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Bartonella henselae and Bartonella clarridgeiae infection in domestic cats from The Philippines.

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One hundred seven domestic cats from The Philippines were serologically tested to establish the prevalence of Bartonella infection. A subset of 31 of these cats also had whole blood collected to tentatively isolate Bartonella strains. Bartonella henselae and B. clarridgeiae were isolated from 19 (61%) of these cats. Bartonella henselae type I was isolated from 17 (89%) of the 19 culture-positive cats. Six cats (31%) were infected with B. clarridgeiae, of which four were coinfected with B. henselae. Sixty-eight percent (73 of 107) and 65% (70 of 107) of the cats had antibodies to B. henselae and B. clarridgeiae, respectively, detected by an immunofluorescence antibody (IFA) test at a titer > or = 1:64. When tested by enzyme immunoassay (EIA), 67 cats (62.6%) had antibodies to B. henselae and 71 cats (66.4%) had antibodies to B. clarridgeiae. Compared with the IFA test, the B. henselae EIA had a sensitivity of 90.4% and a specificity of 97%, with positive and negative predictive values of 98.5% and 82.5%, respectively. Similarly, the B. clarridgeiae EIA had a sensitivity of 97% and a specificity of 92% specificity, with positive and negative predictive values of 95.8% and 94.4%, respectively. The presence of antibodies to Bartonella was strongly associated with flea infestation. Domestic cats represent a large reservoir of Bartonella infection in the Philippines.
Title: Bartonella henselae and Bartonella clarridgeiae infection in domestic cats from The Philippines.
Description:
One hundred seven domestic cats from The Philippines were serologically tested to establish the prevalence of Bartonella infection.
A subset of 31 of these cats also had whole blood collected to tentatively isolate Bartonella strains.
Bartonella henselae and B.
clarridgeiae were isolated from 19 (61%) of these cats.
Bartonella henselae type I was isolated from 17 (89%) of the 19 culture-positive cats.
Six cats (31%) were infected with B.
clarridgeiae, of which four were coinfected with B.
henselae.
Sixty-eight percent (73 of 107) and 65% (70 of 107) of the cats had antibodies to B.
henselae and B.
clarridgeiae, respectively, detected by an immunofluorescence antibody (IFA) test at a titer > or = 1:64.
When tested by enzyme immunoassay (EIA), 67 cats (62.
6%) had antibodies to B.
henselae and 71 cats (66.
4%) had antibodies to B.
clarridgeiae.
Compared with the IFA test, the B.
henselae EIA had a sensitivity of 90.
4% and a specificity of 97%, with positive and negative predictive values of 98.
5% and 82.
5%, respectively.
Similarly, the B.
clarridgeiae EIA had a sensitivity of 97% and a specificity of 92% specificity, with positive and negative predictive values of 95.
8% and 94.
4%, respectively.
The presence of antibodies to Bartonella was strongly associated with flea infestation.
Domestic cats represent a large reservoir of Bartonella infection in the Philippines.

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