Frese M, Kochs G, Meier-Dieter U, Siebler J, Haller O
Abteilung Virologie, Institut für Medizinische Mikrobiologie und Hygiene, Universität Freiburg, Germany.
J Virol. 1995 Jun;69(6):3904-9. doi: 10.1128/JVI.69.6.3904-3909.1995.
Thogoto and Dhori viruses are tick-borne orthomyxoviruses infecting humans and livestock in Africa, Asia, and Europe. Here, we show that human MxA protein is an efficient inhibitor of Thogoto virus but is inactive against Dhori virus. When expressed in the cytoplasm of stably transfected cell lines, MxA protein interfered with the accumulation of Thogoto viral RNA and proteins. Likewise, MxA(R645), a mutant MxA protein known to be active against influenza virus but inactive against vesicular stomatitis virus, was equally efficient in blocking Thogoto virus growth. Hence, a common antiviral mechanism that is distinct from the antiviral action against vesicular stomatitis virus may operate against both influenza virus and Thogoto virus. When moved to the nucleus with the help of a foreign nuclear transport signal, MxA(R645) remained active against Thogoto virus, indicating that a nuclear step of virus replication was inhibited. In contrast, Dhori virus was not affected by wild-type or mutant MxA protein, indicating substantial differences between these two tick-transmitted orthomyxoviruses. Human MxB protein had no antiviral activity against either virus.
托高托病毒和多里病毒是蜱传正黏病毒,在非洲、亚洲和欧洲感染人类和家畜。在此,我们表明人类Mx A蛋白是托高托病毒的有效抑制剂,但对多里病毒无活性。当在稳定转染的细胞系细胞质中表达时,Mx A蛋白干扰了托高托病毒RNA和蛋白质的积累。同样,Mx A(R645),一种已知对流感病毒有活性但对水疱性口炎病毒无活性的突变型Mx A蛋白,在阻断托高托病毒生长方面同样有效。因此,一种不同于针对水疱性口炎病毒的抗病毒作用的共同抗病毒机制可能对流感病毒和托高托病毒都起作用。当借助外源核转运信号转移到细胞核时,Mx A(R645)对托高托病毒仍有活性,表明病毒复制的一个核步骤受到抑制。相比之下,多里病毒不受野生型或突变型Mx A蛋白的影响,表明这两种蜱传正黏病毒之间存在实质性差异。人类Mx B蛋白对这两种病毒均无抗病毒活性。