Evolving Strategies against Antibiotic Resistance in Gram-Positive Pathogens: The Never-Ending Story of Multiple-Drug Resistant Staphylococci and Enterococci

A special issue of Microorganisms (ISSN 2076-2607). This special issue belongs to the section "Medical Microbiology".

Deadline for manuscript submissions: closed (31 October 2022) | Viewed by 5458

Special Issue Editors


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Guest Editor
Department of Biomedical and Biotechnological Sciences, University of Catania, Via S. Sofia 97, 95123 Catania, Italy
Interests: multidrug-resistant gram-positive isolates; mechanisms of antibiotic resistance; Staphylococcus aureus internalization; mechanism of action of novel drugs
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Guest Editor
Instituto de Tecnologia Química e Biológica, Universidade Nova de Lisboa (ITQB-NOVA), Lisbon, Portugal
Interests: multidrug resistant bacteria; evolution of clones; origin and evolution of antibiotic resistance; pathogenicity; coagulase-negative staphylococci; genomics

Special Issue Information

Dear Colleagues,

The major challenge that clinicians face when treating infections is antibiotic resistance. Over the past three decades, severe infections in healthcare environments caused by multiresistant Gram-positive bacteria have been making headlines worldwide. The success of these pathogens lies mainly in their changing epidemiology and genetic flexibility, frequently leading to alterations in their genetic repertoire, namely the gain or loss of antimicrobial resistance (AMR) and virulence genes carried in mobile genetic elements, or the emergence of compensatory mutations mediating fitness and adaptation.

What is so special about these multidrug-resistant bacteria? Where do staphylococci and enterococci rank in the top-ten hospital-associated pathogens? Which are the factors promoting the continuous evolution and maintenance of well-adapted and high-risk clones?

S. aureus, particularly methicillin-resistant S. aureus (MRSA), occurs in clonal waves of multidrug-resistant clones. The reason for the rise and fall of specific strain types remains poorly understood. Coagulase-negative staphylococci are important reservoirs of antibiotic resistance and virulence for S. aureus and have been involved in the evolution and emergence of new antibiotic resistance determinants.

Enterococci are intrinsically resistant, may harbor different degrees of resistance to several antimicrobial classes, and have acquired resistance multiple times over their evolutionary history. The occurrence of the so called “van-alphabet” through the acquisition of plasmid-encoded vancomycin resistance, has become the paradigm of the post-antibiotic era. The transfer of plasmids and large genomic regions is the basis of their genomic plasticity and adaptability to the ever-changing hospital environment.

This Special Issue will focus on the phenotypic and molecular strategies adopted by staphylococci and enterococci that allow for fast adaptation, the development of multidrug resistance, and refractoriness to effective therapy.

Knowledge in this field will help in understanding the emergence of pathogenic clones and the genetic variation underlying clinically relevant changes, as well as in pinpointing novel targets for antibiotics, vaccines or immunotherapy.

Dr. Floriana Campanile
Dr. Maria Miragaia
Guest Editors

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Keywords

  • hospital-acquired pathogens
  • multidrug-resistant Gram-positive isolates
  • genotypic characteristics of staphylococci and enterococci
  • mechanisms of antibiotic resistance
  • evolving antibacterial strategies

Published Papers (1 paper)

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Research

19 pages, 6639 KiB  
Article
Changes in the Ultrastructure of Staphylococcus aureus Treated with Cationic Peptides and Chlorhexidine
by Alina Grigor’eva, Alevtina Bardasheva, Anastasiya Tupitsyna, Nariman Amirkhanov, Nina Tikunova, Dmitrii Pyshnyi and Elena Ryabchikova
Microorganisms 2020, 8(12), 1991; https://0-doi-org.brum.beds.ac.uk/10.3390/microorganisms8121991 - 14 Dec 2020
Cited by 19 | Viewed by 3607
Abstract
Antimicrobial peptides, including synthetic ones, are becoming increasingly important as a promising tool to fight multidrug-resistant bacteria. We examined the effect of cationic peptides H2N-Arg9-Phe2-C(O)NH2 and H2N-(Lys-Phe-Phe)3-Lys-C(O)NH2 on Staphylococcus aureus, [...] Read more.
Antimicrobial peptides, including synthetic ones, are becoming increasingly important as a promising tool to fight multidrug-resistant bacteria. We examined the effect of cationic peptides H2N-Arg9-Phe2-C(O)NH2 and H2N-(Lys-Phe-Phe)3-Lys-C(O)NH2 on Staphylococcus aureus, which remains one of the most harmful pathogens. Antiseptic chlorhexidine served as reference preparation. We studied viability of S. aureus and examined its ultrastructure under treatment with 100 µM of R9F2 or (KFF)3K peptides or chlorhexidine using transmission electron microscopy of ultrathin sections. Bacterial cells were sampled as kinetic series starting from 1 min up to 4 h of treatment with preparations. Both peptides caused clearly visible damage of bacteria cell membrane within 1 min. Incubation of S. aureus with R9F2 or (KFF)3K peptides led to cell wall thinning, loss of cytoplasm structure, formation of mesosome-derived multimembrane structures and “decorated fibers” derived from DNA chains. The effect of R9F2 peptides on S. aureus was more severe than the effect of (KFF)3K peptides. Chlorhexidine heavily damaged the bacteria cell wall, in particular in areas of septa formation, while cytoplasm kept its structure within the observation time. Our study showed that cell membrane damage is critical for S. aureus viability; however, we believe that cell wall disorders should also be taken into account when analyzing the effects of the mechanisms of action of antimicrobial peptides (AMPs). Full article
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