Valat Charlotte, Forest Karine, Auvray Frédéric, Métayer Véronique, Méheut Thomas, Polizzi Charlène, Gay Emilie, Haenni Marisa, Oswald Eric, Madec Jean-Yves
Anses, Laboratoire de Lyon, Unité Antibiorésistance et Virulence Bactériennes, Lyon, France
Anses, Laboratoire de Lyon, Unité Antibiorésistance et Virulence Bactériennes, Lyon, France.
Appl Environ Microbiol. 2014 Dec;80(23):7230-4. doi: 10.1128/AEM.02365-14. Epub 2014 Sep 12.
The CS31A, F17, and F5 adhesins are usually targeted by serology-based methods to detect pathogenic Escherichia coli associated with calf enteritis. However, the virulence traits of the selected isolates are still poorly described. Here, from a set of 349 diarrheagenic E. coli isolates from cattle, we demonstrated a 70.8% concordance rate (Cohen's kappa, 0.599) between serology- and PCR-based approaches for the detection of adhesins under field conditions. A 79% to 82.4% correspondence between the two methods was found for fimbrial adhesins, whereas major discrepancies (33%) were observed for CS31A-type antigens. Various F17A variants were found, such as F17Ac (20K) (50%), F17Aa (FY) (18.9%), F17Ab (8.1%), and F17Ad (111K) (5.4%), including a high proportion (17.6%) of new F17A internal combinations (F17Aab, F17Aac, and F17Abc) or untypeable variants. In addition, the highest proportion of pathovar-associated virulence factor (VF) genes was observed among E. coli isolates that produced F5/F41 adhesins. A specific link between the heat-stable toxins related to the enterotoxigenic E. coli (ETEC) pathovar and adhesins was identified. STa was significantly linked to F5/F41 and EAST1 to CS31A adhesins (P < 0.001), respectively, whereas NTEC was associated with F17 adhesin (P = 0.001). Clustering between phylogroups according to the adhesin types was also observed. Also, few Shiga toxin-producing E. coli (STEC) or enteropathogenic E. coli (EPEC) pathovars were identified. Finally, no statistically significant difference was observed in the occurrence of extended-spectrum beta lactamase (ESBL) production according to the adhesins expressed by the isolates (P = 0.09). Altogether, this study gives new insights into the relationship between adhesins, VF, and antimicrobial resistance in calf enteritis and supports the need for further standardization of methodologies for such approaches.
CS31A、F17和F5黏附素通常是基于血清学方法检测与犊牛肠炎相关的致病性大肠杆菌的目标。然而,所选分离株的毒力特征仍描述甚少。在此,我们从一组349株牛源致泻性大肠杆菌分离株中发现,在现场条件下,基于血清学和基于PCR的黏附素检测方法之间的一致性率为70.8%(科恩kappa系数,0.599)。两种方法对菌毛黏附素的对应率为79%至82.4%,而对于CS31A类型抗原观察到较大差异(33%)。发现了多种F17A变体,如F17Ac(20K)(50%)、F17Aa(FY)(18.9%)、F17Ab(8.1%)和F17Ad(111K)(5.4%),包括高比例(17.6%)的新型F17A内部组合(F17Aab、F17Aac和F17Abc)或无法分型的变体。此外,在产生F5/F41黏附素的大肠杆菌分离株中观察到与致病变种相关的毒力因子(VF)基因比例最高。确定了与产肠毒素性大肠杆菌(ETEC)致病变种相关的热稳定毒素与黏附素之间的特定联系。STa分别与F5/F41显著相关,EAST1与CS31A黏附素显著相关(P < 0.001),而非产肠毒素性大肠杆菌(NTEC)与F17黏附素相关(P = 0.001)。还观察到根据黏附素类型在系统发育群之间的聚类情况。此外,鉴定出的产志贺毒素大肠杆菌(STEC)或肠致病性大肠杆菌(EPEC)致病变种很少。最后,根据分离株表达的黏附素,在超广谱β-内酰胺酶(ESBL)产生的发生率上未观察到统计学上的显著差异(P = 0.09)。总之,本研究为犊牛肠炎中黏附素、VF和抗菌药物耐药性之间的关系提供了新见解,并支持对此类方法的方法学进行进一步标准化的必要性。