Prokaryotic cell structure, essential and non-essential organelles
Prokaryotic cell structure
* Based on morphology, we can classify prokaryotes as cocci (chain–> Streptococcus, cluster
–> Staphylococcus), rods (chain –> Streptobacillus), coccobacilli, vibrios (curved rods),
spirilla (rigid coils), and spirochetes (flexible coils)
Essential organelles
1) Nucleoid
- DNA is circular, haploid (allows for more rapid growth and quicker adaptation to the
environment than diploid)
- Plasmids are extra-circular DNA that can confer antibiotic resistance and encode for
virulence factors
2) Cytoplasm
- 80% water, 20% salts and proteins
- No organelles (mitochondria, Golgi, etc.)
3) Cytoplasmic membrane
- Bilayer of phospholipid
- Flexible and impermeable to water
- Site of biosynthesis of DNA, cell wall polymers, and membrane lipids
- Selective permeability and transport of solutes into cell
4) Cell wall
- Determines the shape of bacteria
- Strength prevents osmotic rupture
- Plays an essential role in cell division and is unique to bacteria
- Gram(+) cell walls are composed of peptidoglycans, lipoteichoic acids, and wall
teichoic acids
- Gram(–) cell walls are composed of an outer bilayered phospholipid membrane
(containing lipopolysaccharides/lipooligosaccharide and proteins) and peptidoglycan
5) Polyribosomes
- Numerous and distributed throughout the cytoplasm, 15-20 nm in diameter
- Composed of a small 30S subunit and a large 50S subunit that together make up the
70S structure
Non-essential organelles
1) Flagellae
- Provide motility and movement to bacteria (e.g. P. mirabilis, V. cholerae)
- Arrangement is the basis for classification (monotrichous – 1 flagellum;
lophotrichous – tuft at one end; amphitrichous – both ends; peritrichous; all around
bacteria)
2) Pili
- Short protein appendages that are smaller than flagellae
- Adhere bacteria (e.g. E. coli) to surfaces
- F-pilus is used in conjugation for the exchange of genetic information
3) Capsule
- Adheres the bacteria (e.g. S. mutans) to a surface and prevents phagocytosis
4) Inclusions
- Discrete structures that are generally intracytoplasmic
- Function as metabolic reserves, cell positioners, or as metabolic organelles
5) Spores
- Resistant structures that protects the bacteria (e.g. B. anthracis, C. difficile) from heat,
irradiation, and cold
Antibiotics inhibiting bacterial cell wall synthesis. Mechanism of action, spectrum of effect,
resistance mechanisms
β-lactams
1) Natural penicillins
- Penicillin G has a narrow spectrum and is susceptible to inactivation by β-lactamase
- Penicillin V is more acid stable
- Mainly used for the treatment of meningitis caused by susceptible organism
2) β-lactamase resistant β-lactams
- Methicillin, nafcillin, and oxacillin
- Have a narrow spectrum and are mainly used against β-lactamase producing
Staphylococci
3) Aminopenicillins
- Ampicillin and amoxicillin
- Broader spectrum against Gram(–), but are susceptible to β-lactamase producing
bacteria (e.g. Klebsiella)
- Reach therapeutic concentration in the CSF
4) Ureidopenicillins
- Piperacillin is the main one
- Effective against P. aeruginosa
- Reach therapeutic concentration in the CSF
5) Carbapenems
- Meropenem, imipenem, doripenem, and ertapenem
- Can resist many β-lactamases
- Good efficacy against facultative anaerobe Gram(–) (such as P. aeruginosa) and ESBL
(extended spectrum β-lactamase) producing Gram(–)
- Ineffective against MRSA, E. faecium and others
- Carbapenemases belong to 2 major groups:
a) Metallo-β-lactamases (MBLs) – e.g. P. aeruginosa
b) Serine-β-lactamases – e.g. K. pneumoniae
6) Cephalosporins
- Related to penicillins structurally and functionally, but are more resistant to
β-lactamases
- Five generations:
7) Monobactams
- Narrow spectrum, only effective against Enterobacteriaceae and Pseudomonas spp.
