This document discusses the emerging issue of antimicrobial resistance in microorganisms. It provides an overview of antibiotics and multi-drug resistance. Common multi-drug resistant organisms include MRSA, ESBL-producing bacteria, and carbapenem-resistant Enterobacteriaceae. The mechanisms of antibiotic resistance include reduced permeability, enzymatic inactivation, efflux pumps, and target modification. Inappropriate antibiotic usage accelerates the development of resistance. If not addressed, antimicrobial resistance could lead to untreatable infections and increased mortality.
SYNTHETIC PEPTIDE VACCINES AND RECOMBINANT ANTIGEN VACCINED.R. Chandravanshi
What is a Vaccine?
A vaccine is a substance that is introduced into the body to prevent infection or to control disease due to a certain pathogen (a disease-causing organism, such as a virus, bacteria or parasite). The vaccine “teaches” the body how to defend itself against the pathogen by creating an immune response.
1 Unlike traditional pharmaceuticals, vaccines are biologics since they are made from living organisms (biological sources).
2 Specifically, vaccines are preparations of components derived from (or related to) a pathogen; they can typically induce a protective effect through one to three very small doses, in the range of micrograms to milligrams.
3 Immunity lasts for an extended period, from one year up to lifetime protection, including prevention of disease and/or related sequelae.
Synthetic peptide vaccines represent fragments of protein antigen sequences, synthesizing specific B cell and T cell epitopes offer the potential to induce diseases neutralizing immuno response with completely synthetic structure. Now it is well established that short chain peptides can be used to mimic antigenic sites of viruses and thus can be used the basics for vaccines and development. therefore, attempts have been made to synthesize such peptides which act as the serrogate immuunogens, as an alternative to the existing conventional vaccines.
SYNTHETIC PEPTIDE VACCINES AND RECOMBINANT ANTIGEN VACCINED.R. Chandravanshi
What is a Vaccine?
A vaccine is a substance that is introduced into the body to prevent infection or to control disease due to a certain pathogen (a disease-causing organism, such as a virus, bacteria or parasite). The vaccine “teaches” the body how to defend itself against the pathogen by creating an immune response.
1 Unlike traditional pharmaceuticals, vaccines are biologics since they are made from living organisms (biological sources).
2 Specifically, vaccines are preparations of components derived from (or related to) a pathogen; they can typically induce a protective effect through one to three very small doses, in the range of micrograms to milligrams.
3 Immunity lasts for an extended period, from one year up to lifetime protection, including prevention of disease and/or related sequelae.
Synthetic peptide vaccines represent fragments of protein antigen sequences, synthesizing specific B cell and T cell epitopes offer the potential to induce diseases neutralizing immuno response with completely synthetic structure. Now it is well established that short chain peptides can be used to mimic antigenic sites of viruses and thus can be used the basics for vaccines and development. therefore, attempts have been made to synthesize such peptides which act as the serrogate immuunogens, as an alternative to the existing conventional vaccines.
Mechanism Antibiotic Resistance
Intrinsic (Natural)
Acquired
Chromosomal
Extra chromosomal
Intrinsic Resistance
Lack target : No cell wall; innately resistant to penicillin
2. Drug inactivation: Cephalosporinase in Klebsiella
3. Innate efflux pumps:
It is an active transport mechanism. It requires ATP.
Eg. E. coli, P. aeruginosa
Altered target sites
PBP alteration
Ribosomal target alteration
Decreased affinity by target modification
Beta-lactamase
Beta-lactamases are enzymes produced by bacteria that provide resistance to β-lactam antibiotics such as penicillins, cephamycins, and carbapenems
Major resistant Pathogen
1. PRSP- Penicillin resistant Streptococcus pneumoniae2. MRSA/ORSA- Methicillin-resistant Staphylococcus Aureus (Super bug)3. VRE -Vancomycin-Resistant Enterococci4. Carbapenem resistant pseudomonas aeruginosa5. Carbapenem resistant Carbapenem resistant 6. Extended spectrum beta-lactamase (ESBL)-producing bacteria
Antibiotic originally was intended to cure and treat disease. However, because of lack of proper education and awareness campaign, antibiotics now are widely abuse and misuse. Such abuse and misuse of antibiotics today are the culprit why we have emergence of new diseases and Bacterial Resistance.
