Xiao S Y, Leduc J W, Chu Y K, Schmaljohn C S
Virology Division, U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland 21702.
Virology. 1994 Jan;198(1):205-17. doi: 10.1006/viro.1994.1023.
We constructed a phylogenic tree by pairwise comparison of the deduced amino acid sequences encoded in the medium (M) genome segments of 13 hantaviruses. Five distinct branches were identified, four of which are represented by Hantaan, Seoul, Puumala, and Prospect Hill viruses. These groups corresponded to those previously established by serological and genetic means. In addition, we present sequence information for the M segment of Thailand virus and demonstrate that it represents a unique, fifth branch on the dendrogram. We show that a tree nearly identical to that constructed from the deduced amino acids encoded in the M segments of these viruses can be constructed by comparing nucleotide sequences of a 333-bp region of the M segments of the same hantaviruses. This region can be amplified, for most hantaviruses, by reverse transcriptase-polymerase chain reaction (RT-PCR) techniques, using a single primer pair. By using this method, we constructed a consensus tree for 30 hantaviruses, including 15 isolates for which we PCR-amplified and sequenced the 333-bp region. In addition to the five branches described above, we identified a sixth unique hantavirus group represented by Dobrava virus, an Apodemus isolate from Slovenia. Although we were unable to PCR-amplify the M segment of Thottapalayam virus, a distantly related hantavirus isolated from a shrew captured in India, we were able to amplify, clone, and sequence a portion of the small (S) segment of that virus. When we compared our Thottapalayam sequence to corresponding S segment sequences of other hantaviruses, the results indicated that this virus may represent a seventh, distinct group of hantaviruses.
我们通过对13种汉坦病毒中膜(M)基因组片段编码的推导氨基酸序列进行两两比较,构建了系统发育树。确定了五个不同的分支,其中四个由汉坦病毒、汉城病毒、普马拉病毒和展望山病毒代表。这些组与先前通过血清学和遗传学方法确定的组相对应。此外,我们提供了泰国病毒M片段的序列信息,并证明它在树状图上代表一个独特的第五分支。我们表明,通过比较相同汉坦病毒M片段333bp区域的核苷酸序列,可以构建一棵与由这些病毒M片段编码的推导氨基酸构建的树几乎相同的树。对于大多数汉坦病毒来说,使用一对引物,通过逆转录聚合酶链反应(RT-PCR)技术可以扩增该区域。通过这种方法,我们为30种汉坦病毒构建了一棵共识树,其中包括15个分离株,我们对其333bp区域进行了PCR扩增和测序。除了上述五个分支外,我们还确定了第六个独特的汉坦病毒组,由来自斯洛文尼亚的姬鼠分离株多布拉瓦病毒代表。尽管我们无法对从印度捕获的一只鼩鼱中分离出的远缘汉坦病毒托塔帕拉亚姆病毒的M片段进行PCR扩增,但我们能够扩增、克隆并测序该病毒小(S)片段的一部分。当我们将托塔帕拉亚姆病毒序列与其他汉坦病毒的相应S片段序列进行比较时,结果表明该病毒可能代表第七个不同的汉坦病毒组。