Rodriguez-Valverde Diana, Leon-Montes Nancy, Belmont-Monroy Laura, Ruiz-Perez Fernando, Santiago Araceli E
University of Virginia, School of Medicine, Department of Pediatrics, Child Health Research Center, 409 Lane Road, MR-4 Building, P.O Box 801326, Charlottesville, VA, 22908, USA.
Laboratorio de Microbiología Molecular, Instituto Nacional de Pediatría, Mexico City, Mexico.
Sci Rep. 2025 Apr 22;15(1):13988. doi: 10.1038/s41598-025-96373-0.
Enteroaggregative Escherichia coli (EAEC) is a diarrheagenic pathotype associated with traveler's diarrhea, foodborne outbreaks, and sporadic diarrhea in industrialized and developing countries. Regulation of virulence factors in EAEC is mediated by the master regulator AggR, an AraC/XylS family member controlling the expression of more than 44 genes associated with metabolism and virulence. Although the AggR regulon is well-characterized, the mechanism and upstream signaling cascades that regulate its activation are poorly understood. This study demonstrates that Lpp (Braun's lipoprotein) and L, D-transpeptidases are required for AggR activation. We found that deletion lpp in EAEC resulted in the downregulation of more than 100 genes involved in transport, metabolism, and virulence. Among the genes, fourteen transcriptional factors, including AggR, were differentially expressed in 042Δlpp. Our findings also showed that Lpp anchoring to the peptidoglycan is a requisite for AggR-activation. Hence, chemical inhibition or genetic deletion of L, D-transpeptidases encoding genes involved in the crosslink of Lpp to the peptidoglycan abolished AggR activation. Moreover, the 042Δlpp mutant exhibited reduced biofilm formation on abiotic surfaces and reduced colonization of human intestinal colonoids. This is the first study to demonstrate the tight regulation of the AraC/XylS transcriptional regulator AggR, essential in EAEC virulence and intestinal colonization by components of the bacterial cell envelope.
肠集聚性大肠杆菌(EAEC)是一种致泻性致病型细菌,与工业化国家和发展中国家的旅行者腹泻、食源性疾病暴发以及散发性腹泻有关。EAEC中毒力因子的调控由主要调节因子AggR介导,AggR是AraC/XylS家族成员,控制着44多个与代谢和毒力相关基因的表达。尽管AggR调控子已得到充分表征,但其激活的机制和上游信号级联反应仍知之甚少。本研究表明,Lpp( Braun脂蛋白)和L,D-转肽酶是AggR激活所必需的。我们发现,EAEC中lpp基因的缺失导致100多个参与转运、代谢和毒力的基因表达下调。在这些基因中,包括AggR在内的14个转录因子在042Δlpp中差异表达。我们的研究结果还表明,Lpp锚定在肽聚糖上是AggR激活的必要条件。因此,化学抑制或基因敲除参与Lpp与肽聚糖交联的L,D-转肽酶编码基因可消除AggR激活。此外,042Δlpp突变体在非生物表面的生物膜形成减少,在人肠道类器官中的定殖减少。这是第一项证明AraC/XylS转录调节因子AggR受到严格调控的研究,AggR对于EAEC的毒力和细菌细胞壁成分在肠道中的定殖至关重要。