Dr. Sachin Verma is a young, diligent and dynamic physician. He did his graduation from IGMC Shimla and MD in Internal Medicine from GSVM Medical College Kanpur. Then he did his Fellowship in Intensive Care Medicine (FICM) from Apollo Hospital Delhi. He has done fellowship in infectious diseases by Infectious Disease Society of America (IDSA). He has also done FCCS course and is certified Advance Cardiac Life support (ACLS) and Basic Life Support (BLS) provider by American Heart Association. He has also done a course in Cardiology by American College of Cardiology and a course in Diabetology by International Diabetes Centre. He specializes in the management of Infections, Multiorgan Dysfunctions and Critically ill patients and has many publications and presentations in various national conferences under his belt. He is currently working in NABH Approved Ivy super-specialty Hospital Mohali as Consultant Intensivists and Physician.
Mechanism Antibiotic Resistance
Intrinsic (Natural)
Acquired
Chromosomal
Extra chromosomal
Intrinsic Resistance
Lack target : No cell wall; innately resistant to penicillin
2. Drug inactivation: Cephalosporinase in Klebsiella
3. Innate efflux pumps:
It is an active transport mechanism. It requires ATP.
Eg. E. coli, P. aeruginosa
Altered target sites
PBP alteration
Ribosomal target alteration
Decreased affinity by target modification
Beta-lactamase
Beta-lactamases are enzymes produced by bacteria that provide resistance to β-lactam antibiotics such as penicillins, cephamycins, and carbapenems
Major resistant Pathogen
1. PRSP- Penicillin resistant Streptococcus pneumoniae2. MRSA/ORSA- Methicillin-resistant Staphylococcus Aureus (Super bug)3. VRE -Vancomycin-Resistant Enterococci4. Carbapenem resistant pseudomonas aeruginosa5. Carbapenem resistant Carbapenem resistant 6. Extended spectrum beta-lactamase (ESBL)-producing bacteria
Antibiotic originally was intended to cure and treat disease. However, because of lack of proper education and awareness campaign, antibiotics now are widely abuse and misuse. Such abuse and misuse of antibiotics today are the culprit why we have emergence of new diseases and Bacterial Resistance.
Dr. Sachin Verma is a young, diligent and dynamic physician. He did his graduation from IGMC Shimla and MD in Internal Medicine from GSVM Medical College Kanpur. Then he did his Fellowship in Intensive Care Medicine (FICM) from Apollo Hospital Delhi. He has done fellowship in infectious diseases by Infectious Disease Society of America (IDSA). He has also done FCCS course and is certified Advance Cardiac Life support (ACLS) and Basic Life Support (BLS) provider by American Heart Association. He has also done a course in Cardiology by American College of Cardiology and a course in Diabetology by International Diabetes Centre. He specializes in the management of Infections, Multiorgan Dysfunctions and Critically ill patients and has many publications and presentations in various national conferences under his belt. He is currently working in NABH Approved Ivy super-specialty Hospital Mohali as Consultant Intensivists and Physician.
Multi Drug Resistant Bacteria.
multidrug resistance is a condition enabling a disease causing organism to resist distinct drug or chemical of a wide variety of structure & function targeted at eradicating the organism
ANTIBIOTIC RESISTANCE
BY- RICHA KRISHNA
(M.PHARMACY)
Antibiotic resistance occurs when bacteria change in response to the use of these medicines. Bacteria, not humans or animals, become antibiotic-resistant. These bacteria may infect humans and animals, and the infections they cause are harder to treat than those caused by non-resistant bacteria.
Phenomics assisted breeding in crop improvementIshaGoswami9
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the complex characteristics of multiple gene, owing to a lack of crop phenotypic data. Efficient, automatic, and accurate technologies and platforms that can capture phenotypic data that can
be linked to genomics information for crop improvement at all growth stages have become as important as genotyping. Thus,
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during crop growing stages at the organism level, including the cell, tissue, organ, individual plant, plot, and field levels. With the rapid development of novel sensors, imaging technology,
and analysis methods, numerous infrastructure platforms have been developed for phenotyping.
