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Serratia marcescens
Gram-negative, rod-shaped, facultative anaerobe.
Serratia marcescens
Motile: Uses peritrichous flagella for movement.
Serratia marcescens
Produces a distinctive red pigment called prodigiosin, especially when cultured at room temperature.
Serratia marcescens
Belongs to the Enterobacteriaceae family.
Opportunistic Pathogen
Causes disease mainly in immunocompromised individuals or those with underlying medical conditions.
Respiratory tract, Urinary tract, May also infect wounds, bloodstream and eye
Common Infection Sites of Serratia marcescens
Respiratory tract
Can cause pneumonia, particularly ventilator-associated pneumonia (VAP).
Urinary tract
Frequently causes catheter-associated urinary tract infections (CAUTIs).
Red Pigment
o Gives colonies a red or pink appearance.
o Useful for identification in the laboratory.
o Pigment production may be inhibited at higher incubation temperatures (e.g., 37°C).
Nosocomial Infections:
o Often associated with outbreaks in intensive care units (ICUs) and among patients with invasive
devices (e.g., catheters, ventilators).
o Found in moist environments, including respiratory equipment, intravenous fluids, and
disinfectants.
Many strains show resistance to multiple antibiotics, including:
o Beta-lactams (via beta-lactamase production)
o Aminoglycosides
o Some fluoroquinolones
Antibiotic susceptibility testing is essential for guiding effective therapy.
Antibiotic Resistance of Serratia marcescens
Due to its ability to survive in hospital environments, resist disinfectants, and form biofilms, Serratia
marcescens is considered a significant cause of nosocomial infections; Infection control practices (e.g., hand hygiene, sterilization) are critical in preventing outbreaks.
Clinical importance of Serratia marcescens:
Yersinia pestis
Gram-negative, non-motile, bipolar-staining bacillus
Yersinia pestis
High Virulence: Responsible for the plague,
Yersinia pestis
Non-enteric pathogen
• Primary reservoir: Rodents (e.g., rats)
• Vector: Flea bites (especially Xenopsylla cheopis)
• Direct contact with infected animals or tissues
• Inhalation of infectious respiratory droplets
transmission of Yersinia pestis:
Bubonic Plague, Pneumonic Plague, Septicemic Plague
Clinical Forms of Plague:
o Bite from an infected flea
o Direct contact with infected animals or tissues
Portal of Entry of Bubonic Plague
Buboes
Painful, swollen lymph nodes
o Buboes: Painful, swollen lymph nodes
o Fever, chills, malaise
o May progress to:
▪ Bacteremia
▪ Septicemia
symptoms of Bubonic Plague:
50–60% if untreated
Mortality Rate of Bubonic Plague
o Early antibiotic therapy significantly improves outcomes
o Effective antibiotics:
▪ Streptomycin
▪ Tetracycline (TCN)
▪ Chloramphenicol
▪ Gentamicin
Treatment for Bubonic Plague:
Streptomycin, Tetracycline (TCN), Chloramphenicol, Gentamicin
antibiotics for Bubonic Plague:
o Inhalation of respiratory droplets from an infected person
o Secondary complication from untreated bubonic or septicemic plague
portal of entry of Pneumonic Plague:
o High fever
o Severe cough with bloody sputum
o Dyspnea (shortness of breath), chest pain
o Rapid deterioration and potential for respiratory failure
symptoms of pneumonic plague:
Prodigiosin
red pigment produced by Serratia marcescens
Black death
other name for Bubonic plague
Yersinia pestis
safety pin looking
hemoptisis
bloody sputum
o Person-to-person via respiratory droplets
o Highly contagious and the most fatal form if left untreated
transmission of pneumonic plague
Near 100% if untreated within 24 hours of symptom onset
mortality rate of pneumonic plague
