Zhang Zhiyi, Li Baisheng, Huang Huitao, Fang Yanmei, Yang Wenqiang
School of Public Health, Guangdong Pharmaceutical University, Guangzhou, People's Republic of China.
Faculty of Health Sciences, University of Macau, Macao, People's Republic of China.
Infect Drug Resist. 2024 May 6;17:1751-1762. doi: 10.2147/IDR.S452295. eCollection 2024.
This study was to identify and analyze the pathogen responsible for food poisoning in a tourist group traveling from Macao to Zhuhai.
Samples were obtained from 27 patients of 96 cases, as well as samples of contaminated food in Macau. The collected samples were subjected to serological identification, drug sensitivity analysis, drug resistance gene identification, virulence factor analysis, and tracing.
Twenty-six isolates and the salad isolate were ST11. Isolates from patients were exhibited significant resistance to Penicillin AMP (Ampicillin) and quinolones NAL (Nalidixic acid). Among these isolates, 21 strains were resistant to two or more antibiotics, indicating the multi-drug resistance (MDR). Genomic characteristics and phylogenetic analysis were performed on 9 of the isolates using whole genome sequencing (WGS). The analysis revealed that the resistance to AMP and NAL was primarily caused by a gryA mutation D87Y (9/9, 100%), and the presence of beta-lactam resistance genes blaOXA-1 (1/9, 11.11%), blaTEM-141 (1/9, 11.11%), and blaTEM-1B (8/9, 88.89%). It was also found a strains isolated from patients had two resistance genes to quinolones or beta-lactam drugs (1/8, 12.5%), respectively. The strains were found to possess 165 virulence genes, one adherence class virulence factor, one invasion class virulence factor and various pathogenicity islands, including SPI-1, SPI-2, SPI-3, SPI-4, SPI-5, SPI-9, SPI-10, SPI-13, SPI-14, SPI-15, SGI 1, CS54_island, and C63PI-1. Additionally, the virulence plasmids were detected, including IncFIB(s)-IncFII(s)-IncX1 (55.56%), IncFIB(s)-IncFII(s) (33.33%), and IncFIB(s)-IncFII(s)-IncHI2-IncHI2A (11.11%). PFGE (Pulsed Field Gel Electrophoresis) and phylogenetic tree analysis revealed a high degree of similarity between Salmonella isolates from patients and food samples from Macao.
This study identified Salmonella ST11 as the cause of the food poisoning outbreak. The findings highlight the importance of phenotypic characterization and next-generation sequencing (NGS) tools in epidemiological studies and emphasize the potential risk of a new emerging multi-antibiotic ST11 clone for .
本研究旨在鉴定和分析一起从澳门前往珠海的旅游团食物中毒事件的病原体。
从96例患者中的27例采集样本,以及澳门受污染食物的样本。对收集的样本进行血清学鉴定、药敏分析、耐药基因鉴定、毒力因子分析及溯源。
26株分离株及沙拉分离株均为ST11型。患者分离株对青霉素类AMP(氨苄西林)和喹诺酮类NAL(萘啶酸)表现出显著耐药性。在这些分离株中,21株对两种或更多抗生素耐药,表明存在多重耐药(MDR)。使用全基因组测序(WGS)对9株分离株进行了基因组特征和系统发育分析。分析显示,对AMP和NAL的耐药主要由gryA基因D87Y突变(9/9,100%)引起,同时存在β-内酰胺耐药基因blaOXA-1(1/9,11.11%)、blaTEM-141(1/9,11.11%)和blaTEM-1B(8/9,88.89%)。还发现1株患者分离株分别对喹诺酮类或β-内酰胺类药物有两个耐药基因(1/8,12.5%)。这些菌株被发现拥有165个毒力基因、1个黏附类毒力因子、1个侵袭类毒力因子以及各种致病岛,包括SPI-1、SPI-2、SPI-3、SPI-4、SPI-5、SPI-9、SPI-10、SPI-13、SPI-14、SPI-15、SGI 1、CS54_island和C63PI-1。此外,检测到毒力质粒,包括IncFIB(s)-IncFII(s)-IncX1(55.56%)、IncFIB(s)-IncFII(s)(33.33%)和IncFIB(s)-IncFII(s)-IncHI2-IncHI2A(11.11%)。脉冲场凝胶电泳(PFGE)和系统发育树分析显示,患者沙门氏菌分离株与澳门食物样本中的分离株高度相似。
本研究确定沙门氏菌ST11型为此次食物中毒暴发的病因。研究结果凸显了表型特征分析和新一代测序(NGS)工具在流行病学研究中的重要性,并强调了新兴的多重耐药ST11克隆对……的潜在风险。