Gjj. Chang et al., NUCLEOTIDE-SEQUENCE VARIATION OF THE ENVELOPE PROTEIN GENE IDENTIFIES2 DISTINCT GENOTYPES OF YELLOW-FEVER VIRUS, Journal of virology, 69(9), 1995, pp. 5773-5780
The evolution of yellow fever virus over 67 years was investigated by
comparing the nucleotide sequences of the envelope (E) protein genes o
f 20 viruses isolated in Africa, the Caribbean, and South America. Uni
formly weighted parsimony algorithm analysis defined two major evoluti
onary yellow fever virus lineages designated E genotypes I and II. E g
enotype I contained viruses isolated from East and Central Africa. E g
enotype II viruses were divided into two sublineages: IIA viruses from
West Africa and IIB viruses from America, except for a 1979 virus iso
lated from Trinidad (TRINID79A). Unique signature patterns were identi
fied at 111 nucleotide and 12 amino acid positions within the yellow f
ever virus E gene by signature pattern analysis. Yellow fever viruses
from East and Central Africa contained unique signatures at 60 nucleot
ide and five amino acid positions, those from West Africa contained un
ique signatures at 25 nucleotide and two amino acid positions, and vir
uses from America contained such signatures at 30 nucleotide and five
amino acid positions in the E gene. The dissemination of yellow fever
viruses from Africa to the Americas is supported by the close genetic
relatedness of genotype IIA and LLB viruses and genetic evidence of a
possible second introduction of yellow fever virus from West Africa, a
s illustrated by the TRINID79A virus isolate. The E protein genes of A
merican IIB yellow fever viruses had higher frequencies of amino acid
substitutions than did genes of yellow fever viruses of genotypes I an
d IIA on the basis of comparisons with a consensus amino acid sequence
for the yellow fever E gene. The great variation in the E proteins of
American yellow fever virus probably results from positive selection
imposed by virus interaction with different species of mosquitoes or n
onhuman primates in the Americas.