o Immediate administration of antibiotics is critical
o Effective antibiotics:
▪ Streptomycin
▪ Gentamicin
▪ Doxycycline
▪ Chloramphenicol
treatment for pneumonic plague:
▪ Streptomycin
▪ Gentamicin
▪ Doxycycline
▪ Chloramphenicol
antibiotics for pneumonic plague:
Septicemic Plague
Occurs when the bacteria multiply in the bloodstream without forming buboes
Septicemic Plague
May arise primarily or as a complication of the other two forms
Septicemic Plague
Symptoms include disseminated intravascular coagulation (DIC), necrosis, shock
• Vector control: Flea and rodent management
• Personal protective measures in endemic areas
• Post-exposure prophylaxis for close contacts (e.g., doxycycline)
• Isolation of pneumonic plague cases
• No widely available vaccine for general use, but some exist for high-risk groups
Prevention and Control of Septicemic plague
Proteus mirabilis
Gram-negative, facultative anaerobe, rod-shaped
Proteus mirabilis
Opportunistic pathogen that causes various human infections, especially in compromised hosts
Proteus mirabilis
Highly motile due to peritrichous flagella
swarming motility
a rapid, coordinated movement across solid surfaces
Actively Motile
o Exhibits "swarming motility" — a rapid, coordinated movement across solid surfaces
o Characteristic "waves" or concentric rings on agar media
Urease-positive
Converts urea to ammonia → raises urine pH → promotes struvite stone formation
Lactose-negative
Does not ferment lactose (colonies appear colorless on MacConkey agar)
Actively Motile, Urease-positive, Lactose-negative
Key Characteristics of Proteus mirabilis:
Urinary Tract Infections (UTIs)
• Especially in patients with catheters or structural urinary tract abnormalities
• Can lead to complicated UTIs, pyelonephritis, or urolithiasis
Wound Infections
• Occur in postsurgical sites or traumatic wounds
• More common in patients with weakened immune systems or poor wound care
Diarrhea
• May be associated with gastrointestinal disturbances, though less commonly than with E. coli or Shigella
• Infections can be nosocomial in origin
Urinary Tract Infections (UTIs), Wound Infections, Diarrhea
Pathogenic Capabilities of Proteus mirabilis
Proteus mirabilis
has innate and acquired resistance to several classes of antibiotics.
o Beta-lactam resistance (via beta-lactamase production)
o Resistance to tetracyclines and fluoroquinolones in some strains
Common resistance patterns of Proteus mirabilis:
• Empiric antibiotic therapy should be guided by local resistance trends
• Common antibiotics (if susceptible):
o Ciprofloxacin
o Trimethoprim-sulfamethoxazole (TMP-SMX)
o Third-generation cephalosporins (e.g., ceftriaxone)
o Aminoglycosides (e.g., gentamicin)
treatment of Proteus mirabilis
Ciprofloxacin
Trimethoprim-sulfamethoxazole (TMP-SMX)
Third-generation cephalosporins (e.g., ceftriaxone)
Aminoglycosides (e.g., gentamicin)
antibiotics for proteus mirabilis:
• Proper catheter care and wound hygiene
• Infection control practices in healthcare settings
• Judicious use of antibiotics to prevent emergence of resistant strains
Prevention and Control of Proteus mirabilis:
Genus Erwinia
Gram-negative, facultatively anaerobic, rod-shaped bacteria
Genus Erwinia
Primarily known as plant pathogens rather than human pathogens
Erwinia species
are significant phytopathogens
Plant Pathogenicity
o Erwinia species are significant phytopathogens
o They invade plant tissues and cause a range of destructive symptoms, especially in soft plant parts.
Host Specificity
o Species often have specific plant hosts they infect.
o Spread can occur through insects, mechanical wounds, rain splash, or contaminated tools.
