Echeverria P, Seriwatana J, Sethabutr O, Taylor D N
Clin Lab Med. 1985 Sep;5(3):447-62.
DNA hybridization with either cloned genes for enteropathogenic determinants or DNA segments that are species-specific is a valuable tool to identify certain bacterial enteric pathogens. Thus far, only E. coli and V. cholerae enterotoxin gene probes have been used to identify ETEC and V. cholerae in clinical specimens. DNA probes developed for Salmonella, Shigella, Campylobacter, and enteroinvasive and enteropathogenic E. coli need to be evaluated with clinical specimens. The major contribution of this system so far has been to examine large numbers of specimens in epidemiologic studies. Once nonradioactive DNA probes are developed, this system will have potential application in clinical laboratories and in research laboratories in the developing world where diarrheal disease causes its greatest impact.
使用针对肠道致病决定因素的克隆基因或物种特异性DNA片段进行DNA杂交,是鉴定某些肠道病原菌的一种有价值的工具。到目前为止,仅使用大肠杆菌和霍乱弧菌肠毒素基因探针来鉴定临床标本中的产肠毒素大肠杆菌和霍乱弧菌。针对沙门氏菌、志贺氏菌、弯曲杆菌以及侵袭性大肠杆菌和致病性大肠杆菌开发的DNA探针,需要用临床标本进行评估。到目前为止,该系统的主要作用是在流行病学研究中检测大量标本。一旦开发出非放射性DNA探针,该系统将在腹泻病影响最为严重的发展中世界的临床实验室和研究实验室中具有潜在应用价值。