- Resistant to β-lactamases
β-lactamase inhibitors (large molecules, do not penetrate into the CSF)
Glycopeptides
* Vancomycin, teicoplanine, dalbavancin, and telavancin
* Bind firmly to and inhibit transglycosylase, inhibiting cell wall synthesis
* Have no effect against Gram(–)
* Narrow spectrum against MRSA, penicillin-resistant S. pneumoniae, C. jekeium, and
C. difficile
* Some species of S. aureus, Enterococci, and C. difficile show acquired resistance
Other agents
1) Daptomycin
- Novel cyclic lipopeptide that is similar to vancomycin
- Active against vancomycin resistant strains of Enterococci, and S. aureus
2) Fosfomycin
- Analog of phosphoenolpyruvate
- Active against both Gram(+) and Gram(–)
3) Cycloserine
- Used against M. tuberculosis
4) Bacitracin
- Effective against Gram(+)
- Topical application due to nephrotoxicity, often used for traumatic abrasions
Antibiotics inhibiting bacterial protein synthesis. Mechanism of action, spectrum of effect,
resistance mechanisms
30S subunit inhibitors
1) Aminoglycosides
2) Tetracyclines
3) Glycylcyclines
- Tigecyclin
- Same mode of action as tetracyclines (bacteriostatic)
- Broad spectrum (except for Pseudomonas and Proteus spp.)
- Can be used against Acinetobacter and C. difficile
50S subunit inhibitors
1) Chloramphenicol
- Old and toxic agent that is now used for the treatment of meningitis in case of
penicillin-allergic patients
- Side effects include dose-dependent bone marrow suppression and doseindependent aplastic anemia
2) Macrolides
- Erythromycin, clarithromycin, spiramycine, azithromycin (preferred), and
fidaxomicin (inhibits C. difficile sporulation)
- Inhibit translocation of polypeptides to the 50S subunit (bacteriostatic)
- Narrow spectrum, mainly Gram (+) but also Campylobacter spp. and causative agents
of atypical pneumonia
- Alternative agents for the treatment of tonsillitis caused by S. pyogenes
3) Lincosamides
- Lincomycin and clindamycin
- Same mechanism of action as macrolides (bacteriostatic)
- Narrow spectrum, mainly Gram(+) facultative anaerobes (Staphylococci,
Streptococci) but also Gram(+) and Gram(-) obligate anaerobes
- Used in the treatment of osteomyelitis
- Can easily cause pseudomembranous colitis
4) Ketolides
- Telitromycin
- Similar to macrolides
5) Streptogramins
- Quinopristin+dalfopristin=Synercid
- Same mechanism of action as macrolides
- Effective against vancomycin-resistant E. faecium, MSSA, and MRSA
6) Oxazolidinons
- Linezolid and tedizolid
- Effective against MRSA, VISA, VRSA, and VRE
- Not effective for the treatment of bacteremia
Antibiotics inhibiting bacterial folate, DNA, or RNA synthesis. Mechanism of action,
spectrum of effect, resistance mechanisms
Fluoroquinolones
Sulfonamides and trimethoprim
Rifamycines
* Rifampicin, rifapentin, rifabutin
* Inhibit RNA synthesis by inhibiting RNA polymerase (bactericidal)
* Good penetration into tissues, peritoneal and pleural cavity, bile, bones, and abscesses
* Reach therapeutic concentration in the CSF
* Prophylactic use against N. meningitidis and H. influenzae
* Active against mycobacteria
* Cause the urine, saliva, and sweat to become orange
Antituberculotic agents. Mechanism of action
Tuberculosis infection is treated with a multiple-drug therapy for 6-9 months consisting of
isoniazid (INH), rifampin, pyrazinamide, and ethambutol.
It is important to treat tuberculosis
with several drugs due to the long treatment period, which can yield strains of M. tuberculosis
that are resistant against one of the drugs but not the others.
