Literature DB >> 17942611

Prevalence and protein specificity of human antibodies to Inkoo virus infection.

Niina Putkuri1, Antti Vaheri, Olli Vapalahti.   

Abstract

Inkoo virus (INKV), a member of the California serogroup orthobunyaviruses, is circulating widely in northern Europe. Although the virus was discovered over 40 years ago, the disease associations and immune responses in human infection are poorly characterized. We first developed an immunofluorescence assay (IFA) for the detection of INKV antibodies in humans, and then we studied a panel of 1,292 sera in patients with a febrile illness in Finland. We found four acute (immunoglobulin M [IgM] positive) INKV infections and an IgG seroprevalence of 51.3%. The data indicate that the infection has become more common than it was in the 1960s, especially in southern Finland. Two distinct IgG IFA fluorescence patterns were observed: a granular pattern in sera from patients with acute INKV infection and a diffuse pattern in those with long-standing immunity. Further analysis with a panel of INKV-positive sera (n = 18; verified by neutralization assay) of protein-specific responses, using immunoprecipitation and IFA based on baculovirus-expressed INK N, Gn, and Gc proteins, demonstrated a strong IgG response predominantly towards N protein in the acute phase. In contrast, in patients with long-standing immunity, the Gc response was more prominent and the N response was weaker. In conclusion, a diagnostic IgG IFA pattern distinguishing between acute infection and long-standing immunity was observed. N protein seems to be the optimal antigen for the serodiagnosis of acute infection, and the Gc protein could be appropriate for the serosurveillance of INKV.

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Year:  2007        PMID: 17942611      PMCID: PMC2168378          DOI: 10.1128/CVI.00288-07

Source DB:  PubMed          Journal:  Clin Vaccine Immunol        ISSN: 1556-679X


  27 in total

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Authors:  Matthew L Plassmeyer; Samantha S Soldan; Karen M Stachelek; Susan M Roth; Julio Martín-García; Francisco González-Scarano
Journal:  Virology       Date:  2006-10-05       Impact factor: 3.616

3.  Biological activities of monoclonal antibodies reactive with antigenic sites mapped on the G1 glycoprotein of La Crosse virus.

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Journal:  Virology       Date:  1983-09       Impact factor: 3.616

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Journal:  Prog Clin Biol Res       Date:  1983

5.  Monoclonal antibodies against La Crosse virus.

Authors:  L J Grady; S Srihongse; M A Grayson; R Deibel
Journal:  J Gen Virol       Date:  1983-08       Impact factor: 3.891

6.  La Crosse virus G1 glycoprotein undergoes a conformational change at the pH of fusion.

Authors:  F Gonzalez-Scarano
Journal:  Virology       Date:  1985-01-30       Impact factor: 3.616

7.  La Crosse bunyavirus can mediate pH-dependent fusion from without.

Authors:  F Gonzalez-Scarano; N Pobjecky; N Nathanson
Journal:  Virology       Date:  1984-01-15       Impact factor: 3.616

8.  Characterization of monoclonal antibodies against the G1 and N proteins of LaCrosse and Tahyna, two California serogroup bunyaviruses.

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Journal:  Virology       Date:  1982-07-15       Impact factor: 3.616

9.  Arboviruses in Finland. IV. Isolation and characterization of Inkoo virus, a Finnish representative of the California group.

Authors:  M Brummer-Korvenkontio; P Saikku; P Korhonen; I Ulmanen; T Reunala; J Karvonen
Journal:  Am J Trop Med Hyg       Date:  1973-05       Impact factor: 2.345

10.  The effect of proteolytic cleavage of La Crosse virus G1 glycoprotein on antibody neutralization.

Authors:  L Kingsford; D W Hill
Journal:  J Gen Virol       Date:  1983-10       Impact factor: 3.891

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