Mumps virus: Difference between revisions
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== Background == |
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* Presents with a prodrome followed by parotitis |
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*Presents with a prodrome followed by parotitis |
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== Microbiology == |
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===Microbiology=== |
|||
* Enveloped single-stranded RNA virus in the genus ''Rubulavirus'' and family Paramyxovirus |
|||
* Only one serotype but 13 genotypes (A to M) |
|||
* Genome encodes eight proteins: hemagglutinin-neuraminidase (HN), fusion (F), nucleocapsid (NP), phosphoprotein (P), matrix (M), hydrophobic (SH) and L protein |
|||
** P contains V and I proteins |
|||
* Irregular spherical shape with nucleocapsid enclosed by a three-layered envelope |
|||
** Surface studded with glycoproteins: HN and F, which are the most important for immunity |
|||
** Middle layer is lipid bilayer from the host cell |
|||
** Inner layer in membrane protein |
|||
*Enveloped single-stranded RNA virus in the genus ''Rubulavirus'' and family Paramyxovirus |
|||
== Epidemiology == |
|||
*Only one serotype but 13 genotypes (A to M) |
|||
*Genome encodes eight proteins: hemagglutinin-neuraminidase (HN), fusion (F), nucleocapsid (NP), phosphoprotein (P), matrix (M), hydrophobic (SH) and L protein |
|||
**P contains V and I proteins |
|||
*Irregular spherical shape with nucleocapsid enclosed by a three-layered envelope |
|||
**Surface studded with glycoproteins: HN and F, which are the most important for immunity |
|||
**Middle layer is lipid bilayer from the host cell |
|||
**Inner layer in membrane protein |
|||
===Epidemiology=== |
|||
* Worldwide distribution |
|||
* Epidemics every 2 to 5 years in unimmunized settings, with a peak between January and May |
|||
* Spread primarily by schoolchildren |
|||
* Outbreaks have happened amongst immunized people, suggesting that a third dose of MMR may be needed to confer ongoing immunity |
|||
* Before vaccination, it was the leading cause of viral encephalitis and a common cause of viral meningitis |
|||
*Worldwide distribution |
|||
== Pathophysiology == |
|||
*Epidemics every 2 to 5 years in unimmunized settings, with a peak between January and May |
|||
*Spread primarily by schoolchildren |
|||
*Outbreaks have happened amongst immunized people, suggesting that a third dose of MMR may be needed to confer ongoing immunity |
|||
*Before vaccination, it was the leading cause of viral encephalitis and a common cause of viral meningitis |
|||
===Pathophysiology=== |
|||
* Acquired through virus (contact, droplet, fomites) entering nose or mouth, with tropism for endo/exocrine glands |
|||
** Salivary, pancreatis, testicular |
|||
* Less infectious that measles or varicella |
|||
* Peak contagion is just before parotitis |
|||
* Immune response begins with antibodies against NP protein (S antigen), and may be detectable at presentation, but decline quickly over months |
|||
* Antibodies against HN protein (V antigen) follow, peaking at 2 to 4 weeks and persist for years |
|||
** IgM antibodies fall within 2 to 6 months |
|||
* Neutralizing antibodies to HN and F are detectable during convalescence |
|||
*Acquired through virus (contact, droplet, fomites) entering nose or mouth, with tropism for endo/exocrine glands |
|||
== Differential Diagnosis == |
|||
**Salivary, pancreatis, testicular |
|||
*Less infectious that measles or varicella |
|||
*Peak contagion is just before parotitis |
|||
*Immune response begins with antibodies against NP protein (S antigen), and may be detectable at presentation, but decline quickly over months |
|||
*Antibodies against HN protein (V antigen) follow, peaking at 2 to 4 weeks and persist for years |
|||
**IgM antibodies fall within 2 to 6 months |
|||
*Neutralizing antibodies to HN and F are detectable during convalescence |
|||
==Clinical Manifestations== |
|||
* Infectious parotitis |
|||
** Parainfluenza 3 virus, coxsackieviruses, and influenza A |
|||
** HIV infection (bilateral, parotid) |
|||
** Staph. aureus or GNBs |
|||
* Drugs (bilateral, mild) |
|||
* Metabolic disorders, including diabetes, malnutrition, cirrhosis, and CKD (bilateral, mild) |
|||
* Tumours, cysts, sialolithiasis, and stricture (unilateral) |
|||
* Eosinophilic parotitis, often as a drug reaction |
|||
*Incubation period of [[Usual incubation period::16 to 18 days]] (range [[Incubation period range::2 to 4 weeks]]) |
|||
== Clinical Presentation == |
|||