Treatment of strains of M. tuberculosis resistant to multiple drugs (MDR strains) involves the use
of four or five drugs, including ciprofloxacin, amikacin, ethionamide, and cycloserine
Isoniazid (INH)
Rifampin
* Inhibits RNA synthesis by inhibiting RNA polymerase (bactericidal)
* Good penetration into tissues, peritoneal and pleural cavity, bile, bones, and abscesses
* Reaches therapeutic concentration in the CSF
* Cause the urine, saliva, and sweat to become orange
Pyrazinamide
* Bactericidal
* Mechanism of action is uncertain, but it is thought to involve inhibition of a fatty acid
synthase that prevents the synthesis of mycolic acid
* Particularly effective against semidormant organisms in the lesion, which are not affected
by INH or rifampin
Ethambutol
* Bacteriostatic
* Acts by inhibiting the synthesis of arabinogalactan, which functions as a link between the
mycolic acids and the peptidoglycan of the organism
Sterilization
Sterilisation is the killing of all microorganisms in a material or on the surface of an object.
Typically the last thing to die when one attempts sterilization is the highly heat- (and chemical-,
etc.) resistant endospores.
Heat sterilization and decontamination
2) Autoclave
- 121°C for 20-30 min at 1 bar overpressure
3) Pasteurization
Electromagnetic irradiation
* At 254 nm wavelength (ultraviolet) electromagnetic irradiation damages DNA but can exert
its effect only on surfaces and in the air, which makes it unsuitable for sterilization
* “Hard X-rays“ (less than ~0.01 nm wavelength) and gamma rays are reliable methods of
sterilization
Filtration
* The preferred method of sterilizing certain solutions (e.g. those with heat-sensitive
components)
* The most commonly used filter is composed of nitrocellulose and has a pore size of 0.22 μm
Gas sterilization
* Ethylene oxide gas is used extensively in hospitals for the sterilization of heat-sensitive
materials such as surgical instruments and plastics
* It is classified as a mutagen and a carcinogen
*Incomplete method of sterilization
Disinfectants
Disinfection means reducing the number of viable microorganisms present in a sample.
A disinfectant is a chemical or physical agent that is applied to inanimate objects to kill microbes.
Not all disinfectants are capable of sterilizing, and therefore spores and some bacteria, viruses,
and fungi may survive. Typically, an antiseptic is a chemical disinfectant agent that is applied on
skin or mucous membranes to kill microbes.
Disruption of cell membranes
1) Alcohol
- Ethanol is widely used to clean the skin before immunization or venipuncture
- Requires the presence of water for maximal activity (i.e. it is far more effective at 70%
than 100%)
2) Detergents
- Composed of a long-chain, lipid-soluble, hydrophobic portion and a polar hydrophilic
group
- Quaternary ammonium compounds are cationic detergents widely used for skin
antisepsis
3) Phenols
- Chlorhexidine is a chlorinated phenol that is widely used as a hand disinfectant prior
to surgery and in the cleaning of wounds
- Hexaclorophene is used in germicidal soaps, but may be neurotoxic
Modification of proteins
1) Chlorine
- Used as a disinfectant to purify the water supply and to treat swimming pools, as well
as being the active component of bleach
2) Iodine
- The most effective skin antiseptic used in medical practice and should be used prior
to obtaining a blood culture and installing intravenous catheters because
contamination with skin flora such as S. epidermidis can be a problem
3) Heavy metals
- Mercury and silver have the greatest antibacterial activity of the heavy metals and
are the most widely used in medicine
4) Hydrogen peroxide
- Used as an antiseptic to clean wounds and to disinfect contact lenses
- Its effectiveness is limited by the organism‘s ability to produce catalase, an enzyme
that degrades H2O
