Laskey Alexander, Ottenbrite Marie, Devenish John, Kang Mingsong, Savic Mirjana, Nadin-Davis Susan, Chmara John, Lin Min, Robertson James, Bessonov Kyrylo, Gurnik Simone, Liu Kira, Nash John H E, Scott Andrew, Topp Edward, Guan Jiewen
Ottawa Laboratory, Fallowfield, Canadian Food Inspection Agency, Ottawa, ON, Canada.
National Microbiology Laboratory, Public Health Agency of Canada, Guelph, ON, Canada.
Front Microbiol. 2020 Jul 7;11:1591. doi: 10.3389/fmicb.2020.01591. eCollection 2020.
Ingestion of food- or waterborne antibiotic-resistant bacteria may lead to the dissemination of antibiotic-resistance genes in the gut microbiota and the development of antibiotic-resistant bacterial infection, a significant threat to animal and public health. Food or water may be contaminated with multiple resistant bacteria, but animal models on gene transfer were mainly based on single-strain infections. In this study, we investigated the mobility of β-lactam resistance following infection with single- versus multi-strain of resistant bacteria under ampicillin treatment. We characterized three bacterial strains isolated from food-animal production systems, O80:H26 and serovars Bredeney and Heidelberg. Each strain carries at least one conjugative plasmid that encodes a β-lactamase. We orally infected mice with each or all three bacterial strain(s) in the presence or absence of ampicillin treatment. We assessed plasmid transfer from the three donor bacteria to an introduced CV601gfp recipient in the mouse gut, and evaluated the impacts of the bacterial infection on gut microbiota and gut health. In the absence of ampicillin treatment, none of the donor or recipient bacteria established in the normal gut microbiota and plasmid transfer was not detected. In contrast, the ampicillin treatment disrupted the gut microbiota and enabled . Bredeney and Heidelberg to colonize and transfer their plasmids to the CV601gfp recipient. O80:H26 on its own failed to colonize the mouse gut. However, during co-infection with the two strains, O80:H26 colonized and transferred its plasmid to the CV601gfp recipient and a residential O2:H6 strain. The co-infection significantly increased plasmid transfer frequency, enhanced Proteobacteria expansion and resulted in inflammation in the mouse gut. Our findings suggest that single-strain infection models for evaluating gene transfer may underrepresent the consequences of multi-strain infections following the consumption of heavily contaminated food or water.
摄入食物或水源性抗生素耐药菌可能导致肠道微生物群中抗生素耐药基因的传播以及抗生素耐药细菌感染的发生,这对动物和公共卫生构成重大威胁。食物或水可能被多种耐药菌污染,但基因转移的动物模型主要基于单菌株感染。在本研究中,我们调查了在氨苄青霉素治疗下,单菌株与多菌株耐药菌感染后β-内酰胺耐药性的转移情况。我们对从食用动物生产系统中分离出的三种细菌菌株进行了特性分析,分别是O80:H26以及布雷德尼和海德堡血清型。每个菌株都携带至少一个编码β-内酰胺酶的接合质粒。我们在有或没有氨苄青霉素治疗的情况下,用每种或所有三种细菌菌株口服感染小鼠。我们评估了质粒从三种供体细菌转移到小鼠肠道中引入的CV601gfp受体菌的情况,并评估了细菌感染对肠道微生物群和肠道健康的影响。在没有氨苄青霉素治疗的情况下,供体菌或受体菌均未在正常肠道微生物群中定植,也未检测到质粒转移。相比之下,氨苄青霉素治疗破坏了肠道微生物群,使布雷德尼和海德堡菌株能够定植并将其质粒转移到CV601gfp受体菌。单独的O80:H26未能在小鼠肠道中定植。然而,在与另外两种菌株共同感染期间,O80:H26定植并将其质粒转移到CV601gfp受体菌和常驻的O2:H6菌株。共同感染显著增加了质粒转移频率,增强了变形菌的扩张,并导致小鼠肠道炎症。我们的研究结果表明,用于评估基因转移的单菌株感染模型可能无法充分代表食用严重污染的食物或水后多菌株感染的后果。