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Identification of syncytial mutations in a clinical isolate of herpes simplex virus 2

Journal Article · · Virology
 [1];  [2];  [3]
  1. Department of Microbiology and Immunology, Louisiana State University Health Sciences Center, Shreveport, LA 71130 (United States) and Center for Molecular and Tumor Virology, Louisiana State University Health Sciences Center, Shreveport, LA 71130 (United States) and Feist-Weiller Cancer Center, Louisiana State University Health Sciences Center, Shreveport, LA 71130 (United States)
  2. Department of Microbiology and Immunology, Louisiana State University Health Sciences Center, Shreveport, LA 71130 (United States)
  3. Department of Microbiology and Molecular Biology, Brigham Young University, Provo, UT 84602 (United States)

Small polykaryocytes resulting from cell fusion are found in herpes simplex virus (HSV) lesions in patients, but their significance for viral spread and pathogenesis is unclear. Although syncytial variants causing extensive fusion in tissue culture can be readily isolated from laboratory strains, they are rarely found in clinical isolates, suggesting that extensive cell fusion may be deleterious in vivo. Syncytial mutations have previously been identified for several laboratory strains, but not for clinical isolates of HSV type 2. To address this deficiency, we studied a recent syncytial clinical isolate, finding it to be a mixture of two syncytial and one nonsyncytial strain. The two syncytial strains have novel mutations in glycoprotein B, and in vitro cell fusion assays confirmed that they are responsible for syncytium formation. This panel of clinical strains may be ideal for examining the effect of increased cell fusion on pathogenesis.

OSTI ID:
20634887
Journal Information:
Virology, Journal Name: Virology Journal Issue: 2 Vol. 328; ISSN VIRLAX; ISSN 0042-6822
Country of Publication:
United States
Language:
English