Razzauti Maria, Plyusnina Angelina, Henttonen Heikki, Plyusnin Alexander
Finnish Forest Research Institute, Vantaa Research Unit, PO Box 18, FI-01301 Vantaa, Finland.
Department of Virology, Haartman Institute, PO Box 21, FI-00014 University of Helsinki, Finland.
J Gen Virol. 2008 Jul;89(Pt 7):1649-1660. doi: 10.1099/vir.0.2008/001248-0.
The genetic diversity of Puumala hantavirus (PUUV) was studied in a local population of its natural host, the bank vole (Myodes glareolus). The trapping area (2.5 x 2.5 km) at Konnevesi, Central Finland, included 14 trapping sites, at least 500 m apart; altogether, 147 voles were captured during May and October 2005. Partial sequences of the S, M and L viral genome segments were recovered from 40 animals. Seven, 12 and 17 variants were detected for the S, M and L sequences, respectively; these represent new wild-type PUUV strains that belong to the Finnish genetic lineage. The genetic diversity of PUUV strains from Konnevesi was 0.2-4.9 % for the S segment, 0.2-4.8 % for the M segment and 0.2-9.7 % for the L segment. Most nucleotide substitutions were synonymous and most deduced amino acid substitutions were conservative, probably due to strong stabilizing selection operating at the protein level. Based on both sequence markers and phylogenetic clustering, the S, M and L sequences could be assigned to two groups, 'A' and 'B'. Notably, not all bank voles carried S, M and L sequences belonging to the same group, i.e. S(A)M(A)L(A) or S(B)M(B)L(B). A substantial proportion (8/40, 20 %) of the newly characterized PUUV strains possessed reassortant genomes such as S(B)M(A)L(A), S(A)M(B)L(B) or S(B)M(A)L(B). These results suggest that at least some of the PUUV reassortants are viable and can survive in the presence of their parental strains.
在普马拉汉坦病毒(PUUV)的天然宿主——棕背䶄(Myodes glareolus)的本地种群中,对该病毒的遗传多样性进行了研究。芬兰中部科内韦西的诱捕区域(2.5×2.5千米)包括14个诱捕点,彼此相距至少500米;2005年5月和10月期间,共捕获了147只棕背䶄。从40只动物中获得了病毒基因组S、M和L片段的部分序列。分别在S、M和L序列中检测到7个、12个和17个变体;这些代表了属于芬兰遗传谱系的新型野生型PUUV毒株。来自科内韦西的PUUV毒株的遗传多样性,S片段为0.2 - 4.9%,M片段为0.2 - 4.8%,L片段为0.2 - 9.7%。大多数核苷酸替换是同义的,大多数推导的氨基酸替换是保守的,这可能是由于在蛋白质水平上存在强大的稳定选择。基于序列标记和系统发育聚类,S、M和L序列可分为“A”和“B”两组。值得注意的是,并非所有棕背䶄携带的S、M和L序列都属于同一组,即S(A)M(A)L(A)或S(B)M(B)L(B)。相当一部分(8/40,20%)新鉴定的PUUV毒株具有重配基因组,如S(B)M(A)L(A)、S(A)M(B)L(B)或S(B)M(A)L(B)。这些结果表明,至少一些PUUV重配体是有活力的,并且能够在其亲本毒株存在的情况下存活。