Purpose. The relationship between host microbiota and infective endocarditis (IE) has been investigated by few studies. We compared the oral, gut and skin microbiota profiles of patients awaiting heart valve replacement, both with and without IE, and correlated the profiles with the patients’ clinical data, including the aetiological agents and antibiotics received. Patients and Methods. Thirty-six patients were enrolled in a prospective, observational pilot study: 25 with IE (cases) and 11 with non-infective valve disease requiring surgery (controls). Clinical data and oral, faecal and skin samples were collected before surgical treatment. Microbiota was profiled using 16S rRNA amplicon sequencing. Results. Cases and controls were comparable, except for inflammatory parameters and prevalence of prosthetic valves, which were higher in cases. Causative IE pathogens were Staphylococcus spp., Streptococcus spp. and Enterococcus spp. Compared to controls, cases showed dysbiotic features in their oral, gut and skin microbiota, including lower diversity in oral and skin communities, and overall community depletion. Only a few bacteria were enriched, such as Oxalobacteraceae in the oral cavity and Bacteroides in the gut. There was low concordance between bacterial changes and blood isolates for most IE-causing pathogens, suggesting that dysbiosis may have effects beyond merely acting as a reservoir for specific pathogens. Conclusions. Dysbiosis may be a relevant yet under explored factor associated with IE. Further studies are needed to clarify the underlying pathogenetic mechanisms.
ORAL, GUT AND SKIN MICROBIOTA CHARACTERIZATION IN PATIENTS WITH HEART VALVE DISEASE WITH OR WITHOUT INFECTIVE ENDOCARDITIS: A PILOT STUDY / Boccia, Filomena. - (2025 Jan 24).
ORAL, GUT AND SKIN MICROBIOTA CHARACTERIZATION IN PATIENTS WITH HEART VALVE DISEASE WITH OR WITHOUT INFECTIVE ENDOCARDITIS: A PILOT STUDY
BOCCIA, FILOMENA
2025
Abstract
Purpose. The relationship between host microbiota and infective endocarditis (IE) has been investigated by few studies. We compared the oral, gut and skin microbiota profiles of patients awaiting heart valve replacement, both with and without IE, and correlated the profiles with the patients’ clinical data, including the aetiological agents and antibiotics received. Patients and Methods. Thirty-six patients were enrolled in a prospective, observational pilot study: 25 with IE (cases) and 11 with non-infective valve disease requiring surgery (controls). Clinical data and oral, faecal and skin samples were collected before surgical treatment. Microbiota was profiled using 16S rRNA amplicon sequencing. Results. Cases and controls were comparable, except for inflammatory parameters and prevalence of prosthetic valves, which were higher in cases. Causative IE pathogens were Staphylococcus spp., Streptococcus spp. and Enterococcus spp. Compared to controls, cases showed dysbiotic features in their oral, gut and skin microbiota, including lower diversity in oral and skin communities, and overall community depletion. Only a few bacteria were enriched, such as Oxalobacteraceae in the oral cavity and Bacteroides in the gut. There was low concordance between bacterial changes and blood isolates for most IE-causing pathogens, suggesting that dysbiosis may have effects beyond merely acting as a reservoir for specific pathogens. Conclusions. Dysbiosis may be a relevant yet under explored factor associated with IE. Further studies are needed to clarify the underlying pathogenetic mechanisms.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


