Profiling Listeria monocytogenes in Hummus, Fresh Produce, and Food Processing Environments in the Western Cape, South Africa

IF 4.6 3区 生物学 Q2 MICROBIOLOGY
Samantha Anne du Toit, Pieter A. Gouws, Diane Rip
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引用次数: 0

Abstract

Listeria monocytogenes is pervasive in agricultural environments and difficult to eradicate from food-processing facilities. Consequently, various foods become contaminated, posing health risks to immunocompromised individuals. This surveillance study aimed to enhance the understanding of the genetic diversity, virulence, plasmid content, sanitizer tolerance, and antibiotic resistance of L. monocytogenes from ready-to-eat (RTE) hummus, fresh produce and food-processing environments in the Western Cape, South Africa (2018–2021). Sixty L. monocytogenes isolates were classified as lineage I or lineage II using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Lineage I was notably prevalent overall (57%; n = 34) and significantly associated with fresh produce (88%; n = 7) (p = 0.04). Whole-genome sequencing (WGS) and bioinformatic analysis characterized a subset of 20 L. monocytogenes isolates into seven sequence types (STs) (ST1, ST2, ST3, ST5, ST101, ST121, ST204), and three serotypes (1/2a, 1/2b, 4b). ST204 (38%; n = 3) was most prevalent in the food-processing environment, ST5 (50%; n = 3) in fresh produce, and ST5 (33%; n = 2), ST101 (33%; n = 2) and ST121 (33%; n = 2), in RTE hummus. However, no single serotype or ST was significantly overrepresented in any category (p > 0.05). All isolates carried both Listeria pathogenicity island (LIPI)-1 and LIPI-2 gene clusters. Two isolates (ST1 and ST3) contained all genes comprising LIPI-3. Two ST5 isolates from RTE hummus contained the tetM gene. Isolates from different origins contained the emrC, bcrABC or qacH genes conferring tolerance to benzalkonium chloride, a quaternary ammonium compound class of sanitizer. RTE hummus, fresh produce and the food-processing environment are susceptible to contamination by diverse and virulent L. monocytogenes strains.

Abstract Image

南非西开普省鹰嘴豆泥、新鲜农产品和食品加工环境中的单核细胞增生李斯特菌分析
单核细胞增生李斯特菌在农业环境中普遍存在,难以从食品加工设施中根除。因此,各种食物受到污染,对免疫功能低下的人构成健康风险。本监测研究旨在加强对南非西开普省(2018-2021)即食鹰嘴豆泥、新鲜农产品和食品加工环境中单核细胞增多乳杆菌的遗传多样性、毒力、质粒含量、消毒剂耐受性和抗生素耐药性的了解。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)技术将60株单核增生乳杆菌分离株分类为I系和II系。谱系I总体上非常普遍(57%,n = 34),与新鲜农产品显著相关(88%,n = 7) (p = 0.04)。全基因组测序(WGS)和生物信息学分析表征了20 L的亚群。分离到7个序列型(ST1、ST2、ST3、ST5、ST101、ST121、ST204)和3个血清型(1/2a、1/2b、4b)。ST204 (38%, n = 3)在食品加工环境中最常见,ST5 (50%, n = 3)在新鲜农产品中最常见,ST5 (33%, n = 2)、ST101 (33%, n = 2)和ST121 (33%, n = 2)在RTE鹰嘴豆泥中最常见。然而,没有单一血清型或ST在任何类别中显着过度代表(p > 0.05)。所有分离株均携带李斯特菌致病性岛(LIPI)-1和LIPI-2基因簇。两个分离株(ST1和ST3)含有LIPI-3的所有基因。从RTE鹰嘴豆泥中分离的2株ST5菌株含有tetM基因。来自不同来源的菌株含有emrC、bcrABC或qacH基因,这些基因赋予了对季铵盐类消毒剂苯扎氯铵的耐受性。RTE鹰嘴豆泥、新鲜农产品和食品加工环境容易受到多种毒力强的单核细胞增生乳杆菌的污染。
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来源期刊
MicrobiologyOpen
MicrobiologyOpen MICROBIOLOGY-
CiteScore
8.00
自引率
0.00%
发文量
78
审稿时长
20 weeks
期刊介绍: MicrobiologyOpen is a peer reviewed, fully open access, broad-scope, and interdisciplinary journal delivering rapid decisions and fast publication of microbial science, a field which is undergoing a profound and exciting evolution in this post-genomic era. The journal aims to serve the research community by providing a vehicle for authors wishing to publish quality research in both fundamental and applied microbiology. Our goal is to publish articles that stimulate discussion and debate, as well as add to our knowledge base and further the understanding of microbial interactions and microbial processes. MicrobiologyOpen gives prompt and equal consideration to articles reporting theoretical, experimental, applied, and descriptive work in all aspects of bacteriology, virology, mycology and protistology, including, but not limited to: - agriculture - antimicrobial resistance - astrobiology - biochemistry - biotechnology - cell and molecular biology - clinical microbiology - computational, systems, and synthetic microbiology - environmental science - evolutionary biology, ecology, and systematics - food science and technology - genetics and genomics - geobiology and earth science - host-microbe interactions - infectious diseases - natural products discovery - pharmaceutical and medicinal chemistry - physiology - plant pathology - veterinary microbiology We will consider submissions across unicellular and cell-cluster organisms: prokaryotes (bacteria, archaea) and eukaryotes (fungi, protists, microalgae, lichens), as well as viruses and prions infecting or interacting with microorganisms, plants and animals, including genetic, biochemical, biophysical, bioinformatic and structural analyses. The journal features Original Articles (including full Research articles, Method articles, and Short Communications), Commentaries, Reviews, and Editorials. Original papers must report well-conducted research with conclusions supported by the data presented in the article. We also support confirmatory research and aim to work with authors to meet reviewer expectations. MicrobiologyOpen publishes articles submitted directly to the journal and those referred from other Wiley journals.
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