Erwinia amylovora, Erwinia carotovora (now as Pectobacterium), Erwinia chrysanthemi (also reclassified)
Common Species and Associated Diseases of genus erwinia:
Fire blight
disease of Erwinia amylovora
Soft rot, blackleg
disease of Erwinia carotovora (now as Pectobacterium)
Soft rot
Erwinia chrysanthemi (also reclassified)
Apple, pear, and other rosaceae
host plants of Erwinia amylovora:
Potatoes, carrots, and many vegetables
host plants of Erwinia carotovora (now as Pectobacterium)
Ornamentals and vegetables
host plants of Erwinia chrysanthemi (also reclassified)
• Wilting
• Soft Rot
• Leaf Spots
• Cankers or Oozing Lesions
Symptoms of Erwinia Infections in Plants:
Wilting
Caused by blockage or destruction of xylem vessels
Soft Rot
Tissue degradation and foul odor due to enzyme secretion (e.g., pectinases)
Leaf Spots
Necrotic lesions or discolorations
Cankers or Oozing Lesions
Bacterial ooze from stems or fruits
• Can cause major crop losses and economic damage
• Common in temperate climates, especially in humid and warm conditions
• Control and prevention involve:
o Crop rotation
o Sanitation of tools and equipment
o Use of resistant cultivars
o Application of bactericides (e.g., copper-based sprays)
agricultural importance of genus erwinia:
Genus Enterobacter
Gram-negative, facultatively anaerobic, motile (with peritrichous flagella)
Genus Enterobacter
Widely distributed in soil, water, sewage, and intestinal tracts of animals and humans
Genus Enterobacter
Includes species that are opportunistic pathogens in humans
Enterobacter species
are part of the normal flora, especially in the gastrointestinal tract, they can
cause disease under certain conditions, particularly in immunocompromised individuals or those in
healthcare settings.
Urinary Tract Infections (UTIs), Nosocomial Infections (Healthcare-associated infections)
Common Infections Caused by Enterobacter:
Urinary Tract Infections (UTIs)
Enterobacter cloacae and Enterobacter aerogenes (now reclassified as Klebsiella aerogenes) are
frequent culprits.
Urinary Tract Infections (UTIs)
Can occur in both community-acquired and hospital-acquired settings.
Urinary Tract Infections (UTIs)
Catheter-associated UTIs (CAUTIs) are common in hospitalized patients.
Enterobacter cloacae and Enterobacter aerogenes (now Klebsiella aerogenes)
are frequent culprits of UTI
Nosocomial Infections (Healthcare-associated infections)
Wound infections
Nosocomial Infections (Healthcare-associated infections)
Bloodstream infections (sepsis)
Nosocomial Infections (Healthcare-associated infections)
Lower respiratory tract infections (e.g., ventilator-associated pneumonia)
Nosocomial Infections (Healthcare-associated infections)
Common in ICU settings and among patients with invasive devices or prolonged hospital stays.
Enterobacter species (SOME)
possess inducible AmpC beta-lactamases, which confer resistance to:
o Penicillins
o First- to third-generation cephalosporins
Penicillins, First- to third-generation cephalosporins
Some Enterobacter species possess inducible AmpC beta-lactamases, which confer resistance to:
Enterobacter species
May also acquire extended-spectrum beta-lactamases (ESBLs) or carbapenemases, making them multi-drug resistant (MDR).
Carbapenems, Fluoroquinolones, Aminoglycosides
Common treatments of Enterobacter species (if susceptible) may include:
• Strict adherence to hand hygiene, disinfection protocols, and device management in hospitals can help prevent spread.
• Surveillance and antibiotic stewardship are essential to combat resistance.
Infection Control of Enterobacter species:
Family Vibrionaceae
Gram-negative, facultatively anaerobic, curved rods (comma-shaped)
Family Vibrionaceae
Motile with polar flagella
Family Vibrionaceae
Oxidase-positive (distinguishing them from Enterobacteriaceae)
Family Vibrionaceae
Halophilic or salt-tolerant – commonly found in marine or estuarine environments
Family Vibrionaceae
Includes several genera, but most notably:
• Vibrio (e.g., V. cholerae, V. parahaemolyticus, V. vulnificus)
Vibrio cholerae, Vibrio parahaemolyticus, Vibrio vulnificus
family Vibrionaceae Includes several genera, but most notably:
Vibrio cholerae
Gram-negative, comma-shaped (curved rod), facultative anaerobe
Vibrio cholerae
Motile with a single polar flagellum