Cytomegalovirus: Difference between revisions

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=== Epidemiology ===
 
=== Epidemiology ===
* Transferred by respiratory droplets and blood transfusions that lies dormant in white blood cells
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* Transferred by droplets and blood transfusions
 
* 80% of people are CMV-IgG positive
 
* 80% of people are CMV-IgG positive
   

Revision as of 17:26, 23 October 2019

Background

Microbiology

  • A dsDNA virus and the largest member of the human herpesvirus family
  • DNA in the nucleoprotein core is embedded in matrix proteins and pp65 antigen, which is surrounded by lipid envelope
  • UL54 encodes DNA polymerase and is highly conserved
  • UL97 encodes a phosphotransferase enzymes required to phosphorylate (and therefore activate) ganciclovir
  • May have four genotypes

Epidemiology

  • Transferred by droplets and blood transfusions
  • 80% of people are CMV-IgG positive

Risk Factors

  • Crowding

Clinical Presentation

  • Asymptomatic when young

Infectious mononucleosis syndrome

  • CMV causes 21% of IM
  • Fever, lymphadenopathy, and lymphocytosis

Stem cell transplantation

  • Low risk until day 21 post-transplantation, when cell lines begin to return
  • May presents as asymptomatic viremia
  • Most common symptomatic presentation is pneumonitis
    • Can also present with GI involvement

Solid-organ transplantation

  • Tends to reactivate within the transplanted organ
  • However, all can have GI involvement

Investigations

  • CBC showing leukopenia or pancytopenia
  • Mild elevation in liver enzymes
  • CMV-IgG positive
  • Detectable CMV DNA in peripheral blood, though it can rise during intercurrent illness

Diagnosis

  • Serology for IgG only useful for prior exposure (suggesting latent infection)
  • Quantitative PCR is most useful for diagnosis and monitoring response to treatment
    • Can be done on blood, BAL, urine, saliva, etc.
    • Standards for reporting are defined by WHO
    • However, can shed CMV asymptomatically during an acute illness, so must be taken within the clinical context
    • Sensitivity/specificity for CMV disease depends on the laboratory methods and cutoff used
  • Microscopy of tissue biopsy or cytology may demonstrate large nuclear inclusions, and can use immunofluorescence to pp65 antigen to confirm diagnosis
  • Viral culture can be done with human fibroblast cells, but is slow

Management

Resistance

  • Inherent acyclovir resistance
  • Tyrosine kinase mutation UL97? confers resistance to (val)ganciclovir
  • Polymerase mutation U54? confers resistance to (val)ganciclovir and foscarnet
  • Consider resistance if CMV DNA titres not decreasing despite appropriate treatment
  • Resistance genotyping available

Prophylaxis

  • Solid-organ transplant
    • Donor+/Recipient– high risk for reactivation, the the donor organ infecting the recipient
    • Donor–/Recipient+ intermediate risk
    • Donor+/Recipient+ intermediate risk
    • Donor–/Recipient– lowest risk
    • High and intermediate risk patients get prophylaxis with valganciclovir 900 mg po bid for some amount of duration...
  • Hematologic stem cell transplant
    • Donor+/Recipient+ high risk for reactivation
    • Donor–/Recipient+ high risk
    • Donor+/Recipient– intermediate risk
    • Donor–/Recipient– lowest risk
    • Preemptive monitoring with weekly CMV DNA PCR starting week 2
  • Treat if greater than threshold (1425 at McMaster) or if rising titre with symptoms

Complications

  • Even when dormant, can cause mild immunosuppression that predisposes to fungal infections
  • Asymptomatic shedding in lungs during intercurrent illness
  • Viremia with influenza-like illness
  • End-orgam damage
    • CMV colitis
    • Retinitis in AIDS patient (CD4 < 50-100)
    • Organ inflammation of solid-organ transplants
    • Pneumonitis in stem cell transplants

References

  1. ^  Michael J. Cannon, D. Scott Schmid, Terri B. Hyde. Review of cytomegalovirus seroprevalence and demographic characteristics associated with infection. Reviews in Medical Virology. 2010;20(4):202-213. doi:10.1002/rmv.655.
  2. ^  Jutta K. Preiksaitis, R. P. Bryce Larke, Glory J. Froese. Comparative seroepidemiology of cytomegalovirus infection in the Canadian Arctic and an Urban center. Journal of Medical Virology. 1988;24(3):299-307. doi:10.1002/jmv.1890240307.