Kersulyte Dangeruta, Rossi Mirko, Berg Douglas E
Department of Molecular Microbiology, Washington University Medical School, St Louis, Missouri, United States of America.
Faculty of Veterinary Medicine, University of Helsinki, Helsinki, Finland.
PLoS One. 2013 Dec 17;8(12):e83177. doi: 10.1371/journal.pone.0083177. eCollection 2013.
Strains of Helicobacter cetorum have been cultured from several marine mammals and have been found to be closely related in 16 S rDNA sequence to the human gastric pathogen H. pylori, but their genomes were not characterized further.
The genomes of H. cetorum strains from a dolphin and a whale were sequenced completely using 454 technology and PCR and capillary sequencing.
These genomes are 1.8 and 1.95 mb in size, some 7-26% larger than H. pylori genomes, and differ markedly from one another in gene content, and sequences and arrangements of shared genes. However, each strain is more related overall to H. pylori and its descendant H. acinonychis than to other known species. These H. cetorum strains lack cag pathogenicity islands, but contain novel alleles of the virulence-associated vacuolating cytotoxin (vacA) gene. Of particular note are (i) an extra triplet of vacA genes with ≤50% protein-level identity to each other in the 5' two-thirds of the gene needed for host factor interaction; (ii) divergent sets of outer membrane protein genes; (iii) several metabolic genes distinct from those of H. pylori; (iv) genes for an iron-cofactored urease related to those of Helicobacter species from terrestrial carnivores, in addition to genes for a nickel co-factored urease; and (v) members of the slr multigene family, some of which modulate host responses to infection and improve Helicobacter growth with mammalian cells.
Our genome sequence data provide a glimpse into the novelty and great genetic diversity of marine helicobacters. These data should aid further analyses of microbial genome diversity and evolution and infection and disease mechanisms in vast and often fragile ocean ecosystems.
已从数种海洋哺乳动物中培养出鲸型幽门螺杆菌菌株,发现其16S rDNA序列与人类胃部病原体幽门螺杆菌密切相关,但尚未对其基因组进行进一步表征。
利用454技术、PCR和毛细管测序对来自一只海豚和一头鲸的鲸型幽门螺杆菌菌株基因组进行了全序列测定。
这些基因组大小分别为1.8 Mb和1.95 Mb,比幽门螺杆菌基因组大约7%-26%,在基因含量以及共享基因的序列和排列上彼此显著不同。然而,每个菌株总体上与幽门螺杆菌及其后代沙猫幽门螺杆菌的关系比与其他已知物种的关系更为密切。这些鲸型幽门螺杆菌菌株缺乏cag致病岛,但含有与毒力相关的空泡毒素(vacA)基因的新等位基因。特别值得注意的是:(i)在宿主因子相互作用所需基因的5'三分之二区域内,有一组额外的vacA基因三联体,彼此间蛋白质水平同一性≤50%;(ii)不同的外膜蛋白基因集;(iii)一些与幽门螺杆菌不同的代谢基因;(iv)除了镍辅助因子脲酶基因外,还有与陆生食肉动物幽门螺杆菌物种相关的铁辅助因子脲酶基因;(v)slr多基因家族成员,其中一些成员可调节宿主对感染的反应并促进幽门螺杆菌在哺乳动物细胞中的生长。
我们的基因组序列数据让我们得以一窥海洋螺杆菌的新奇性和巨大的遗传多样性。这些数据应有助于进一步分析广阔且往往脆弱的海洋生态系统中的微生物基因组多样性与进化以及感染和疾病机制。