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Cytological and molecular detection of Leishmania infantum in different tissues of clinically normal and sick cats

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dc.contributor.author Chatzis, MK en
dc.contributor.author Andreadou, M en
dc.contributor.author Leontides, L en
dc.contributor.author Kasabalis, D en
dc.contributor.author Mylonakis, M en
dc.contributor.author Koutinas, AF en
dc.contributor.author Rallis, T en
dc.contributor.author Ikonomopoulos, J en
dc.contributor.author Saridomichelakis, MN en
dc.date.accessioned 2014-06-06T06:53:00Z
dc.date.available 2014-06-06T06:53:00Z
dc.date.issued 2014 en
dc.identifier.issn 18732550 en
dc.identifier.uri http://dx.doi.org/10.1016/j.vetpar.2014.02.044 en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/6302
dc.subject Cat en
dc.subject Cytology en
dc.subject Greece en
dc.subject Leishmania infantum en
dc.subject PCR en
dc.title Cytological and molecular detection of Leishmania infantum in different tissues of clinically normal and sick cats en
heal.type journalArticle en
heal.identifier.primary 10.1016/j.vetpar.2014.02.044 en
heal.publicationDate 2014 en
heal.abstract Natural infection of domestic cats by Leishmania infantum (synonym: L. chagasi) has been demonstrated in several European, Latin American, and Asian countries, and the estimated prevalence of infection, based mainly on blood PCR, ranges from 0.3% up to 60.6%. In this study we aimed to: (a) estimate the prevalence of the infection by L. infantum in clinically normal cats (group A; n = 50) and in cats with various clinical signs (group B; n = 50), living in an endemic region, by both cytological examination of four different tissues (lymph node, skin, bone marrow, and conjunctiva) and by PCR in four different tissues (blood, skin biopsies, bone marrow, and conjunctiva); (b) compare the diagnostic sensitivity of the above methods and evaluate for possible associations between their results; and (c) investigate the possible associations between infection by L. infantum and signalment, living conditions, season of sampling, and health status of the cats. The prevalence of the infection in the study population was 41% and did not differ (P = 0.839) between group A (42%) and B (40%) cats. Lymph node, skin, bone marrow and conjunctiva cytology was always negative. Therefore, the diagnosis of the infection was based only on PCR in blood, skin biopsy, bone marrow and conjunctiva, which was positive in 13%, 18.2%, 16% and 3.1% of the cats, respectively. PCR was positive in only one of the four tissues in 80.5% of the infected cats. The results differed (P = 0.014) among the four tissues and were less frequently positive in conjunctiva compared to skin biopsies and bone marrow (P = 0.007 for both comparisons), thus highlighting the need for multiple tissue PCR testing in order to minimize false-negative results. More PCR-positive cats were found when sampling was performed during the period of sandfly activity (odds ratio: 2.44; P = 0.022). Also, in group B cats, the likelihood of PCR-positivity was higher (odds ratio: 3.93; P = 0.042) among those presenting at least one systemic clinical sign that had been previously reported in cats with leishmaniosis. © 2014 Elsevier B.V. en
heal.publisher Elsevier en
heal.journalName Veterinary Parasitology en
dc.identifier.issue 3-4 en
dc.identifier.volume 202 en
dc.identifier.doi 10.1016/j.vetpar.2014.02.044 en
dc.identifier.spage 217 en
dc.identifier.epage 225 en


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