Department of Food Science and Technology, University of California, Davis, California, United States of America.
Western Center for Food Safety, University of California, Davis, California, United States of America.
PLoS One. 2023 Sep 7;18(9):e0291109. doi: 10.1371/journal.pone.0291109. eCollection 2023.
A comparative genomic analysis was conducted for 171 Salmonella isolates recovered from raw inshell almonds and raw almond kernels between 2001 and 2013 and for 30 Salmonella Enteritidis phage type (PT) 30 isolates recovered between 2001 and 2006 from a 2001 salmonellosis outbreak-associated almond orchard. Whole genome sequencing was used to measure the genetic distance among isolates by single nucleotide polymorphism (SNP) analyses and to predict the presence of plasmid DNA and of antimicrobial resistance (AMR) and virulence genes. Isolates were classified by serovars with Parsnp, a fast core-genome multi aligner, before being analyzed with the CFSAN SNP Pipeline (U.S. Food and Drug Administration Center for Food Safety and Applied Nutrition). Genetically similar (≤18 SNPs) Salmonella isolates were identified among several serovars isolated years apart. Almond isolates of Salmonella Montevideo (2001 to 2013) and Salmonella Newport (2003 to 2010) differed by ≤9 SNPs. Salmonella Enteritidis PT 30 isolated between 2001 and 2013 from survey, orchard, outbreak, and clinical samples differed by ≤18 SNPs. One to seven plasmids were found in 106 (62%) of the Salmonella isolates. Of the 27 plasmid families that were identified, IncFII and IncFIB plasmids were the most predominant. AMR genes were identified in 16 (9%) of the survey isolates and were plasmid encoded in 11 of 16 cases; 12 isolates (7%) had putative resistance to at least one antibiotic in three or more drug classes. A total of 303 virulence genes were detected among the assembled genomes; a plasmid that harbored a combination of pef, rck, and spv virulence genes was identified in 23% of the isolates. These data provide evidence of long-term survival (years) of Salmonella in agricultural environments.
对 2001 年至 2013 年间从生杏仁和生杏仁仁中回收的 171 株沙门氏菌分离株和 2001 年至 2006 年间从与 2001 年沙门氏菌病暴发相关的杏仁果园中回收的 30 株肠炎沙门氏菌噬菌体型 (PT) 30 分离株进行了比较基因组分析。全基因组测序用于通过单核苷酸多态性 (SNP) 分析测量分离株之间的遗传距离,并预测质粒 DNA 的存在以及抗生素耐药性 (AMR) 和毒力基因。使用 Parsnp(一种快速核心基因组多重对齐器)根据血清型对分离株进行分类,然后使用 CFSAN SNP Pipeline(美国食品和药物管理局食品安全和应用营养中心)进行分析。在相隔数年分离的几种血清型中发现了遗传上相似(≤18 个 SNP)的沙门氏菌分离株。2001 年至 2013 年分离的沙门氏菌蒙特维多(Montevideo)和 2003 年至 2010 年分离的沙门氏菌纽波特(Newport)分离株相差≤9 个 SNP。2001 年至 2013 年从调查、果园、暴发和临床样本中分离的肠炎沙门氏菌 PT 30 相差≤18 个 SNP。在 106 株(62%)沙门氏菌分离株中发现了 1 到 7 个质粒。在所鉴定的 27 个质粒家族中,IncFII 和 IncFIB 质粒最为常见。在 16 株(9%)调查分离株中发现了 AMR 基因,其中 11 株存在于 16 株中的 11 株中;12 株(7%)在三种或三种以上药物类别中至少对一种抗生素具有推定耐药性。在组装的基因组中检测到 303 个毒力基因;在 23%的分离株中发现了一个携带 pef、rck 和 spv 毒力基因组合的质粒。这些数据提供了沙门氏菌在农业环境中长期(数年)存活的证据。