Human cytomegalovirus genetic variability in strains isolated from Japanese children during 1983-2003

Kaori Tanaka1, Kei Numazaki, Hiroyuki Tsutsumi

  • 1Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, Japan.

Insights

Investigating human cytomegalovirus (HCMV) genetic variability in Japanese children revealed distinct UL144 clades in congenital infections. Studying multiple genes is crucial for understanding HCMV epidemiology and developing vaccines.

Area of Science:

  • Virology
  • Molecular Epidemiology
  • Genetics

Background:

  • Human cytomegalovirus (HCMV) is a common pathogen with significant genetic diversity.
  • Understanding HCMV genetic variability is essential for tracking its spread and developing effective interventions.

Purpose of the Study:

  • To investigate the genetic variability of HCMV clinical isolates in Japanese infants and children.
  • To correlate genetic variations with clinical manifestations.
  • To assess the utility of studying single genes for HCMV molecular epidemiology.

Main Methods:

  • Analysis of the hypervariable regions (a sequence, UL144) and glycoprotein B (gB) gene of 74 HCMV clinical isolates using PCR.
  • Construction of unrooted phylogenetic trees to group isolates.
  • Comparison of genetic clades/genotypes with clinical outcomes.

Main Results:

  • HCMV isolates were grouped into 5 clades based on the a sequence and 3 clades based on the UL144 region.
  • Three genotypes of HCMV glycoprotein B were identified.
  • No correlation was found between specific genotypes/clades and clinical forms, except for congenital infections clustering within UL144 clades.
  • Variability in the studied genes was not correlated with each other.

Conclusions:

  • Studying a single HCMV gene is insufficient for comprehensive molecular epidemiology.
  • Congenital HCMV infections show specific UL144 clade associations.
  • This study provides foundational data on HCMV genetic diversity in an Asian population, aiding vaccine strain selection.

Related Concept Videos

Viral Recombination00:57

Viral Recombination

Cells are sometimes infected by more than one virus at once. When two viruses disassemble to expose their genomes for replication in the same cell, similar regions of their genomes can pair together and exchange sequences in a process called recombination. Alternatively, viruses with segmented genomes can swap segments in a process called reassortment.
Viral Mutations00:36

Viral Mutations

A mutation is a change in the sequence of bases of DNA or RNA in a genome. Some mutations occur during replication of the genome due to errors made by the polymerase enzymes that replicate DNA or RNA. Unlike DNA polymerase, RNA polymerase is prone to errors because it is not capable of “proofreading” its work. Viruses with RNA-based genomes, like HIV, therefore accrue mutations faster than viruses with DNA-based genomes. Because mutation and recombination provide the raw material for adaptive...
Genetic Variation01:25

Genetic Variation

Genetic variation is the diversity in DNA sequences found among individuals of the same species. This diversity is crucial for a species' survival because it helps organisms adapt to environmental changes. Genetic variation begins with fertilization, where an egg and sperm cell merge. Each of these cells carries 23 chromosomes, up to 46 in the fertilized egg. Chromosomes are long DNA strands that contain genes, the basic units of heredity.
Genes exist in different versions called alleles, which...
Horizontal Gene Transfer01:27

Horizontal Gene Transfer

Horizontal gene transfer (HGT) is a process where genetic material moves between organisms within the same generation, unlike vertical gene transfer, which occurs from parent to offspring. HGT plays a crucial role in microbial evolution, adaptation, and survival, particularly in shared environments like the human gut.Mobile genetic elements such as plasmids, prophages, integrons, insertion sequences, and transposons facilitate this process. HGT occurs through three primary mechanisms:...
Cytomegalovirus Disease01:27

Cytomegalovirus Disease

Cytomegalovirus (CMV) disease is caused by human cytomegalovirus, a double-stranded DNA virus of the Herpesviridae family. While primary CMV infection is often asymptomatic in immunocompetent individuals, the virus can cause severe disease in neonates and immunocompromised patients. CMV is the most common cause of congenital viral infection in the United States, and a major pathogen in solid organ and hematopoietic stem cell transplant recipients.CMV is transmitted via bodily fluids, sexual...