Comparing Evolved Extractive Text Summary Scores of Bidirectional Encoder Rep...University of Maribor
Slides from:
11th International Conference on Electrical, Electronics and Computer Engineering (IcETRAN), Niš, 3-6 June 2024
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https://www.etran.rs/2024/en/home-english/
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Carbonyls undergo addition reactions with a large range of nucleophiles.
Comparing the relative basicity of the nucleophile and the product is extremely helpful in determining how reversible the addition reaction is. Reactions with Grignards and hydrides are irreversible. Reactions with weak bases like halides and carboxylates generally don’t happen.
Electronic effects (inductive effects, electron donation) have a large impact on reactivity.
Large groups adjacent to the carbonyl will slow the rate of reaction.
Neutral nucleophiles can also add to carbonyls, although their additions are generally slower and more reversible. Acid catalysis is sometimes employed to increase the rate of addition.
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Monitor common gases, weather parameters, particulates.
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Inspired by David Donoho's vision, this talk aims to revisit the three crucial pillars of frictionless reproducibility (data sharing, code sharing, and competitive challenges) with the perspective of deep software variability.
Our observation is that multiple layers — hardware, operating systems, third-party libraries, software versions, input data, compile-time options, and parameters — are subject to variability that exacerbates frictions but is also essential for achieving robust, generalizable results and fostering innovation. I will first review the literature, providing evidence of how the complex variability interactions across these layers affect qualitative and quantitative software properties, thereby complicating the reproduction and replication of scientific studies in various fields.
I will then present some software engineering and AI techniques that can support the strategic exploration of variability spaces. These include the use of abstractions and models (e.g., feature models), sampling strategies (e.g., uniform, random), cost-effective measurements (e.g., incremental build of software configurations), and dimensionality reduction methods (e.g., transfer learning, feature selection, software debloating).
I will finally argue that deep variability is both the problem and solution of frictionless reproducibility, calling the software science community to develop new methods and tools to manage variability and foster reproducibility in software systems.
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💥 Let’s dive into the future of science and shed light on PraxiLabs’ crucial role in transforming this field!
Remote Sensing and Computational, Evolutionary, Supercomputing, and Intellige...University of Maribor
Slides from talk:
Aleš Zamuda: Remote Sensing and Computational, Evolutionary, Supercomputing, and Intelligent Systems.
11th International Conference on Electrical, Electronics and Computer Engineering (IcETRAN), Niš, 3-6 June 2024
Inter-Society Networking Panel GRSS/MTT-S/CIS Panel Session: Promoting Connection and Cooperation
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The use of Nauplii and metanauplii artemia in aquaculture (brine shrimp).pptxMAGOTI ERNEST
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Brine shrimp (Artemia spp.) are used in marine aquaculture worldwide. Annually, more than 2,000 metric tons of dry cysts are used for cultivation of fish, crustacean, and shellfish larva. Brine shrimp are important to aquaculture because newly hatched brine shrimp nauplii (larvae) provide a food source for many fish fry (Mozanzadeh et al., 2021). Culture and harvesting of brine shrimp eggs represents another aspect of the aquaculture industry. Nauplii and metanauplii of Artemia, commonly known as brine shrimp, play a crucial role in aquaculture due to their nutritional value and suitability as live feed for many aquatic species, particularly in larval stages (Sorgeloos & Roubach, 2021).
2. OVERVIEW
Multi drug resistivity of the microorganisms is an
emerging one ,that almost all microbes are being
developed a type of resistance within their cell to
certain groups of drugs.
These drugs are nothing but the antibiotics that we
use or developing in our immune system
Due to this resistivity character of microbes there will
be no curation or less curation of the diseases, hence
the pathogen gets adapted to our immune system
This topic will gives an idea about the drug resistivity
of various microbes with a fine description
3. DRUGS RESEMBLES
ANTIBIOTICS:
Antibiotics, also called antibacterials, are a type
of antimicrobial drug used in
the treatment and prevention of bacterial
infections. They may either kill or inhibit the
growth of bacteria
There are different routes of administration for antibiotic
treatment.
