101. Multidrug efflux pumps as main players in intrinsic and acquired resistance to antimicrobials
- Author
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María Blanca Sánchez, Fernando Corona, José L. Martínez, Paula Blanco, Sara Hernando-Amado, Jose Antonio Reales-Calderon, and Manuel Alcalde-Rico
- Subjects
0301 basic medicine ,Cell physiology ,Cancer Research ,medicine.drug_class ,030106 microbiology ,Antibiotics ,Pharmacology ,Biology ,Gram-Positive Bacteria ,Microbiology ,Fungal Proteins ,03 medical and health sciences ,Antibiotic resistance ,Anti-Infective Agents ,Bacterial Proteins ,In vivo ,Drug Resistance, Multiple, Bacterial ,Drug Resistance, Multiple, Fungal ,Gene Expression Regulation, Fungal ,Gram-Negative Bacteria ,medicine ,Humans ,Pharmacology (medical) ,Effector ,Fungi ,Transporter ,Bacterial Infections ,Gene Expression Regulation, Bacterial ,Antimicrobial ,Infectious Diseases ,Mycoses ,Oncology ,Efflux ,Genes, MDR - Abstract
Multidrug efflux pumps constitute a group of transporters that are ubiquitously found in any organism. In addition to other functions with relevance for the cell physiology, efflux pumps contribute to the resistance to compounds used for treating different diseases, including resistance to anticancer drugs, antibiotics or antifungal compounds. In the case of antimicrobials, efflux pumps are major players in both intrinsic and acquired resistance to drugs currently in use for the treatment of infectious diseases. One important aspect not fully explored of efflux pumps consists on the identification of effectors able to induce their expression. Indeed, whereas the analysis of clinical isolates have shown that mutants overexpressing these resistance elements are frequently found, less is known on the conditions that may trigger expression of efflux pumps, hence leading to transient induction of resistance in vivo , a situation that is barely detectable using classical susceptibility tests. In the current article we review the structure and mechanisms of regulation of the expression of bacterial and fungal efflux pumps, with a particular focus in those for which a role in clinically relevant resistance has been reported.
- Published
- 2016