*One-day prodrome of low-grade fever, anorexia, malaise, and headache |
|||
*Earache and parotitis soon follow |
|||
**Parotitis progresses over 2 to 3 days, with severe pain |
|||
**The other parotid usually follows, but it can be unilateral |
|||
**Stensen's duct is edematous and erythematous |
|||
**Pain exacerbated by citrus |
|||
**Can involve other salivary glands in 10% |
|||
*Temperature can be as high as 40º C |
|||
*Pain, fever, tenderness resolve, with parotid returning to normal within 1 week |
|||
*Can lead to sialectasia resulting in recurrent or chronic sialadenitis |
|||
===Mumps epididymo-orchitis=== |
|||
* Incubation period of 16 to 18 days (range 2 to 4 weeks) |
|||
* One-day prodrome of low-grade fever, anorexia, malaise, and headache |
|||
* Earache and parotitis soon follow |
|||
** Parotitis progresses over 2 to 3 days, with severe pain |
|||
** The other parotid usually follows, but it can be unilateral |
|||
** Stensen's duct is edematous and erythematous |
|||
** Pain exacerbated by citrus |
|||
** Can involve other salivary glands in 10% |
|||
* Temperature can be as high as 40º C |
|||
* Pain, fever, tenderness resolve, with parotid returning to normal within 1 week |
|||
* Can lead to sialectasia resulting in recurrent or chronic sialadenitis |
|||
*The most common extrasalivary gland manifestation, occuring in 20-30% of postpubertal men (bilateral in 15%) |
|||
=== Mumps epididymo-orchitis === |
|||
*Occurs in first 1-2 weeks after parotitis |
|||
*Fevers up to 41º C, chills, headache, vomiting, and testicular pain |
|||
*Swollen warm testicles with scrotal erythema |
|||
*Fever resolves within 5 days, followed by slower resolution of the orchitis |
|||
**Tenderness can sometimes last longer than 2 weeks |
|||
*Longterm testicular atrophy in 50% |
|||
**If unilateral, no concerns |
|||
**If bilateral, sterility is rare, and impotence is not a sequela |
|||
===Mumps oopheritis=== |
|||
* The most common extrasalivary gland manifestation, occuring in 20-30% of postpubertal men (bilateral in 15%) |
|||
* Occurs in first 1-2 weeks after parotitis |
|||
* Fevers up to 41º C, chills, headache, vomiting, and testicular pain |
|||
* Swollen warm testicles with scrotal erythema |
|||
* Fever resolves within 5 days, followed by slower resolution of the orchitis |
|||
** Tenderness can sometimes last longer than 2 weeks |
|||
* Longterm testicular atrophy in 50% |
|||
** If unilateral, no concerns |
|||
** If bilateral, sterility is rare, and impotence is not a sequela |
|||
*In 5% of cases in postpubertal women |
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=== Mumps oopheritis === |
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*May cause impaired fertility |
|||
===Mumps meningitis=== |
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* In 5% of cases in postpubertal women |
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* May cause impaired fertility |
|||
*Fever, headache, vomiting, and nuchal rigidity, with an aseptic CSF (lymphocyte-predominant more often than neutrophil-predominant) |
|||
=== Mumps meningitis === |
|||
**Amylase may be elevated |
|||
*Onset usually after parotitis, but can be 1 week before or up to 2 weeks after |
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*Can also occur without parotitis |
|||
*Lasts 3 to 10 days, with complete recovery |
|||
===Mumps encephalitis=== |
|||
* Fever, headache, vomiting, and nuchal rigidity, with an aseptic CSF (lymphocyte-predominant more often than neutrophil-predominant) |
|||
** Amylase may be elevated |
|||
* Onset usually after parotitis, but can be 1 week before or up to 2 weeks after |
|||
* Can also occur without parotitis |
|||
* Lasts 3 to 10 days, with complete recovery |
|||
*Non-focal encephalitis, high fever, altered LOC, seizures, paresis, aphasia, and involuntary movements, with an aseptic CSF |
|||
=== Mumps encephalitis === |
|||
**Fever can be up to 41º C |
|||
*Can occur concurrent with or up to 10 days after onset of parotitis |
|||
*Early-onset is from virus; late-onset is a postinfectious autoimmune demyelinating disease; but there is likely a continuum between these two extremes |
|||
*Gradually resolves over 1 to 2 weeks |
|||
*Can cause sequelae, including psychomotor retardation, seizures, and death |
|||
===Other complications=== |
|||
* Non-focal encephalitis, high fever, altered LOC, seizures, paresis, aphasia, and involuntary movements, with an aseptic CSF |
|||
** Fever can be up to 41º C |
|||
* Can occur concurrent with or up to 10 days after onset of parotitis |
|||
