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MICP LAB (WEEK - 5) Antimicrobial Agents in Therapydoc
MICP LAB (WEEK - 5) Antimicrobial Agents in Therapydoc
MICP LAB (WEEK - 5) Antimicrobial Agents in Therapydoc
MICP
Implement a study habit to read and comprehend the following prior to online class
proper: unit objectives; lab module and lab learning videos.
Actively search for unfamiliar medical terminologies and relate to discussions.
Establish effective teacher- student interactions through participation in the
synchronous online class discussion. through LMS discussion board or through Online
Lab Class chat box. Ask relevant questions.
Answer and submit lab unit tasks online if there is any.
For additional direction read study guide prior to class proper
1
LAB INTRODUCTION
A
NTIMICROBIAL AGENTS
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According to absorbability from site of administration:
1.locally-acting – ex: topical agents (topical ointments & eyedrops)
2.systemically - acting- affects several body systems
(ex:antibiotics administered intravenously)
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3. agents that act on the nucleic acid
They inhibit DNA replication- (quinolones, novobiocin & metronidazole)
Inhibit the synthesis of folic acid -(trimethropim, sulfonamides and sulfones)
Inhibits RNA synthesis- (rifampicin)
Antimicrobial Resistance (AMR) occurs when bacteria, viruses, fungi and parasites change over time
and no longer respond to medicines making infections harder to treat and increasing the risk of
disease spread, severe illness and death.
common bacterial infections such as urinary tract infections, sepsis, sexually transmitted infections,
and some forms of diarrhoea have high rates of resistance against antibiotics.
For example, the rate of resistance to ciprofloxacin, an antibiotic commonly used to treat urinary
tract infection
Escherichia coli for Klebsiella pneumoniaefluoroquinolone antibiotics for E. coli, (treatment of
urinary tract infections)
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Drug resistance in mycobacterium tuberculosis - new cases of rifampicin-resistant TB (RR-TB).
Majority have multi-drug resistant TB (MDR-TB), a form of tuberculosis that is resistant to the
two most powerful anti-TB drugs
- Drug resistance in viruses - an increasing concern in immunocompromised patient with drug-
resistant HIV (HIVDR). People receiving antiretroviral therapy can acquire HIVDR. Latest WHO
ARV guidelines now recommend the adoption of a new drug, dolutegravir, as the preferred
first-line treatment for adults and children.
Drug resistance in malaria parasites . Artemisinin-based combination therapies (ACTs) are the
recommended first-line treatment for uncomplicated P. falciparum malaria and are used by
most malaria endemic countries. In the WHO Eastern Mediterranean Region, P.
falciparum resistance to sulfadoxine-pyrimethamine led to artesunate-sulfadoxine-
pyrimethamine failures in some countries, necessitating a chang
Drug resistance in fungi. Drug-resistant Candida auris, one of the most common invasive fungal
infections, is already widespread with increasing resistance reported to fluconazole,
amphotericin B and voriconazole as well as emerging caspofungin resistance.
Video Link
Part 1 Microbiology - Antibiotics Mechanisms of Action https://www.youtube.com/watch?v=IVB
Video A CrzjOl40
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LAB TASKS
The terms listed below are crucial for this lab module. Some of it needs to be actively
looked for.
TERMINOLOGIES
Antagonism -
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Antifungal agents -A drug that selectively eliminates fungal pathogens from a host with
minimal toxicity to the host
Antiviral agents -Agents that are used to inhibit production of viruses that causes disease. Most
antiviral agents are only effective while the virus is replicating
Commensal bacteria: the skin and mucous membranes are continuously colonized by
commensal bacteria that do not cause disease unless the subject is weakened
Empiric therapy -
Multi-resistant bacteria - bacteria are said to be multi-resistant to antibiotics when they are
sensitive only to a small number of the antibiotics customarily used in therapy, as a
consequence of the accumulation of natural and acquired resistances.
PCR (Polymerase Chain Reaction) - molecular biology technology for in vitro amplification of
genetic sequences, used to copy known DNA or RNA sequences in large quantities (by an order
of magnitude of a billion) from an initially small quantity. This technology is particularly useful
for detecting the presence of viruses
Superbug -
Superinfection -
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Synergism -
Engelkirk, Paul G. (2019). Burton's microbiology for the health sciences, 8th ed. .
Philadelphia : LWW.616.01 E3 2007
www.cdc.com
www.googlesearch
https://www.who.com
Useful website:
Mcq online
https://microbeonline.com/mcqs-in-microbiology-for-m-sc-entrance-examination/
/ avg-val