5) Formaldehyde and glutaraldehyde
- Formaldehyde is an alkylating agent available as a 37% solution in water (formalin)
- Glutaraldehyde has two reactive aldehyde groups and is 10 times more effective than
formaldehyde and is less toxic
6) Ethylene oxide
- Gas that is used extensively in hospitals for the sterilization of heat-sensitive
materials such as surgical instruments and plastics
- It is classified as a mutagen and a carcinogen
7) Acids and alkalis
- Although most bacteria are susceptible, it is important to note that M. tuberculosis
and other mycobacteria are relatively resistant
- Weak acids, such as benzoic, propionic, and citric acids, are frequently used as food
preservatives because they are bacteriostatic
Modification of nucleic acids
* A variety of stains not only stain microorganisms, but also inhibit their growth
- Crystal violet is used as a skin antiseptic
- Malachite green is used for the culturing of M. tuberculosis on Löwenstein-Jensen‘s
medium, because it inhibits the growth of unwanted organisms in the sputum during
the 6-week incubation period
Bacterial virulence factors
Bacterial virulence factors can be toxic (exotoxins, endotoxins) or non-toxic (adherence factors,
invasive factors, other factors)
Exotoxins
* Excreted by living cells
* Produced by both Gram(+) and Gram(–)
* Heat labile, highly antigenic, and highly toxic polypeptides that have specific effects and can
generally be converted to toxoids with formalin
* Unique exotoxins include erythrogen toxin of S. pyogenes(cannot be converted to toxoid by
formalin), heat stable enterotoxin of E. coli, botulinus toxin of C. botulinum (resistant to
digestive enzymes), and heat-resistant enterotoxin of S. aureus
* We can differentiate between two types of exotoxins:
) Toxic enzymes (cytolysins)
- Phospholipase: destroy membranes, e.g. lecithinase (alpha toxin)
(C. perfringens)
- Pore forming cytolysins: destroy membranes, e.g. streptolysin O (S. pyogenes)
and alpha toxin (S. aureus)
- Detergents: destroy membranes, e.g. delta toxin (S. aureus)
2) Exotoxins with 2 subunits (A and B)
- Inhibition of protein synthesis: inhibit EF-2 by ADP-ribosylation, e.g.
diphtheria toxin (C. diphtheriae) and “A“ toxin (P. aeruginosa)
Endotoxins
Extracellular enzymes
* Coagulase (S. aureus), fibrinolysin (streptokinase) (S. pyogenes), urease (K. pneumoniae,
Proteus spp., H. pylori), lipase (S. aureus), protease (P. aeruginosa, Proteus spp.), IgA
protease (H. influenzae, S. pneumoniae, N. meningitidis, N. gonorrhoeae)
Surface components
1) Antiphagocytic factors
* Capsule (S. pneumoniae, K. pneumoniae, H. influenzae, N. meningitidis, B. anthracis),
LPS (O specific chain), cord factor (mycolic acid) (M. tuberculosis), M protein
(S. pyogenes), protein A (S. aureus), soluble chemotaxis inhibiting factor (B. pertussis)
2) Adhesion factors
* Pili (N. gonorrhoeae), adhesive fimbriae (E. coli, V. cholerae, S. dysenteriae,
B. pertussis), afimbrial adhesins (chlamydia, mycoplasma, S. pyogenes)
Invasion factors
* Invasins (shigella, E. coli, yersinia, L. monocytogenes), flagellae, enzymes (lecithinase,
hyaluronidase etc.), S fimbriae (bind to sialic acid receptors –> sepsis, meningitis caused by
E. coli)
Siderophores
* Aerobactin (E. coli) and enterobactin (Enterobacteriaceae)
* Pick up iron from transferrin, lactoferrin
Transmission of infections, the portals of entry of pathogenic microbes
An understanding of the mode of transmission of bacteria and other infectious agents is
extremely important from a public health perspective, because interrupting the chain of
transmission is an excellent way to prevent infectious diseases.
Fomites are inanimate objects, such as towels, that serve as a source of microorganisms that can
cause infectious diseases.
Human to human transmission
A. Direct contact
B. No direct contact
- e.g. dysentery (S. dysenteriae, EIEC, etc.)
