An Isolate of Streptococcus mitis Displayed In Vitro Antimicrobial Activity and Deleterious Effect in a Preclinical Model of Lung Infection.
Elliot MathieuQuentin MarquantFlorian ChainEdwige BouguyonVinciane Saint-CriqRonan Le GofficDelphyne DescampsPhilippe LangellaThomas A TompkinsSylvie BindaMuriel ThomasPublished in: Nutrients (2023)
Microbiota studies have dramatically increased over these last two decades, and the repertoire of microorganisms with potential health benefits has been considerably enlarged. The development of next generation probiotics from new bacterial candidates is a long-term strategy that may be more efficient and rapid with discriminative in vitro tests. Streptococcus strains have received attention regarding their antimicrobial potential against pathogens of the upper and, more recently, the lower respiratory tracts. Pathogenic bacterial strains, such as non-typable Haemophilus influenzae ( NTHi ), Pseudomonas aeruginosa ( P. aeruginosa ) and Staphylococcus aureus ( S. aureus ), are commonly associated with acute and chronic respiratory diseases, and it could be interesting to fight against pathogens with probiotics. In this study, we show that a Streptococcus mitis ( S. mitis ) EM-371 strain, isolated from the buccal cavity of a human newborn and previously selected for promising anti-inflammatory effects, displayed in vitro antimicrobial activity against NTHi , P. aeruginosa or S. aureus . However, the anti-pathogenic in vitro activity was not sufficient to predict an efficient protective effect in a preclinical model. Two weeks of treatment with S. mitis EM-371 did not protect against, and even exacerbated, NTHi lung infection.
Keyphrases
- biofilm formation
- staphylococcus aureus
- pseudomonas aeruginosa
- escherichia coli
- candida albicans
- human health
- endothelial cells
- public health
- healthcare
- cystic fibrosis
- liver failure
- gram negative
- mental health
- working memory
- methicillin resistant staphylococcus aureus
- respiratory failure
- antimicrobial resistance
- risk assessment
- respiratory tract
- induced pluripotent stem cells
- acinetobacter baumannii
- combination therapy
- hepatitis b virus
- replacement therapy
- bone marrow
- case control