Micafungin and amphotericin B synergy against Candida auris. 2020

Siddharth Jaggavarapu, and Eileen M Burd, and David S Weiss
Emory Antibiotic Resistance Center, Atlanta, GA 30329, USA; Emory Vaccine Center, Atlanta, GA, USA; Emory University School of Medicine, Atlanta, GA, USA; Research Service, Atlanta VA Medical Center, Decatur, GA, USA.

UI MeSH Term Description Entries
D002175 Candida A genus of yeast-like mitosporic Saccharomycetales fungi characterized by producing yeast cells, mycelia, pseudomycelia, and blastophores. It is commonly part of the normal flora of the skin, mouth, intestinal tract, and vagina, but can cause a variety of infections, including CANDIDIASIS; ONYCHOMYCOSIS; VULVOVAGINAL CANDIDIASIS; and CANDIDIASIS, ORAL (THRUSH). Candida guilliermondii var. nitratophila,Candida utilis,Cyberlindnera jadinii,Hansenula jadinii,Lindnera jadinii,Monilia,Pichia jadinii,Saccharomyces jadinii,Torula utilis,Torulopsis utilis,Monilias
D000077551 Micafungin A cyclic lipo-hexapeptide echinocandin antifungal agent that is used for the treatment and prevention of CANDIDIASIS. FK 463,FK-463,FK463,Micafungin Sodium,Mycamine
D000088063 Candida auris A species of yeast in genus Candida. C. auris infection is most often associated with immunocompromised patients in healthcare settings. INVASIVE CANDIDIASIS and colonization pose a treatment challenge when multidrug resistant strains are involved. C auris
D000666 Amphotericin B Macrolide antifungal antibiotic produced by Streptomyces nodosus obtained from soil of the Orinoco river region of Venezuela. Amphocil,Amphotericin,Amphotericin B Cholesterol Dispersion,Amphotericin B Colloidal Dispersion,Fungizone
D000935 Antifungal Agents Substances that destroy fungi by suppressing their ability to grow or reproduce. They differ from FUNGICIDES, INDUSTRIAL because they defend against fungi present in human or animal tissues. Anti-Fungal Agents,Antifungal Agent,Fungicides, Therapeutic,Antibiotics, Antifungal,Therapeutic Fungicides,Agent, Antifungal,Anti Fungal Agents,Antifungal Antibiotics
D054714 Echinocandins Cyclic hexapeptides of proline-ornithine-threonine-proline-threonine-serine. The cyclization with a single non-peptide bond can lead them to be incorrectly called DEPSIPEPTIDES, but the echinocandins lack ester links. Antifungal activity is via inhibition of 1,3-beta-glucan synthase production of BETA-GLUCANS. Aculeacin,Echinocandin,Pneumocandin,Aculeacins,Mulundocandins,Pneumocandins

Related Publications

Siddharth Jaggavarapu, and Eileen M Burd, and David S Weiss
September 2019, Antimicrobial agents and chemotherapy,
Siddharth Jaggavarapu, and Eileen M Burd, and David S Weiss
August 2006, Antimicrobial agents and chemotherapy,
Siddharth Jaggavarapu, and Eileen M Burd, and David S Weiss
March 2024, Journal of fungi (Basel, Switzerland),
Siddharth Jaggavarapu, and Eileen M Burd, and David S Weiss
May 2022, Journal of fungi (Basel, Switzerland),
Siddharth Jaggavarapu, and Eileen M Burd, and David S Weiss
October 2021, Pharmaceutics,
Siddharth Jaggavarapu, and Eileen M Burd, and David S Weiss
September 2016, The Journal of antimicrobial chemotherapy,
Siddharth Jaggavarapu, and Eileen M Burd, and David S Weiss
August 2019, The Journal of antimicrobial chemotherapy,
Siddharth Jaggavarapu, and Eileen M Burd, and David S Weiss
August 2021, Pathogens (Basel, Switzerland),
Siddharth Jaggavarapu, and Eileen M Burd, and David S Weiss
April 2008, Antimicrobial agents and chemotherapy,
Siddharth Jaggavarapu, and Eileen M Burd, and David S Weiss
January 2013, Indian journal of medical microbiology,
Copied contents to your clipboard!