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Updated: Jun 26, 2026

Plaquing of Herpes Simplex Viruses
Published on: November 5, 2021
Utilization of microsatellite polymorphism for differentiating herpes simplex virus type 1 strains
C Deback1, D Boutolleau, C Depienne
1UPMC Université Paris 06, UPRES EA 2387, Paris F-75013, France. claire.deback@psl.aphp.fr
Herpes simplex virus type 1 (HSV-1) microsatellites, identified through in silico analysis and PCR, serve as stable genetic markers. A multiplex PCR method enables rapid HSV-1 strain characterization and tracking of infections.
Area of Science:
- Virology
- Genetics
- Molecular Biology
Background:
- The herpes simplex virus type 1 (HSV-1) genome contains microsatellites, which are short tandem repeats.
- Microsatellite variability suggests potential as molecular markers for HSV-1 strain differentiation.
Purpose of the Study:
- To identify and characterize microsatellites within the HSV-1 genome.
- To develop a method for rapid and accurate genetic characterization of HSV-1 strains using microsatellites.
Main Methods:
- In silico analysis of the complete HSV-1 genome to identify microsatellites.
- Polymerase chain reaction (PCR) and length polymorphism analysis of 12 distinct HSV-1 strains.
- Development of a multiplex PCR assay targeting polymorphic microsatellites.
Main Results:
- Identified 79 microsatellites in the HSV-1 genome, with 45 in noncoding regions and 34 in open reading frames.
- Discovered 23 polymorphic and 6 monomorphic microsatellites among 12 HSV-1 strains.
- Developed a stable multiplex PCR method for rapid HSV-1 strain genotyping, revealing unique microsatellite haplotypes.
Conclusions:
- Microsatellites are valuable, stable genetic markers for differentiating HSV-1 strains.
- The developed multiplex PCR tool facilitates accurate genetic characterization and investigation of HSV-1 infections, including recurrent and nosocomial cases.
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