Ahmed Wedad, Neubauer Heinrich, Tomaso Herbert, El Hofy Fatma Ibrahim, Monecke Stefan, Abd El-Tawab Ashraf Awad, Hotzel Helmut
Friedrich-Loeffler-Institut, Institute of Bacterial Infections and Zoonoses, Naumburger Str. 96a, 07743 Jena, Germany.
Department of Microbiology, Faculty of Veterinary Medicine, Benha University, Moshtohor Toukh P.O. Box 13736, Benha 13511, Egypt.
Pathogens. 2021 Jan 21;10(2):97. doi: 10.3390/pathogens10020097.
This study aimed to investigate the prevalence and antimicrobial resistance of enterococci- and ESBL-producing isolated from milk of bovine mastitis cases in Egypt. Fifty milk samples of dairy animals were collected from localities in the Nile Delta region of Egypt. Isolates were identified using MALDI-TOF MS, and antibiotic susceptibility testing was performed by the broth microdilution method. PCR amplifications were carried out, targeting resistance-associated genes. Seventeen isolates and eight coliform isolates could be cultivated. Vancomycin resistance rate was high in The VITEK 2 system confirmed all isolates as ESBL-producing. All . isolates harbored (B), L and D genes. The A gene was detected in isolate, B was found in other while one isolate of exhibited the A gene. isolates exhibited high prevalence of erm(B) and tetL. isolates were analyzed by DNA microarray analysis. Four isolates were determined by O-serotyping as O8 (n = 1), O86 (n = 2) and O157 (n = 1). H-serotyping resulted in H11, H12, H21 (two isolates each) and one was of H16 type. Different virulence-associated genes were detected in isolates including A, A, B, L, I1 and I2, and the N gene was identified by DNA microarray analysis.
本研究旨在调查从埃及奶牛乳房炎病例的乳汁中分离出的肠球菌和产超广谱β-内酰胺酶(ESBL)菌的流行情况及抗菌药物耐药性。从埃及尼罗河三角洲地区的不同地点采集了50份奶牛的乳汁样本。使用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)对分离菌进行鉴定,并采用肉汤微量稀释法进行药敏试验。进行聚合酶链反应(PCR)扩增,靶向耐药相关基因。共培养出17株分离菌和8株大肠菌群分离菌。万古霉素耐药率较高。VITEK 2系统确认所有分离菌均产ESBL。所有分离菌均携带(B)、L和D基因。在1株分离菌中检测到A基因,在其他分离菌中发现B基因,而1株分离菌表现出A基因。分离菌中erm(B)和tetL的流行率较高。通过DNA微阵列分析对分离菌进行分析。通过O血清型鉴定,4株分离菌分别为O8(n = 1)、O86(n = 2)和O157(n = 1)。H血清型鉴定结果为H11、H12、H21(各2株),1株为H16型。在分离菌中检测到不同的毒力相关基因,包括A、A、B、L、I1和I2,通过DNA微阵列分析鉴定出N基因。