BackViral Diseases of the Respiratory System: Influenza, SARS-CoV2, and Related Viruses
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Viral Diseases of the Respiratory System
Influenza Virus
The influenza virus is a major cause of acute respiratory illness worldwide. It is highly infectious and can lead to seasonal epidemics and occasional pandemics. Understanding its structure, transmission, and clinical features is essential for microbiology students.
Etiology:
Influenza virus is a single-stranded, negative-sense RNA virus (ssRNA-).
Genome consists of 8 separate RNA segments.
Capsid shape is variable.
Virus is enveloped.
Virulence Factors:
Hemagglutinin (H): Enables virus to attach to host cell; 18 variants exist in nature; H1, H2, H3 most common in human infection.
Neuraminidase (N): Essential for virus replication and release; 11 variants exist; N1, N2 most common in human infection.
Types of Influenza Viruses
Influenza viruses are divided into three main groups: A, B, and C.
Influenza Type | Hosts |
|---|---|
Type A | Humans, birds, pigs, horses |
Type B | Humans only |
Type C | Humans only |
Type A viruses are responsible for most epidemics and all pandemics, and can infect multiple animal species. Type B and Type C infect humans only.
Clinical Features and Symptoms
Acute onset of illness
Highly infectious; rapid person-to-person spread
Symptoms: sudden fever, headache, muscle aches, severe weakness, cough, sore throat, difficulty breathing
Influenza typically causes more severe symptoms than the common cold (caused by coronavirus or rhinovirus)
Comparison: Flu vs. Cold
Symptom | Cold | Flu |
|---|---|---|
Headache | Rare | Achy |
Fever | Rare | High (102-104°F) |
Muscle aches | Slight | Usual, often severe |
Onset | Slow | Sudden |
Incubation Period
Estimates vary: 1 to 4 days
Most commonly 2-3 days
Contagiousness may linger beyond symptom onset
Transmission
Spread via respiratory droplets (coughing, sneezing, talking)
Contact with contaminated surfaces followed by touching face
Groups at Increased Risk
Infants/toddlers (6-59 months), adults ≥50 years
Chronic pulmonary, cardiovascular, renal, hepatic, neurologic, hematologic, or metabolic disorders
Immunosuppressed individuals
Pregnant women
Children/adolescents on aspirin/salicylate medications (risk for Reye syndrome)
Residents of nursing homes/long-term care
Antigenic Variation
Influenza A viruses undergo frequent changes in their surface antigens, leading to new strains and potential pandemics.
Antigenic Drift: Minor changes due to natural mutations; results in new variants each year.
Antigenic Shift: Major changes due to reassortment of RNA segments between viruses; can lead to pandemics.
Antigenic Drift vs. Shift
Type | Description | Impact |
|---|---|---|
Drift | Point mutations in genes encoding surface proteins | Seasonal epidemics |
Shift | Reassortment of RNA segments between different viruses | Pandemics |
Epidemiology
Major antigenic changes result in little/no immunity in the population
Rapid and widespread transmission
Historical examples: 1957 Asian flu (shift), 2003 Panama/Fujian strain (drift)
Flu Pandemics
Global epidemics of newly emerged influenza A subtypes
Three major pandemics in the last century; worst killed 20-40 million
2009 H1N1 pandemic (swine flu)
Prevention
Vaccines:
Trivalent: protects against three strains (H1N1, H3N2, B)
Quadrivalent: protects against four strains (H1N1, H3N2, B, additional B)
Types: Inactivated (IIV), Recombinant (RIV), Attenuated (LAIV)
Guidelines: all persons ≥6 months without contraindications
Diagnosis
Rapid antigen tests
Lab assays (PCR, viral culture)
Further analysis for strain identification
Treatment
Antivirals (oseltamivir, zanamivir, peramivir, baloxavir)
Chemoprophylaxis within 48 hours of exposure
Neuraminidase inhibitors: block release of new virus
Endonuclease inhibitors: block viral RNA transcription
Antiviral Agent | Activity | Use | Recommended For | Not Recommended | Adverse Events |
|---|---|---|---|---|---|
Oseltamivir | Influenza A & B | Chemoprophylaxis, Treatment | 3 months and older | NA | Nausea, vomiting |
Zanamivir | Influenza A & B | Chemoprophylaxis, Treatment | 7 years and older | People with respiratory disease (asthma, COPD) | Bronchospasm |
Peramivir | Influenza A & B | Treatment | 2 years and older | NA | Diarrhea |
Baloxavir | Influenza A & B | Treatment | 12 years and older | Pregnant, breastfeeding, severe illness | Diarrhea |
SARS-CoV2 (COVID-19)
Etiology
SARS-CoV2 is the causative agent of COVID-19, a severe acute respiratory syndrome. It is a single-stranded, positive-sense RNA virus with a nucleocapsid and an envelope. The virus uses its spike protein to attach to ACE2 receptors on human cells.
