Bacterial Vaccines Flashcards

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1
Q

Most common type of vac

A

Inactivated

Bacterins- where the whole culture or bacterial cells are enriched with pathogenic determinants or pars of a bacterial cell

Contain sufficient antigen to stimulate antibody production- generally requires 2 doses in order to generate sufficient response for protection

Formaldehyde inactivates/denatures pro (may modify surface antigens)
Preserved with phenol
Mixed with adjuvant

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2
Q

Antigens preserved in inactivated vac

A
Fimbrae
Capsules
Outer membrane pros
Cell wall lipopolysaccharides
Iron binding proteins and heat shock proteins
Prototoxins and toxins/toxoids
Other secreted antigens
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3
Q

Use of inactivated vaccines

A
Im
2 or more injections 
IgM and IgG
Poor mucosal and cellular immunity
Poor duration of immunity
Passive immunity for offspring
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4
Q

Toxoids

A

Stimulate the formation of toxin neutralizing antibodies
Usually contain adjuvants

Good for clostridial bc they rely on toxins for infection

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5
Q

Adjuvants

A

Inactivated vac contain to enhance the immune response

Induce inflammation at the site of vaccination, may cause local irritation at inj site

AlOH, Aluminum phosphate, mineral oil/liquid paraffin

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6
Q

Component vaccines

A

one or more protective antigens - toxoid secreted antigen and/or structural proteins

Use is becoming more common
Require a moderate amount of antigen, so cost decreases and decreased side effects

Administer with adjuvant

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7
Q

Live

A

Not many at the present, many have been withdrawn. Control of attenuation is difficult, and may revery to virulence in vivo. Give via natural route

Live microorganisms that have lost the ability to cause disease/non -pathogenic forms of infecting organism. Allows them to retain many/all surface antigens. Replicate in host, but dont cause disease

Stimulate CMI and antibody both locally and systemically- colonize and replicate on the surface of appropriate mucosa

Immunity long lasting, but generally less than that of a natural infection

Canine bordatella, Cattle bacillus anthracis (no capsule, but still has toxin), Salmonella enteritidis for poultry (oral), and fungal for ring worm in cattle

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8
Q

Passive immunity

A

Provided by the dam

Requires first administration and boost, given before parturition

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9
Q

Hyperimmune antisera

A

Commercially available preparations of antisera produced by immunizing horses/cattle

Sera contain the appropriate antibodies or antitoxins- provide passive protection when unimmunised and exposed

May produce hypersensitivity in recipient of sera

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10
Q

Subunit vac

A

Critical epitope(s) destroyed by inactivation
Poorly immunogenic
May still be toxic if insufficiently treated

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11
Q

Target genes for attenuating bac

A

Genes coding for virulence factors
Regulatory genes
Metabolic pathway genes
Stress-response genes

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12
Q

Rational attenuation of bacterial pathogens

A

Clone target gene
Inactivated gene (deleted portion of gene)
Introduce mutated gene into bacteria
Homologous recombination replaces wild type with mutates
Check genotype and phenotype of mutant bacteria
Check attenuation and immunogenicity

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13
Q

Pre chorismate (aro) pathway

A

Required for synthesis of aromatic compounds in bacteria, fungi, and plants

Precursors- phosphoenol pyruvate + erythrose-4-PO4
Chorismate, branch point for the biosynthesis of aromatic amino acids, PABA (not produced by vert, must obtain from diet but bac cant use exogenous folate), DHBA, vitamins, and modified nucleosides (tRNA)

Mutation in one or more aro gene is highly attenuation

Potentially virulent in immunocompromised individuals

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14
Q

Salmonella aro mutants

A

Mutation in one or more aro genes are highly attenuated, and under go limited replication in vivo

S. typhi aro mutants are safe and immunogenic in humans, as S.typhimurium aro mutants are in many animals

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15
Q

Oral vac of calves with live recombinant salmonella vac

A

S. typhinimurium aroA and aroD, give orally at 7 days, 3 weeks later they were challenged and all vac were fully protected

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16
Q

Strangles vac

A

Genetically modified S. equi aro mutant vac. Admin inside of upper lip

Higher risk get 2 vac 4 weeks apart every 3 months (over attenuated), for med risk 2 vac 4 weeks apart every 6 months

17
Q

Live salmonella for oral delivery

A

Stimulate all arms of immune system, reside in antigen presenting cells, oral immunization

18
Q

Genetically inactivated toxins

A

Conformation and critical epitopes preserved
Improved immunogenicity
Safe- no chance of incomplete inactivation or reversion
dont need adjuvants

19
Q

Shiga like toxin

A

causes edema disease in pigs

Inhibits pro synth in eukaryotic cells

Vacs based on this- traditionally, inactivate with formaldehyde and becomes inactive in vitro but vac pigs had reduced growth wt compared to controls
Molecular change to AA in active site of A subunit (so you have a genetically altered no toxic toxin) and none of the inoculated pigs experienced weight gain

20
Q

Recombinant Pasteurella multocida toxin vac

A

Frame deletion- and give sow non toxic molecule before farrowing- challenged piglets had decreased snout deformity, increased weight gain, and recovered from P. multocida

21
Q

Cholera toxin + E. coli

A

Most potent soluble oral immunogens, mucosal adjvants, can overcome oral tolerance

Can add toxins to vac and get mucosal vac

22
Q

Naked DNA vac

A

Injection of naked DNA using plasmids encoding genes with functional eukaryotic promoters, results in expression of the gene in striated muscle at site of injection

Potential safety issues- autoimmune diseases

Isolate gene from protective antigen of bac