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Presence of broadly reactive and group-specific neutralizing epitopes on newly described isolates of Crimean-Congo hemorrhagic fever virus

Asim AhmedDepartment of Microbiology, University of Pennsylvania, Philadelphia, PA 19104, USAJeanne McFallsDepartment of Microbiology, University of Pennsylvania, Philadelphia, PA 19104, USAChristian HoffmannDepartment of Microbiology, University of Pennsylvania, Philadelphia, PA 19104, USAClaire Marie FiloneDepartment of Microbiology, University of Pennsylvania, Philadelphia, PA 19104, USAShaun StewartDepartment of Microbiology, University of Pennsylvania, Philadelphia, PA 19104, USAJason ParagasVirology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702, USAS. KhodjaevInstitute of Virology, Ministry of Health, Tashkent, UzbekistanDilbar ShermukhamedovaInstitute of Virology, Ministry of Health, Tashkent, UzbekistanConnie S. SchmaljohnVirology Division, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, MD 21702, USARobert W. DomsDepartment of Microbiology, University of Pennsylvania, Philadelphia, PA 19104, USAAndrea Bertolotti‐CiarletDepartment of Microbiology, University of Pennsylvania, Philadelphia, PA 19104, USA
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Аннотация

Crimean-Congo hemorrhagic fever virus (CCHFV), a member of the genus Nairovirus of the family Bunyaviridae, causes severe disease in humans with high rates of mortality. The virus has a tripartite genome composed of a small (S), a medium (M) and a large (L) RNA segment; the M segment encodes the two viral glycoproteins, G(N) and G(C). Whilst relatively few full-length M segment sequences are available, it is apparent that both G(N) and G(C) may exhibit significant sequence diversity. It is unknown whether considerable antigenic differences exist between divergent CCHFV strains, or whether there are conserved neutralizing epitopes. The M segments derived from viral isolates of a human case of CCHF in South Africa (SPU 41/84), an infected tick (Hyalomma marginatum) in South Africa (SPU 128/81), a human case in Congo (UG 3010), an infected individual in Uzbekistan (U2-2-002) and an infected tick (Hyalomma asiaticum) in China (Hy13) were sequenced fully, and the glycoproteins were expressed. These novel sequences showed high variability in the N-terminal region of G(N) and more modest differences in the remainder of G(N) and in G(C). Phylogenetic analyses placed these newly identified strains in three of the four previously described M segment groups. Studies with a panel of mAbs specific to G(N) and G(C) indicated that there were significant antigenic differences between the M segment groups, although several neutralizing epitopes in both G(N) and G(C) were conserved among all strains examined. Thus, the genetic diversity exhibited by CCHFV strains results in significant antigenic differences that will need to be taken into consideration for vaccine development.

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