Department of Entomology and Plant Pathology, North Carolina State University, Raleigh, North Carolina, United States of America.
Comparative Medicine Institute, North Carolina State University, Raleigh, North Carolina, United States of America.
PLoS One. 2018 Dec 6;13(12):e0208327. doi: 10.1371/journal.pone.0208327. eCollection 2018.
Scrub typhus is a mites-borne rickettsiosis caused by the obligate intracellular Gram-negative bacterium Orientia tsutsugamushi. The disease is potentially life threatening and is prevalent in tropical Asia, islands of the western Pacific Ocean and northern Australia where an estimated one million cases occur annually. Orientia tsutsugamushi is transmitted by the bite of larval mites in the genus Leptotrombidium. In the present study, the composition of the microbiome in larvae, deutonymphs and adult males and females from laboratory colonies of L. imphalum that were infected as well as uninfected with O. tsutsugamushi were investigated by high-throughput sequencing of the bacterial 16S rRNA gene. Notably, the bacterial microbiomes of infected adult females were dominated by sequences of O. tsutsugamushi and an unidentified species of Amoebophilaceae, which together comprised 98.2% of bacterial sequences. To improve the taxonomic resolution of the Amoebophilaceae OTU a nearly full length sequence of the 16S rRNA gene was amplified, cloned, and Sanger sequenced. Infected female mites had 89 to 92% nucleotide identity with the Amoebophilaceae family, indicating that the bacterium was likely to be a species of a novel genus. The species composition of bacterial communities varied between mite life stages regardless of their infection status. Uninfected adults exhibited greater species diversity than adults infected with O. tsutsugamushi. In the infected colony, the rate of filial infection with Orientia was less than 100%. Larval and male mites that were PCR-negative for Orientia contained low numbers of sequences of Amoebophilaceae (0.01 and 0.06%, respectively) in their taxonomic profiles, suggesting that a mutualistic relationship exists between the novel species of Amoebophilaceae and O. tsutsugamushi. Our study findings provide the basis for further research to determine the influence of the novel Amoebophilaceae species on the bacterial microbiome and on vector susceptibility to and transovarial transmission of O. tsutsugamushi.
恙虫病是一种由专性细胞内革兰氏阴性细菌恙虫东方体引起的螨虫传播立克次体病。该疾病可能危及生命,流行于热带亚洲、西太平洋岛屿和澳大利亚北部,估计每年有 100 万例病例。恙虫东方体通过幼虫螨虫属的幼虫叮咬传播。在本研究中,通过高通量测序细菌 16S rRNA 基因,研究了感染和未感染恙虫东方体的实验室群体幼虫、若虫和成年雄性和雌性中的微生物组组成。值得注意的是,感染成年雌性的细菌微生物组主要由恙虫东方体和未鉴定的变形菌目阿米巴科的序列组成,这两种序列共同占细菌序列的 98.2%。为了提高阿米巴科 OTU 的分类分辨率,扩增、克隆并对 16S rRNA 基因进行了 Sanger 测序。感染的雌性螨虫与阿米巴科家族的核苷酸同一性为 89%至 92%,表明该细菌可能是一种新型属的物种。无论感染状态如何,螨虫生命阶段的细菌群落的物种组成都有所不同。未感染的成虫比感染恙虫东方体的成虫表现出更高的物种多样性。在感染的群体中, Orientia 的亲代感染率低于 100%。PCR 检测 Orientia 阴性的幼虫和雄性螨虫在其分类特征中含有低数量的阿米巴科序列(分别为 0.01%和 0.06%),这表明新型阿米巴科物种与恙虫东方体之间存在共生关系。我们的研究结果为进一步研究确定新型阿米巴科物种对细菌微生物组以及对媒介对恙虫东方体的易感性和经卵传播的影响提供了基础。