Viruses of the respiratory tract
Replicate In upper airways, nasal passages, to lower lung bronchioles
> 200 kinds ranging from mild rhinitis (cough, congestion) to severe pneumonia
seasonal distribution (winter vs summer)
Common mode of transmission (direct or indirect)
Efficient and difficult to control in community
Influenza Virus
Enveloped RNA virus with segmented genome
-8 separate pieces of nucleic acid
Two kinds of spike proteins on envelope
Both proteins essential to virus, immune system targets these to give protective immunity
Three types of Influenza Virus
Influenza Type A
Influenza B
Influenza C
-rare, very mild symptoms (not a global threat with no vaccines)
Evolution of influenza type A: Antigenic Drifting Vs Shifting
Antigenic Drifting:
During virus replication, random mutations of H or N genes (minor change)
-New virus is only slightly different from parent (variant strain)
-Long period of time
Virus 1 to 1A
Antigenic Shifting:
H and N Genes mix two different flu sub types if they infect same cell
-New cell is a hybrid
-shifting common near close human-animal-avian contact (agriculture)
End result is continuous creation of new stains we have no immunity to
Influenza Type A clinical Features
-virus replicates causing host cell damg, inflammation and immune response
1-3 day incubation period before symptoms
RIsk for secondary bacterial infections
-Dmg to ciliated cells in lungs compromises lung defenses (immunocompromised, elderly)
How do you know if you really have the flu (type A) and not a cold
Flu
Lab diagnosis
Specimens using nasopharyngeal swab
Main lab test is nucleic acid amplification (PCR) for viral nucleic acid (Detects A and B)
(restricted to critical pts during flu season)
Influenza: Care and Treatment
Rest, fever-relief, good nutrition and hydration (other wise healthy people)
Anti-Virals: Oseltamivir (Tamiflu), Zanaivir (Relenza)
Older drugs (amantadine) resistant
Influenza: Infection Prevention and Control
Droplet precautions for atleast 7 days
Flu Vaccination
Influenza Vaccination and Immunity
Body produce antibodies to H protein (best also N protein)
-Produced after exposure to virus
Immunity is strain specific (one strain not different ones)
The Flu Vaccine
-Contain killed or purified H and N proteins (cant cause flu cause not alive)
-Different formulation for populations
-all contain same virus components
50-60% protection
why is protection 50-60% (or sometimes much lower)
Why do I need to get a flu shot again this year
Antibodies you developed last year are gone
New influenza strains for the new year
Who should be vaccinated
Who should strongly consider being vaccinated?
Healthy people who don’t want to get the flu( or pass it)
Ebola Virus
Enveloped RNA virus with a
“pleomorphic” morphology
No distinct shape
Africa
Broad host range (bats, monkeys, humans)
Hemorrhagic virus
Mechanism of disease (ebola)
Symptoms appear 8 days after becoming infected and rapidly worsen
-large number of virus found everywhere
Transmission via blood or bodily fluids
-Entry into bloodstream through small breaks in skin, ingestion, or contact with mucosal membranes
Replicates in various white blood cells and spreads via lymphatic system
Other cells become secondarily infected
Therefore: → Uncontrolled blood loss (esp. mucosal tissues and gut), electrolyte imbalance, rash + edema, hypotension = Multi-organ failure leading to death
Treatment/ Prevention ebola)
No anti-virals (supportive care only)
→ Maintain electrolyte balance
→ Aggressive fluid replacement
→ Maintain blood pressure and oxygenation
→ Nutritional support, pain control, etc
Two vaccines in clinical trials (none used)
History
What can history say about new viral diseases start and spread