McDougall Fiona, Gordon David, Robins-Browne Roy, Bennett-Wood Vicki, Boardman Wayne S J, Graham Petra L, Power Michelle
School of Natural Sciences, Faculty of Science and Engineering, Macquarie University, NSW 2109, Australia.
Research School of Biology, Australian National University, ACT 2601, Australia.
Sci Total Environ. 2023 Dec 1;902:166336. doi: 10.1016/j.scitotenv.2023.166336. Epub 2023 Aug 15.
Enteropathogenic Escherichia coli (EPEC) is an important cause of diarrhoeal disease in human infants. EPEC strains are defined by the presence of specific virulence factors including intimin (encoded by the eae gene) and bundle forming pili (Bfp). Bfp is encoded by the bfp operon and includes the bfpA gene for the major pilus subunit. By definition, Bfp are only present in typical EPEC (tEPEC), for which, humans are considered to be the only known natural host. This study detected tEPEC in faecal samples from a wild Australian fruit bat species, the grey-headed flying-fox (Pteropus poliocephalus). Whole genome sequencing of 61 E. coli isolates from flying-foxes revealed that 21.3 % (95%CI: 13 %-33 %) were tEPEC. Phylogenetic analyses showed flying-fox tEPEC shared evolutionary lineages with human EPEC, but were predominantly novel sequence types (9 of 13) and typically harboured novel bfpA variants (11 of 13). HEp-2 cell adhesion assays showed adherence to human-derived epithelial cells by all 13 flying-fox tEPEC, indicating that they all carried functional Bfp. Using an EPEC-specific duplex PCR, it was determined that tEPEC comprised 17.4 % (95%CI: 13 %-22 %) of 270 flying-fox E. coli isolates. Furthermore, a tEPEC-specific multiplex PCR detected the eae and bfpA virulence genes in 18.0 % (95%CI: 8.0 %-33.7 %) of 506 flying-fox faecal DNA samples, with occurrences ranging from 1.3 % to 87.0 % across five geographic areas sampled over a four-year period. The identification of six novel tEPEC sequence types and five novel bfpA variants suggests flying-foxes carry bat-specific tEPEC lineages. However, their close relationship with human EPEC and functional Bfp, indicates that flying-fox tEPEC have zoonotic potential and that dissemination of flying-fox tEPEC into urban environments may pose a public health risk. The consistent detection of tEPEC in flying-foxes over extensive geographical and temporal scales indicates that both wild grey-headed flying-foxes and humans should be regarded as natural tEPEC hosts.
肠致病性大肠杆菌(EPEC)是人类婴儿腹泻疾病的重要病因。EPEC菌株由特定毒力因子的存在来定义,包括紧密黏附素(由eae基因编码)和成束菌毛(Bfp)。Bfp由bfp操纵子编码,包括主要菌毛亚基的bfpA基因。根据定义,Bfp仅存在于典型EPEC(tEPEC)中,而人类被认为是其唯一已知的天然宿主。本研究在澳大利亚野生果蝠物种灰头狐蝠(Pteropus poliocephalus)的粪便样本中检测到了tEPEC。对来自狐蝠的61株大肠杆菌分离株进行全基因组测序发现,21.3%(95%置信区间:13% - 33%)为tEPEC。系统发育分析表明,狐蝠tEPEC与人类EPEC共享进化谱系,但主要是新的序列类型(13株中有9株),并且通常含有新的bfpA变体(13株中有11株)。HEp - 2细胞黏附试验表明,所有13株狐蝠tEPEC均能黏附于人源上皮细胞,这表明它们都携带功能性Bfp。使用EPEC特异性双重PCR检测发现,在270株狐蝠大肠杆菌分离株中,tEPEC占17.4%(95%置信区间:13% - 22%)。此外,一种tEPEC特异性多重PCR在506份狐蝠粪便DNA样本中的18.0%(95%置信区间:8.0% - 33.7%)中检测到了eae和bfpA毒力基因,在四年期间对五个地理区域进行采样,其出现频率在1.3%至87.0%之间。六种新的tEPEC序列类型和五种新的bfpA变体的鉴定表明狐蝠携带蝙蝠特异性的tEPEC谱系。然而,它们与人类EPEC和功能性Bfp的密切关系表明,狐蝠tEPEC具有人畜共患病潜力,并且狐蝠tEPEC传播到城市环境中可能构成公共卫生风险。在广泛的地理和时间尺度上对狐蝠中tEPEC的持续检测表明,野生灰头狐蝠和人类都应被视为tEPEC的天然宿主。