4.6 Article

Ubericin K, a New Pore-Forming Bacteriocin Targeting mannose-PTS

期刊

MICROBIOLOGY SPECTRUM
卷 9, 期 2, 页码 -

出版社

AMER SOC MICROBIOLOGY
DOI: 10.1128/Spectrum.00299-21

关键词

bacteriocin; ubericin; mastitis; in vitro translation; pore formation; quorum sensing; pHluorin

资金

  1. Research Council of Norway [275190]
  2. National Centre for Research and Development [NOR/POLNOR/PrevEco/0021/2019-00]
  3. Norwegian Foundation for Research Levy on Agricultural Products (FFL)
  4. Norwegian Agricultural Agreement Research Fund (JA) [267623]
  5. JPIAMR grant from the Research Council of Norway [296906]

向作者/读者索取更多资源

Bovine mastitis infection in dairy cattle poses a significant economic burden globally, prompting the search for alternative treatments to reduce antibiotic usage. A novel bacteriocin, ubericin K, was discovered from a Streptococcus uberis strain in Norwegian bovine raw milk, showing potent antimicrobial activity. Whole-genome sequencing revealed a gene cluster encoding multiple bacteriocins, with ubericin K targeting bacteria causing mastitis by membrane disruption. The study suggests that ubericin K and the methodology employed could potentially aid in reducing antibiotic use in the dairy industry.
Bovine mastitis infection in dairy cattle is a significant economic burden for the dairy industry globally. To reduce the use of antibiotics in treatment of clinical mastitis, new alternative treatment options are needed. Antimicrobial peptides from bacteria, also known as bacteriocins, are potential alternatives for combating mastitis pathogens. In search of novel bacteriocins against mastitis pathogens, we screened samples of Norwegian bovine raw milk and found a Streptococcus uberis strain with potent antimicrobial activity toward Enterococcus, Streptococcus, Listeria, and Lactococcus. Whole-genome sequencing of the strain revealed a multibacteriocin gene cluster encoding one class IIb bacteriocin, two class IId bacteriocins, in addition to a three-component regulatory system and a dedicated ABC transporter. Isolation and purification of the antimicrobial activity from culture supernatants resulted in the detection of a 6.3-kDa mass peak by matrix-assisted laser desorption ionization-time of flight (MALDI-TOF) mass spectrometry, a mass corresponding to the predicted size of one of the class IId bacteriocins. The identification of this bacteriocin, called ubericin K, was further confirmed by in vitro protein synthesis, which showed the same inhibitory spectrum as the purified antimicrobial compound. Ubericin K shows highest sequence similarity to the class IId bacteriocins bovicin 255, lactococcin A, and garvieacin Q. We found that ubericin K uses the sugar transporter mannose phosphotransferase (PTS) as a target receptor. Further, by using the pHlourin sensor system to detect intracellular pH changes due to leakage across the membrane, ubericin K was shown to be a pore former, killing target cells by membrane disruption. IMPORTANCE Bacterial infections in dairy cows are a major burden to farmers worldwide because infected cows require expensive treatments and produce less milk. Today, infected cows are treated with antibiotics, a practice that is becoming less effective due to antibiotic resistance. Compounds other than antibiotics also exist that kill bacteria causing infections in cows; these compounds, known as bacteriocins, are natural products produced by other bacteria in the environment. In this work, we discover a new bacteriocin that we call ubericin K, which kills several species of bacteria known to cause infections in dairy cows. We also use in vitro synthesis as a novel method for rapidly characterizing bacteriocins directly from genomic data, which could be useful for other researchers. We believe that ubericin K and the methods described in this work will aid in the transition away from antibiotics in the dairy industry.

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