Bailly Jean-Luc, Brosson Damien, Archimbaud Christine, Chambon Martine, Henquell Cécile, Peigue-Lafeuille Hélène
UFR Médecine, Laboratoire de Virologie-EA2148, Clermont-Ferrand, France.
J Med Virol. 2002 Dec;68(4):558-67. doi: 10.1002/jmv.10235.
Echovirus 30 is one of the enterovirus serotypes isolated most frequently in meningitis cases. The genetic diversity of echovirus 30 was investigated in patients hospitalised during an outbreak in 2000 in Clermont-Ferrand, France. A nested reverse transcription-PCR (RT-PCR) assay was developed for qualitative analysis of the echovirus 30 VP1 encoding sequence directly from cerebrospinal fluid. The viral sequences obtained for 22 patients were compared with those of virus isolates obtained from nine patients with echovirus 30 meningitis admitted to hospital in 1996-1997 and with echovirus 30 sequences from international databases. In 2000, meningitis cases were caused by two virus variants (C3 and C4) distinct genetically from the other two variants (C1 and C2) identified during the period 1996-1997. A detailed phylogenetic analysis established that the C1, C2, and C3 variants had close relatives among viruses previously identified in other geographical areas. The C4 variant had not been described earlier. The genomic differences observed between the four echovirus 30 variants arose at synonymous sites indicating that the viruses shared similar antigenic sites in the VP1 encoding sequence. Overall, these observations suggest wide circulation of different echovirus 30 variants and periodic importation of new viruses. The apparent displacement observed between virus variants did not result from a selective advantage caused by antigenic variation.
埃可病毒30型是在脑膜炎病例中分离出的最常见肠道病毒血清型之一。对2000年法国克莱蒙费朗一次疫情期间住院患者的埃可病毒30型的遗传多样性进行了调查。开发了一种巢式逆转录聚合酶链反应(RT-PCR)检测方法,用于直接从脑脊液中对埃可病毒30型VP1编码序列进行定性分析。将22例患者获得的病毒序列与1996 - 1997年收治的9例埃可病毒30型脑膜炎患者的病毒分离株序列以及国际数据库中的埃可病毒30型序列进行比较。2000年,脑膜炎病例由两种病毒变体(C3和C4)引起,它们在基因上与1996 - 1997年期间鉴定出的另外两种变体(C1和C2)不同。详细的系统发育分析表明,C1、C2和C3变体在先前在其他地理区域鉴定出的病毒中有近亲。C4变体此前未被描述过。在四个埃可病毒30型变体之间观察到的基因组差异出现在同义位点,表明这些病毒在VP1编码序列中共享相似的抗原位点。总体而言,这些观察结果表明不同的埃可病毒30型变体广泛传播,并且新病毒会定期传入。病毒变体之间观察到的明显替代并非由抗原变异导致的选择优势引起。