Geographic distribution and evolution of yellow fever viruses based on direct sequencing of genomic cDNA fragments

• Published in: Journal of general virology Vol. 75; no. 2; pp. 417 - 423
• Main Authors: Lepiniec, Loic, Dalgarno, Lynn, Huong, Vu Thi Que, Monath, Thomas P, Digoutte, Jean-Pierre, Deubel, Vincent
• Format: Journal Article
• Language: English
• Published: Reading Soc General Microbiol 01-02-1994; Society for General Microbiology; Microbiology Society
• Subjects: Amino Acid Sequence; Animals; Base Sequence; Biological and medical sciences; DNA, Complementary - chemistry; Fundamental and applied biological sciences. Psychology; Genetics; Humans; Life Sciences; Microbiology; Microbiology and Parasitology; Molecular Sequence Data; Phylogeny; RNA, Viral - chemistry; Virology; yellow fever virus; Yellow fever virus - classification; Yellow fever virus - genetics; Genetic variability; Nucleotide sequence; Homology; Dendrogram; Flavivirus; Virus; Molecular evolution; Gene; Geographic distribution; Flaviviridae; Virus envelope; Aminoacid sequence; Structural analysis; Yellow fever virus; ADNC
• ISSN: 0022-1317; 1465-2099
• DOI: 10.1099/0022-1317-75-2-417

1 Institut Pasteur, Department of Virology, 25 rue du Dr Roux, 75724 Paris cedex 15, France,
2 Division of Biochemistry and Molecular Biology, Faculty of Science, The Australian National University, Canberra, Australia 2601
3 OraVax Inc., 230 Albany Street, Cambridge, Massachusetts 02139, U.S.A.
and 4 Institut Pasteur, BP 220, Dakar, Senegal
We have compared the nucleotide sequence of an envelope protein gene fragment encoding amino acids 291 to 406 of 22 yellow fever (YF) virus strains of diverse geographic and host origins isolated over a 63 year time span. The nucleotide fragment of viral RNA was examined by direct sequencing of a PCR product derived from complementary DNA. Alignment with the prototype Asibi strain sequence showed divergence of 0 to 21.5% corresponding to a maximum of 5.2% divergence in the amino acid sequence. Taking 10% nucleotide divergence as a cut-off point, the 22 YF virus strains fell into three topotypes which corresponded to different geographical areas, namely West Africa, Central-East Africa, and South America. Two subgroups were defined in West Africa, a genotypic group circulating in the sylvatic zone of the western part of Africa, from western Ivory Coast-Mali to Senegal, and a group responsible for large outbreaks from eastern Ivory Coast-Burkina Faso to Cameroon. Strains from Central-East Africa showed a low ratio of transition:transversion of about 1 instead of 8 to 10 for other strains, when their nucleotide sequences were compared with those of other African strains. This may reflect a more distant relationship between the former strains and the others. No change was observed in the highly conserved amino acid domain encompassing the TGD sequence, and important determinant of flavivirus tropism and pathogenesis. Our results support earlier observations on the genetic relationships between YF isolates established by T1 oligonucleotide fingerprinting and offer a useful tool for the understanding of YF virus distribution and evolution.
Received 28 June 1993;
accepted 6 October 1993.