Cytomegalovirus: Difference between revisions
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* DNA in the nucleoprotein core is embedded in matrix proteins and pp65 antigen, which is surrounded by lipid envelope |
* DNA in the nucleoprotein core is embedded in matrix proteins and pp65 antigen, which is surrounded by lipid envelope |
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* UL54 encodes DNA polymerase and is highly conserved |
* UL54 encodes DNA polymerase and is highly conserved |
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* UL97 encodes a |
* UL97 encodes a tyrosine kinase required to phosphorylate (and therefore activate) ganciclovir |
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* May have four genotypes |
* May have four genotypes |
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=== Antiviral resistance === |
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* Inherent acyclovir resistance |
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* Tyrosine kinase mutation UL97 confers resistance to (val)ganciclovir |
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* Polymerase mutation UL54 confers resistance to (val)ganciclovir and to foscarnet |
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=== Epidemiology === |
=== Epidemiology === |
Revision as of 02:05, 24 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 tyrosine kinase required to phosphorylate (and therefore activate) ganciclovir
- May have four genotypes
Antiviral resistance
- Inherent acyclovir resistance
- Tyrosine kinase mutation UL97 confers resistance to (val)ganciclovir
- Polymerase mutation UL54 confers resistance to (val)ganciclovir and to foscarnet
Epidemiology
- Transferred by droplets and blood transfusions
- 80% of people are CMV-IgG positive
Risk Factors
- Crowding
Clinical Presentation
- Often asymptomatic when young
Infectious mononucleosis syndrome
- CMV causes 21% of IM
- Fever, lymphadenopathy, and lymphocytosis
- Often mild liver abnormalities
- Occasionally cold agglutinin disease, RF positivity, cryoglobulinemia, and ANA positivity
- Symptoms can persist or relapse over months (average 2 months, but up to 8)
Stem cell transplantation
- Low risk until day 21 post-transplantation, when cell lines begin to return
- May present as asymptomatic viremia
- Most common symptomatic presentation is pneumonitis (an interstitial pneumonia)
- Can also present with GI involvement
Solid-organ transplantation
- Tends to reactivate within the transplanted organ
- However, all can have GI involvement
Advanced HIV
- Coinfection is common, with 90% CMV seropositivity in HIV-positive men
- Advanced HIV disease carries increased risk of severe CMV disease
- CMV retinitis is the most common form in AIDS
- Classic white fluffy retinal infiltrate with areas of hemorrhage
- Can cause polyradiculopathy and myopathy, with back pain and subacute flaccid paralysis
- CSF will be abnormal
- Can cause esophagitis
- Can cause colitis, with diarrhea, often fever, and occasionally hematochezia
- On sigmoidoscopy, has plaque-like pseudomembranes, serpiginous ulcers, and erosions
- Can occasionally present with a mass lesion that can cause partial obstruction
- Rarely, pancreatitis, cholecystitis,
Complications
- Pneumonitis
- Can cause an interstitial pneumonia
- Severe in SCT patients, mild in mononucleosis patients
- Hepatitis
- Usually mild
- Can include granulomatous hepatitis in the context of mononucleosis
- Guillain-Barré syndrome
- Sensory and motor palsies in the extremities and cranial nerves
- Resolves over months
- Meningoencephalitis
- Headache, photophobia, lethargy, and pyramidal tract dysfunction
- May have concurrent motor and sensory palsies
- Myocarditis
- Rare
- Thrombocytopenia and hemolytic anemia
- Common in congenital infection, and occasionally seen in adults
- Rashes
- Can cause maculopapular or rubelliform rashes following treatment with amipicillin
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
- IgG useful for prior exposure (suggesting latent infection)
- IgG avidity can confirm recent infection
- IgM >300 U/mL can help diagnose acute 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
- 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
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.