Rönnberg B, Söderlind O, Wadström T
J Clin Microbiol. 1985 Dec;22(6):893-6. doi: 10.1128/jcm.22.6.893-896.1985.
A competitive enzyme-linked immunosorbent assay (ELISA) was compared with the conventional suckling mouse assay for the identification of heat-stable enterotoxin (STa) in samples from piglets suffering from diarrhea. A total of 110 Escherichia coli isolates, 22 primary cultures, and 26 fecal samples from piglets up to 8 weeks of age with diarrhea were compared in parallel by both assays. Of the 110 isolates tested, all gave consistent results by the ELISA and the suckling mouse assay; 60 strains were negative and 50 strains produced STa by both tests. Identical results were obtained when 22 primary agar cultures were screened for STa production by both methods; 6 were found to produce STa, while 16 did not. When 26 fecal samples were tested for the presence of STa, 10 were negative and 12 were positive by both assays. One of the remaining four samples gave questionable positive results by both the suckling mouse assay and the ELISA, but E. coli isolated from this sample gave positive results by both tests. The remaining three samples were negative by the suckling mouse assay, but gave questionable positive results by the ELISA. E. coli isolates from these three samples were always negative by both assays. The ELISA used in this study provides a reliable and convenient method for diagnosing STa-producing enterotoxigenic E. coli of porcine origin.
采用竞争性酶联免疫吸附测定法(ELISA)与传统乳鼠试验对腹泻仔猪样本中的热稳定肠毒素(STa)进行鉴定比较。对110株大肠杆菌分离株、22份初代培养物以及26份来自8周龄以内腹泻仔猪的粪便样本,同时采用这两种方法进行平行比较。在检测的110株分离株中,ELISA法和乳鼠试验结果一致;两种检测方法均显示60株为阴性,50株产生STa。对22份初代琼脂培养物进行STa产生情况的两种方法筛查,结果相同;6份产生STa,16份未产生。对26份粪便样本进行STa检测时,两种检测方法均显示10份为阴性,12份为阳性。其余4份样本中的1份,乳鼠试验和ELISA法均给出可疑阳性结果,但从该样本中分离出的大肠杆菌两种检测均呈阳性。其余3份样本乳鼠试验为阴性,但ELISA法给出可疑阳性结果。这3份样本分离出的大肠杆菌两种检测始终为阴性。本研究中使用的ELISA法为诊断猪源产STa的产肠毒素大肠杆菌提供了一种可靠且便捷的方法。