Thus, both healthy and diarrhoeic calves younger than 1 month may represent a risk for the transmission of cryptosporidiosis in humans and animals.</description><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>calves</subject><subject>Cattle</subject><subject>Cattle Diseases - epidemiology</subject><subject>Cattle Diseases - parasitology</subject><subject>Cryptosporidiosis</subject><subject>Cryptosporidiosis - epidemiology</subject><subject>Cryptosporidiosis - parasitology</subject><subject>Cryptosporidium</subject><subject>Cryptosporidium - classification</subject><subject>Cryptosporidium - genetics</subject><subject>Cryptosporidium - isolation & purification</subject><subject>Cryptosporidium parvum</subject><subject>Disinfectants</subject><subject>DNA, Protozoan - genetics</subject><subject>Factor analysis</subject><subject>Farms</subject><subject>feces</subject><subject>Feces - parasitology</subject><subject>Female</subject><subject>floors</subject><subject>genes</subject><subject>glycoproteins</subject><subject>herds</subject><subject>humans</subject><subject>Immunology</subject><subject>Infection</subject><subject>Italy</subject><subject>Italy - epidemiology</subject><subject>Male</subject><subject>Medical Microbiology</subject><subject>Microbiology</subject><subject>milk replacer</subject><subject>Oocysts</subject><subject>Oocysts - classification</subject><subject>Oocysts - genetics</subject><subject>Oocysts - isolation & purification</subject><subject>Original Paper</subject><subject>polymerase chain reaction</subject><subject>Prevalence</subject><subject>Protozoa</subject><subject>questionnaires</subject><subject>regression analysis</subject><subject>Risk Factors</subject><subject>RNA</subject><subject>RNA, Ribosomal - genetics</subject><subject>rRNA</subject><subject>Sardinia</subject><subject>sequence analysis</subject><subject>suckling</subject><subject>Suckling behavior</subject><subject>Surveys</subject><subject>Weaning</subject><subject>Zoonoses</subject><issn>0932-0113</issn><issn>1432-1955</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkl9rFDEUxYModq1-AF8k4Isvs978z74IZWlroeKLPsdsJtmmzkzGZKZ0v71ZtrZWFCQPyb35nUNyOQi9JrAkAOp9AeBMNkB0IwGguX2CFoQz2pCVEE_RAlb1DISwI_SilGsAoiTnz9ERq7QmjC_Qt0-p827ubMbuymbrJp9jsVNMA7ZDi2vxHYfaTrnWttuVWHAKeJ1345TKmHJs49zjMo5LHAfsbHfjCw459fhiqvxL9CzYrvhXd_sx-np2-mX9sbn8fH6xPrlsnFAwNS3x3motmW61p8FKHahSnmvtCQhONnQlpLZaSB42JASqndsEu2mlt23rAjtGHw6-47zpfev8MGXbmTHH3uadSTaaxzdDvDLbdGMUaE0Zrwbv7gxy-jH7Mpk-Fue7zg4-zcVQIphkjMJ_oKBAraSUUNG3f6DXac51kHtD0ByYVPKB2trOmziEVJ_o9qbmRAguFVVCVWr5F6qu1vfRpcGHWPuPBOQgcDmVkn24HwcBs0-QOSTI1ASZfYLMbdW8-X2O94pfkakAPQClXg1bnx9-9G_Xn8rq0gI</recordid><startdate>20181001</startdate><enddate>20181001</enddate><creator>Díaz, P.</creator><creator>Varcasia, A.</creator><creator>Pipia, A. P.</creator><creator>Tamponi, C.</creator><creator>Sanna, G.</creator><creator>Prieto, A.</creator><creator>Ruiu, A.</creator><creator>Spissu, P.</creator><creator>Díez-Baños, P.</creator><creator>Morrondo, P.</creator><creator>Scala, A.</creator><general>Springer Berlin Heidelberg</general><general>Springer</general><general>Springer Nature B.V</general><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>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-2445-1095</orcidid></search><sort><creationdate>20181001</creationdate><title>Molecular characterisation and risk factor analysis of Cryptosporidium spp. in calves from Italy</title><author>Díaz, P. ; Varcasia, A. ; Pipia, A. P. ; Tamponi, C. ; Sanna, G. ; Prieto, A. ; Ruiu, A. ; Spissu, P. ; Díez-Baños, P. ; Morrondo, P. ; Scala, A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c570t-d1eea88638d8e2fa68f277e488e10541b29568a8564fb1ff28ccbfabd6eaddcf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animals</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>calves</topic><topic>Cattle</topic><topic>Cattle Diseases - epidemiology</topic><topic>Cattle Diseases - parasitology</topic><topic>Cryptosporidiosis</topic><topic>Cryptosporidiosis - epidemiology</topic><topic>Cryptosporidiosis - parasitology</topic><topic>Cryptosporidium</topic><topic>Cryptosporidium - classification</topic><topic>Cryptosporidium - genetics</topic><topic>Cryptosporidium - isolation & purification</topic><topic>Cryptosporidium parvum</topic><topic>Disinfectants</topic><topic>DNA, Protozoan - genetics</topic><topic>Factor analysis</topic><topic>Farms</topic><topic>feces</topic><topic>Feces - parasitology</topic><topic>Female</topic><topic>floors</topic><topic>genes</topic><topic>glycoproteins</topic><topic>herds</topic><topic>humans</topic><topic>Immunology</topic><topic>Infection</topic><topic>Italy</topic><topic>Italy - epidemiology</topic><topic>Male</topic><topic>Medical Microbiology</topic><topic>Microbiology</topic><topic>milk replacer</topic><topic>Oocysts</topic><topic>Oocysts - classification</topic><topic>Oocysts - genetics</topic><topic>Oocysts - isolation & purification</topic><topic>Original Paper</topic><topic>polymerase chain reaction</topic><topic>Prevalence</topic><topic>Protozoa</topic><topic>questionnaires</topic><topic>regression analysis</topic><topic>Risk Factors</topic><topic>RNA</topic><topic>RNA, Ribosomal - genetics</topic><topic>rRNA</topic><topic>Sardinia</topic><topic>sequence analysis</topic><topic>suckling</topic><topic>Suckling behavior</topic><topic>Surveys</topic><topic>Weaning</topic><topic>Zoonoses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Díaz, P.