Federal State Budgetary Scientific Institution "Institute of Experimental Medicine", St. Petersburg 197022, Russia.
Institute of Biomedical Systems and Biotechnology, Peter the Great St. Petersburg Polytechnic University, St. Petersburg 194021, Russia.
Int J Mol Sci. 2023 Dec 12;24(24):17386. doi: 10.3390/ijms242417386.
Influenza virus strain A/South Africa/3626/2013 (H1N1)pdm09 (SA-WT) is a non-mouse-adapted model strain that has naturally high pathogenic properties in mice. It has been suggested that the high pathogenicity of this strain for mice could be due to the three strain-specific substitutions in the polymerase complex (Q687R in PB1, N102T in PB2, and E358E/K heterogeneity in PB2). To evaluate the role of these replacements, SA-WT was passaged five times in mouse lungs, and the genome of the mouse-adapted version of the SA-WT strain (SA-M5) was sequenced. SA-M5 lost E358E/K heterogeneity and retained E358, which is the prevalent amino acid at this position among H1N1pdm09 strains. In addition, in the hemagglutinin of SA-M5, two heterogeneous substitutions (G155G/E and S190S/R) were identified. Both viruses, SA-M5 and SA-WT, were compared for their toxicity, ability to replicate, pathogenicity, and immunogenicity in mice. In mice infected with SA-M5 or SA-WT strains, toxicity, virus titer in pulmonary homogenates, and mouse survival did not differ significantly. In contrast, an increase in the immunogenicity of SA-M5 compared to SA-WT was observed. This increase could be due to the substitutions G155G/E and S190S/R in the HA of SA-M5. The prospects for using SA-M5 in studying the immunogenicity mechanisms were also discussed.
甲型流感病毒南非/3626/2013(H1N1)pdm09(SA-WT)株是非适应鼠株,在小鼠中具有天然的高致病性。有人认为,该株在小鼠中具有高致病性,可能是由于聚合酶复合物中的三个株特异性替换(PB1 中的 Q687R、PB2 中的 N102T 和 PB2 中的 E358E/K 异质性)。为了评估这些替换的作用,将 SA-WT 在小鼠肺部传代 5 次,并对适应鼠株的 SA-WT 株(SA-M5)的基因组进行测序。SA-M5 失去了 E358E/K 异质性,保留了 E358,这是 H1N1pdm09 株中该位置普遍存在的氨基酸。此外,在 SA-M5 的血凝素中,鉴定出两个异质性替换(G155G/E 和 S190S/R)。比较了 SA-M5 和 SA-WT 两种病毒在小鼠中的毒性、复制能力、致病性和免疫原性。在感染 SA-M5 或 SA-WT 株的小鼠中,毒性、肺匀浆中的病毒滴度和小鼠存活率没有显著差异。相比之下,与 SA-WT 相比,SA-M5 的免疫原性显著增加。这种增加可能是由于 SA-M5 的 HA 中的 G155G/E 和 S190S/R 替换。还讨论了使用 SA-M5 研究免疫原性机制的前景。