Pisanelli Giuseppe, Laurent-Rolle Maudry, Manicassamy Balaji, Belicha-Villanueva Alan, Morrison Juliet, Lozano-Dubernard Bernardo, Castro-Peralta Felipa, Iovane Giuseppe, García-Sastre Adolfo
Department of Microbiology, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, New York, NY 10029, United States; Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, New York, NY 10029, United States; Department of Veterinary Medicine and Animal Production, University of Naples Federico II, Via Federico Delpino 1, 80137 Naples, Italy.
Department of Microbiology, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, New York, NY 10029, United States; Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai, One Gustave L. Levy Place, New York, NY 10029, United States.
Virus Res. 2016 Feb 2;213:11-22. doi: 10.1016/j.virusres.2015.10.027. Epub 2015 Nov 3.
La Piedad Michoacán Mexico Virus (LPMV) is a member of the Rubulavirus genus within the Paramyxoviridae family. LPMV is the etiologic agent of "blue eye disease", causing a significant disease burden in swine in Mexico with long-term implications for the agricultural industry. This virus mainly affects piglets and is characterized by meningoencephalitis and respiratory distress. It also affects adult pigs, causing reduced fertility and abortions in females, and orchitis and epididymitis in males. Viruses of the Paramyxoviridae family evade the innate immune response by targeting components of the interferon (IFN) signaling pathway. The V protein, expressed by most paramyxoviruses, is a well-characterized IFN signaling antagonist. Until now, there were no reports on the role of the LPMV-V protein in inhibiting the IFN response. In this study we demonstrate that LPMV-V protein antagonizes type I but not type II IFN signaling by binding STAT2, a component of the type I IFN cascade. Our results indicate that the last 18 amino acids of LPMV-V protein are required for binding to STAT2 in human and swine cells. While LPMV-V protein does not affect the protein levels of STAT1 or STAT2, it does prevent the IFN-induced phosphorylation and nuclear translocation of STAT1 and STAT2 thereby inhibiting cellular responses to IFN α/β.
米却肯州拉皮德城墨西哥病毒(LPMV)是副粘病毒科腮腺炎病毒属的成员。LPMV是“蓝眼病”的病原体,给墨西哥的养猪业带来了巨大的疾病负担,并对农业产业产生长期影响。这种病毒主要感染仔猪,其特征为脑膜脑炎和呼吸窘迫。它也会感染成年猪,导致母猪繁殖力下降和流产,以及公猪睾丸炎和附睾炎。副粘病毒科的病毒通过靶向干扰素(IFN)信号通路的成分来逃避先天免疫反应。大多数副粘病毒表达的V蛋白是一种特征明确的IFN信号拮抗剂。到目前为止,尚无关于LPMV-V蛋白在抑制IFN反应中作用的报道。在本研究中,我们证明LPMV-V蛋白通过结合I型IFN级联反应的一个成分STAT2来拮抗I型而非II型IFN信号。我们的结果表明,LPMV-V蛋白的最后18个氨基酸是在人和猪细胞中与STAT2结合所必需的。虽然LPMV-V蛋白不影响STAT1或STAT2的蛋白水平,但它确实能阻止IFN诱导的STAT1和STAT2的磷酸化及核转位,从而抑制细胞对IFNα/β的反应。