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Review
. 2016 Mar 24:7:381.
doi: 10.3389/fmicb.2016.00381. eCollection 2016.

Induced Bacterial Cross-Resistance toward Host Antimicrobial Peptides: A Worrying Phenomenon

Affiliations
Review

Induced Bacterial Cross-Resistance toward Host Antimicrobial Peptides: A Worrying Phenomenon

Osmel Fleitas et al. Front Microbiol. .

Abstract

Bacterial resistance to conventional antibiotics has reached alarming levels, threatening to return to the pre-antibiotic era. Therefore, the search for new antimicrobial compounds that overcome the resistance phenomenon has become a priority. Antimicrobial peptides (AMPs) appear as one of the most promising antibiotic medicines. However, in recent years several AMP-resistance mechanisms have been described. Moreover, the AMP-resistance phenomenon has become more complex due to its association with cross-resistance toward AMP effectors of the host innate immune system. In this context, the use of AMPs as a therapeutic option could be potentially hazardous, since bacteria could develop resistance toward our innate immune system. Here, we review the findings of major studies that deal with the AMP cross-resistance phenomenon.

Keywords: antibiotics; antimicrobial peptides; bacterial infection; cross-resistance.

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Figures

FIGURE 1
FIGURE 1
The challenge of Vibrio cholerae with sub-lethal concentrations of polymyxin B induced the release of outer membrane vesicles that bind the protein Bap1, which in turn binds LL-37.

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References

    1. Bayer A. S., Mishra N. N., Chen L., Kreiswirth B. N., Rubio A., Yang J. S. (2015). Frequency and distribution of single-nucleotide polymorphisms within mprf in methicillin-resistant Staphylococcus aureus clinical isolates: role in cross-resistance between daptomycin and host defense antimicrobial peptides. Antimicrob. Agents Chemother. 59 4930–4937. 10.1128/AAC.00970-15 - DOI - PMC - PubMed
    1. Bayer A. S., Mishra N. N., Sakoulas G., Nonejuie P., Nast C. C., Pogliano J. (2014). Heterogeneity of mprF sequences in methicillin-resistant Staphylococcus aureus clinical isolates: role in cross-resistance between daptomycin and host defense antimicrobial peptides. Antimicrob. Agents Chemother. 58 7462–7467. 10.1128/AAC.03422-14 - DOI - PMC - PubMed
    1. Bell G., Gouyon P. H. (2003). Arming the enemy: the evolution of resistance to self-proteins. Microbiology 149 1367–1375. 10.1099/mic.0.26265-0 - DOI - PubMed
    1. Chen H. D., Groisman E. A. (2013). The biology of the PmrA/PmrB two component system: the major regulator of lipopolysaccharide modifications. Annu. Rev. Microbiol. 67 83–112. 10.1146/annurev-micro-092412-155751 - DOI - PMC - PubMed
    1. Chernysh S., Gordya N., Suborova T. (2015). Insect antimicrobial peptide complexes prevent resistance development in bacteria. PLoS ONE 10:e0130788 10.1371/journal.pone.0130788 - DOI - PMC - PubMed

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