1994
DOI: 10.1128/jcm.32.4.942-948.1994
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Detection of Rochalimaea henselae DNA in specimens from cat scratch disease patients by PCR

Abstract: A PCR assay was developed by using degenerate primers that allow amplification of a 414-bp fragment of DNA from the rickettsia-like organisms Rochalimaea henselae and R. quintana. Internal oligonucleotides were used as hybridization probes, permitting rapid differentiation of these two Rochalimaea species. DNAs from 12 different isolates of R. henselae were amplified with the PCR primers, and the resulting 414-bp PCR product hybridized only with the R. henselae-specific probe. DNAs from four different isolates… Show more

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Cited by 263 publications
(91 citation statements)
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“…Most CSD cases in the past have been diagnosed by clinical and pathologic criteria, confirmed in later studies by a nonstandardized skin test (14). It is only since the identification of B henselae as the etiologic agent of CSD in the early 1990s that more sensitive, specific, and readily available diagnostic tests, particularly serology (9, 18) and PCR (11, 19), have been introduced, allowing for the association of new clinical syndromes, such as arthropathy, with CSD.…”
Section: Discussionmentioning
confidence: 99%
“…Most CSD cases in the past have been diagnosed by clinical and pathologic criteria, confirmed in later studies by a nonstandardized skin test (14). It is only since the identification of B henselae as the etiologic agent of CSD in the early 1990s that more sensitive, specific, and readily available diagnostic tests, particularly serology (9, 18) and PCR (11, 19), have been introduced, allowing for the association of new clinical syndromes, such as arthropathy, with CSD.…”
Section: Discussionmentioning
confidence: 99%
“…Isolation of B. henselae from patients is extremely difficult (La Scola & Raoult, 1999). The diagnosis of CSD relies on clinical manifestations, history of contact with cats, serology, or the detection of bacterial DNA in tissue specimens by PCR (Regnery et al, 1992;Anderson et al, 1994;Murakami et al, 2002;Woestyn et al, 2004;Tsuneoka & Tsukahara, 2006). Bartonella henselae strains are divided into two 16S rRNA (rrs) genotypes (16S type I/Houston-1 and 16S type II/Marseille), which correspond to two distinct human serotypes (Drancourt et al, 1996;La Scola et al, 2002).…”
Section: Introductionmentioning
confidence: 99%
“…In 1931 Debré observed the occurrence of regional lymphadenopathy following cat scratches, then 20 years later published a report of "la maladie des griffe du chat", establishing CSD as a clinical entity (1)(2)(3). Serological testing for this organism in humans and their cats, as well as the culture of B henselae and the detection of B henselae DNA from lymph nodes in patients with clinical disease, supports the role of this organism in CSD (4)(5)(6)(7). Formerly known as Rochalimaea henselae, the organism was reclassified as B henselae in 1993, following 16S rRNA sequence analysis (8).…”
mentioning
confidence: 88%
“…The IFA test currently available has shown significant crossreactivity between B henselae and B quintana (79). While BA, BP and trench fever are caused by B quintana, this organism has not been identified in specimens from patients with CSD by culture or PCR (6,48,79). Interpretation of a positive IFA test for Bartonella species should therefore be made in the context of clinical presentation.…”
Section: Diagnosis Of Csdmentioning
confidence: 99%
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