BackInfectious Diseases Manifesting in the Respiratory System: Microbiology Study Notes
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Chapter 22: Infectious Diseases Manifesting in the Respiratory System
22.1 The Respiratory Tract, Its Defenses, and Normal Biota
The respiratory tract is a major portal of entry for pathogens and is divided into upper and lower sections, each with specialized defenses and resident microbiota. Understanding these components is essential for recognizing how infections develop and are prevented.
Upper respiratory tract: Includes the mouth, nose, nasal cavity, sinuses, throat (pharynx), epiglottis, and larynx.
Lower respiratory tract: Comprises the trachea, bronchi, bronchioles, and alveoli within the lungs.
Anatomical Defenses
Nasal hairs: Trap larger particles and pathogens.
Ciliated epithelium (ciliary escalator): Moves mucus and trapped particles upward toward the throat for removal.
Mucus: Traps microbes and debris.
Coughing and sneezing: Expel irritants and pathogens.
Swallowing: Moves trapped microbes to the stomach for destruction.
Normal Biota of the Respiratory Tract
The respiratory tract harbors a diverse microbiome, with certain bacteria considered part of the normal flora but capable of causing disease under specific conditions.
Streptococcus pyogenes
Haemophilus influenzae
Streptococcus pneumoniae
Neisseria meningitidis
Staphylococcus aureus
Research indicates that the composition of the lung microbiome can be altered in patients with certain lung disorders.
Defenses | Normal Biota |
|---|---|
Nasal hair, ciliary escalator, mucus, involuntary responses (coughing, sneezing), secretory IgA, alveolar macrophages, cytokines, complement | Large number of genera. Most abundant: Streptococcus, Prevotella, Sphingomonas, Pseudomonas, Acinetobacter, Fusobacterium, Megasphaera, Veillonella, Staphylococcus. Note: Streptococcus pyogenes, Streptococcus pneumoniae, Haemophilus influenzae, Neisseria meningitidis, and Staphylococcus aureus often present as "normal biota". |
22.2 Infectious Diseases Manifesting in the Upper Respiratory Tract
Several infectious diseases primarily affect the upper respiratory tract, including the common cold, sinusitis, otitis media, and pharyngitis.
The Common Cold
Causative organisms: Approximately 200 viruses (rhinoviruses, adenoviruses, coronaviruses)
Transmission: Indirect contact, droplet contact
Virulence factors: Attachment proteins; symptoms mainly due to host immune response
Prevention: Hygiene practices
Treatment: Symptomatic relief only
Epidemiology: Highest incidence among preschool and elementary schoolchildren; adults average 2–4 colds/year
Causative Organism(s) | Most Common Modes of Transmission | Virulence Factors | Culture/Diagnosis | Prevention | Treatment | Epidemiological Features |
|---|---|---|---|---|---|---|
~200 viruses (rhinoviruses, adenoviruses, coronaviruses) | Indirect contact, droplet contact | Attachment proteins; host response | Not necessary | Hygiene | Symptomatic | Preschool/elementary: 3–8 colds/year; adults: 2–4/year |
Sinusitis
Causative organisms: Viruses, various bacteria (often mixed), various fungi
Transmission: Direct/indirect contact (viruses), endogenous (bacteria), trauma/opportunistic (fungi)
Distinctive features: Viral and bacterial much more common than fungal; suspect fungi in immunocompromised patients
Causative Organism(s) | Most Common Modes of Transmission | Culture/Diagnosis | Prevention | Treatment | Distinctive Features | Epidemiological Features |
|---|---|---|---|---|---|---|
Viruses | Direct/indirect contact | Not usually performed; diagnosis based on clinical presentation | Hygiene | None | Viral/bacterial more common than fungal | Commonly follows cold |
Bacteria | Endogenous (opportunism) | Clinical presentation; imaging if needed | N/A | Antibiotics for severe cases | Viral/bacterial more common than fungal | 1/7 adults in US; 12–30 million diagnoses/year |
Fungi | Trauma/opportunistic | Same as above | N/A | Antifungals if needed | Suspect in immunocompromised | Rare in healthy; more common in India, North Africa, Middle East |
Otitis Media (Middle Ear Infection)
Causative organisms: Streptococcus pneumoniae, Haemophilus influenzae, Moraxella catarrhalis, Streptococcus pyogenes, Staphylococcus aureus, Candida auris
Transmission: Endogenous (may follow upper respiratory tract infection)
Virulence factors: Capsule, hemolysin (bacteria); biofilm formation (Candida auris)
Prevention: Pneumococcal conjugate vaccine (PCV13)
Treatment: Wait for resolution or antibiotics if needed; consult CDC for Candida auris
Epidemiology: 30% of cases in US children; Candida auris increasing globally
Causative Organism(s) | Most Common Modes of Transmission | Virulence Factors | Culture/Diagnosis | Prevention | Treatment | Epidemiological Features |
|---|---|---|---|---|---|---|
Streptococcus pneumoniae | Endogenous | Capsule, hemolysin | Clinical symptoms, failure to resolve in 72 hr | PCV13 vaccine | Wait/antibiotics | 30% of US cases |
Candida auris | Not known | Biofilm formation | MALDI-TOF/PCR | Consult CDC | Consult CDC | First reported 2009; increasing |
Pharyngitis
Definition: Inflammation of the throat causing pain and swelling
Causative organisms: Viruses, Streptococcus pyogenes, Fusobacterium necrophorum
Symptoms: White packets on throat, difficulty swallowing, foul breath; viral is mild, bacterial is more severe with fever, headache, nausea
Causative Organism(s) | Most Common Modes of Transmission | Virulence Factors | Culture/Diagnosis | Prevention | Treatment | Distinctive Features | Epidemiological Features |
|---|---|---|---|---|---|---|---|
Streptococcus pyogenes | Droplet/direct contact | LTA, M protein, hyaluronic acid capsule, SLS/SLO, superantigens | Beta-hemolytic on blood agar, rapid tests | Hygiene | Penicillin, cephalexin | More severe than viral | 20–30% of pharyngitis in children |
Fusobacterium necrophorum | Endogenous | Invasiveness, endotoxin | Cultured anaerobically, CT for abscess | Hygiene | Penicillin | Can lead to Lemierre’s syndrome | 15% of teens/adults |
Viruses | All forms of contact | N/A | Rule out S. pyogenes/F. necrophorum | Hygiene | Symptomatic | Hoarseness accompanies viral | 40–60% of all pharyngitis |
Streptococcus pyogenes and Its Complications
Characteristics: Gram-positive coccus, grows in chains, facultative anaerobe, produces capsules and slime layer
Complications if untreated: Scarlet fever, rheumatic fever, glomerulonephritis
Virulence Factors of Streptococcus pyogenes
Surface antigens mimic host proteins
M protein resists phagocytosis and aids adhesion
Surface antigens protect from lysozyme
Streptolysin O and S: injure cells/tissues
Erythrogenic toxin (lysogenic strains): key for scarlet fever
Some toxins act as superantigens
Fusobacterium necrophorum
Gram-negative bacterium
Causes 15% of acute pharyngitis in >15 years group
Can cause Lemierre’s syndrome (peritonsillar abscess, life-threatening)
22.3 Infectious Diseases Manifesting in Both the Upper and Lower Respiratory Tracts
Some pathogens can affect both upper and lower respiratory tracts, leading to more severe or systemic disease.
