- Cause of smallpox (i.e. variola)
Background
Microbiology
- Variola virus is a dsDNA virus in Orthopoxvirus genus
- Virus replicats in the cell cytoplasm rather than nucleus
Pathophysiology
- Virus enters through a respiratory route, a mucosal surface, or a break in the skin
- Replicates locally then spreads through local lymphatics, causing a primary viremia
- Then spreads to the reticuloendothelial system, where replication results in secondary viremia
- The virus then ultimately seeds skin, causing a characteristic “pock” rash
Epidemiology
- Human are only known hosts (no animal reservoir)
- Droplet transmission, can be transmitted on fomites (survives 6 to 24 hours on surfaces or cloth)
- There have been outbreaks among hospital laundry staff
- Virus in scabs can survive longer
- Period of communicability is about 3 weeks, from just before first lesions to disappearance of all scabs
- Highest during first week of rash
Eradication
- Contagious during prodrome, but most highly infectious for the first 7 to 10 days following rash and continues until all the lesions have crusted over
- Eradicated worldwide with the last case in Somalia in 1977
Differential Diagnosis
- Varicella zoster virus
- Enterovirus
- Monkeypox: generally more lymphadenopathy
- Other causes of a vesicular rash
Risk Classification Algorithm
- Applied to patients with an acute generalized vesicular or pustular rash (AGVPR)
- Source: Hutchins SS, et al. CID. 2008:46(Suppl 3):S195-S203
High risk
- A febrile prodrome (a temperature 38.3C occurring 1–4 days before rash accompanied by prostration, headache, backache, chills, vomiting, or severe abdominal pain);
- Characteristic lesions, described as deep-seated, firm, hard, well-circumscribed vesicles or pustules; and
- Vesicles or pustules all at the same stage of development on any 1 body part (e.g., face, leg, or arm).
Moderate risk
- A febrile prodrome, an AGVPR, and at least 1 other major criterion; or
- Afebrile prodrome, an AGVPR, and ≥4 minor criteria
Low risk
- An AGVPR with a febrile prodrome and <4 minor clinical criteria; or
- Only an AGVPR
Minor clinical criteria
Use to distinguish ordinary-type variola from varicella in the prevaccine era:
- Centrifugal rash distribution
- First lesions on the oral mucosa, face, or forearms
- A toxic or moribund appearance
- A slow rash evolution from macules to papules to pustules (1–2 days for each stage)
- Lesions on palms and soles
Clinical Presentation
Variola major
- Most common clinical form, with a mortality of about 30%
- Four presentations: ordinary (most common), modified (if vaccinated), flat, and hemorrhagic
Ordinary
- Most common (90%), with 3 phases (incubation, prodrome, and pox)
- Incubation period 12-14 days (range 7-17 days)
- Prodrome lasts 2 to 4 days, with fever, headache, backache, chills, and vomiting
- Followed by rash, starting as a small red spot in the mouth or on the face (called herald spots)
- Rash spreads centrifugally from the face to arms and legs (more distal than trunk)
- Includes palms and soles
- Usually spread to entire body within about 24 hours
- Lesions initially maculopapular, followed by firm, well-defined vesicles, often with a central depression
- Vesicles develop into pustules during the second week, then they flatten and scab over by third or fourth week
- Lesions may become confluent
- Lesions progress synchronously, unlike chicken pox
- Mortality
Modified
- Modified form occurs in patients with previous immunization
- Milder illness
- Atypical rash, with fewer lesions that evolve more rapidly
- Mortalilty <10%
Flat/malignant
- Rare and severe, usually fatal (50%)
- Similarly severe prodrome
- However, rash is slower to develop, and remains soft and flat and velvety
- Like fine-grained, reddish-coloured crepe rubber
- Sometimes hemorrhages
Hemorrhagic
- Rare and severe, usually fatal (~100%)
- Pregnancy is a risk factor, but occurs in all age groups and sexes
- Shorter incubation period with severe, prostrating prodrome with high fever, headache, back pain, and abdominal pain
- Erythema follows, then petechiae and skin and mucosal hemorrhages
- Death within 5 to 6 days
Variola minor
- Lower mortality rate ~1%
- Fewer constitutional symptoms, fewer skin lesions
Bioterrorism
- Last case globally in 1977, with no routine vaccination in Canada since 1972, and in Canadian armed forces personel since 1988
- The majority of people living in the US (and likely Canada) have not been vaccinated
- Limited vaccine reserves still exist in the US; a new horsepox-derived vaccine was developed in Canada in the 2010s
- In case of an outbreak
- Healthcare workers should be vaccinated and, ideally, a single hospital designated for smallpox patients
- Patients should be in negative-pressure isolation with HEPA filter
- Standard precautions using gloves, gowns, and masks
- All laundry and waste should be placed in biohazard bags and autoclaved before being laundered or incinerated
- Rooms should be decontaminated after they are vacated
Diagnosis
- Samples should be collected by unroofing a lesion and soaking a swab
- RG-4 infection, must be processed in a CL-4 lab (i.e. the national micro lab)
- Viral swab with viral transport medium (e.g. NPS swab)
- PCR can be done for routine viruses as well as Orthopoxviridae
- Tissue
- Tzanck smear for intracellular inclusion bodies for HSV/VZV
- Direct immunofluorescence
- Electron microscopy
- Smallpox and monkeypox virions may be indistinguishable, naturally occurring monkeypox is found only in tropical rain forest areas of Africa
- Viral culture: technically the gold standard
Management
- No specific treatment; supportive care
- May try cidofovir
- Patients should be maintained in negative-pressure isolation with HEPA filters (airborne/contact)
Post-exposure prophylaxis
- Contacts may be given vaccine within 4 days of exposure to lessen the severity of symptoms
- Canada has developed a new vaccine derived from horsepox (fewer adverse events)