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Molecular Survey of Species in Shelter Cats in Rio De Janeiro: Clinical, Hematological, and Risk Factors

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Specialty Tropical Medicine
Date 2019 Apr 25
PMID 31017080
Citations 6
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Abstract

The present study aimed to detect DNA in cats belonging to shelters, and to evaluate risk factors, clinical signs, and hematological abnormalities associated with infection. Complete blood counts and screening for the presence of DNA were performed on cats' ethylenediamine tetraacetic acid anticoagulant-blood samples. Eighty-three cats (39.9%) were positive for species. DNA was also detected in fleas and in the blood of cats infested by positive flea. Cats that had not been sterilized, had outdoor access, had histories of fights, and had concurrent flea infestation were more likely to be infected by species ( < 0.05). Age and sex were not associated with infection. Fifty-one (38.6%) symptomatic cats were positive to species ( > 0.05). Clinical conditions most commonly observed were signs of respiratory abnormality and S species coinfection ( > 0.05). Regarding hematological changes, eosinophilia was associated with infection ( < 0.05). A high frequency of species infection was found in shelter cats and highlights the importance of adequate flea-control programs to prevent infection in cats and consequently in adopters and other animals.

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References
1.
Miceli N, Gavioli F, Goncalves L, Andre M, Sousa V, de Sousa K . Molecular detection of feline arthropod-borne pathogens in cats in Cuiabá, state of Mato Grosso, central-western region of Brazil. Rev Bras Parasitol Vet. 2013; 22(3):385-90. DOI: 10.1590/S1984-29612013000300011. View

2.
Breitschwerdt E, Broadhurst J, Cherry N . as a cause of acute-onset febrile illness in cats. JFMS Open Rep. 2017; 1(2):2055116915600454. PMC: 5362002. DOI: 10.1177/2055116915600454. View

3.
Guptill L . Bartonellosis. Vet Microbiol. 2009; 140(3-4):347-59. DOI: 10.1016/j.vetmic.2009.11.011. View

4.
Tsai Y, Lin C, Chomel B, Chuang S, Tsai K, Wu W . Bartonella infection in shelter cats and dogs and their ectoparasites. Vector Borne Zoonotic Dis. 2010; 11(8):1023-30. DOI: 10.1089/vbz.2010.0085. View

5.
Mostl K, Egberink H, Addie D, Frymus T, Boucraut-Baralon C, Truyen U . Prevention of infectious diseases in cat shelters: ABCD guidelines. J Feline Med Surg. 2013; 15(7):546-54. PMC: 11148948. DOI: 10.1177/1098612X13489210. View