Clinical and Diagnostic Laboratory Immunology, January 1999, p. 41-44, Vol. 6, No. 1
1071-412X/99/$00.00+0
Centers for Disease Control and Prevention,
Public Health Service, U.S. Department of Health and Human
Services, Atlanta, Georgia,1 and
United
States Naval Medical Research Unit-2 (US NAMRU-2),
Received 28 May 1998/Returned for modification 22 September
1998/Accepted 10 November 1998
We studied evidence of Bartonella henselae and
Bartonella clarridgeiae infection in 54 cats living in
Jakarta, Indonesia. By using an indirect immunofluorescence assay, we
found immunoglobulin G antibody to B. henselae in 40 of 74 cats (54%). The blood of 14 feral cats was cultured on rabbit
blood agar plates for 28 days. Bartonella-like colonies
were identified as B. henselae or B. clarridgeiae by using restriction fragment length polymorphism analysis and direct sequencing of the PCR amplicons. Of the cats sampled in the study, 6 of 14 (43%; all feral) were culture positive for B. henselae; 3 of 14 (21%; 2 feral and 1 pet)
culture positive for B. clarridgeiae. This is the
first report that documents B. henselae and
B. clarridgeiae infections in Indonesian cats.
*
Corresponding author. Mailing address: Centers for
Disease Control and Prevention, Viral and Rickettsial Zoonoses Branch, Mailstop G13, 1600 Clifton Rd., Atlanta, GA 30333. Phone: (404) 639-1075. Fax: (404) 639-4436. E-mail: JGO0{at}CDC.GOV.
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