- Fecal-oral (e.g. excreted in human feces and then ingested in food or water)
C. Transplacental
- e.g. congenital syphilis (T. pallidum)
- Bacteria cross the placenta and infect the fetus
D. Bloodborne
- e.g. syphilis (T. pallidum)
- Transfused blood or intravenous drug use can transmit bacteria and viruses;
screening of blood for transfusions has greatly reduced this risk
Nonhuman to human transmission
A. Soil source
- e.g. tetanus (C. tetani)
- Spores in soil enter wound in skin
B. Water source
- e.g. Legionnaire‘s disease (L. pneumophila)
- Bacteria in water aerosol are inhaled into lungs
C. Animal source
a) Directly:
- e.g. cat-scratch fever (B. henselae)
- Bacteria enter into the blood stream through a cat scratch
b) Via insect vector:
- e.g. Lyme disease (B. burgdorferi)
- Bacteria enter into the blood stream through a tick bite
c) Via animal excreta:
- e.g. hemolytic-uremic syndrome (EHEC O157:H7)
- Bacteria in cattle feces are ingested in undercooked hamburger
D. Fomite source
- e.g. staphylococcal skin infection
- Bacteria on an object (e.g. a towel) are transferred onto the skin
Portals of entry of some common pathogens
* There are four important portals of entry: respiratory tract, gastrointestinal tract, genital
tract, and skin
1) Respiratory tract
- S. pneumoniae –> pneumonia
- N. meningitidis, H. influenzae –> meningitis
- Influenza virus –> influenza
2) Gastrointestinal tract
- S. dysenteriae –> dysentery
- Norovirus –> gastroenteritis
- Trichinella spiralis –> trichinosis
3) Genital tract
- N. gonorrhoeae –> gonorrhea
- C. trachomatis –> urethritis
- Human papillomavirus –> genital warts
4) Skin
- C. tetani –> tetanus
- Rabies virus –> rabies
- Plasmodium vivax –> malaria
Non-specific defenses against pathogenic microbes
Innate (non-specific) defenses protect against microorganisms in general. They can be classified
into three major categories: (1) physical barriers, such as intact skin and mucous membranes;
(2) phagocytic cells, such as neutrophils, macrophages, and natural killer cells; and (3) proteins,
such as complement, lysozyme, and interferon.
Skin and mucous membranes
Inflammatory response and phagocytosis
* Neutrophils predominate in the acute pyogenic infections, whereas macrophages are
more prevalent in the chronic or granulomatous infections
Specific immune responses against pathogenic microbes
Adaptive (specific) immunity protects against a particular microorganism and results either from
exposure to the organism (active immunity) or from receipt of preformed antibody made in
another host (passive immunity)
Passive adaptive immunity
Active adaptive immunity
* Protection based on exposure to the organism in the form of overt disease, subclinical
infection, or a vaccine
* Protective abilities have a delay of a few days to a few weeks
* Mediated by both antibodies (immunoglobulins) and T cells:
1) Antibodies
- Neutralization of toxins
- Lysis of bacteria in the presence of complement
- Opsonization of bacteria to facilitate phagocytosis
- Interference with adherence of bacteria and viruses to cell surfaces
2) T cells
- Cytotoxic destruction of virus-infected cells and bacteria
- Activation of macrophages
- Delayed hypersensitivity
- Stimulation of B cells to produce antibodies
Hypersensitivity reactions in infectious diseases, serum sickness
Hypersensitivity is the term used when an immune response results in exaggerated or
inappropriate reactions harmful to the host. Hypersensitivity reactions can be subdivided into
four main types.
Types I, II, and III are antibody-mediated, whereas type IV is cell-mediated.
