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Bartonella spp. Prevalence (Serology, Culture, and PCR) in Sanitary Workers in La Rioja Spain.


ABSTRACT: Bartonella spp. are increasingly implicated in association with a spectrum of zoonotic infectious diseases. One hundred sanitary workers in La Rioja, Spain completed a questionnaire and provided blood specimens for Bartonella spp. serology and Bartonella alpha-Proteobacteria growth medium (BAPGM) enrichment blood culture/PCR. Six immunofluorescence assays (IFA) were performed and aseptically obtained blood specimens were inoculated into liquid BAPGM and subcultured onto blood agar plates. Bartonella DNA was amplified using conventional and real-time PCR assays. The Bartonella spp., strain, or genotype was determined by DNA sequencing. Bartonella seroreactivity was documented in 83.1% and bloodstream infection in 21.6% of participants. Bartonella henselae, B. vinsonii subsp. berkhoffii genotypes I and III, and B. quintana were identified. IFA seroreactivity and PCR positivity were not statistically associated with self-reported symptoms. Our results suggest that exposure to and non-clinical infection with Bartonella spp. may occur more often than previously suspected in the La Rioja region.

SUBMITTER: Portillo A 

PROVIDER: S-EPMC7157737 | biostudies-literature | 2020 Mar

REPOSITORIES: biostudies-literature

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<i>Bartonella</i> spp. Prevalence (Serology, Culture, and PCR) in Sanitary Workers in La Rioja Spain.

Portillo Aránzazu A   Maggi Ricardo R   Oteo José A JA   Bradley Julie J   García-Álvarez Lara L   San-Martín Montserrat M   Roura Xavier X   Breitschwerdt Edward E  

Pathogens (Basel, Switzerland) 20200304 3


<i>Bartonella</i> spp. are increasingly implicated in association with a spectrum of zoonotic infectious diseases. One hundred sanitary workers in La Rioja, Spain completed a questionnaire and provided blood specimens for <i>Bartonella</i> spp. serology and <i>Bartonella</i> alpha-Proteobacteria growth medium (BAPGM) enrichment blood culture/PCR. Six immunofluorescence assays (IFA) were performed and aseptically obtained blood specimens were inoculated into liquid BAPGM and subcultured onto bloo  ...[more]

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