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使用替代基质对牡蛎中副溶血性弧菌进行实时荧光定量PCR检测

Real-time PCR quantification of Vibrio parahaemolyticus in oysters using an alternative matrix.

作者信息

Kaufman G E, Blackstone G M, Vickery M C L, Bej A K, Bowers J, Bowen Michael D, Meyer Richard F, DePaola A

机构信息

Department of Biology, University of Alabama at Birmingham, Birmingham, Alabama 35294-1170, USA.

出版信息

J Food Prot. 2004 Nov;67(11):2424-9. doi: 10.4315/0362-028x-67.11.2424.

Abstract

This study examined the relationship between levels of total Vibrio parahaemolyticus found in oyster tissues and mantle fluid with the goal of using mantle fluid as a template matrix in a new quantitative real-time PCR assay targeting the thermolabile hemolysin (tlh) gene for the enumeration of total V. parahaemolyticus in oysters. Oysters were collected near Mobile Bay, Ala., in June, July, and September and tested immediately after collection and storage at 26 degrees C for 24 h. Initial experiments using DNA colony hybridization targeting tlh demonstrated that natural V. parahaemolyticus levels in the mantle fluid of individual oysters were strongly correlated (r = 0.85, P < 0.05) with the levels found in their tissues. When known quantities of cultured V. parahaemolyticus cells were added to real-time PCR reactions that contained mantle fluid and oyster tissue matrices separately pooled from multiple oysters, a strong linear correlation was observed between the real-time PCR cycle threshold and the log concentration of cells inoculated into each PCR reaction (mantle fluid: r = 0.98, P < 0.05; and oyster: r = 0.99, P < 0.05). However, the mantle fluid exhibited less inhibition of the PCR amplification than the homogenized oyster tissue. Analysis of natural V. parahaemolyticus populations in mantle fluids using both colony hybridization and real-time PCR demonstrated a significant (P < 0.05) but reduced correlation (r = -0.48) between the two methods. Reductions in the efficiency of the real-time PCR that resulted from low population densities of V. parahaemolyticus and PCR inhibitors present in the mantle fluid of some oysters (with significant oyster-to-oyster variation) contributed to the reduction in correlation between the methods that was observed when testing natural V. parahaemolyticus populations. The V. parahaemolyticus-specific real-time PCR assay used for this study could estimate elevated V. parahaemolyticus levels in oyster mantle fluid within 1 h from sampling time.

摘要

本研究检测了牡蛎组织和外套膜液中副溶血性弧菌总数水平之间的关系,目的是将外套膜液用作一种模板基质,用于一种新的定量实时PCR检测方法,该方法针对不耐热溶血素(tlh)基因来计数牡蛎中的副溶血性弧菌总数。牡蛎于6月、7月和9月在阿拉巴马州莫比尔湾附近采集,并在采集后立即进行检测,以及在26摄氏度下储存24小时后进行检测。最初使用针对tlh的DNA菌落杂交实验表明,单个牡蛎外套膜液中的天然副溶血性弧菌水平与它们组织中的水平呈强相关(r = 0.85,P < 0.05)。当将已知数量的培养副溶血性弧菌细胞分别添加到包含从多个牡蛎中汇集的外套膜液和牡蛎组织基质的实时PCR反应中时,在实时PCR循环阈值与接种到每个PCR反应中的细胞对数浓度之间观察到强线性相关(外套膜液:r = 0.98,P < 0.05;牡蛎:r = 0.99,P < 0.05)。然而,外套膜液对PCR扩增的抑制作用比匀浆后的牡蛎组织小。使用菌落杂交和实时PCR分析外套膜液中的天然副溶血性弧菌群体表明,两种方法之间存在显著(P < 0.05)但降低的相关性(r = -0.48)。由于一些牡蛎(牡蛎个体间存在显著差异)的外套膜液中副溶血性弧菌种群密度低以及存在PCR抑制剂,导致实时PCR效率降低,这促成了在检测天然副溶血性弧菌群体时观察到的两种方法之间相关性的降低。本研究中使用的副溶血性弧菌特异性实时PCR检测方法可以在采样时间起1小时内估计牡蛎外套膜液中升高的副溶血性弧菌水平。

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