Cytomegalovirus: Difference between revisions
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=== Microbiology === |
=== Microbiology === |
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* A |
* A dsDNA virus and the largest member of the [[Human herpesviruses|human herpesvirus]] family |
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* UL54 encodes DNA polymerase and is highly conserved |
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* UL97 encodes a phosphotransferase enzymes required to phosphorylate (and therefore activate) ganciclovir |
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* DNA in the nucleoprotein core embedded in matrix proteins and pp65 antigen, surrounded by lipid encelope |
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=== Epidemiology === |
=== Epidemiology === |
Revision as of 20:52, 23 October 2019
Background
Microbiology
- A dsDNA virus and the largest member of the human herpesvirus family
- UL54 encodes DNA polymerase and is highly conserved
- UL97 encodes a phosphotransferase enzymes required to phosphorylate (and therefore activate) ganciclovir
- DNA in the nucleoprotein core embedded in matrix proteins and pp65 antigen, surrounded by lipid encelope
Epidemiology
- Transferred by respiratory droplets and blood transfusions that lies dormant in white blood cells
- 80% of people are CMV-IgG positive
Risk Factors
- Crowding
Clinical Presentation
- Asymptomatic when young
- Mono-like or influenza-like illness when older
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)
- PCR most useful for diagnosis
- Can be done on blood and BAL
- However, can shed CMV asymptomatically during an acute illness, so must be taken within the clinical context
Management
- Antivirals
- First-line: valganciclovir or ganciclovir
- Measure baseline CBC first due to risk of cytopenias
- Second-line, if cytopenias: foscarnet
- Third-line: cidofovir, maribavir, letermovir
- First-line: valganciclovir or ganciclovir
- At McMaster, expect 1-log drop within 2 weeks (lab-dependent)
- Continue treatment until PCR is negative
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
- ^ 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.
- ^ 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.