An organism's ability to establish an infection. The proportion of individuals exposed to a pathogen through horizontal transmission who will become infected
Pathogenicity
The inherent capacity of an organism to cause disease. A qualitative trait determined by its genetic makeup
Virulence
A quantitative trait that refers to the extent of damage, or pathology, caused by the organism
Plasmids
Self-replicating genetic elements located in the bacteria's cytoplasm that contain a limited number of genes. The location where the genetic information needed to produce virulence factors is found
Bacterial Evasion Mechanisms
Avoiding antibodies by altering antigens (antigenic variation)
Blocking phagocytosis by inhibiting binding of neutrophils and macrophages
Blocking/inactivating complement activation
Methods to detect causative agent of bacterial infection
Culture or growth of the causative agent
Microscopy
Detection of bacterial antigens in the clinical sample
Molecular detection of bacterial DNA or RNA
Serology, or detection of antibodies produced in response to the infection
Serology disadvantage
Delay between start of infection and production of antibodies
Serology for Group A Streptococci
1. Culture or rapid screening methods are useful for acute pharyngitis diagnosis
2. Serological diagnosis must be used to identify rheumatic fever and glomerulonephritis
Streptococcal antigen detection
Rapid assays like lateral flow immunochromatographic assays (LFA) are used to detect Group A streptococcal antigens directly from throat swabs
Streptozyme Kit Testing
Sheep RBCs are coated with streptococcal antigens so antibodies to any of them can be detected by hemagglutination
Anti-DNase Testing
1. Classic Neutralization method - Anti-DNase B antibodies neutralize reagent DNase B, preventing DNA depolymerization
2. Nephelometry method - Immune complexes between antibodies and DNase B reagent generate light scatter
Anti-Streptolysin O (ASO)
Presence of antibodies indicates recent streptococcal infection. ASO titers usually do not increase with skin infections
Traditional/Classic ASO titer tube method
Involves dilution of patient serum, addition of streptolysin O reagent, and indicator RBCs. No hemolysis indicates presence of anti-streptolysin O antibody
Helicobacter pylori is now recognized as a major cause of both gastric and duodenal ulcers
Helicobacter pylori virulence factors
Production of CagA protein, vacuolating cytotoxin (VacA)
Production of large amounts of urease to protect against stomach acid
Can detect presence of H. pylori in fecal samples, but cannot distinguish between living and dead bacteria
Urea Breath Test
Patient ingests urea labeled with radioactive or nonradioactive carbon. Measures exhaled labeled carbon dioxide to detect H. pylori infection
Serological testing for H. pylori
Measures IgG antibodies, which are the primary antibody found in chronic infections. ELISA is the method of choice
CLOtest
Detects urease activity in gastric mucosal biopsies. Turns pink in presence of urease, indicating H. pylori infection
Mycoplasma pneumoniae infections are referred to as "atypical pneumonia" because the organism lacks a cell wall and cannot be treated with penicillin
Mycoplasma pneumoniae is a leading cause of community-acquired pneumonia, often referred to as "walking pneumonia"
Mycoplasma pneumoniae infections are associated with dermatological manifestations
Yellow gel
Turns hot pink color due to increase in pH in the presence of urease
Gel
Remains yellow if urease is not present
Majority of the tests will turn positive within 20 minutes
Test should be held and reexamined after 24 hours to allow time for detection of a low-level infection
Test
Easy to use and ideal for rapid diagnosis of H pylori infections
Pneumonia caused by M pneumoniae
Originally referred to as "atypical pneumonia" because the infection could not be treated with penicillin
M pneumoniae lacks the cell wall to which penicillin is directed against
M pneumoniae
A leading cause of community acquired pneumonia
Infection caused by M pneumoniae
Often referred to as "walking pneumonia" because individuals often do not stay home from work or school and still participate in their daily activities
Dermatological manifestations associated with M pneumoniae infection
Stevens–Johnson syndrome, or erythema multiforme major
Raynaud syndrome
M. pneumoniae is associated with a cold agglutinin that is directed against altered I antigens (I blood group system) in the RBCs
Laboratory means of detecting Mycoplasma infection
Culturing of the organism
Detection of M pneumoniae-specific antibodies in serum
Detection of M pneumoniae-specific antigens or nucleotide sequences directly in patient specimens
Culture
Considered as the gold standard for diagnosis
Growth of M pneumoniae in culture
Produces a "mulberry" colony with a typical "fried egg" appearance
Serology
Detection of M pneumoniae-specific IgM immunoglobulin is the most useful diagnostic test
Enzyme-linked immunoassays
The most widely used methods for antibodies and can detect IgM or IgG directed against M pneumonia
Cold agglutinin titer test is no longer recommended because the development of cold agglutinins occurs in other circumstances, including some viral infections and collagen vascular diseases