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Analysis of the Costs and Economic Feasibility of Requiring Postharvest Processing for Raw Oysters.对生牡蛎采后加工要求的成本及经济可行性分析。
Compr Rev Food Sci Food Saf. 2013 Nov;12(6):652-661. doi: 10.1111/1541-4337.12031.
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A systematic review of post-harvest interventions for Vibrio parahaemolyticus in raw oysters.对生食牡蛎中副溶血性弧菌的采后干预措施的系统评价。
Sci Total Environ. 2020 Nov 25;745:140795. doi: 10.1016/j.scitotenv.2020.140795. Epub 2020 Jul 12.
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The role of the gut microbiome in sustainable teleost aquaculture.肠道微生物组在可持续鱼类养殖中的作用。
Proc Biol Sci. 2020 May 13;287(1926):20200184. doi: 10.1098/rspb.2020.0184. Epub 2020 May 6.
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Oyster disease in a changing environment: Decrypting the link between pathogen, microbiome and environment.牡蛎病害在变化环境下的相关研究:解析病原体、微生物组和环境之间的关系。
Mar Environ Res. 2019 Jan;143:124-140. doi: 10.1016/j.marenvres.2018.11.007. Epub 2018 Nov 16.
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A Comparative Review on Microbiota Manipulation: Lessons From Fish, Plants, Livestock, and Human Research.微生物群调控的比较综述:来自鱼类、植物、家畜和人类研究的经验教训
Front Nutr. 2018 Sep 5;5:80. doi: 10.3389/fnut.2018.00080. eCollection 2018.
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Experimental and Histological Studies of Four Life-History Stages of the Eastern Oyster, Crassostrea virginica, Exposed to a Cultured Strain of the Dinoflagellate Prorocentrum minimum.
Biol Bull. 1995 Jun;188(3):313-328. doi: 10.2307/1542308.
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The gastrointestinal microbiome and its association with the control of pathogens in broiler chicken production: A review.肠道微生物组及其与肉鸡生产中病原体控制的关系:综述。
Poult Sci. 2018 Mar 1;97(3):1006-1021. doi: 10.3382/ps/pex359.
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Bile Sensing: The Activation of Virulence.胆汁感知:毒力的激活
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Incidence and prevalence of Vibrio parahaemolyticus in seafood: a systematic review and meta-analysis.海产品中副溶血性弧菌的发病率和患病率:一项系统评价和荟萃分析。
Springerplus. 2016 Apr 14;5:464. doi: 10.1186/s40064-016-2115-7. eCollection 2016.
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Vibrio bacteria in raw oysters: managing risks to human health.生牡蛎中的弧菌:管理对人类健康的风险。
Philos Trans R Soc Lond B Biol Sci. 2016 Mar 5;371(1689). doi: 10.1098/rstb.2015.0209.

建立一种可控的实验室规模接种系统以研究副溶血性弧菌-牡蛎相互作用。

Development of a Controlled Laboratory-scale Inoculation System to Study Vibrio parahaemolyticus-oyster Interactions.

机构信息

Department of Biological Sciences, Virginia Tech, Blacksburg, VA 24061, United States.

Center for Emerging, Zoonotic, and Arthropod-borne Pathogens, Virginia Tech, Blacksburg, VA 24061, United States.

出版信息

FEMS Microbiol Lett. 2022 Jul 21;369(1). doi: 10.1093/femsle/fnac055.

DOI:10.1093/femsle/fnac055
PMID:35687396
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11506194/
Abstract

Prevalence of seafood-borne gastroenteritis caused by the human pathogen Vibrio parahaemolyticus is increasing globally despite current preventative measures. The United States Centers for Disease Control have designated V. parahaemolyticus as a reportable emerging human pathogen. The Eastern oyster (Crassostrea virginica) is a natural reservoir of the bacterium in marine environments, but little is actually known regarding interactions between oysters and V. parahaemolyticus. Therefore, a laboratory-scale Biosafety Level-2 (BSL2) inoculation system was developed wherein Chesapeake Bay region oysters harvested during summer or winter months, were exposed to the clinical RIMD2210633 strain carrying a chloramphenicol-selective marker (VP RIMDmC). Homogenized whole oyster tissues were spread on selective and differential agar medium to measure viable VP RIMDmC levels. Endogenous Vibrio spp. cell numbers were significantly reduced followed chloramphenicol treatment and this likely contributed to higher VP RIMDmC oyster-associated levels, especially using winter-harvested animals. Summer-harvested oysters had significantly higher existing Vibrio levels and a lower level of artificial oyster-associated VP RIMDmC. Thus, the pre-existing microbiome appears to afford some protection from an external V. parahaemolyticus challenge. Overall, this system successfully enabled controlled manipulation of parameters influencing V. parahaemolyticus-oyster interactions and will be useful in safely testing additional pertinent environmental variables and potential mitigation strategies.

摘要

尽管目前采取了预防措施,但由人类病原体副溶血性弧菌引起的食源性肠胃炎的全球流行率仍在上升。美国疾病控制与预防中心已将副溶血性弧菌列为应报告的新兴人类病原体。东方牡蛎(Crassostrea virginica)是海洋环境中该细菌的天然宿主,但实际上人们对牡蛎与副溶血性弧菌之间的相互作用知之甚少。因此,开发了一种实验室规模的生物安全 2 级(BSL2)接种系统,在该系统中,夏季或冬季收获的切萨皮克湾地区牡蛎暴露于携带氯霉素选择性标记物(VP RIMDmC)的临床 RIMD2210633 菌株中。将匀浆的整个牡蛎组织铺在选择性和差异琼脂培养基上,以测量活的 VP RIMDmC 水平。在用氯霉素处理后,内源性弧菌属细胞数量明显减少,这可能导致 VP RIMDmC 牡蛎相关水平升高,尤其是使用冬季收获的动物时。夏季收获的牡蛎具有明显更高的现有弧菌水平和更低的人工牡蛎相关 VP RIMDmC 水平。因此,先前存在的微生物组似乎为外部副溶血性弧菌的挑战提供了一些保护。总体而言,该系统成功地实现了对影响副溶血性弧菌-牡蛎相互作用的参数的可控操作,将有助于安全测试其他相关环境变量和潜在的缓解策略。