Sequence analysis of rabies virus in humans exhibiting encephalitic or paralytic rabies

被引:25
作者
Hemachudha, T
Wacharapluesadee, S
Lumlertdaecha, B
Orciari, LA
Rupprecht, CE
La-ongpant, M
Juntrakul, S
Denduangboripant, J
机构
[1] Chulalongkorn Univ Hosp, Dept Med, Mol Biol Lab Neurol Dis, Bangkok 10330, Thailand
[2] Ctr Dis Control & Prevent, Rabies Sect, Atlanta, GA USA
[3] Chulalongkorn Univ, Fac Sci, Dept Biol, Bangkok, Thailand
[4] Chulalongkorn Univ, Queen Saovabha Mem Inst, Bangkok, Thailand
关键词
D O I
10.1086/378415
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Two distinct clinical patterns, encephalitic ( furious) and paralytic ( dumb), have been recognized in human rabies. It has been postulated that different rabies virus variants associated with particular vectors may be responsible for these different clinical manifestations. Analysis of the glycoprotein (G), nucleoprotein (N), and phosphoprotein ( P) genes of rabies viruses from 2 human cases of encephalitic rabies and from 2 human cases of paralytic rabies demonstrated only minor nucleotide differences. Deduced amino-acid patterns of the N protein were identical in both human and canine samples that came from the same geographic location, regardless of the clinical form. All differences in amino-acid patterns of the G protein were found outside the ectodomain, in either the signal peptide or the transmembrane and endodomains. None of the amino-acid differences of the P protein was within the interactive site with dynein. These findings support the concept that clinical manifestations of rabies are not explained solely by the associated rabies virus variant.
引用
收藏
页码:960 / 966
页数:7
相关论文
共 15 条
[1]   PARALYTIC RABIES - A CLINICOPATHOLOGICAL STUDY [J].
CHOPRA, JS ;
BANERJEE, AK ;
MURTHY, JMK ;
PAL, SR .
BRAIN, 1980, 103 (DEC) :789-802
[2]   Molecular characterization of rabies virus isolates from Mexico:: Implications for transmission dynamics and human risk [J].
de Mattos, CC ;
de Mattos, CA ;
Loza-Rubio, E ;
Aguilar-Setién, A ;
Orciari, LA ;
Smith, JS .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1999, 61 (04) :587-597
[3]   Human rabies: a disease of complex neuropathogenetic mechanisms and diagnostic challenges [J].
Hemachudha, T ;
Laothamatas, J ;
Rupprecht, CE .
LANCET NEUROLOGY, 2002, 1 (02) :101-109
[4]  
Hemachudha Thiravat, 2003, International Journal of Infectious Diseases, V7, P76, DOI 10.1016/S1201-9712(03)90046-4
[5]  
Laothamatas J, 2003, AM J NEURORADIOL, V24, P1102
[6]  
LOPEZ A, 1992, LANCET, V339, P408, DOI 10.1016/0140-6736(92)90088-K
[7]   Extensive attenuation of rabies virus by simultaneously modifying the dynein light chain binding site in the P protein and replacing Arg333 in the G protein [J].
Mebatsion, T .
JOURNAL OF VIROLOGY, 2001, 75 (23) :11496-11502
[8]   Characterization of a unique variant of bat rabies virus responsible for newly emerging human cases in North America [J].
Morimoto, K ;
Patel, M ;
Corisdeo, S ;
Hooper, DC ;
Fu, ZF ;
Rupprecht, CE ;
Koprowski, H ;
Dietzschold, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (11) :5653-5658
[9]   Phylogeographic patterns exhibited by Ontario rabies virus variants [J].
Nadin-Davis, SA ;
Sampath, MI ;
Casey, GA ;
Tinline, RR ;
Wandeler, AI .
EPIDEMIOLOGY AND INFECTION, 1999, 123 (02) :325-336
[10]   Polymorphism of rabies viruses within the phosphoprotein and matrix protein genes [J].
NadinDavis, SA ;
Huang, W ;
Wandeler, AI .
ARCHIVES OF VIROLOGY, 1997, 142 (05) :979-992