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In Vitro Evaluation of Antimicrobial Peptide Tridecaptin M in Combination with Other Antibiotics against Multidrug Resistant Acinetobacter baumannii
by
Raka, Vrushali
, Jangra, Manoj
, Nandanwar, Hemraj
in
Acinetobacter baumannii
/ Acinetobacter baumannii - drug effects
/ Acinetobacter baumannii - pathogenicity
/ Acinetobacter Infections - drug therapy
/ Acinetobacter Infections - microbiology
/ Acinetobacter Infections - pathology
/ Anti-Bacterial Agents - pharmacology
/ antibiotic-resistance
/ Antibiotics
/ Antimicrobial agents
/ Bacteria
/ Bacterial infections
/ Ceftazidime - pharmacology
/ combination therapy
/ Drug resistance
/ Drug Resistance, Multiple - drug effects
/ Drug Resistance, Multiple, Bacterial - drug effects
/ Gram-negative bacteria
/ Humans
/ Intensive care
/ Microbial Sensitivity Tests
/ Multidrug resistant organisms
/ Nosocomial infections
/ Pathogens
/ Peptides
/ Peptides - chemistry
/ Peptides - pharmacology
/ persisters
/ Pore Forming Cytotoxic Proteins - pharmacology
/ Rifampin - pharmacology
/ Tridecaptin M
/ Vancomycin - pharmacology
2020
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In Vitro Evaluation of Antimicrobial Peptide Tridecaptin M in Combination with Other Antibiotics against Multidrug Resistant Acinetobacter baumannii
by
Raka, Vrushali
, Jangra, Manoj
, Nandanwar, Hemraj
in
Acinetobacter baumannii
/ Acinetobacter baumannii - drug effects
/ Acinetobacter baumannii - pathogenicity
/ Acinetobacter Infections - drug therapy
/ Acinetobacter Infections - microbiology
/ Acinetobacter Infections - pathology
/ Anti-Bacterial Agents - pharmacology
/ antibiotic-resistance
/ Antibiotics
/ Antimicrobial agents
/ Bacteria
/ Bacterial infections
/ Ceftazidime - pharmacology
/ combination therapy
/ Drug resistance
/ Drug Resistance, Multiple - drug effects
/ Drug Resistance, Multiple, Bacterial - drug effects
/ Gram-negative bacteria
/ Humans
/ Intensive care
/ Microbial Sensitivity Tests
/ Multidrug resistant organisms
/ Nosocomial infections
/ Pathogens
/ Peptides
/ Peptides - chemistry
/ Peptides - pharmacology
/ persisters
/ Pore Forming Cytotoxic Proteins - pharmacology
/ Rifampin - pharmacology
/ Tridecaptin M
/ Vancomycin - pharmacology
2020
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In Vitro Evaluation of Antimicrobial Peptide Tridecaptin M in Combination with Other Antibiotics against Multidrug Resistant Acinetobacter baumannii
by
Raka, Vrushali
, Jangra, Manoj
, Nandanwar, Hemraj
in
Acinetobacter baumannii
/ Acinetobacter baumannii - drug effects
/ Acinetobacter baumannii - pathogenicity
/ Acinetobacter Infections - drug therapy
/ Acinetobacter Infections - microbiology
/ Acinetobacter Infections - pathology
/ Anti-Bacterial Agents - pharmacology
/ antibiotic-resistance
/ Antibiotics
/ Antimicrobial agents
/ Bacteria
/ Bacterial infections
/ Ceftazidime - pharmacology
/ combination therapy
/ Drug resistance
/ Drug Resistance, Multiple - drug effects
/ Drug Resistance, Multiple, Bacterial - drug effects
/ Gram-negative bacteria
/ Humans
/ Intensive care
/ Microbial Sensitivity Tests
/ Multidrug resistant organisms
/ Nosocomial infections
/ Pathogens
/ Peptides
/ Peptides - chemistry
/ Peptides - pharmacology
/ persisters
/ Pore Forming Cytotoxic Proteins - pharmacology
/ Rifampin - pharmacology
/ Tridecaptin M
/ Vancomycin - pharmacology
2020
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In Vitro Evaluation of Antimicrobial Peptide Tridecaptin M in Combination with Other Antibiotics against Multidrug Resistant Acinetobacter baumannii
Journal Article
In Vitro Evaluation of Antimicrobial Peptide Tridecaptin M in Combination with Other Antibiotics against Multidrug Resistant Acinetobacter baumannii
2020
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Overview
The rapid emergence of antimicrobial resistance in Acinetobacter baumannii coupled with the dried pipeline of novel treatments has driven the search for new therapeutic modalities. Gram-negative bacteria have an extra outer membrane that serves as a permeability barrier for various hydrophobic and/or large compounds. One of the popular approaches to tackle this penetration barrier is use of potentiators or adjuvants in combination with traditional antibiotics. This study reports the in vitro potential of an antimicrobial peptide tridecaptin M in combination with other antibiotics against different strains of A. baumannii. Tridecaptin M sensitized the bacteria to rifampicin, vancomycin, and ceftazidime. Further, we observed that a tridecaptin M and rifampicin combination killed the bacteria completely in 4 h in an ex vivo blood infection model and was superior to rifampicin monotherapy. The study also found that concomitant administration of both compounds is not necessary to achieve the antimicrobial effect. Bacteria pre-treated with tridecaptin M (for 2–4 h) followed by exposure to rifampicin showed similar killing as obtained for combined treatment. Additionally, this combination hampered the survival of persister development in comparison to rifampicin alone. These findings encourage the future investigation of this combination to treat severe infections caused by extremely drug-resistant A. baumannii.
Publisher
MDPI AG,MDPI
Subject
/ Acinetobacter baumannii - drug effects
/ Acinetobacter baumannii - pathogenicity
/ Acinetobacter Infections - drug therapy
/ Acinetobacter Infections - microbiology
/ Acinetobacter Infections - pathology
/ Anti-Bacterial Agents - pharmacology
/ Bacteria
/ Drug Resistance, Multiple - drug effects
/ Drug Resistance, Multiple, Bacterial - drug effects
/ Humans
/ Multidrug resistant organisms
/ Peptides
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