Antibiotics are usually taken by mouth. In more severe
cases, particularly systemic infections, antibiotics can be
given intravenously or by injection.
6. WHAT IS MULTI DRUG RESISTANCE?
Multiple drug resistance (MDR), or drug
resistance or multi resistance is antimicrobial
resistance shown by a species of microorganism to various
antimicrobial drugs.
MDR bacteria that resist multiple antibiotics; other types
include MDR viruses, fungi, and parasites
7.
8. Resistance is accelerated through inappropriate
use of antimicrobials
Standard treatment guidelines is not
provided by physicians or provided
but not adhered to.
Drugs taken without prescription
Inadequate monitoring of diseases
(AMR surveillance programs)
Irrational self-administration or
prescription
9. Resistanceof microbeshas huge
negativeimpacton human health
• Longer duration of illness
• Longer treatment
• Higher mortality
• Increased burden on health system
• Patient acts as reservoir of resistant organisms
which are passed to community and health-
care workers
• Huge economic impact
10. Mechanisms of antibiotic resistance:
Reduced permeability or uptake
Enzymatic inactivation
Enhanced efflux
Alternation or over expression of target
Loss of enzymes involved in drug metabolism
Enzymatic inactivation - β-lactamase(EC No
3.5.2.6) releases the β-lactam ring and inactivates
the β-lactam antibiotics.
14. ESCHERICHIA COLI – RESISTANCE TO
CEPHALOSPORINS
AND TO FLUOROQUINOLONES:
• E. coli is part of the normal flora in the intestine in humans and
animals.
• cephalosporins is mainly conferred by enzymes known as
extended spectrum beta-lactamases (ESBLs); these enzymes
destroy many beta-lactam antibacterial drugs.
• E. coli strains that have ESBL are generally also resistant to several
other antibacterial drugs
• E. coli resistance to fluoroquinolones were similar to those found
for resistance to third-generation cephalosporins.
15. KLEBSIELLA PNEUMONIAE –
RESISTANCE
TO CEPHALOSPORINS
AND TO CARBAPENEMS• Klebsiella are frequent colonizers of the gut in humans and
other vertebrates Causes urinary tract, respiratory tract
infections, bloodstream infections.
• pneumoniae carries a resistance gene (chromosomally located
betalactamase) that have resistance to ampicillin and
amoxicillin
• The presence of extended spectrum
beta lactamase in klebsiella give
resistance to cephalosporins and the
carbapenems
16. STAPHYLOCOCCUS AUREUS –
RESISTANCE
TO METHICILLIN:
• S.aureus is a Gram-positive bacterium that can be a part
of the normal flora on the skin and in the nose and causes
notable infections- skin, soft tissue, bone and bloodstream
infections
• S.aureus gets the resistance by the production of a
betalactamase enzyme that inactivates drugs such as
penicillin, ampicillin and amoxicillin.
17. STREPTOCOCCUS PNEUMONIAE –
RESISTANCE TO
PENICILLIN:
• S. pneumoniae ( also known as pneumococci) is the leading
cause worldwide of community-acquired pneumonia
• It is resistant to penicillin
18. SALMONELLA –
RESISTANCE TO FLUOROQUINOLONES
• Bacteria of the genus Salmonella are a major cause of
foodborne illness throughout the world(zoonotic pathogen)
• These species are resistant to anti microbials like ampicillin,
chloramphenicol,
• streptomycin,
• sulfonamides and
• tetracycline
19. SHIGELLA SPECIES – RESISTANCE TO
FLUOROQUINOLONES
• Shigella species area major cause of diarrhoea
and dysentery
• These bacteria aretransmitted by ingestion of contaminated food orwater
• Formerly, Shigellastrains wereless susceptible to cotrimoxazole, ciprofloxacin and
fluoroquinolones
21. MULTIDRUG-RESISTANT
TUBERCULOSIS
• Tuberculosis (TB) is caused by the bacterium Mycobacterium
tuberculosis
• Has slight resistance to rifampicin, isoniazid, ethambutol
and pyrazinamide
• MDR (multi drug resistant) TB is the name given to TB when
the bacteria that are causing it are resistant to at least isoniazid
and rifampicin
• XDR TB (extensively drug resistant TB) resistant to at least
rifampicin and isoniazid,fluoroquinolones,amikacin,
kanamycin, capreomycin.
