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Sökning: WFRF:(Bergström Petra) > (1999) > Variability of the ...

Variability of the glycoprotein G gene in clinical isolates of herpes simplex virus type 1.

Rekabdar, Elham, 1971 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för laboratoriemedicin, Avdelningen för klinisk virologi,Institute of Laboratory Medicine, Dept of Clinical Virology
Tunbäck, Petra, 1965 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för särskilda specialiteter, Avdelningen för dermatologi och venereologi,Institute of Selected Clinical Sciences, Department of Dermatology and Venereology
Liljeqvist, Jan-Åke, 1954 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för laboratoriemedicin, Avdelningen för klinisk virologi,Institute of Laboratory Medicine, Dept of Clinical Virology
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Bergström, Tomas, 1950 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för laboratoriemedicin, Avdelningen för klinisk virologi,Institute of Laboratory Medicine, Dept of Clinical Virology
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 (creator_code:org_t)
1999
1999
Engelska.
Ingår i: Clinical and diagnostic laboratory immunology. - 1071-412X. ; 6:6, s. 826-31
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Glycoprotein G (gG) of herpes simplex virus type 1 (HSV-1) has been used as a prototype antigen for HSV-1 type-specific serodiagnosis, but data on the sequence variability of the gene coding for this protein in wild-type strains are lacking. In this study, direct DNA sequencing of the gG-1 genes from PCR products was performed with clinical HSV-1 isolates from 11 subjects as well as with strains Syn 17(+), F, and KOS 321. The reference strains Syn 17(+) and F showed a high degree of conservation, while KOS 321 carried 13 missense mutations and, in addition, 12 silent mutations. Three clinical isolates showed mutations leading to amino acid alterations: one had a mutation of K(122) to N, which is a gG-1-to-gG-2 alteration; another contained all mutations which were observed in KOS 321 except two silent mutations; and the third isolate carried five missense mutations. Two clinical isolates as well as strain KOS 321 showed a mutation (F(111)-->V) within the epitope of a gG-1-reactive monoclonal antibody (MAb). When all viruses were tested for reactivity with the anti-gG-1 MAb, the three strains with the F(111)-->V mutation were found to be unreactive. Furthermore, gG-1 antibodies purified from sera from the two patients carrying strains mutated in this epitope were less reactive when they were tested by an HSV-1-infected-cell assay. Therefore, our finding that the sequence variability of the gG-1 gene also affects B-cell epitope regions of this protein in clinical isolates may have consequences for the use of this protein as a type-specific antigen for serodiagnosis.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Dermatologi och venereologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Dermatology and Venereal Diseases (hsv//eng)

Nyckelord

Adult
Aged
Amino Acid Sequence
Amino Acid Substitution
Animals
Antibodies
Monoclonal
Antibodies
Viral
immunology
Antigens
Surface
analysis
immunology
Cells
Cultured
Cercopithecus aethiops
DNA Mutational Analysis
DNA
Viral
analysis
Enzyme-Linked Immunosorbent Assay
Epitopes
immunology
Female
Genetic Variation
Herpes Simplex
genetics
immunology
Herpesvirus 1
Human
genetics
immunology
Humans
Immunoglobulin G
immunology
Kidney
cytology
Male
Middle Aged
Molecular Sequence Data
Polymerase Chain Reaction
Sensitivity and Specificity
Serologic Tests
Viral Envelope Proteins
genetics
immunology

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