Kim Il-Hwan, Kwon Hyuk-Joon, Lee Su-Hyung, Kim Dae-Yong, Kim Jae-Hong
Laboratory of Avian Diseases, College of Veterinary Medicine, Seoul National University, Seoul, Republic of Korea; Research Institute for Veterinary Science, College of Veterinary Medicine, Seoul National University, Seoul, Republic of Korea.
Research Institute for Veterinary Science, College of Veterinary Medicine, Seoul National University, Seoul, Republic of Korea; Laboratory of Poultry Clinical Science, College of Veterinary Medicine, Seoul National University, Pyeongchang, Gangwon-do, Republic of Korea.
Vet Microbiol. 2015 Jan 30;175(1):17-25. doi: 10.1016/j.vetmic.2014.11.010. Epub 2014 Nov 18.
To examine the effects of the NS1 and NEP genes of avian influenza viruses (AIVs) on pathogenicity in mice, we generated recombinant PR8 viruses containing 3 different NS genes of AIVs. In contrast to the reverse genetics-generated PR8 (rPR8) strain and other recombinant viruses, the recombinant virus rPR8-NS(0028), which contained the NS gene of A/chicken/KBNP-0028/2000 (H9N2) (0028), was non-pathogenic to mice. The novel single mutations of 0028 NS1 to corresponding amino acid of PR8 NS1, G139D and S151T increased the pathogenicity of rPR8-NS(0028). The replacement of the PL motifs (EPEV or RSEV) of pathogenic recombinant viruses with that of 0028 (GSEV) did not reduce the pathogenicity of the viruses. However, a recombinant virus with an EPEV-grafted 0028 NS gene was more pathogenic than rPR8-NS(0028) but less than rPR8. The lower pathogenicity of rPR8-NS(0028) might be associated with the lower virus titer and IFN-β level in the lungs of infected mice, and be attributed to G139, S151 and GSEV-PL motif of NS1 gene of 0028. In conclusion we defined new amino acid residues of NS1 related to mice pathogenicity and the presence of pathogenic NS genes among low pathogenic AIVs may encourage continuous monitoring of their mammalian pathogenicity.
为研究禽流感病毒(AIV)的NS1和NEP基因对小鼠致病性的影响,我们构建了含有3种不同AIV NS基因的重组PR8病毒。与反向遗传学产生的PR8(rPR8)毒株及其他重组病毒不同,含有A/鸡/KBNP - 0028/2000(H9N2)(0028)NS基因的重组病毒rPR8 - NS(0028)对小鼠无致病性。0028 NS1中与PR8 NS1相应氨基酸的新型单突变G139D和S151T增加了rPR8 - NS(0028)的致病性。将致病性重组病毒的PL基序(EPEV或RSEV)替换为0028的PL基序(GSEV)并未降低病毒的致病性。然而,带有嫁接EPEV的0028 NS基因的重组病毒比rPR8 - NS(0028)致病性更强,但比rPR8弱。rPR8 - NS(0028)致病性较低可能与感染小鼠肺内较低的病毒滴度和IFN -β水平有关,并归因于0028 NS1基因的G139、S151和GSEV - PL基序。总之,我们确定了与小鼠致病性相关的NS1新氨基酸残基,低致病性AIV中致病性NS基因的存在可能促使持续监测其对哺乳动物的致病性。