22. DRUG RESISTANCE
IN MALARIA:
• Malaria is caused by the protozoan parasite
Plasmodium which is transmitted via the bite of
female Anopheles mosquitoes.
• Among the five species of Plasmodium parasites [P.
falciparum, P. vivax, P. ovale,P. malariae and P.
knowlesi] that infect humans are P. falciparum and P.
vivax
• Malaria has slow resistant to chloroquine,
mefloquine or piperaquine
• P. falciparum to amodiaquine and sulfadoxine-
pyrimethamine
23. DRUG RESISTANCE IN
HIV:
• Human immunodeficiency virus (HIV) infects cells of the immune system,
destroying or impairing their function.
• HIV treatments with some drugs are failure
• This have resistance to artesunate-mefloquine,dihydroartemisinin-
piperaquine,
atovaquone-proguanil
• These drugs supress the viral load but don’t kill the virus
24. DRUG RESISTANCE IN
INFLUENZA
VIRUSES
• Influenza imposes a global public health and economic burden for all populations
• Influenza A and B viruses causes acute respiratory illness
• TheA(H1N1) and A(H3N2) subtypes are currently in general circulation in human
populations
• Influenza has a less resistance to adamantanes and neuraminidase
25. CANCER
MULTIDRUG
RESISTANCE
• Canceris a group of diseases involving abnormal cell growth with the potential to
invade or spread to other parts of the body.
• The cancercells actively expel chemotherapy drugs from the interior and thus
resists the drugs
• They have resistance to mechlorethamine,methotrexate, Bendamustine,
Busulfan,Carmustine
Asparagin,Capecitabine etc.
26. ANTIBIOTIC RESISTANT INFECTIONS
Diseases Agent Resistances
Pneumonia S pneumoniae Penicillin
Dysentery S dysenteriae Multiple resistances
Typhoid S typhi Multiple resistances
Gonorrhea N gonorrhoeae Penicillin and
tetracycline
Tuberculosis M tuberculosis Rifampicine and INH
Nosocomial infections S aureus Methicillin, vancomycin
E species Vancomycin
Klebsiella,
Pseudomonas
Multiple resistances
27. ANTIBIOTIC SURVEILLANCE STUDIES
IN VIRUDHUNAGAR DISTRICT
• 100% resistant to penicillin
• 100% of resistance to monobactam group except
Enterococcus
• Pseudomonas sp. showed resistance to both third and
fourth generation cephalosporins at higher rates
• 99.9% of the selected isolates were sensitive to
imipenem during 2013
• 80% of isolates were sensitive to imipenem during 2014
28. LEADING GLOBAL DISEASES
0
1
2
3
4
Respiratory infections HIV Diarrheal diseases Tuberculosis Malaria
Millionsofdeaths,worldwide,1998
S. pneumonia: Up to 55%
resistance to penicillin in some
regions
HIV: Report of
resistance to all
marketed agents
S. dyentariae: 90% resistance to
cotrimoxazole S.Typhi: Outbreaks of
multi-resistant strains in 11 countries
M. tuberculosis:
Multi-drug resistant
tuberculosis
P. falciparum:
Chloroquine resistance in
81/92 countries
30. Superbugs* are visible manifestations of our prolonged failure to preserve antibiotics
Note: Methicillin resistant Staph aureus, MDR-and XDR Mycobacteria, ESBL producing Gram negative
bacteria and NDM-1 producing
enterobacteriaceae bacteria are few examples of superbugs because these fail to respond to large
number of commonly used antibiotics
Known but neglected.
Need immediate action
Known but
inevitable