Studies with bioengineered Nisin peptides highlight the broad-spectrum potency of Nisin V

被引:86
作者
Field, Des [2 ]
Quigley, Lisa [2 ]
O'Connor, Paula M. [1 ]
Rea, Mary C. [1 ]
Daly, Karen [2 ]
Cotter, Paul D. [1 ,3 ]
Hill, Colin [2 ,3 ]
Ross, R. Paul [1 ,3 ]
机构
[1] TEAGASC, Moorepk Food Res Ctr, Fermoy, Cork, Ireland
[2] Univ Coll Cork, Dept Microbiol, Cork, Ireland
[3] Univ Coll Cork, Alimentary Pharmabiot Ctr, Cork, Ireland
基金
爱尔兰科学基金会;
关键词
RESISTANT STAPHYLOCOCCUS-AUREUS; PRECURSOR LIPID-II; MOLECULAR EPIDEMIOLOGIC ANALYSIS; GRAM-POSITIVE PATHOGENS; LACTIC-ACID BACTERIA; LISTERIA-MONOCYTOGENES; IN-VITRO; LANTIBIOTIC LACTICIN-3147; CLOSTRIDIUM-DIFFICILE; STREPTOCOCCUS-MUTANS;
D O I
10.1111/j.1751-7915.2010.00184.x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Nisin A is the most thoroughly investigated member of the lantibiotic family of antimicrobial peptides. In addition to a long history of safe use as a food antimicrobial, its activity against multi-drug resistant pathogens has resulted in a renewed interest in applying nisin as a chemotherapeutic to treat bacterial infections. The wealth of Nisin-related information that has been generated has also led to the development of the biotechnological capacity to engineer novel Nisin variants with a view to improving the function and physicochemical properties of this already potent peptide. However, the identification of bioengineered Nisin derivatives with enhanced antimicrobial activity against Gram-positive targets is a recent event. In this study, we created stable producers of the most promising derivatives of Nisin A generated to date [M21V (hereafter Nisin V) and K22T (hereafter Nisin T)] and assessed their potency against a range of drug-resistant clinical, veterinary and food pathogens. Nisin T exhibited increased activity against all veterinary isolates, including streptococci and staphylococci, and against a number of multi-drug resistant clinical isolates including MRSA, but not vancomycin-resistant enterococci. In contrast, Nisin V displayed increased potency against all targets tested including hVISA strains and the hyper-virulent Clostridium difficile ribotype 027 and against important food pathogens such as Listeria monocytogenes and Bacillus cereus. Significantly, this enhanced activity was validated in a model food system against L. monocytogenes. We conclude that Nisin V possesses significant potential as a novel preservative or chemotherapeutic compound.
引用
收藏
页码:473 / 486
页数:14
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