Department of Pediatrics, Division of Infectious Diseases, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
RK Mellon Institute for Pediatric Research, UPMC Children's Hospital of Pittsburgh, Pittsburgh, Pennsylvania, USA.
J Virol. 2023 May 31;97(5):e0193022. doi: 10.1128/jvi.01930-22. Epub 2023 Apr 24.
Inbred mouse lines vary in their ability to mount protective antiretroviral immune responses, and even closely related strains can exhibit opposing phenotypes upon retroviral infection. Here, we found that 129S mice inherit a previously unknown mechanism for the production of anti-murine leukemia virus (MLV) antibodies and control of infection. The resistant phenotype in 129S1 mice is controlled by two dominant loci that are independent from known MLV resistance genes. We also show that production of anti-MLV antibodies in 129S7 mice, but not 129S1 mice, is independent of interferon gamma signaling. Thus, our data indicate that 129S mice inherit an unknown mechanism for control of MLV infection and demonstrate that there is genetic variability in 129S substrains that affects their ability to mount antiviral immune responses. Understanding the genetic basis for production of protective antiviral immune responses is crucial for the development of novel vaccines and adjuvants. Additionally, characterizing the genetic and phenotypic variability in inbred mice has implications for the selection of strains for targeted mutagenesis, choice of controls, and for broader understanding of the requirements for protective immunity.
近交系小鼠在产生保护性抗病毒免疫反应的能力上存在差异,即使是密切相关的品系,在逆转录病毒感染后也可能表现出相反的表型。在这里,我们发现 129S 小鼠继承了一种先前未知的产生抗鼠白血病病毒 (MLV) 抗体和控制感染的机制。129S1 小鼠的抗性表型由两个独立于已知 MLV 抗性基因的显性基因座控制。我们还表明,129S7 小鼠而非 129S1 小鼠产生抗 MLV 抗体的能力与干扰素 γ信号无关。因此,我们的数据表明 129S 小鼠继承了一种控制 MLV 感染的未知机制,并表明 129S 亚系存在影响其产生抗病毒免疫反应能力的遗传变异。了解产生保护性抗病毒免疫反应的遗传基础对于新型疫苗和佐剂的开发至关重要。此外,描述近交系小鼠的遗传和表型变异对于靶向诱变的品系选择、对照品的选择以及更广泛地理解保护性免疫的要求都具有重要意义。