Jans Christoph, Boleij Annemarie
Laboratory of Food Biotechnology, Institute of Food Nutrition and Health, Department of Health Science and Technology, ETH Zurich, Zurich, Switzerland.
Department of Pathology, Radboud Institute for Molecular Life Sciences, Radboudumc, Nijmegen, Netherlands.
Front Microbiol. 2018 Apr 10;9:603. doi: 10.3389/fmicb.2018.00603. eCollection 2018.
The complex (SBSEC) comprises several species inhabiting the animal and human gastrointestinal tract (GIT). They match the pathobiont description, are potential zoonotic agents and technological organisms in fermented foods. SBSEC members are associated with multiple diseases in humans and animals including ruminal acidosis, infective endocarditis (IE) and colorectal cancer (CRC). Therefore, this review aims to re-evaluate adhesion and colonization abilities of SBSEC members of animal, human and food origin paired with genomic and functional host-microbe interaction data on their road from colonization to infection. SBSEC seem to be a marginal population during GIT symbiosis that can proliferate as opportunistic pathogens. Risk factors for human colonization are considered living in rural areas and animal-feces contact. Niche adaptation plays a pivotal role where subsp () retained the ability to proliferate in various environments. Other SBSEC members have undergone genome reduction and niche-specific gene gain to yield important commensal, pathobiont and technological species. Selective colonization of CRC tissue is suggested for , possibly related to increased adhesion to cancerous cell types featuring enhanced collagen IV accessibility. can colonize, proliferate and may shape the tumor microenvironment to their benefit by tumor promotion upon initial neoplasia development. Bacteria cell surface structures including lipotheichoic acids, capsular polysaccharides and pilus loci (, and govern adhesion. Only human blood-derived contain complete pilus loci and other disease-associated surface proteins. Rumen or feces-derived and other SBSEC members lack or harbor mutated pili. Pili also contribute to binding to fibrinogen upon invasion and translocation of cells from the GIT into the blood system, subsequent immune evasion, human contact system activation and collagen-I-binding on damaged heart valves. Only carrying complete pilus loci seem to have highest IE potential in humans with significant links between bacteremia/IE and underlying diseases including CRC. Other SBSEC host-microbe combinations might rely on currently unknown mechanisms. Comparative genome data of blood, commensal and food isolates are limited but required to elucidate the role of pili and other virulence factors, understand pathogenicity mechanisms, host specificity and estimate health risks for animals, humans and food alike.
该复合体(SBSEC)包含几种栖息于动物和人类胃肠道(GIT)的菌种。它们符合病理共生体的描述,是发酵食品中的潜在人畜共患病原体和技术生物体。SBSEC成员与人类和动物的多种疾病相关,包括瘤胃酸中毒、感染性心内膜炎(IE)和结直肠癌(CRC)。因此,本综述旨在重新评估动物、人类和食物来源的SBSEC成员的黏附与定殖能力,并结合从定殖到感染过程中基因组和功能性宿主-微生物相互作用数据进行分析。SBSEC在GIT共生过程中似乎是边缘菌群,可作为机会性病原体增殖。人类定殖的风险因素包括生活在农村地区和接触动物粪便。生态位适应起着关键作用,其中亚种()保留了在各种环境中增殖的能力。其他SBSEC成员经历了基因组缩减和特定生态位基因获得,从而产生了重要的共生、病理共生和技术菌种。有人提出,可能会选择性定殖于CRC组织,这可能与对具有增强的IV型胶原可及性的癌细胞类型的黏附增加有关。在肿瘤形成初期,可定殖、增殖,并可能通过促进肿瘤生长来塑造有利于自身的肿瘤微环境。细菌细胞表面结构,包括脂磷壁酸、荚膜多糖和菌毛位点(、和)决定黏附。只有源自人类血液的含有完整的菌毛位点和其他与疾病相关的表面蛋白。源自瘤胃或粪便的和其他SBSEC成员缺乏菌毛或含有突变的菌毛。菌毛在细胞从GIT侵入并转移到血液系统、随后的免疫逃避、人类接触系统激活以及在受损心脏瓣膜上结合I型胶原方面也发挥着作用。只有携带完整菌毛位点的在人类中似乎具有最高的IE潜力,菌血症/IE与包括CRC在内的潜在疾病之间存在显著联系。其他SBSEC宿主-微生物组合可能依赖目前未知的机制。血液、共生和食物分离株的比较基因组数据有限,但对于阐明菌毛和其他毒力因子的作用、理解致病机制、宿主特异性以及评估动物、人类和食物的健康风险是必需的。