4.7 Article

Bio-Engineered Nisin with Increased Anti-Staphylococcus and Selectively Reduced Anti-Lactococcus Activity for Treatment of Bovine Mastitis

期刊

出版社

MDPI
DOI: 10.3390/ijms22073480

关键词

antimicrobial; lantibiotic; bacteriocin; peptide engineering; nisin; bovine mastitis; staphylococci; S; aureus

资金

  1. Pfizer Animal Health
  2. Irish Government under the National Development Plan through a Science Foundation Ireland (SFI) Technology and Innovation Development Award (TIDA) [14/TIDA/2286]
  3. SFI Investigator awards [10/IN.1/B3027]
  4. SFI-PI fund [11/PI/1137]
  5. APC Microbiome Ireland [SFI/12/RC/2273, SFI/12/RC/2273 P2]
  6. Science Foundation Ireland (SFI) [14/TIDA/2286] Funding Source: Science Foundation Ireland (SFI)

向作者/读者索取更多资源

This article discusses the application and improvement of nisin in the treatment of bovine mastitis. Through bioengineering strategies, the specific activity of nisin against pathogens has been enhanced, and three nisin derivatives with improved activity have been proposed.
Bovine mastitis is a significant economic burden for dairy enterprises, responsible for premature culling, prophylactic and therapeutic antibiotic use, reduced milk production and the withholding (and thus wastage) of milk. There is a desire to identify novel antimicrobials that are expressly directed to veterinary applications, do not require a lengthy milk withholding period and that will not have a negative impact on the growth of lactic acid bacteria involved in downstream dairy fermentations. Nisin is the prototypical lantibiotic, a family of highly modified antimicrobial peptides that exhibit potent antimicrobial activity against many Gram-positive microbes, including human and animal pathogens including species of Staphylococcus and Streptococcus. Although not yet utilized in the area of human medicine, nisin is currently applied as the active agent in products designed to prevent bovine mastitis. Over the last decade, we have harnessed bioengineering strategies to boost the specific activity and target spectrum of nisin against several problematic microorganisms. Here, we screen a large bank of engineered nisin derivatives to identify novel derivatives that exhibit improved specific activity against a selection of staphylococci, including mastitis-associated strains, but have unchanged or reduced activity against dairy lactococci. Three such peptides were identified; nisin A M17Q, nisin A T2L and nisin A HTK.

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