Molecular typing and antimicrobial susceptibility profiles of Campylobacter jejuni and Campylobacter coli Isolates from Patients and raw meat in Huzhou, China, 2021-2022. [PDF]
Wu X +5 more
europepmc +1 more source
Six-Year Prescription Pattern of Antimicrobial Use in Cats at the Veterinary Teaching Hospital of the University of Pisa. [PDF]
De Marchi L +6 more
europepmc +1 more source
The Paradox of Healthcare in the 'Superbugs' Era: Current Challenges and Future Directions. [PDF]
Sole E +7 more
europepmc +1 more source
Prevalence, antibiotic resistance, resistance and virulence determinants of Campylobacter jejuni in China: A systematic review and meta-analysis. [PDF]
Li Z +8 more
europepmc +1 more source
Postoperative Empyema Due to Leclercia adecarboxylata Following Mesothelioma Surgery: A Case Report. [PDF]
Montenegro JF +6 more
europepmc +1 more source
Resistance to ketolide antibiotics by coordinated expression of rRNA methyltransferases in a bacterial producer of natural ketolides [PDF]
Ketolides are promising new antimicrobials effective against a broad range of Gram-positive pathogens, in part because of the low propensity of these drugs to trigger the expression of resistance genes.
Sung Ryeol Park +2 more
exaly +7 more sources
Ketolides are the most recent generation of antimicrobials derived from the 14-membered ring macrolide, erythromycin A. The main structural feature that differentiates ketolides from erythromycin is the keto group, which replaces the L-cladinose moiety ...
Stephen Douthwaite +2 more
exaly +2 more sources
Ketolides—telithromycin, an example of a new class of antibacterial agents
Ketolides are new medicinal chemical entities. They are obtained by removing the 3-L-cladinose sugar moiety from erythronolide A and oxidation of the resulting 3-hydroxyl.
A Bryskier
exaly +2 more sources
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Ketolides are a new class of macrolides designed particularly to combat respiratory tract pathogens that have acquired resistance to macrolides. The ketolides are semi-synthetic derivatives of the 14-membered macrolide erythromycin A, and retain the erythromycin macrolactone ring structure as well as the D-desosamine sugar attached at position 5.
George G, Zhanel +8 more
openaire +4 more sources

