» Articles » PMID: 24558222

Genomic and Phylogenetic Characterization of Viruses Included in the Manzanilla and Oropouche Species Complexes of the Genus Orthobunyavirus, Family Bunyaviridae

Abstract

A thorough characterization of the genetic diversity of viruses present in vector and vertebrate host populations is essential for the early detection of and response to emerging pathogenic viruses, yet genetic characterization of many important viral groups remains incomplete. The Simbu serogroup of the genus Orthobunyavirus, family Bunyaviridae, is an example. The Simbu serogroup currently consists of a highly diverse group of related arboviruses that infect both humans and economically important livestock species. Here, we report complete genome sequences for 11 viruses within this group, with a focus on the large and poorly characterized Manzanilla and Oropouche species complexes. Phylogenetic and pairwise divergence analyses indicated the presence of high levels of genetic diversity within these two species complexes, on a par with that seen among the five other species complexes in the Simbu serogroup. Based on previously reported divergence thresholds between species, the data suggested that these two complexes should actually be divided into at least five species. Together these five species formed a distinct phylogenetic clade apart from the rest of the Simbu serogroup. Pairwise sequence divergences among viruses of this clade and viruses in other Simbu serogroup species complexes were similar to levels of divergence among the other orthobunyavirus serogroups. The genetic data also suggested relatively high levels of natural reassortment, with three potential reassortment events present, including two well-supported events involving viruses known to infect humans.

Citing Articles

Addressing the emerging threat of Oropouche virus: implications and public health responses for healthcare systems.

Okesanya O, Amisu B, Adigun O, Ahmed M, Agboola A, Kab T Trop Dis Travel Med Vaccines. 2025; 11(1):1.

PMID: 39748388 PMC: 11694362. DOI: 10.1186/s40794-024-00236-x.


Genomic Epidemiology of 2023-2024 Oropouche Outbreak in Iquitos, Peru reveals independent origin from a concurrent outbreak in Brazil.

Paredes Olortegui M, Schiaffino F, Penataro Yori P, Colston J, Shapiama Lopez V, Pinedo Vasquez T medRxiv. 2024; .

PMID: 39711716 PMC: 11661442. DOI: 10.1101/2024.12.08.24318674.


Efficient Expression of Oropouche Virus Nonstructural Proteins NSs and NSm.

Jurado-Cobena E, Ikegami T Methods Mol Biol. 2024; 2893:273-283.

PMID: 39671044 DOI: 10.1007/978-1-0716-4338-9_20.


OROPOUCHE VIRUS: MORE QUESTIONS THAN ANSWERS.

Jurado-Cobena E Zoonoses (Burlingt). 2024; 4(1).

PMID: 39575443 PMC: 11580152. DOI: 10.15212/zoonoses-2024-0006.


Full Genome Characterization of the First Oropouche Virus Isolate Imported in Europe from Cuba.

Deiana M, Malago S, Mori A, Accordini S, Matucci A, Mantovani R Viruses. 2024; 16(10).

PMID: 39459919 PMC: 11512199. DOI: 10.3390/v16101586.


References
1.
Gentsch J, Rozhon E, Klimas R, El Said L, Shope R, Bishop D . Evidence from recombinant bunyavirus studies that the M RNA gene products elicit neutralizing antibodies. Virology. 1980; 102(1):190-204. DOI: 10.1016/0042-6822(80)90080-x. View

2.
Xu F, Liu D, Nunes M, Travassos da Rosa A, Tesh R, Xiao S . Antigenic and genetic relationships among Rift Valley fever virus and other selected members of the genus Phlebovirus (Bunyaviridae). Am J Trop Med Hyg. 2007; 76(6):1194-200. View

3.
Djikeng A, Halpin R, Kuzmickas R, DePasse J, Feldblyum J, Sengamalay N . Viral genome sequencing by random priming methods. BMC Genomics. 2008; 9:5. PMC: 2254600. DOI: 10.1186/1471-2164-9-5. View

4.
Seymour C, Peralta P, Montgomery G . Viruses isolated from Panamanian sloths. Am J Trop Med Hyg. 1983; 32(6):1435-44. DOI: 10.4269/ajtmh.1983.32.1435. View

5.
Nelson M, Holmes E . The evolution of epidemic influenza. Nat Rev Genet. 2007; 8(3):196-205. DOI: 10.1038/nrg2053. View