* Early-onset is from virus; late-onset is a postinfectious autoimmune demyelinating disease; but there is likely a continuum between these two extremes |
|||
* Gradually resolves over 1 to 2 weeks |
|||
* Can cause sequelae, including psychomotor retardation, seizures, and death |
|||
*Cerebellar ataxia, facial palsy, transverse myelitis, Guillain-Barré syndrome, and poliomyelitis-lik syndrome |
|||
=== Other complications === |
|||
*Migratory polyarthritis, usually starting 10-14 days after parotitis and lasting up to 5 weeks |
|||
*Pancreatitis |
|||
*ECG changes with ST depression and T-wave changes, 1st degree heart block |
|||
**Myocarditis is rare |
|||
===Pregnancy=== |
|||
* Cerebellar ataxia, facial palsy, transverse myelitis, Guillain-Barré syndrome, and poliomyelitis-lik syndrome |
|||
* Migratory polyarthritis, usually starting 10-14 days after parotitis and lasting up to 5 weeks |
|||
* Pancreatitis |
|||
* ECG changes with ST depression and T-wave changes, 1st degree heart block |
|||
** Myocarditis is rare |
|||
*Pregnant women who are infected have increased risk of spontaneous abortion in the first trimester, as well as low birth weight |
|||
=== Pregnancy === |
|||
*Not clearly related to any significant birth defects |
|||
== Differential Diagnosis == |
|||
*Infectious [[parotitis]] |
|||
* Pregnant women who are infected have increased risk of spontaneous abortion in the first trimester, as well as low birth weight |
|||
**[[Parainfluenza]] 3 virus, [[coxsackievirus]], and [[Influenza virus|influenza A]] |
|||
* Not clearly related to any significant birth defects |
|||
**[[HIV]] infection (bilateral, parotid) |
|||
**[[Staphylococcus aureus]] or [[Gram-negative bacilli]] |
|||
*Drugs (bilateral, mild) |
|||
*Metabolic disorders, including [[diabetes]], [[malnutrition]], [[cirrhosis]], and [[CKD]] (bilateral, mild) |
|||
*Tumours, cysts, [[sialolithiasis]], and stricture (unilateral) |
|||
*[[Eosinophilic parotitis]], often as a drug reaction |
|||
== |
==Diagnosis== |
||
* |
*Traditionally a clinical diagnosis |
||
* |
*CBC and diff are normal or mild leukopenia; amylase may be up from parotitis, or lipase from pancreatitis |
||
* |
*Can be diagnosed with serology or PCR |
||
* |
*ELISA for IgM, or a fourfold rise from acute to convalescent ELISA or HAI serologies, are diagnostic |
||
** |
**HAI may be affected by parainfluenza |
||
* |
*PCR or culture detectable in saliva, though relatively low level after 5 days; also found in CSF |
||
** |
**Can be detected in urine up to 2 weeks after onset |
||
== |
==Management== |
||
* |
*Symptomatic |
||
* |
*Immune globulin not helpful |
||
* |
*Post-exposure immunization may not be helpful, though in an outbreak situation, may consider giving an MMR booster |
||
* |
*Isolation for 5 days after onset of parotitis to reduce spread |
||
* |
*Reportable disease, public health may do outbreak investigation and consider booster MMR in high-risk populations |
||
== |
==Prevention== |
||
* |
*Live attenuated vaccine in the MMR is given at 12-15 months and again at 4-6 years |
||
* |
*Vaccine 65-70% effective, so need high vaccination rate to achieve herd immunity |
||
* |
*Titres positive for at least 10 years, but immunity wanes |
||
* |
*Contraindicated in pregnant women |
||
[[Category:Paramyxoviridae]] |
[[Category:Paramyxoviridae]] |
Latest revision as of 14:05, 5 August 2020
Background
- Presents with a prodrome followed by parotitis
Microbiology
- Enveloped single-stranded RNA virus in the genus Rubulavirus and family Paramyxovirus
- Only one serotype but 13 genotypes (A to M)
- Genome encodes eight proteins: hemagglutinin-neuraminidase (HN), fusion (F), nucleocapsid (NP), phosphoprotein (P), matrix (M), hydrophobic (SH) and L protein
- P contains V and I proteins
- Irregular spherical shape with nucleocapsid enclosed by a three-layered envelope
- Surface studded with glycoproteins: HN and F, which are the most important for immunity
- Middle layer is lipid bilayer from the host cell
- Inner layer in membrane protein
Epidemiology
- Worldwide distribution
- Epidemics every 2 to 5 years in unimmunized settings, with a peak between January and May
- Spread primarily by schoolchildren
- Outbreaks have happened amongst immunized people, suggesting that a third dose of MMR may be needed to confer ongoing immunity
- Before vaccination, it was the leading cause of viral encephalitis and a common cause of viral meningitis
Pathophysiology
- Acquired through virus (contact, droplet, fomites) entering nose or mouth, with tropism for endo/exocrine glands
- Salivary, pancreatis, testicular
