Molecular Virology Laboratory, VA-MD Regional College of Veterinary Medicine and Maryland Pathogen Research Institute, University of Maryland, College Park, MD 20742, USA.
Virology. 2012 Oct 25;432(2):261-70. doi: 10.1016/j.virol.2012.05.015. Epub 2012 Jun 15.
Porcine reproductive and respiratory syndrome virus (PRRSV) is known to interfere with the signaling of type I interferons (IFNs). Here we found PRRSV A2MC2 induced type I IFNs in cultured cells. A2MC2 replication in MARC-145 cells resulted in the synthesis of IFN-α2 protein, transcript elevation of the IFN-stimulated genes ISG15 and ISG56, and the proteins of the signal transducer and activator of transcription 2 (STAT2) and ISG56. A2MC2 infection of primary porcine pulmonary alveolar macrophages (PAMs) also led to the elevation of the two proteins, but had little cytopathic effect. Furthermore, A2MC2 infection of MARC-145 or PAM cells had no detectable inhibitory effect on the ability of IFN-α to induce an antiviral response. Sequencing analysis indicated that A2MC2 was closely related to VR-2332 and Ingelvac PRRS MLV with an identity of 99.8% at the nucleotide level. The identification of this IFN-inducing PRRSV isolate may be beneficial for vaccine development against PRRS.
猪繁殖与呼吸综合征病毒(PRRSV)已知会干扰 I 型干扰素(IFNs)的信号转导。在这里,我们发现 PRRSV A2MC2 可在培养的细胞中诱导 I 型 IFNs。A2MC2 在 MARC-145 细胞中的复制导致 IFN-α2 蛋白的合成、IFN 刺激基因 ISG15 和 ISG56 的转录水平升高,以及信号转导和转录激活因子 2(STAT2)和 ISG56 的蛋白升高。A2MC2 感染原代猪肺泡巨噬细胞(PAMs)也导致这两种蛋白的升高,但几乎没有细胞病变效应。此外,A2MC2 感染 MARC-145 或 PAM 细胞对 IFN-α 诱导抗病毒反应的能力没有检测到抑制作用。序列分析表明,A2MC2 在核苷酸水平上与 VR-2332 和 Ingelvac PRRS MLV 密切相关,同源性为 99.8%。这种诱导 IFN 的 PRRSV 分离株的鉴定可能有助于 PRRS 疫苗的开发。