Johnson Timothy J, Giddings Catherine W, Horne Shelley M, Gibbs Penelope S, Wooley Richard E, Skyberg Jerod, Olah Pam, Kercher Ronda, Sherwood Julie S, Foley Steven L, Nolan Lisa K
Department of Veterinary and Microbiological Sciences, North Dakota State University, Fargo 58105, USA.
Avian Dis. 2002 Apr-Jun;46(2):342-52. doi: 10.1637/0005-2086(2002)046[0342:LOISSG]2.0.CO;2.
Avian colibacillosis is a costly disease for the poultry industry. The mechanisms of virulence employed by the etiologic agent of this disease remain ill defined. However, accumulated evidence suggests that complement resistance and the presence of the increased serum survival gene (iss) in an avian Escherichia coli isolate may be indicative of its ability to cause disease. This association of iss with the E. coli implicated in avian disease may mean that iss and/or, perhaps, the genes associated with it are important contributors to avian E. coli virulence. For this reason, we have begun a search for iss's location in the bacterial genome. Thus far, iss in an avian E coli isolate has been localized to a conjugative R plasmid and estimated to be about 100 kilobase (kb) in size, encoding resistance to tetracycline and ampicillin. Hybridization studies have revealed that this plasmid contains sequences with homology to tsh, a gene associated with virulence of avian E coli; intI 1, a gene encoding the integrase of Class 1 integrons; and certain genes of the aerobactin- and CoIV-encoding operons. Sequences homologous to merA, a gene of the mercury resistance operon, were not identified on this R plasmid. This plasmid, when transferred into an avirulent, recipient strain by conjugation, enhanced the transconjugant's resistance to complement but not its virulence, in spite of the plasmid's possession of several putative virulence genes and traits. Such results may reflect the multifactorial nature of virulence, the degree of the recipient's impairment for virulence, or an inability of the embryo assay used here to detect this plasmid's contribution to virulence. Additionally, this plasmid contains genes encoding antimicrobial resistances, which may provide a selective advantage to virulent E. coli in the production environment. Further study will be needed to determine whether this plasmid is widespread among virulent E. coli and to ascertain the implications that this link between virulence and antimicrobial resistance genes may have for poultry management.
禽大肠杆菌病对家禽业来说是一种代价高昂的疾病。这种疾病的病原体所采用的毒力机制仍不清楚。然而,越来越多的证据表明,禽源大肠杆菌分离株对补体的抗性以及血清存活增强基因(iss)的存在可能表明其致病能力。iss与禽病相关大肠杆菌之间的这种关联可能意味着iss和/或与其相关的基因是禽源大肠杆菌毒力的重要促成因素。因此,我们开始寻找iss在细菌基因组中的位置。到目前为止,禽源大肠杆菌分离株中的iss已定位到一个接合性R质粒上,估计大小约为100千碱基(kb),编码对四环素和氨苄青霉素的抗性。杂交研究表明,该质粒包含与tsh(一种与禽源大肠杆菌毒力相关的基因)、intI 1(一种编码1类整合子整合酶的基因)以及气杆菌素编码操纵子和CoIV编码操纵子的某些基因具有同源性的序列。在这个R质粒上未鉴定到与汞抗性操纵子基因merA同源的序列。尽管该质粒拥有几个假定的毒力基因和特性,但通过接合将其转移到无毒的受体菌株中时,增强了接合子对补体的抗性,但没有增强其毒力。这样的结果可能反映了毒力的多因素性质、受体菌株毒力受损的程度,或者这里使用的胚胎试验无法检测到该质粒对毒力的贡献。此外,该质粒包含编码抗菌抗性的基因,这可能为生产环境中的有毒大肠杆菌提供选择优势。需要进一步研究以确定该质粒在有毒大肠杆菌中是否广泛存在,并确定毒力与抗菌抗性基因之间的这种联系对家禽管理可能产生的影响。