The non-structural leader protein gene of foot-and-mouth disease virus is highly variable between serotypes
被引:28
作者:
George, M
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机构:
Indian Vet Res Inst, All India Coordinated Res Project Epidemiol Studi, Cent Lab, Mukteswar Kumaon 263138, Nainital, IndiaIndian Vet Res Inst, All India Coordinated Res Project Epidemiol Studi, Cent Lab, Mukteswar Kumaon 263138, Nainital, India
George, M
[1
]
Venkataramanan, R
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Indian Vet Res Inst, All India Coordinated Res Project Epidemiol Studi, Cent Lab, Mukteswar Kumaon 263138, Nainital, IndiaIndian Vet Res Inst, All India Coordinated Res Project Epidemiol Studi, Cent Lab, Mukteswar Kumaon 263138, Nainital, India
Venkataramanan, R
[1
]
B, GC
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Indian Vet Res Inst, All India Coordinated Res Project Epidemiol Studi, Cent Lab, Mukteswar Kumaon 263138, Nainital, IndiaIndian Vet Res Inst, All India Coordinated Res Project Epidemiol Studi, Cent Lab, Mukteswar Kumaon 263138, Nainital, India
B, GC
[1
]
Hemadri, D
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Indian Vet Res Inst, All India Coordinated Res Project Epidemiol Studi, Cent Lab, Mukteswar Kumaon 263138, Nainital, IndiaIndian Vet Res Inst, All India Coordinated Res Project Epidemiol Studi, Cent Lab, Mukteswar Kumaon 263138, Nainital, India
Hemadri, D
[1
]
机构:
[1] Indian Vet Res Inst, All India Coordinated Res Project Epidemiol Studi, Cent Lab, Mukteswar Kumaon 263138, Nainital, India
FMDV;
leader gene sequence variability;
non-structural L protein;
D O I:
10.1023/A:1011153904910
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
Aphthoviruses are unique among picornaviruses in that they alone encode a functional L proteinase as the first component of the viral polyprotein. The L genes of a few Indian foot-and-mouth disease viruses were sequenced and compared with those available to study the extent of variation in this gene. Besides the two in-frame start codons present in all FMDV L genes, the Asia-I vaccine virus had an additional in-frame AUG (start) codon, at codon position 3. Amino acid sequence comparison revealed that 39.8% of positions were capable of accepting replacements, yet the residues of the catalytic dyad were totally conserved. Sequence comparison at the C-terminus of the protein indicated that K/R down arrow GAGQS is sufficient for L/P1 cleavage. Phylogenetic analysis based on the L gene sequences did not reveal any serotype-specific clustering. The probable implications of the observed high variability in this non-structural gene is briefly discussed.