Department of Infectious Diseases, Hangzhou First People's Hospital, Hangzhou, 310006, China.
Key Laboratory of Microbial Technology and Bioinformatics of Zhejiang Province, Hangzhou, 310016, China.
Ann Clin Microbiol Antimicrob. 2024 Sep 28;23(1):86. doi: 10.1186/s12941-024-00748-6.
This study explored the molecular epidemiology and resistance mechanisms of 271 non-duplicate Salmonella enterica (S. enterica) strains, isolated mainly from adults (209/271) in a tertiary hospital in Hangzhou between 2020 and 2021. Through whole-genome sequencing and bioinformatics, the bacterial strains were classified into 46 serotypes and 54 sequence types (ST), with S. Enteritidis, S. 1,4,[5],12:i:-, and S. Typhimurium being the most prevalent serotypes and ST11, ST34, and ST19 the most common STs. The strains isolated from adults were primarily S. Enteritidis (59/209), while from children were mainly S. 1,4,[5],12:i:- (20/62). Worryingly, 12.55% strains were multi-drug resistant (MDR), with resistance rates to cefepime (FEP), ceftazidime (CAZ), ceftriaxone (CRO) and cefotaxime (CTX) of 7.38%, 9.23%, 15.87% and 16.24%, respectively, and resistance rates to levofloxacin (LEV) and ciprofloxacin (CIP) of 8.49% and 19.19%, respectively. It is worth noting that the resistance rates of CRO and CTX in children reached 30.65%. A total of 34 strains carried extended-spectrum β-lactamase (ESBL) genes, dominated by bla (13/34) and bla (12/34); it is notable that one strain of S. Saintpaul carried both bla and bla. The resistance mechanism to cephalosporins was mainly due to ESBL genes (20/43), and other genes included AmpC and β-lactamase genes. The strains resistant to quinolones mainly carried qnrS1 (27/53), and others included qnrB6, aac(6')-Ib-cr, and mutations in gyrA and parC. One strain did not carry common quinolone resistance genes but had a parC (p.T57S) mutation to cause CIP resistance. This research provides vital insights into the molecular epidemiology and resistance mechanisms of clinical S. enterica, implicating possible infection control strategies.
本研究探索了 2020 年至 2021 年期间,杭州一家三级医院从成人(209/271)中分离的 271 株非重复的沙门氏菌(S. enterica)的分子流行病学和耐药机制。通过全基因组测序和生物信息学,将细菌株分为 46 种血清型和 54 种序列型(ST),其中肠炎沙门氏菌、1、4、[5]、12:i:-和鼠伤寒沙门氏菌是最常见的血清型和 ST11、ST34 和 ST19 是最常见的 ST。从成人分离的菌株主要是肠炎沙门氏菌(59/209),而从儿童分离的菌株主要是 1、4、[5]、12:i:-(20/62)。令人担忧的是,12.55%的菌株为多药耐药(MDR),对头孢吡肟(FEP)、头孢他啶(CAZ)、头孢曲松(CRO)和头孢噻肟(CTX)的耐药率分别为 7.38%、9.23%、15.87%和 16.24%,对左氧氟沙星(LEV)和环丙沙星(CIP)的耐药率分别为 8.49%和 19.19%。值得注意的是,儿童 CRO 和 CTX 的耐药率分别达到 30.65%。共有 34 株菌携带超广谱β-内酰胺酶(ESBL)基因,主要为 bla(13/34)和 bla(12/34);值得注意的是,一株圣路易斯沙门氏菌携带 bla 和 bla。头孢菌素类耐药的主要机制是 ESBL 基因(20/43),其他基因包括 AmpC 和β-内酰胺酶基因。对喹诺酮类耐药的菌株主要携带 qnrS1(27/53),其他基因包括 qnrB6、aac(6')-Ib-cr 和 gyrA 和 parC 的突变。一株菌不携带常见的喹诺酮类耐药基因,但存在 parC(p.T57S)突变导致对 CIP 的耐药性。本研究为临床沙门氏菌的分子流行病学和耐药机制提供了重要的见解,暗示了可能的感染控制策略。