Multipotent mesenchymal stromal cells are fully permissive for human cytomegalovirus infection

Guan-Hua Qiao1, Fei Zhao1, Shuang Cheng2

  • 1State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, 430071, China.

Virologica Sinica
|April 24, 2016
PubMed

Insights

Congenital human cytomegalovirus (HCMV) infects multipotent mesenchymal stromal cells (MSCs). This susceptibility may explain multi-organ maldevelopment seen in infants with congenital HCMV infection.

Area of Science:

  • Virology
  • Stem Cell Biology
  • Developmental Biology

Background:

  • Congenital human cytomegalovirus (HCMV) infection is a primary cause of birth defects, often leading to multi-organ maldevelopment.
  • Multipotent mesenchymal stromal cells (MSCs) are crucial for organ formation and development.
  • The susceptibility of MSCs to HCMV infection remains largely unexplored.

Purpose of the Study:

  • To investigate whether multipotent mesenchymal stromal cells (MSCs) are susceptible to human cytomegalovirus (HCMV) infection.
  • To explore the role of MSCs in the pathogenesis of congenital HCMV infection and associated birth defects.

Main Methods:

  • Isolation and characterization of MSCs from human umbilical cord Wharton's jelly.
  • Infection of MSCs with the HCMV Towne strain.
  • Assessment of viral entry, replication, protein expression, and infectious virion release using western blotting, immunofluorescence, and plaque assays.

Main Results:

  • Isolated MSCs demonstrated full permissiveness to HCMV infection.
  • Evidence of viral entry, replication initiation, protein expression, and release of infectious virions was observed in infected MSCs.
  • These findings indicate MSCs are a viable target for HCMV.

Conclusions:

  • MSCs are fully permissive to HCMV infection.
  • This permissiveness provides a potential mechanism for multi-organ malformation in congenital HCMV infections.
  • Further research into MSCs' role in HCMV pathogenesis is warranted for non-nervous system diseases.

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