Programa de Doctorado, Posgrado Integral en Biotecnología, FCQB, UAS, Culiacan Sinaloa, 80030, Mexico.
School of Medicine, Autonomous University of Sinaloa, Culiacan, Sinaloa, 80019, Mexico.
World J Microbiol Biotechnol. 2024 Nov 2;40(12):371. doi: 10.1007/s11274-024-04176-8.
Recently, cyclomodulins have been identified in Escherichia coli (E. coli), which can induce dysplastic damage. This work aimed to determine the dysplastic activity of cyclomodulin-harboring E. coli isolated from CRC patients, obese and normal-weight subjects in a mouse model. Forty-two mice were pretreated with streptomycin, azoxymethane, and dextran sodium sulfate. Mice were infected with E. coli pks + isolated from a CRC patient, with E. coli pks + cif + isolated from obese or normal-weight subjects, or with E. coli HB101. The presence of cyclomodulin-harboring E. coli in the feces, weight loss, changes in fecal consistency, and the presence of blood in the feces were monitored and used to assess the disease activity index (DAI). After 62 days, the mice were sacrificed to evaluate the presence of intestinal polyps and dysplastic damage by histologic sections. Cyclomodulin-harboring E. coli colonized the mice; these mice exhibited weight loss and watery diarrhea, and isolated normal-weight E. coli had a higher DAI. Polyps were observed in mice infected with cyclomodulin-harboring E. coli in the ileum but to a greater extent in obese isolates. E. coli isolated from CRC showed more significant endothelial damage associated with dysplasia in the ileum in equal proportions from obese and normal-weight isolates. In conclusion, E. coli harboring cyclomodulins isolated from CRC, obesity, or normal weight can cause dysplastic damage in the ileum of mice and may be a risk factor for CRC development.
最近,已在大肠杆菌(E. coli)中鉴定出环调节素,它可诱导发育不良损伤。本研究旨在确定从 CRC 患者、肥胖和正常体重受试者中分离的携带环调节素的大肠杆菌在小鼠模型中的发育不良活性。42 只小鼠经链霉素、氧化偶氮甲烷和葡聚糖硫酸钠预处理。将来自 CRC 患者的 pks+E. coli、来自肥胖或正常体重受试者的 pks+cif+E. coli 或 HB101 感染小鼠。监测粪便中携带环调节素的大肠杆菌的存在、体重减轻、粪便稠度的变化以及粪便中是否有血,并用疾病活动指数(DAI)评估来评估疾病活动。62 天后,处死小鼠,通过组织学切片评估肠道息肉和发育不良损伤的存在。携带环调节素的大肠杆菌定植于小鼠;这些小鼠出现体重减轻和水样腹泻,且分离的正常体重大肠杆菌的 DAI 更高。在回肠感染携带环调节素的大肠杆菌的小鼠中观察到息肉,但在肥胖分离株中更为明显。在肥胖和正常体重分离株中,来自 CRC 的大肠杆菌显示出与发育不良相关的更显著的内皮损伤。总之,从 CRC、肥胖或正常体重中分离出的携带环调节素的大肠杆菌可引起小鼠回肠的发育不良损伤,可能是 CRC 发展的一个危险因素。