Improvement of Bartonella henselae DNA Detection in Cat Blood Samples by Combining Molecular and Culture Methods
Author(s) -
Marina Rovani Drummond,
Bruno Grosselli Lania,
Pedro Paulo Vissotto de Paiva Diniz,
Rovílson Gilioli,
Daniele Masselli Rodrigues Demolin,
Diana G. Scorpio,
Edward B. Breitschwerdt,
Paulo Eduardo Neves Ferreira Velho
Publication year - 2018
Publication title -
journal of clinical microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.349
H-Index - 255
eISSN - 1070-633X
pISSN - 0095-1137
DOI - 10.1128/jcm.01732-17
Subject(s) - bartonella , bartonella henselae , cat scratch disease , bacteremia , biology , nested polymerase chain reaction , cats , polymerase chain reaction , blood culture , virology , microbiology and biotechnology , asymptomatic , natural reservoir , immunology , medicine , pathology , antibiotics , serology , gene , genetics , disease , outbreak , antibody
Bartonella spp. are bacteria of worldwide distribution that cause asymptomatic to fatal infections in animals and humans. The most common zoonotic species isBartonella henselae , for which cats are the major natural reservoir host. To better understandBartonella sp. diagnostic limitations, we determined the frequency of bloodstream infection in 112 cats by comparing and combining the results of multiple conventional and nested PCRs from blood and liquid culture samples. Using liquid culture conventional PCR,Bartonella sp. DNA was amplified from 27.7% of samples (31/112) compared to 90.2% of samples (101/112) by combining nested PCR from blood and liquid culture, indicating that PCR testing of more than one type of sample provides better sensitivity than a standalone PCR and that bloodstream infection is very frequent among cats in southeastern Brazil. This study reinforces the need for multistep testing forBartonella sp. infection to prevent false-negative diagnostic results, even in reservoir hosts such as cats that typically maintain higher bacteremia levels.
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