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

被引:25
作者
Theonest, Ndyetabura O. [1 ,2 ]
Carter, Ryan W. [3 ]
Amani, Nelson [2 ]
Doherty, Sian L. [3 ]
Hugho, Ephrasia [2 ]
Keyyu, Julius D. [4 ]
Mable, Barbara K. [3 ]
Shirima, Gabriel M. [1 ]
Tarimo, Rigobert [1 ,2 ]
Thomas, Kate M. [2 ,5 ]
Haydon, Daniel T. [3 ]
Buza, Joram J. [1 ]
Allan, Kathryn J. [3 ]
Halliday, Jo E. B. [3 ]
机构
[1] Nelson Mandela African Inst Sci & Technol, Sch Life Sci & Bioengn, Arusha, Tanzania
[2] Kilimanjaro Clin Res Inst, Moshi, Tanzania
[3] Univ Glasgow, Coll Med Vet & Life Sci, Boyd Orr Ctr Populat & Ecosyst Hlth, Inst Biodivers Anim Hlth & Comparat Med, Glasgow, Lanark, Scotland
[4] Tanzania Wildlife Res Inst, Arusha, Tanzania
[5] Univ Otago, Ctr Int Hlth, Dunedin Sch Med, Dunedin, New Zealand
来源
PLOS ONE | 2019年 / 14卷 / 10期
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
SMALL MAMMALS; INFECTING RODENTS; FEBRILE ILLNESS; DIVERSITY; PREVALENCE; IDENTIFICATION; RATS; DIFFERENTIATION; THAILAND; PROVINCE;
D O I
10.1371/journal.pone.0223667
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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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