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1.
J Am Anim Hosp Assoc ; 45(3): 118-24, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19411647

RESUMO

Eighty-six dogs were selected based upon Ehrlichia (E.) canis SNAP 3Dx positive results to determine clinical relevance of annual E. canis screening. Immunofluorescence assay showed 72 (84%) of 86 dogs were seroreactive for E. canis. Polymerase chain reaction (PCR) revealed that 12 (14%) of 86 dogs had Ehrlichia deoxyribonucleic acid; seven had E. canis, four had E. ewingii, and one was coinfected with E. chaffeensis and E. ewingii. Thrombocytopenia (<164,000 platelets/microL) was found in 28 (39%) of 72 dogs. In this study, thrombocytopenia was frequently detected in healthy Ehrlichia SNAP 3Dx-positive dogs, whereas active infection was infrequently confirmed by PCR. Therefore, treatment based upon screening results alone is not recommended.


Assuntos
Doenças do Cão/diagnóstico , Ehrlichiose/veterinária , Ensaio de Imunoadsorção Enzimática/veterinária , Imunofluorescência/veterinária , Reação em Cadeia da Polimerase/veterinária , Animais , Diagnóstico Diferencial , Testes Diagnósticos de Rotina/métodos , Testes Diagnósticos de Rotina/normas , Testes Diagnósticos de Rotina/veterinária , Doenças do Cão/sangue , Cães , Ehrlichia/genética , Ehrlichia/imunologia , Ehrlichia/isolamento & purificação , Ehrlichiose/sangue , Ehrlichiose/diagnóstico , Ensaio de Imunoadsorção Enzimática/normas , Imunofluorescência/normas , Reação em Cadeia da Polimerase/normas , Trombocitopenia/sangue , Estados Unidos
2.
Vector Borne Zoonotic Dis ; 7(4): 689-97, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-18021025

RESUMO

For many vector-borne organisms, dogs can be used as sentinels to estimate the risk of human infection. The objective of this study was to use dogs as sentinels for multiple vector-borne organisms in order to evaluate the potential for human infection with these agents in southeastern Brazil. Blood from 198 sick dogs with clinicopathological abnormalities consistent with tick-borne infections were selected at the São Paulo State University Veterinary Teaching Hospital in Botucatu and tested for DNA and/or antibodies against specific vector-borne pathogens. At least one organism was detected in 88% of the dogs, and Ehrlichia canis DNA was amplified from 78% of the blood samples. Bartonella spp. seroreactivity was found in 3.6%. Leishmania chagasi antibodies were detected in 1% of the dogs. There was no serological or polymerase chain reaction evidence of infection with Anaplasma phagocytophilum, Borrelia burgdorferi, Ehrlichia chaffeensis, Ehrlichia ewingii, and Rickettsia rickettsii. The full E. canis 16S rRNA gene sequence of one of the Brazilian strains obtained in this study was identical to the causative agent of human ehrlichiosis in Venezuela. Ehrlichia canis may pose a human health hazard and may be undiagnosed in southeastern Brazil, whereas exposure to the other organisms examined in this study is presumably infrequent.


Assuntos
Infecções por Bartonella/epidemiologia , Doenças do Cão/epidemiologia , Ehrlichiose/epidemiologia , Leishmaniose Visceral/epidemiologia , Vigilância de Evento Sentinela , Zoonoses/epidemiologia , Animais , Anticorpos Antibacterianos/sangue , Anticorpos Antiprotozoários/sangue , Bartonella/isolamento & purificação , Bartonella/fisiologia , Infecções por Bartonella/sangue , Brasil/epidemiologia , DNA Bacteriano/sangue , Doenças do Cão/sangue , Doenças do Cão/microbiologia , Doenças do Cão/parasitologia , Cães , Ehrlichia canis/genética , Ehrlichia canis/isolamento & purificação , Ehrlichia canis/fisiologia , Ehrlichiose/sangue , Feminino , Leishmania infantum/isolamento & purificação , Leishmania infantum/fisiologia , Leishmaniose Visceral/sangue , Masculino , Dados de Sequência Molecular , RNA Ribossômico 16S/genética , Alinhamento de Sequência
3.
PLoS Negl Trop Dis ; 9(1): e0003467, 2015 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-25590435

RESUMO

Bartonella species are blood-borne, re-emerging organisms, capable of causing prolonged infection with diverse disease manifestations, from asymptomatic bacteremia to chronic debilitating disease and death. This pathogen can survive for over a month in stored blood. However, its prevalence among blood donors is unknown, and screening of blood supplies for this pathogen is not routinely performed. We investigated Bartonella spp. prevalence in 500 blood donors from Campinas, Brazil, based on a cross-sectional design. Blood samples were inoculated into an enrichment liquid growth medium and sub-inoculated onto blood agar. Liquid culture samples and Gram-negative isolates were tested using a genus specific ITS PCR with amplicons sequenced for species identification. Bartonella henselae and Bartonella quintana antibodies were assayed by indirect immunofluorescence. B. henselae was isolated from six donors (1.2%). Sixteen donors (3.2%) were Bartonella-PCR positive after culture in liquid or on solid media, with 15 donors infected with B. henselae and one donor infected with Bartonella clarridgeiae. Antibodies against B. henselae or B. quintana were found in 16% and 32% of 500 blood donors, respectively. Serology was not associated with infection, with only three of 16 Bartonella-infected subjects seropositive for B. henselae or B. quintana. Bartonella DNA was present in the bloodstream of approximately one out of 30 donors from a major blood bank in South America. Negative serology does not rule out Bartonella spp. infection in healthy subjects. Using a combination of liquid and solid cultures, PCR, and DNA sequencing, this study documents for the first time that Bartonella spp. bacteremia occurs in asymptomatic blood donors. Our findings support further evaluation of Bartonella spp. transmission which can occur through blood transfusions.


Assuntos
Bacteriemia/epidemiologia , Infecções por Bartonella/transmissão , Bartonella henselae/isolamento & purificação , Doadores de Sangue , Adulto , Infecções por Bartonella/epidemiologia , Bartonella henselae/genética , Bartonella henselae/imunologia , Brasil/epidemiologia , Estudos Transversais , Feminino , Humanos , Masculino , Reação em Cadeia da Polimerase , Análise de Sequência de DNA
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