- Less infectious that measles or varicella
- Peak contagion is just before parotitis
- Immune response begins with antibodies against NP protein (S antigen), and may be detectable at presentation, but decline quickly over months
- Antibodies against HN protein (V antigen) follow, peaking at 2 to 4 weeks and persist for years
- IgM antibodies fall within 2 to 6 months
- Neutralizing antibodies to HN and F are detectable during convalescence
Clinical Manifestations
- Incubation period of 16 to 18 days (range 2 to 4 weeks)
- One-day prodrome of low-grade fever, anorexia, malaise, and headache
- Earache and parotitis soon follow
- Parotitis progresses over 2 to 3 days, with severe pain
- The other parotid usually follows, but it can be unilateral
- Stensen's duct is edematous and erythematous
- Pain exacerbated by citrus
- Can involve other salivary glands in 10%
- Temperature can be as high as 40º C
- Pain, fever, tenderness resolve, with parotid returning to normal within 1 week
- Can lead to sialectasia resulting in recurrent or chronic sialadenitis
Mumps epididymo-orchitis
- The most common extrasalivary gland manifestation, occuring in 20-30% of postpubertal men (bilateral in 15%)
- Occurs in first 1-2 weeks after parotitis
- Fevers up to 41º C, chills, headache, vomiting, and testicular pain
- Swollen warm testicles with scrotal erythema
- Fever resolves within 5 days, followed by slower resolution of the orchitis
- Tenderness can sometimes last longer than 2 weeks
- Longterm testicular atrophy in 50%
- If unilateral, no concerns
- If bilateral, sterility is rare, and impotence is not a sequela
Mumps oopheritis
- In 5% of cases in postpubertal women
- May cause impaired fertility
Mumps meningitis
- Fever, headache, vomiting, and nuchal rigidity, with an aseptic CSF (lymphocyte-predominant more often than neutrophil-predominant)
- Amylase may be elevated
- Onset usually after parotitis, but can be 1 week before or up to 2 weeks after
- Can also occur without parotitis
- Lasts 3 to 10 days, with complete recovery
Mumps encephalitis
- Non-focal encephalitis, high fever, altered LOC, seizures, paresis, aphasia, and involuntary movements, with an aseptic CSF
- Fever can be up to 41º C
- Can occur concurrent with or up to 10 days after onset of parotitis
- Early-onset is from virus; late-onset is a postinfectious autoimmune demyelinating disease; but there is likely a continuum between these two extremes
- Gradually resolves over 1 to 2 weeks
- Can cause sequelae, including psychomotor retardation, seizures, and death
Other complications
- Cerebellar ataxia, facial palsy, transverse myelitis, Guillain-Barré syndrome, and poliomyelitis-lik syndrome
- Migratory polyarthritis, usually starting 10-14 days after parotitis and lasting up to 5 weeks
- Pancreatitis
- ECG changes with ST depression and T-wave changes, 1st degree heart block
- Myocarditis is rare
Pregnancy
- Pregnant women who are infected have increased risk of spontaneous abortion in the first trimester, as well as low birth weight
- Not clearly related to any significant birth defects
Differential Diagnosis
- Infectious parotitis
- Parainfluenza 3 virus, coxsackievirus, and influenza A
- HIV infection (bilateral, parotid)
- Staphylococcus aureus or Gram-negative bacilli
- Drugs (bilateral, mild)
- Metabolic disorders, including diabetes, malnutrition, cirrhosis, and CKD (bilateral, mild)
- Tumours, cysts, sialolithiasis, and stricture (unilateral)
- Eosinophilic parotitis, often as a drug reaction
Diagnosis
- Traditionally a clinical diagnosis
- CBC and diff are normal or mild leukopenia; amylase may be up from parotitis, or lipase from pancreatitis
- Can be diagnosed with serology or PCR
- ELISA for IgM, or a fourfold rise from acute to convalescent ELISA or HAI serologies, are diagnostic
- HAI may be affected by parainfluenza
- PCR or culture detectable in saliva, though relatively low level after 5 days; also found in CSF
- Can be detected in urine up to 2 weeks after onset
Management
- Symptomatic
- Immune globulin not helpful
- Post-exposure immunization may not be helpful, though in an outbreak situation, may consider giving an MMR booster
- Isolation for 5 days after onset of parotitis to reduce spread
- Reportable disease, public health may do outbreak investigation and consider booster MMR in high-risk populations
Prevention
- Live attenuated vaccine in the MMR is given at 12-15 months and again at 4-6 years
- Vaccine 65-70% effective, so need high vaccination rate to achieve herd immunity
- Titres positive for at least 10 years, but immunity wanes
- Contraindicated in pregnant women