PLoS ONE (Jan 2019)

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

  • Ndyetabura O Theonest,
  • Ryan W Carter,
  • Nelson Amani,
  • Siân L Doherty,
  • Ephrasia Hugho,
  • Julius D Keyyu,
  • Barbara K Mable,
  • Gabriel M Shirima,
  • Rigobert Tarimo,
  • Kate M Thomas,
  • Daniel T Haydon,
  • Joram J Buza,
  • Kathryn J Allan,
  • Jo E B Halliday

DOI
https://doi.org/10.1371/journal.pone.0223667
Journal volume & issue
Vol. 14, no. 10
p. e0223667

Abstract

Read online

BackgroundBartonellae 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 resultsSpleen 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 ConclusionsThe 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.