STRATEGY TO DETECT AND IDENTIFY BARTONELLA SPECIES IN ROUTINE CLINICAL LABORATORY YIELDS BARTONELLA-HENSELAE FROM HUMAN IMMUNODEFICIENCY VIRUS-POSITIVE PATIENT AND UNIQUE BARTONELLA STRAIN FROM HIS CAT
Je. Clarridge et al., STRATEGY TO DETECT AND IDENTIFY BARTONELLA SPECIES IN ROUTINE CLINICAL LABORATORY YIELDS BARTONELLA-HENSELAE FROM HUMAN IMMUNODEFICIENCY VIRUS-POSITIVE PATIENT AND UNIQUE BARTONELLA STRAIN FROM HIS CAT, Journal of clinical microbiology, 33(8), 1995, pp. 2107-2113
We wished to develop a cost-effective, rapid strategy to detect and id
entify Bartonella species in the clinical laboratory and to determine
the prevalence of Bartonella infection in the Houston veteran populati
on. Bartonella colonies were identified by colony morphology, Gram sta
in, RapID ANA, repetitive extragenic palindromic-PCR (REP-PCR) and who
le-cell fatty acid (CFA) analysis, and these methods were compared for
their usefulness. A new test order for ''Rochalimaea culture'' (the g
enus Bartonella was previously known as the genus Rochalimaea) was ins
tituted, and in addition, all blood specimens submitted for fungal cul
ture (obtained in an isolator tube) were processed for Bartonella cult
ure. Over a 16-month period we isolated Bartonella henselae from only
0.4% (2 of 533) of total cultures but from 1% (2 of 204) of human immu
nodeficiency virus-positive patients. After sufficient growth, identif
ication of the Bartonella isolates to the species level could be obtai
ned in 2 days. The REP-PCR allowed discrimination of all known species
, whereas CFA analysis distinguished all except B. henselae and Barton
ella quintana. The RapID ANA results failed to differentiate between B
. henselae and B. quintana, and results for other species differed by
only one or two tests. Blood obtained from a kitten which had been int
roduced into the household of one patient 2 months before the onset of
fever yielded a Bartonella strain which was shown to be different fro
m the strain from the patient and distinct from other Bartonella speci
es by a combination of REP-PCR, CFA, and growth characteristics. Subse
quent analysis of the citrate synthase gene sequence showed only an 86
% similarity with any of the other known Bartonella species, suggestin
g that this isolate represents a distinct, previously uncharacterized
species of Bartonella.