Type I: Immediate (anaphylactic) hypersensitivity
Type II: Cytotoxic hypersensitivity
Type III: Immune complex hypersensitivity
1) Arthus reaction is the name given to the inflammation caused by the deposition of
immune complexes at a localized site
2) Serum sickness is a systemic inflammatory response to the presence of immune
complexes deposited in many areas of the body
Type IV: Delayed (cell-mediated) hypersensitivity
Active and passive immunization, principles, side effects. Types of vaccines
Active immunization
* Occurs either naturally during infection or via vaccination with vaccines prepared from
microbes or their products
Passive immunization
1) Tetanus antitoxin is used in the treatment of tetanus and in its prevention
2) Botulinum antitoxin is used in the treatment of botulism
3) Diphtheria antitoxin is used in the treatment of diphtheria
1) Rabies immune globulin (RIG) is used in prevention of rabies in people who may have
been exposed to the virus
2) Hepatitis B immune globulin (HBIG) is used in the prevention of hepatitis B in people
who may have been exposed to the virus
3) Varicella-zoster immune globulin (VZIG) is used in the prevention of disseminated
zoster in people who may have been exposed to the virus and who are
immunocompromised
4) Vaccinia immune globulins (VIG) can be used to treat some of the complications of
smallpox vaccination
5) Hepatitis A or measles immune globulins can be used for the prevention of disease in
people who may have been exposed to these viruses
Types of vaccines
A. Live, attenuated vaccines
* The vaccine against tuberculosis contains a live, attenuated strain of M. bovis called
BCG (Bacillus Calmette-Guérin)
B. Killed/inactivated vaccines
C. Toxoid vaccines
* Corynebacterium diphtheriae vaccine contains the diphtheria toxoid
- Indicated for every child
* Clostridium tetani vaccine contains tetanus toxoid
- Given to everyone both early in life and later as boosters
* Bordetella pertussis vaccine contains pertussis toxoid, but includes other proteins as
well
D. Subunit vaccines
a) Capsular polysaccharide vaccines
Diagnostic immune reactions in microbiology
The basis of diagnostic immune reactions (a.k.a. serological reactions) is the great specificity
between antigens and their antibodies.
Serological tests are of great importance when diagnosing
infectious diseases in several situations:
One problem with this approach is that it takes time for antibodies to form (e.g. 7-10 days in the
primary response).
For this reason, acute and convalescent serum samples are taken, and a
fourfold or greater rise in antibody titer is required to make a diagnosis.
Types of diagnostic tests
1) Agglutination
* Antigen is particulate (e.g. bacteria and RBCs) or is an inert particle (latex beads)
coated with an antigen
2) Precipitation (precipitin)
3) Enzyme-linked immunosorbent assay (ELISA)
* Based on covalently linking an enzyme to a known antigen or antibody, reacting the
enzyme-linked material with the patient‘s specimen, and then assaying for enzyme
activity by adding the substrate of the enzyme
4) Immunofluorescence assay (IFA)
5) Complement fixation
(2) An indicator system, consisting of “sensitized“ RBCs (i.e. RBCs plus anti-RBC
antibody), is added
6) Hemagglutination tests
* Many viruses clump RBCs from one species or another (active hemagglutination) and
this can be inhibited by antibody specifically directed against the virus
* RBCs can also absorb many antigens and, when mixed with matching antibodies, will
clump (passive hemagglutination)
7) Western blot (immunoblot)
8) Fluorescence-activated cell sorting (flow cytometry)
Entameba
Infection by E. histolytica is found worldwide but occurs most frequently in tropical
countries
Naegleria, Acanthamoeba
Acanthamoeba castellanii and Naegleria fowleri are free-living amoebas that cause
meningoencephalitis
Giardia lamblia, Trichomonas
Trypanosoma, Leishmania
Trypanosoma brucei
Leishmania braziliensis and L. donovani
Plasmodia, Babesia
Plasmodium malariae, P. vivax, P. ovale,
and P. falciparum
The life cycle in humans begins with the introduction of sporozoites into the blood
from the saliva of the biting mosquito
Babesia spp.
Toxoplasma gondii
When contained, the organisms persist as cysts within tissues with no inflammation
present, and the individual remains well unless immunosuppression allows activation of
organisms in the cysts
Cryptosporidium, Cyclospora, Cycloisospora
Cryptosporidium spp.
Microsporida are a group of protozoa characterized by obligate intracellular replication
and spore formation
Enterobius vermicularis, Trichuris trichiura
Intestinal nematodes
Enterobius vermicularis
Trichuris trichiura
Ascaris lumbricoides, Toxocara
Ascaris lumbricoides
Toxocara (tissue nematode)
Strongyloides stercolaris, Ancylostoma duodenale, Necator americanus
Strongyloides stercoralis
Most patients are asymptomatic and most infections occur in Southeast Asia
Ancylostoma duodenale and Necator americanus