Salmonella prevalence and serovar distribution in reptiles: a systematic review and meta-analysis.

IF 4 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Claire Muslin, Paula Salas-Brito, Dayana Coello, Diana Morales-Jadán, Carolina Viteri-Dávila, Marco Coral-Almeida
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引用次数: 0

Abstract

Background: Reptiles are recognized as reservoirs of Salmonella bacteria, and the expansion of the global pet reptile trade has led to reptile-associated salmonellosis emerging as a significant public health concern. To characterize the risk posed by reptiles as a source of Salmonella transmission to humans, we conducted the first comprehensive meta-analysis to estimate the worldwide prevalence of Salmonella in both wild and captive reptiles and identify the primary factors influencing this prevalence.

Results: We systematically reviewed publications reporting the prevalence of Salmonella spp. intestinal isolation in reptiles, published between 1986 and 2023, across the PubMed, Scopus and Web of Science databases. The 179 studies included examined a total of 23,411 reptiles from 56 countries across all continents, with 49.9% being free-ranging animals and 48.4% living in captivity, mainly from zoos, pet shops, or households. The overall pooled prevalence of Salmonella spp. in reptiles was estimated at 30.4% (95% confidence interval, CI: 27.4-33.6%). Notably, significant variations in Salmonella spp. colonization rates were observed across different reptile taxa, with snakes exhibiting the highest prevalence at 63.1% (95%CI: 57.4-68.4%), followed by lizards at 33.6% (95%CI: 28.6-39.0%), and turtles and crocodiles with similar rates of 11.2% (95%CI: 8.8-14.2%) and 10.5% (95%CI: 5.7-18.6%), respectively. Furthermore, significant differences in Salmonella spp. prevalence were observed across different reptile families within each taxon. The data suggest that captivity is a contributing factor to Salmonella spp. colonization, as captive reptiles showed significantly higher prevalence rates (37.8%, 95%CI: 34.3-41.4%) compared to their wild counterparts (14.8%, 95%CI: 11.0-19.6%). Additionally, we found that the inclusion of pre-enrichment and selective enrichment steps in culture broths significantly improved the sensitivity of both culture-based and PCR-based Salmonella detection methods. Importantly, the study revealed that reptiles primarily carried Salmonella enterica subspecies enterica, responsible for most human salmonellosis cases. Of particular concern, several human-pathogenic Salmonella serovars of public health relevance, such as Enteritidis, Typhimurium and Newport, were identified among the 10 most common serovars colonizing reptiles.

Conclusions: Collectively, these findings highlight the substantial health threat posed by reptiles as a source of human Salmonella infection and may inform the development of policies and strategies for prevention and public education to mitigate the risk of reptile-associated salmonellosis.

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爬行动物中沙门氏菌的流行和血清分布:一项系统综述和荟萃分析。
背景:爬行动物被认为是沙门氏菌的宿主,全球宠物爬行动物贸易的扩大导致与爬行动物相关的沙门氏菌病成为一个重大的公共卫生问题。为了描述爬行动物作为沙门氏菌传播给人类的来源所构成的风险,我们进行了首次综合荟萃分析,以估计全球范围内野生和圈养爬行动物中沙门氏菌的流行情况,并确定影响这种流行的主要因素。结果:我们系统地回顾了1986年至2023年间发表的关于爬行动物中沙门氏菌肠道分离流行的出版物,这些出版物来自PubMed、Scopus和Web of Science数据库。179项研究共调查了来自各大洲56个国家的23,411种爬行动物,其中49.9%是自由放养的动物,48.4%生活在圈养环境中,主要来自动物园、宠物店或家庭。爬行动物中沙门氏菌的总流行率估计为30.4%(95%置信区间,CI: 27.4-33.6%)。值得注意的是,在不同的爬行动物类群中,沙门氏菌的定殖率存在显著差异,其中蛇的定殖率最高,为63.1% (95%CI: 53.4 -68.4%),其次是蜥蜴,为33.6% (95%CI: 28.6-39.0%),乌龟和鳄鱼的定殖率相似,分别为11.2% (95%CI: 8.8-14.2%)和10.5% (95%CI: 5.7-18.6%)。此外,在每个分类单元内,不同爬行动物科的沙门氏菌流行率也存在显著差异。数据表明,圈养是沙门氏菌定植的重要因素,圈养爬行动物的感染率(37.8%,95%CI: 343 ~ 41.4%)显著高于野生爬行动物(14.8%,95%CI: 11.0 ~ 19.6%)。此外,我们发现在培养液中加入预富集和选择性富集步骤显著提高了基于培养和基于pcr的沙门氏菌检测方法的灵敏度。重要的是,该研究揭示了爬行动物主要携带肠道沙门氏菌亚种,导致大多数人类沙门氏菌病病例。特别值得关注的是,在爬行动物中最常见的10种血清型中发现了几种与公共卫生相关的人类致病性沙门氏菌血清型,如肠炎、鼠伤寒和新港沙门氏菌。结论:总的来说,这些发现突出了爬行动物作为人类沙门氏菌感染源所构成的重大健康威胁,并可能为制定预防和公共教育政策和战略提供信息,以减轻爬行动物相关沙门氏菌病的风险。
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来源期刊
Gut Pathogens
Gut Pathogens GASTROENTEROLOGY & HEPATOLOGY-MICROBIOLOGY
CiteScore
7.70
自引率
2.40%
发文量
43
期刊介绍: Gut Pathogens is a fast publishing, inclusive and prominent international journal which recognizes the need for a publishing platform uniquely tailored to reflect the full breadth of research in the biology and medicine of pathogens, commensals and functional microbiota of the gut. The journal publishes basic, clinical and cutting-edge research on all aspects of the above mentioned organisms including probiotic bacteria and yeasts and their products. The scope also covers the related ecology, molecular genetics, physiology and epidemiology of these microbes. The journal actively invites timely reports on the novel aspects of genomics, metagenomics, microbiota profiling and systems biology. Gut Pathogens will also consider, at the discretion of the editors, descriptive studies identifying a new genome sequence of a gut microbe or a series of related microbes (such as those obtained from new hosts, niches, settings, outbreaks and epidemics) and those obtained from single or multiple hosts at one or different time points (chronological evolution).
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