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Antibody-dependent enhancement of serotype II feline enteric coronavirus infection in primary feline monocytes

机译:原代猫单核细胞中血清型 II 型猫肠道冠状病毒感染的抗体依赖性增强

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Feline coronavirus (FCoV) has been classified into two biotypes: avirulent feline coronavirus (feline enteric coronavirus: FECV) and virulent feline coronavirus (feline infectious peritonitis virus: FIPV). In FIPV infection, antibody-dependent enhancement (ADE) has been reported and was shown to be associated with severe clinical disease. On the other hand, the potential role of ADE in FECV infection has not been examined. In this study, using laboratory strains of serotype II FIPV WSU 79-1146 (FIPV 79-1146) and serotype II FECV WSU 79-1683 (FECV 79-1683), we investigated the relationship between ADE and induction of inflammatory cytokines, which are pathogenesis-related factors, for each strain. As with ADE of FIPV 79-1146 infection, a monoclonal antibody against the spike protein of FCoV (mAb 6-4-2) enhanced FECV 79-1683 replication in U937 cells and primary feline monocytes. However, the ADE activity of FECV 79-1683 was lower than that of FIPV 79-1146. Moreover, mRNA levels of inflammatory cytokines (TNF-alpha, IL-1 beta, and IL-6) significantly increased with ADE of FIPV 79-1146 infection in primary feline monocytes, but FECV 79-1683 did not demonstrate an increase in these levels. In conclusion, infection of monocytes by FECV was enhanced by antibodies, but the efficiency of infection was lower than that of FIPV.
机译:猫冠状病毒 (FCoV) 分为两种生物类型:毒性猫冠状病毒(猫肠道冠状病毒:FECV)和毒力猫冠状病毒(猫传染性腹膜炎病毒:FIPV)。在 FIPV 感染中,抗体依赖性增强 (ADE) 已被报道,并被证明与严重的临床疾病相关。另一方面,ADE 在 FECV 感染中的潜在作用尚未得到检验。在这项研究中,使用血清型 II FIPV WSU 79-1146 (FIPV 79-1146) 和血清型 II FECV WSU 79-1683 (FECV 79-1683) 的实验室菌株,我们研究了每种菌株的 ADE 与炎症细胞因子诱导之间的关系,炎症细胞因子是发病机制相关因素。与 FIPV 79-1146 感染的 ADE 一样,针对 FCoV 刺突蛋白的单克隆抗体 (mAb 6-4-2) 增强了 U937 细胞和原代猫单核细胞中的 FECV 79-1683 复制。然而,FECV 79-1683的ADE活性低于FIPV 79-1146。此外,在原代猫单核细胞中,炎症细胞因子(TNF-α、IL-1 β 和 IL-6)的 mRNA 水平随着 FIPV 79-1146 感染的 ADE 显着增加,但 FECV 79-1683 并未证明这些水平增加。总之,抗体增强了FECV对单核细胞的感染,但感染效率低于FIPV。

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