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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Veröffentlicht in:Parasitology research (1987) 2018-10, Vol.117 (10), p.3081-3090
Hauptverfasser: Díaz, P., Varcasia, A., Pipia, A. P., Tamponi, C., Sanna, G., Prieto, A., Ruiu, A., Spissu, P., Díez-Baños, P., Morrondo, P., Scala, A.
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container_issue 10
container_start_page 3081
container_title Parasitology research (1987)
container_volume 117
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
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P. ; Tamponi, C. ; Sanna, G. ; Prieto, A. ; Ruiu, A. ; Spissu, P. ; Díez-Baños, P. ; Morrondo, P. ; Scala, A.</creator><creatorcontrib>Díaz, P. ; Varcasia, A. ; Pipia, A. P. ; Tamponi, C. ; Sanna, G. ; Prieto, A. ; Ruiu, A. ; Spissu, P. ; Díez-Baños, P. ; Morrondo, P. ; Scala, A.</creatorcontrib><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 . 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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 &amp; 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 &amp; 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 &amp; 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 &amp; 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. 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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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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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