Likely originated in bats; other animals (e.g., pangolins) considered possible reservoirs.
mRNA vaccines are used for prevention.
Structure and Replication
Envelope contains spike (S) protein, membrane (M) protein, and envelope (E) protein.
Spike protein is a glycoprotein responsible for binding to ACE2 receptor.
Replication cycle involves entry via ACE2, translation of viral proteins, assembly, and release.
Clinical Features
Wide range of symptoms: fever, chills, cough, shortness of breath, fatigue, muscle aches, headache, loss of taste/smell, sore throat, congestion, nausea, diarrhea.
Symptoms may appear 2-14 days after exposure.
Diagnosis
Antigen tests (lab or home)
Nucleic acid amplification tests (PCR)
Epidemiology and Prevention
Transmission: airborne aerosols
Prevention: vaccination, distancing, mask use, rapid detection and isolation
Treatment
Antiviral medications: ritonavir-boosted nirmatrelvir, remdesivir, molnupiravir, interferons, ivermectin
Early treatment reduces risk of hospitalization and death
Antigenic Variation
Mutations in spike protein can lead to new variants with altered transmissibility and immune escape
Monkeypox (Pox Virus)
Etiology and Transmission
Monkeypox is a zoonotic disease caused by a DNA virus in the Poxviridae family.
Transmission occurs via contact with infected animals (e.g., rodents, primates) or humans.
Clinical Features
Fever, rash, lymphadenopathy, and pustular lesions
Incubation period: 7-14 days
Treatment and Prevention
Antivirals: tecovirimat, cidofovir
Vaccines: smallpox vaccine provides some protection
Sexually Transmitted Viral Diseases: Human Papillomavirus (HPV)
Etiology
HPV is a DNA virus with many types, some of which are associated with cancer (e.g., HPV-16, HPV-18).
Virulence Factors
Oncogenes E6 and E7 inactivate tumor suppressor genes (p53, Rb), leading to uncontrolled cell growth.
Clinical Features
Most infections are asymptomatic.
Symptoms: warts (condyloma acuminata), cervical cell changes (detected by PAP smear), potential progression to cervical cancer.
Diagnosis, Treatment, and Prevention
Diagnosis: PAP smear, HPV DNA testing
Treatment: no cure for infection; warts may be removed
Prevention: HPV vaccine (Gardasil) protects against high-risk types
Arboviruses
Overview
Arboviruses are transmitted by arthropod vectors (mosquitoes, ticks).
Examples: Yellow fever virus, Equine encephalitis virus, West Nile virus, Dengue virus
Humans are dead-end hosts; most infections are mild, but severe cases can cause encephalitis or hemorrhagic fever.
West Nile Virus
Single-stranded RNA virus with icosahedral capsid
Enveloped; infects birds, horses, humans
80% asymptomatic; severe neurological disease possible
No vaccine or specific treatment for humans
Dengue Virus
Single-stranded RNA virus; icosahedral capsid; enveloped
Transmitted by Aedes mosquitoes
Can cause dengue fever or dengue hemorrhagic fever
Symptoms: high fever, severe pain, rash, bleeding
Latent and Persistent Viral Infections
Definitions
Latent infection: Virus remains dormant in host cells for long periods; can reactivate (e.g., herpes simplex, varicella-zoster)
Persistent infection: Disease process occurs over a long period, often fatal (e.g., subacute sclerosing panencephalitis, prion diseases)
Graphical Representation
Acute infection: rapid onset and resolution
Latent infection: periods of dormancy and reactivation
Persistent infection: slow progression over months/years
Additional info: These notes expand on the original slides by providing definitions, tables, and context for each virus and disease discussed, suitable for exam preparation in a college microbiology course.