Scharinger Eva J, Dietrich Richard, Kleinsteuber Ina, Märtlbauer Erwin, Schauer Kristina
Department of Veterinary Science, Faculty of Veterinary Medicine, Ludwig-Maximilians-Universität München, Oberschleißheim, Germany.
Department of Veterinary Science, Faculty of Veterinary Medicine, Ludwig-Maximilians-Universität München, Oberschleißheim, Germany
Appl Environ Microbiol. 2016 Apr 4;82(8):2300-2311. doi: 10.1128/AEM.04016-15. Print 2016 Apr.
Cronobacter sakazakii is a foodborne pathogen associated with rare but often lethal infections in neonates. Powdered infant formula (PIF) represents the most frequent source of infection. Out of the identified serotypes (O1 to O7), O1, O2, and O3 are often isolated from clinical and PIF samples. Serotype-specific monoclonal antibodies (MAbs) suitable for application in enzyme immunoassays (EIAs) for the rapid detection of C. sakazakii have not yet been developed. In this study, we created specific MAbs with the ability to bind toC. sakazakii of serotypes O1, O2, and O3. Characterization by indirect EIAs, immunofluorescence, motility assays, and immunoblotting identified lipopolysaccharide (LPS) and exopolysaccharide (EPS) as the antigenic determinants of the MAbs. The established sandwich EIAs were highly sensitive and were able to detect between 2 × 10(3)and 9 × 10(6)CFU/ml. Inclusivity tests confirmed that 93% of serotype O1 strains, 100% of O2 strains, and 87% of O3 strains were detected at low cell counts. No cross-reactivity with >100 strains of Cronobacter spp. and other Enterobacter iaceae was observed, except for that with C. sakazakii serotype O3 and Cronobacter muytjensii serotype O1. Moreover, the sandwich EIAs detected C. sakazakii in PIF samples artificially contaminated with 1 to 10 bacterial cells per 10 g of sample after 15 h of preenrichment. The use of these serotype-specific MAbs not only allows the reliable detection of C. sakazakii strains but also enables simultaneous serotyping in a simple sandwich EIA method.
阪崎肠杆菌是一种食源性病原体,与新生儿罕见但往往致命的感染有关。婴儿配方奶粉(PIF)是最常见的感染源。在已鉴定的血清型(O1至O7)中,O1、O2和O3经常从临床和PIF样本中分离出来。尚未开发出适用于酶免疫分析(EIA)以快速检测阪崎肠杆菌的血清型特异性单克隆抗体(MAb)。在本研究中,我们制备了能够结合O1、O2和O3血清型阪崎肠杆菌的特异性单克隆抗体。通过间接EIA、免疫荧光、运动性测定和免疫印迹进行表征,确定脂多糖(LPS)和胞外多糖(EPS)为单克隆抗体的抗原决定簇。建立的夹心EIA高度灵敏,能够检测2×10³至9×10⁶CFU/ml。包容性测试证实,93%的O1血清型菌株、100%的O2血清型菌株和87%的O3血清型菌株在低细胞数时能够被检测到。除了与阪崎肠杆菌O3血清型和穆氏克罗诺杆菌O1血清型有交叉反应外,未观察到与100多种克罗诺杆菌属菌株和其他肠杆菌科细菌有交叉反应。此外,夹心EIA在预富集15小时后,能够检测每10克样本中人工污染1至10个细菌细胞的PIF样本中的阪崎肠杆菌。使用这些血清型特异性单克隆抗体不仅能够可靠地检测阪崎肠杆菌菌株,还能够通过简单的夹心EIA方法同时进行血清分型。