</creatorcontrib><creatorcontrib>Varcasia, A.</creatorcontrib><creatorcontrib>Pipia, A. P.</creatorcontrib><creatorcontrib>Tamponi, C.</creatorcontrib><creatorcontrib>Sanna, G.</creatorcontrib><creatorcontrib>Prieto, A.</creatorcontrib><creatorcontrib>Ruiu, A.</creatorcontrib><creatorcontrib>Spissu, P.</creatorcontrib><creatorcontrib>Díez-Baños, P.</creatorcontrib><creatorcontrib>Morrondo, P.</creatorcontrib><creatorcontrib>Scala, A.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Parasitology research (1987)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Díaz, P.</au><au>Varcasia, A.</au><au>Pipia, A. P.</au><au>Tamponi, C.</au><au>Sanna, G.</au><au>Prieto, A.</au><au>Ruiu, A.</au><au>Spissu, P.</au><au>Díez-Baños, P.</au><au>Morrondo, P.</au><au>Scala, A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular characterisation and risk factor analysis of Cryptosporidium spp. in calves from Italy</atitle><jtitle>Parasitology research (1987)</jtitle><stitle>Parasitol Res</stitle><addtitle>Parasitol Res</addtitle><date>2018-10-01</date><risdate>2018</risdate><volume>117</volume><issue>10</issue><spage>3081</spage><epage>3090</epage><pages>3081-3090</pages><issn>0932-0113</issn><eissn>1432-1955</eissn><abstract>To provide up-to-date information on the occurrence of
Cryptosporidium
in pre-weaned calves from Sardinia (Italy), the species implicated and their zoonotic potential, 147 faecal samples from 22 cattle herds were microscopically examined for
Cryptosporidium
oocysts; positive isolates were molecularly characterised. A questionnaire was developed to identify risk factors for
Cryptosporidium
infection. Overall, the percentage of positive calves and farms was 38.8 and 68.2%, respectively. The SSU rRNA-based PCR identified two
Cryptosporidium
species,
Cryptosporidium parvum
(95.8%) and
C. bovis
(4.2%). Sequence analyses of the glycoprotein (
gp60
) gene revealed that all
C. parvum
isolates belonged to the subtype family IIa (IIaA15G2R1 and IIaA16G3R1), with the exception of three isolates that belonged to the subtype family IId (IIdA20G1b and IIdA20). Mixed logistic regression results indicated that calves aged 15–21 days were more likely to be
Cryptosporidium
-positive. The risk of being positive was also significantly higher in herds from Central Sardinia and in farms using non-slatted flooring. In addition, the application of disinfectants and milk replacers was significantly associated with higher
Cryptosporidium
prevalence. In contrast, the risk of being positive was significantly reduced in halofuginone-treated calves. Our results reveal that a significant percentage of suckling calves are carriers of zoonotic subtypes of
C. parvum
. Thus, both healthy and diarrhoeic calves younger than 1 month may represent a risk for the transmission of cryptosporidiosis in humans and animals.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>30008134</pmid><doi>10.1007/s00436-018-6000-x</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-2445-1095</orcidid><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; SpringerLink Journals - AutoHoldings |
subjects | Animals Biomedical and Life Sciences Biomedicine calves Cattle Cattle Diseases - epidemiology Cattle Diseases - parasitology Cryptosporidiosis Cryptosporidiosis - epidemiology Cryptosporidiosis - parasitology Cryptosporidium Cryptosporidium - classification Cryptosporidium - genetics Cryptosporidium - isolation & purification Cryptosporidium parvum Disinfectants DNA, Protozoan - genetics Factor analysis Farms feces Feces - parasitology Female floors genes glycoproteins herds humans Immunology Infection Italy Italy - epidemiology Male Medical Microbiology Microbiology milk replacer Oocysts Oocysts - classification Oocysts - genetics Oocysts - isolation & purification Original Paper polymerase chain reaction Prevalence Protozoa questionnaires regression analysis Risk Factors RNA RNA, Ribosomal - genetics rRNA Sardinia sequence analysis suckling Suckling behavior Surveys Weaning Zoonoses |
title | Molecular characterisation and risk factor analysis of Cryptosporidium spp. in calves from Italy |
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