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Bioaccumulation Retention and Depuration of Enteric Viruses by Crassostrea virginica and Crassostrea ariakensis Oysters

机译:破伤风和破伤风牡蛎对肠道病毒的生物蓄积保留和净化作用

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摘要

Crassostrea ariakensis oysters are under review for introduction into the Chesapeake Bay. However, the human health implications of the introduction have not been fully addressed. This study evaluated rates of bioaccumulation, retention, and depuration of viruses by Crassostrea virginica and C. ariakensis when the two oyster species were maintained in separate tanks containing synthetic seawater of various salinities (8, 12, or 20 ppt). Oyster bioaccumulation tanks were seeded with 103 PFU/ml of hepatitis A virus (HAV), poliovirus, male-specific bacteriophage (MS2), and murine norovirus 1 (MNV-1) and 103 PCR units/ml of human norovirus (NoV). After 24 h, depuration commenced as oysters (n = 255) were placed in pathogen-free seawater under continuous filtration. Oysters (n = 6) were sampled weekly for 1 month from each tank. Viral RNA was recovered using a modified proteinase K, guanidine, and glassmilk method and analyzed by quantitative reverse transcription-PCR. The odds of C. ariakensis oysters harboring NoV, MNV-1, or HAV were statistically greater than the odds of C. virginica oysters harboring the same viruses (MNV-1 odds ratio [OR], 4.5; P = 0.01; NoV OR, 8.4; P < 0.001; HAV OR, 11.4; P < 0.001). Unlike C. virginica, C. ariakensis bioaccumulated and retained NoV, MNV-1, and HAV for 1 month at all salinities. Additionally, the odds of an oyster testing positive for NoV was 25.5 times greater (P < 0.001) when the oyster also tested positive for MNV-1. This research helps assess the threat of C. ariakensis as a vehicle for viral pathogens due to the consumption of raw oysters and validates the role for MNV-1 as a surrogate for NoV.
机译:Crassostrea ariakensis牡蛎正在接受审核,以引入切萨皮克湾。但是,引言对人体健康的影响尚未得到充分解决。这项研究评估了两种牡蛎分别保存在装有不同盐度(8、12或20 ppt)合成海水的单独储水池中时,Crassostrea virginica和C. ariakensis对病毒的生物积累,保留和净化的速率。牡蛎生物蓄积池中接种了10 3 PFU / ml的甲型肝炎病毒(HAV),脊髓灰质炎病毒,雄性特异性噬菌体(MS2)和鼠诺如病毒1(MNV-1)和10 人类诺如病毒(NoV)的3 PCR单位/ ml。 24小时后,开始净化,将牡蛎(n = 255)置于无病原体的海水中,并进行连续过滤。每周从每个储罐中采样牡蛎(n = 6),持续1个月。使用修饰的蛋白酶K,胍和玻璃奶方法回收病毒RNA,并通过定量逆转录PCR进行分析。统计上,携带NoV,MNV-1或HAV的aria C. ariakensis牡蛎的几率比携带相同病毒的virginica C. virginica牡蛎的几率大(MNV-1的优势比[OR],4.5; P = 0.01; NoV OR, 8.4; P <0.001; HAV OR,11.4; P <0.001)。与维尔纽斯菌不同,ariakensis在所有盐度下都会生物积聚并保留NoV,MNV-1和HAV 1个月。此外,当牡蛎也检测出MNV-1阳性时,牡蛎检测为NoV阳性的几率是25.5倍(P <0.001)。这项研究有助于评估由于食用生牡蛎而导致aria C. ariakensis作为病毒病原体传播媒介的威胁,并验证了MNV-1作为NoV替代品的作用。

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