首页> 外文期刊>Journal of applied microbiology >Evaluating virulence of waterborne and clinical Aeromonas isolates using gene expression and mortality in neonatal mice followed by assessing cell culture's ability to predict virulence based on transcriptional response
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Evaluating virulence of waterborne and clinical Aeromonas isolates using gene expression and mortality in neonatal mice followed by assessing cell culture's ability to predict virulence based on transcriptional response

机译:使用基因表达和死亡率评估新生小鼠的水性和临床气单胞菌分离物的毒力,然后评估细胞培养物根据转录反应预测毒力的能力

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Aims: To assess the virulence of Aeromonas spp. using two models, a neonatal mouse assay and a mouse intestinal cell culture. Methods and Results: After artificial infection with a variety of Aeromonas spp., mRNA extracts from the two models were processed and hydridized to murine microarrays to determine host gene response. Definition of virulence was determined based on host mRNA production in murine neonatal intestinal tissue and mortality of infected animals. Infections of mouse intestinal cell cultures were then performed to determine whether this simpler model system's mRNA responses correlated to neonatal results and therefore be predictive of virulence of Aeromonas spp. Virulent aeromonads up-regulated transcripts in both models including multiple host defense gene products (chemokines, regulation of transcription and apoptosis and cell signalling). Avirulent species exhibited little or no host response in neonates. Mortality results correlated well with both bacterial dose and average fold change of up-regulated transcripts in the neonatal mice. Conclusions: Cell culture results were less discriminating but showed promise as potentially being able to be predictive of virulence. Jun oncogene up-regulation in murine cell culture is potentially predictive of Aeromonas virulence. Significance and Impact of the Study: Having the ability to determine virulence of waterborne pathogens quickly would potentially assist public health officials to rapidly assess exposure risks.
机译:目的:评估毒气单胞菌的毒力。使用两种模型:新生鼠测定和鼠肠细胞培养。方法和结果:在人工感染了多种气单胞菌后,将两种模型的mRNA提取物进行处理并氢化成鼠微阵列,以确定宿主基因的应答。根据鼠新生肠组织中宿主mRNA的产生和感染动物的死亡率来确定毒力的定义。然后进行小鼠肠道细胞培养物的感染以确定该较简单的模型系统的mRNA反应是否与新生儿结果相关,因此可以预测气单胞菌的毒力。在两个模型中,包括多个宿主防御基因产物(趋化因子,转录和细胞凋亡的调控以及细胞信号转导),有毒的气单胞菌上调了转录本。无毒物种在新生儿中几乎没有宿主反应。死亡率结果与新生小鼠中细菌剂量和上调转录本的平均倍数变化均相关。结论:细胞培养结果的区别较少,但显示出有望潜在地预测毒力的前景。鼠细胞培养物中的Jun癌基因上调可能预示了气单胞菌毒力。研究的意义和影响:具有快速确定水生病原体毒力的能力可能会帮助公共卫生官员快速评估接触风险。

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