a Department of Pediatrics , University of Virginia School of Medicine and University of Virginia Children's Hospital , Charlottesville , Virginia.
b Center for Global Health, Division of Infectious Diseases and International Health, Department of Medicine , University of Virginia , Charlottesville , VA , USA.
Gut Microbes. 2018;9(3):264-278. doi: 10.1080/19490976.2018.1429877. Epub 2018 Apr 19.
Enteroaggregative E. coli (EAEC) is associated with food-borne outbreaks of diarrhea and growth faltering among children in developing countries. A Shiga toxin-producing EAEC strain of serotype O104:H4 strain caused one of the largest outbreaks of a food-borne infection in Europe in 2011. The outbreak was traced to contaminated fenugreek sprouts, yet the mechanisms whereby such persistent contamination of sprouts could have occurred are not clear. We found that under ambient conditions of temperature and in minimal media, pathogenic Shiga toxin-producing EAEC O104:H4 227-11 and non-Shiga toxin-producing 042 strains both produce high levels of exopolysaccharide structures (EPS) that are released to the external milieu. The exopolysaccharide was identified as colanic acid (CA). Unexpectedly, Shiga-toxin producing EAEC strain 227-11 produced 3-6-fold higher levels of CA than the 042 strain, suggesting differential regulation of the CA in the two strains. The presence of CA was accompanied by the formation of large biofilm structures on the surface of sprouts. The wcaF-wza chromosomal locus was required for the synthesis of CA in EAEC 042. Deletion in the glycosyltransferase wcaE gene abolished the production of CA in 042, and resulted in diminished adherence to sprouts when co-cultured at ambient temperature. In conclusion, this work suggests that copious production of CA may contribute to persistence of EAEC in the environment and suggests a potential explanation for the large Shiga toxin-producing EAEC outbreak in 2011.
肠聚集性大肠杆菌(EAEC)与发展中国家儿童食源性腹泻和生长迟缓有关。产志贺毒素的 EAEC O104:H4 血清型菌株引起了 2011 年欧洲最大的食源性感染爆发之一。该爆发可追溯到受污染的葫芦巴芽,但豆芽持续污染的机制尚不清楚。我们发现,在环境温度和最小培养基条件下,致病性产志贺毒素的 EAEC O104:H4 227-11 和非产志贺毒素的 042 菌株都产生高水平的胞外多糖结构(EPS),这些结构被释放到外部环境中。该胞外多糖被鉴定为柯兰酸(CA)。出乎意料的是,产志贺毒素的 EAEC 227-11 株比 042 株产生的 CA 高出 3-6 倍,表明这两株菌中 CA 的调控存在差异。CA 的存在伴随着豆芽表面形成大的生物膜结构。CA 在 EAEC 042 中的合成需要 wcaF-wza 染色体基因座。wcaE 基因的糖基转移酶缺失消除了 042 中 CA 的产生,并导致在环境温度下共培养时对豆芽的黏附性降低。总之,这项工作表明,CA 的大量产生可能有助于 EAEC 在环境中的持续存在,并为 2011 年大规模产志贺毒素 EAEC 爆发提供了潜在解释。