Pseudocin 196, a novel lantibiotic produced by Bifidobacterium pseudocatenulatum elicits antimicrobial activity against clinically relevant pathogens.
Rocio Sanchez-GallardoPaula M O'ConnorIan J O'NeillBrian McDonnellCiaran M LeeRebecca L MooreFionnuala M McauliffePaul D CotterDouwe van SinderenPublished in: Gut microbes (2024)
Bacteriocins are broad or narrow-spectrum antimicrobial compounds that have received significant scientific attention due to their potential to treat infections caused by antibiotic-resistant pathogenic bacteria. The genome of Bifidobacterium pseudocatenulatum MM0196, an antimicrobial-producing, fecal isolate from a healthy pregnant woman, was shown to contain a gene cluster predicted to encode Pseudocin 196, a novel lantibiotic, in addition to proteins involved in its processing, transport and immunity. Following antimicrobial assessment against various indicator strains, protease-sensitive Pseudocin 196 was purified to homogeneity from cell-free supernatant. MALDI TOF mass spectrometry confirmed that the purified antimicrobial compound corresponds to a molecular mass of 2679 Da, which is consistent with that deduced from its genetic origin. Pseudocin 196 is classified as a lantibiotic based on its similarity to lacticin 481, a lanthionine ring-containing lantibiotic produced by Lactococcus lactis . Pseudocin 196, the first reported bacteriocin produced by a B. pseudocatenulatum species of human origin, was shown to inhibit clinically relevant pathogens, such as Clostridium spp. and Streptococcus spp. thereby highlighting the potential application of this strain as a probiotic to treat and prevent bacterial infections.
Keyphrases
- mass spectrometry
- cell free
- staphylococcus aureus
- genome wide
- liquid chromatography
- endothelial cells
- escherichia coli
- antimicrobial resistance
- high resolution
- high performance liquid chromatography
- biofilm formation
- ms ms
- working memory
- capillary electrophoresis
- dna methylation
- circulating tumor
- induced pluripotent stem cells
- single molecule
- cystic fibrosis
- resting state
- tandem mass spectrometry
- genetic diversity