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定量实时逆转录聚合酶链反应表明,应激处理可导致斑节对虾鳃相关病毒(GAV)感染水平迅速上升。

Quantitative real-time RT-PCR demonstrates that handling stress can lead to rapid increases of gill-associated virus (GAV) infection levels in Penaeus monodon.

作者信息

de la Vega Enrique, Degnan Bernard M, Hall Michael R, Cowley Jeff A, Wilson Kate J

机构信息

Australian Institute of Marine Science, PMB 3, Townsville, Queensland 4810, Australia.

出版信息

Dis Aquat Organ. 2004 Jun 11;59(3):195-203. doi: 10.3354/dao059195.

Abstract

Gill-associated virus (GAV) of the black tiger prawn Penaeus monodon has been implicated as a cause of periodic production losses in Australia since 1996. We report here the development of a real-time quantitative RT-PCR (qRT-PCR) for GAV. A dilution series of in vitro transcribed RNA was used to determine the sensitivity limit of the qRT-PCR and as a standard for GAV quantification. A linear relationship between cycle threshold (Ct) values and input RNA was obtained over a wide concentration range between 4.86 x 10(9) and 0.5 template copies per reaction, the latter being the test detection limit. The qRT-PCR was used to follow the progression of GAV levels in a group of 15 adult male P. monodon with chronic GAV infections that were super-infected by intramuscular injection of an inoculum containing high levels of GAV. By Day 9 post-injection, cumulative mortalities reached 100% (15/15) in the GAV-injected prawns and 40% (2/5) in placebo-injected prawns. Spermatophores were collected at the beginning, and together with other tissues, at the end of the trial. Prawns were also bled at regular intervals to collect circulating haemocytes. The qRT-PCR revealed that GAV loads increased significantly in haemocytes collected from both the control and super-infected prawns (p = 0.010). This increase was significantly higher in the super-infected prawns (p = 0.047). The rapid increase in GAV levels in super-infected P. monodon was expected. However, the increase in the control prawns was not, and indicates that repetitive bleeding and handling stress can stimulate GAV proliferation in chronically infected P. monodon.

摘要

自1996年以来,黑虎虾(斑节对虾)的鳃相关病毒(GAV)被认为是澳大利亚对虾周期性产量损失的一个原因。我们在此报告一种针对GAV的实时定量逆转录聚合酶链反应(qRT-PCR)方法的开发。使用体外转录RNA的稀释系列来确定qRT-PCR的灵敏度极限,并作为GAV定量的标准。在每个反应4.86×10⁹至0.5个模板拷贝的宽浓度范围内,获得了循环阈值(Ct)值与输入RNA之间的线性关系,后者是检测下限。qRT-PCR用于跟踪一组15只患有慢性GAV感染的成年雄性斑节对虾中GAV水平的变化,这些对虾通过肌肉注射含有高浓度GAV的接种物进行了二次感染。注射后第9天,GAV注射组对虾的累积死亡率达到100%(15/15),安慰剂注射组对虾的累积死亡率为40%(2/5)。在试验开始时收集精荚,并在试验结束时与其他组织一起收集。还定期采集对虾血液以收集循环血细胞。qRT-PCR显示,从对照对虾和二次感染对虾收集的血细胞中GAV载量均显著增加(p = 0.010)。二次感染对虾中的这种增加显著更高(p = 0.047)。二次感染的斑节对虾中GAV水平的快速增加在意料之中。然而,对照对虾中的增加并非如此,这表明反复采血和处理应激可刺激慢性感染的斑节对虾中GAV的增殖。

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