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Molecular detection and genetic characterization of Bartonella species from rodents and their associated ectoparasites from northern Tanzania. | LitMetric

Molecular detection and genetic characterization of Bartonella species from rodents and their associated ectoparasites from northern Tanzania.

PLoS One

The Boyd Orr Centre for Population and Ecosystem Health, Institute of Biodiversity Animal Health and Comparative Medicine, College of Medical Veterinary and Life Sciences, University of Glasgow, Glasgow, Scotland, United Kingdom.

Published: March 2020

AI Article Synopsis

  • The study investigates the prevalence of Bartonella bacteria in rodents and fleas in Tanzania, finding a 15% infection rate in rodents and a 27.5% infection rate in fleas.
  • It identifies that mature Rattus rattus rodents are more likely to be infected compared to immature ones, indicating potential risk factors for infection.
  • Genetic analysis reveals a variety of Bartonella genotypes closely related to known zoonotic species, emphasizing the need for further research on their impact on human health.

Article Abstract

Background: Bartonellae are intracellular bacteria, which can cause persistent bacteraemia in humans and a variety of animals. Several rodent-associated Bartonella species are human pathogens but data on their global distribution and epidemiology are limited. The aims of the study were to: 1) determine the prevalence of Bartonella infection in rodents and fleas; 2) identify risk factors for Bartonella infection in rodents; and 3) characterize the Bartonella genotypes present in these rodent and flea populations.

Methods And Results: Spleen samples collected from 381 rodents representing six different species were tested for the presence of Bartonella DNA, which was detected in 57 individuals (15.0%; 95% CI 11.3-18.5), of three rodent species (Rattus rattus n = 54, Mastomys natalensis n = 2 and Paraxerus flavovottis n = 1) using a qPCR targeting the ssrA gene. Considering R. rattus individuals only, risk factor analysis indicated that Bartonella infection was more likely in reproductively mature as compared to immature individuals (OR = 3.42, p <0.001). Bartonella DNA was also detected in 53 of 193 Xenopsylla cheopis fleas (27.5%: 95% CI 21.3-34.3) collected from R.rattus individuals. Analysis of ssrA and gltA sequences from rodent spleens and ssrA sequences from fleas identified multiple genotypes closely related (≥ 97% similar) to several known or suspected zoonotic Bartonella species, including B. tribocorum, B. rochalimae, B. elizabethae and B. quintana.

Conclusions: The ssrA and gltA sequences obtained from rodent spleens and ssrA sequences obtained from fleas reveal the presence of a diverse set of Bartonella genotypes and increase our understanding of the bartonellae present in Tanzanian. Further studies are needed to fully characterise the prevalence, genotypes and diversity of Bartonella in different host populations and their potential impacts on human health.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6793857PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0223667PLOS

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