Mossel Eric C, Ramig Robert F
Department of Molecular Virology and Microbiology, Baylor College of Medicine, Houston, Texas 77030, USA.
J Virol. 2003 Nov;77(22):12352-6. doi: 10.1128/jvi.77.22.12352-12356.2003.
We used the neonatal mouse model of rotavirus infection and virus strains SA11-clone 4 (SA11-Cl4) and Rhesus rotavirus (RRV) to examine the mechanism of the extraintestinal spread of viruses following oral inoculation. The spread-competent viruses, RRV and reassortant R7, demonstrated a temporal progression from the intestine, to the terminal ileum, to the mesenteric lymph nodes (MLN), and to the peripheral tissues. SA11-Cl4 was not found outside the intestine. Reassortant virus S7, which was unable to reach the liver in previous studies (E. C. Mossel and R. F. Ramig, J. Virol. 76:6502-6509, 2002), was recovered from 60% of the MLN, suggesting that there are multiple determinants for the spread of virus from the intestine to the MLN. Phenotypic segregation analysis identified RRV genome segment 6 (VP6) as a secondary determinant of the spread of virus to the MLN (P = 0.02) in reassortant viruses containing segment 7 from the spread-incompetent parent. These data suggest that in the orally infected neonatal mouse, the extraintestinal spread of rotavirus occurs via a lymphatic pathway, and the spread phenotype is primarily determined by NSP3 and can be modified by VP6.
我们使用轮状病毒感染的新生小鼠模型以及病毒株SA11 - clone 4(SA11 - Cl4)和恒河猴轮状病毒(RRV)来研究口服接种后病毒肠外传播的机制。具有传播能力的病毒RRV和重配病毒R7呈现出从肠道到回肠末端、到肠系膜淋巴结(MLN)以及到外周组织的时间进程。在肠道外未发现SA11 - Cl4。在先前研究中无法到达肝脏的重配病毒S7(E. C. Mossel和R. F. Ramig,《病毒学杂志》76:6502 - 6509,2002),在60%的肠系膜淋巴结中被检测到,这表明病毒从肠道传播到肠系膜淋巴结存在多种决定因素。表型分离分析确定RRV基因组片段六(VP6)是在含有来自无传播能力亲本的片段七的重配病毒中病毒传播到肠系膜淋巴结的次要决定因素(P = 0.02)。这些数据表明,在经口感染的新生小鼠中,轮状病毒的肠外传播通过淋巴途径发生,传播表型主要由NSP3决定,并且可被VP6改变。