Whooping Cough (Pertussis)
Causative agent: Bordetella pertussis (small, gram-negative rod, strictly aerobic, fastidious)
Phases:
Catarrhal: cold symptoms
Paroxysmal: uncontrollable coughing with "whoop" sound, possible complications (hemorrhage, vomiting)
Convalescent: recovery, ciliated epithelia damaged
Virulence factors: Filamentous hemagglutinin (attachment), pertussis toxin (mucus production), tracheal cytotoxin (ciliated cell destruction), endotoxin (cytokine production)
Vaccine: Acellular (DTaP); booster needed after age 11
Causative Organism(s) | Most Common Modes of Transmission | Virulence Factors | Culture/Diagnosis | Prevention | Treatment | Epidemiological Features |
|---|---|---|---|---|---|---|
Bordetella pertussis | Droplet contact | FHA, pertussis toxin, tracheal cytotoxin, endotoxin | PCR/growth on selective media; symptoms | Acellular vaccine (DTaP), azithromycin for contacts | Azithromycin; drug resistance emerging | US: 19,000 cases (2017); global: millions annually |
Respiratory Syncytial Virus (RSV) Disease
Causative agent: Respiratory syncytial virus (RSV)
Transmission: Droplet and indirect contact
Virulence factor: Syncytia formation (fusion of host cells)
Prevention: Passive antibody (monoclonal) in high-risk children
Treatment: Ribavirin plus passive antibody in severe cases
Epidemiology:
Causative Organism(s) | Common Modes of Transmission | Virulence Factors | Culture/Diagnosis | Prevention | Treatment | Epidemiological Features |
|---|---|---|---|---|---|---|
RSV | Droplet, indirect contact | Syncytia formation | RT-PCR | Passive antibody (high-risk) | Ribavirin, passive antibody | US: |
22.4 Infectious Diseases Manifesting in the Lower Respiratory Tract
Lower respiratory tract infections are often more severe and can be life-threatening, especially in vulnerable populations.
Influenza
Causative agents: Influenza viruses A, B, or C (family Orthomyxoviridae)
Reasons for study: High mortality potential, frequent misdiagnosis, rapid viral evolution
Symptoms: Headache, chills, dry cough, body aches, fever, sore throat, extreme fatigue, risk of secondary infections (e.g., pneumonia)
High-risk groups: Very young, elderly, pregnant, or those with chronic diseases
Structure and Virulence Factors
Hemagglutinin (H): Agglutinates red blood cells, binds to host cell receptors
Neuraminidase (N): Breaks down mucus, assists in viral budding/release, host cell fusion
Mutation of Glycoproteins
Antigenic drift: Gradual amino acid changes in antigens; reduces host memory cell recognition
Antigenic shift: Exchange of RNA segments between different influenza viruses; leads to pandemics
Prevention and Epidemiology
Annual vaccination (inactivated, trivalent or quadrivalent)
Vaccine does not cause flu; research ongoing for universal vaccines
Seasonal flu deaths: US (17,000–52,000/year); global (250,000–500,000/year)
Causative Organism(s) | Most Common Modes of Transmission | Virulence Factors | Culture/Diagnosis | Prevention | Treatment | Epidemiological Features |
|---|---|---|---|---|---|---|
Influenza A, B, C viruses | Droplet, direct/indirect contact | Glycoprotein spikes, antigenic drift/shift | RT-PCR (gold standard) | Annual vaccination | Oseltamivir (Tamiflu), baloxavir (Xofluza) | US: 17,000–52,000 deaths/year; global: 250,000–500,000 |
Key Terms and Concepts
Ciliary escalator: Mechanism by which cilia move mucus and trapped particles out of the respiratory tract.
Superantigen: Toxin that causes excessive activation of the immune system.
Antigenic drift: Minor genetic changes in viral antigens.
Antigenic shift: Major genetic reassortment leading to new viral subtypes.
Additional info: These notes are based on textbook slides and are suitable for exam preparation in a college-level microbiology course. For more details on lower respiratory tract diseases (e.g., tuberculosis, pneumonia), refer to subsequent sections of the chapter.