Jennifer N Russell, Min-Kuang Lee, Miguel I Uyaguari-Diaz, Ashton N Sies, Danae M Suchan, William Hsiao, Erin Fraser, Muhammad G Morshed, Andrew D S Cameron
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The bacterial isolates represented three different species from the Lyme disease-causing <i>Borrelia burgdorferi sensu lato</i> genospecies complex [<i>Borrelia burgdorferi sensu stricto</i> (<i>n</i>=47), <i>Borrelia americana</i> (<i>n</i>=3) and <i>Borrelia bissettiae</i> (<i>n</i>=1)]. The traditional eight-gene multi-locus sequence typing (MLST) strategy was applied to facilitate comparisons across studies. This identified 13 known <i>Borrelia</i> sequence types (STs), established 6 new STs, and assigned 5 novel types to the nearest sequence types. <i>B. burgdorferi</i> s. s. isolates were further differentiated into ten <i>ospC</i> types, plus one novel <i>ospC</i> with less than 92 % nucleotide identity to all previously defined <i>ospC</i> types. The MLST types resampled over extended time periods belonged to previously described STs that are distributed across North America. The most geographically widespread ST, ST.12, was isolated from all three tick species. Conversely, new <i>B. burgdorferi</i> s. s. 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引用次数: 0
摘要
气候的变化使得蜱虫及其动物宿主的地理分布不断扩大,增加了加拿大人畜共患包柔氏菌病的风险。然而,人们对加拿大落基山脉西部以及蜱虫载体太平洋伊蚊(Ixodes pacificus)、钝头伊蚊(Ixodes auritulus)和角伊蚊(Ixodes angustus)的鲍氏杆菌基因组多样性知之甚少。在此,我们报告了 1993 年至 2016 年间从多种蜱虫物种中采集的 51 个包柔氏菌分离物的全基因组霰弹枪序列,这些蜱虫主要分布在不列颠哥伦比亚省沿海地区的一系列动物宿主身上。这些细菌分离物代表了莱姆病致病包柔氏菌(Borrelia burgdorferi sensu lato genospecies complex)中的三个不同物种[严格意义上的包柔氏菌(Borrelia burgdorferi sensu stricto,n=47)、美洲包柔氏菌(Borrelia americana,n=3)和鲍氏杆菌(Borrelia bissettiae,n=1)]。采用传统的八基因多焦点序列分型(MLST)策略,以便于对各项研究进行比较。该方法确定了 13 个已知的包柔病毒序列类型(ST),建立了 6 个新的 ST,并将 5 个新类型归入最近的序列类型。B. burgdorferi s. s. 分离物被进一步区分为 10 种 ospC 类型,外加一种与之前定义的所有 ospC 类型的核苷酸同一性低于 92% 的新型 ospC。在较长时期内重新取样的 MLST 类型属于先前描述的 ST,这些 ST 分布在整个北美地区。地理分布最广的 ST(ST.12)从所有三个蜱种中分离出来。相反,来自温哥华岛的新的 B. burgdorferi s.温哥华岛和温哥华地区的新B. burgdorferi s. s.ST仅在短时间内被检测到,揭示了空间、时间和宿主蜱物种的惊人瞬变性,这可能是由于被扩展到北美的长寿命基因型所取代。
Whole-genome sequencing of Western Canadian Borrelia spp. collected from diverse tick and animal hosts reveals short-lived local genotypes interspersed with longer-lived continental genotypes.
Changing climates are allowing the geographic expansion of ticks and their animal hosts, increasing the risk of Borrelia-caused zoonoses in Canada. However, little is known about the genomic diversity of Borrelia from the west of the Canadian Rockies and from the tick vectors Ixodes pacificus, Ixodes auritulus and Ixodes angustus. Here, we report the whole-genome shotgun sequences of 51 Borrelia isolates from multiple tick species collected on a range of animal hosts between 1993 and 2016, located primarily in coastal British Columbia. The bacterial isolates represented three different species from the Lyme disease-causing Borrelia burgdorferi sensu lato genospecies complex [Borrelia burgdorferi sensu stricto (n=47), Borrelia americana (n=3) and Borrelia bissettiae (n=1)]. The traditional eight-gene multi-locus sequence typing (MLST) strategy was applied to facilitate comparisons across studies. This identified 13 known Borrelia sequence types (STs), established 6 new STs, and assigned 5 novel types to the nearest sequence types. B. burgdorferi s. s. isolates were further differentiated into ten ospC types, plus one novel ospC with less than 92 % nucleotide identity to all previously defined ospC types. The MLST types resampled over extended time periods belonged to previously described STs that are distributed across North America. The most geographically widespread ST, ST.12, was isolated from all three tick species. Conversely, new B. burgdorferi s. s. STs from Vancouver Island and the Vancouver region were only detected for short periods, revealing a surprising transience in space, time and host tick species, possibly due to displacement by longer-lived genotypes that expanded across North America.This article contains data hosted by Microreact.
期刊介绍:
Microbial Genomics (MGen) is a fully open access, mandatory open data and peer-reviewed journal publishing high-profile original research on archaea, bacteria, microbial eukaryotes and viruses.