TY - JOUR
T1 - Fecal Microbiome Among Nursing Home Residents with Advanced Dementia and Clostridium difficile
AU - Araos, Rafael
AU - Andreatos, Nikolaos
AU - Ugalde, Juan
AU - Mitchell, Susan
AU - Mylonakis, Eleftherios
AU - D’Agata, Erika M.C.
N1 - Publisher Copyright:
© 2018, Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2018/3/28
Y1 - 2018/3/28
N2 - Background/Objectives: Patients colonized with toxinogenic strains of Clostridium difficile have an increased risk of subsequent infection. Given the potential role of the gut microbiome in increasing the risk of C. difficile colonization, we assessed the diversity and composition of the gut microbiota among long-term care facility (LTCF) residents with advanced dementia colonized with C. difficile. Design: Retrospective analysis of rectal samples collected during a prospective observational study. Setting: Thirty-five nursing homes in Boston, Massachusetts. Participants: Eighty-seven LTCF residents with advanced dementia. Measurements: Operational taxonomic units were identified using 16S rRNA sequencing. Samples positive for C. difficile were matched to negative controls in a 1:3 ratio and assessed for differences in alpha diversity, beta diversity, and differentially abundant features. Results: Clostridium difficile sequence variants were identified among 7/87 (8.04%) residents. No patient had evidence of C. difficile infection. Demographic characteristics and antimicrobial exposure were similar between the seven cases and 21 controls. The overall biodiversity among cases and controls was reduced with a median Shannon index of 3.2 (interquartile range 2.7–3.9), with no statistically significant differences between groups. The bacterial community structure was significantly different among residents with C. difficile colonization versus those without and included a predominance of Akkermansia spp., Dermabacter spp., Romboutsia spp., Meiothermus spp., Peptoclostridium spp., and Ruminococcaceae UGC 009. Conclusion: LTCF residents with advanced dementia have substantial dysbiosis of their gut microbiome. Specific taxa characterized C. difficile colonization status.
AB - Background/Objectives: Patients colonized with toxinogenic strains of Clostridium difficile have an increased risk of subsequent infection. Given the potential role of the gut microbiome in increasing the risk of C. difficile colonization, we assessed the diversity and composition of the gut microbiota among long-term care facility (LTCF) residents with advanced dementia colonized with C. difficile. Design: Retrospective analysis of rectal samples collected during a prospective observational study. Setting: Thirty-five nursing homes in Boston, Massachusetts. Participants: Eighty-seven LTCF residents with advanced dementia. Measurements: Operational taxonomic units were identified using 16S rRNA sequencing. Samples positive for C. difficile were matched to negative controls in a 1:3 ratio and assessed for differences in alpha diversity, beta diversity, and differentially abundant features. Results: Clostridium difficile sequence variants were identified among 7/87 (8.04%) residents. No patient had evidence of C. difficile infection. Demographic characteristics and antimicrobial exposure were similar between the seven cases and 21 controls. The overall biodiversity among cases and controls was reduced with a median Shannon index of 3.2 (interquartile range 2.7–3.9), with no statistically significant differences between groups. The bacterial community structure was significantly different among residents with C. difficile colonization versus those without and included a predominance of Akkermansia spp., Dermabacter spp., Romboutsia spp., Meiothermus spp., Peptoclostridium spp., and Ruminococcaceae UGC 009. Conclusion: LTCF residents with advanced dementia have substantial dysbiosis of their gut microbiome. Specific taxa characterized C. difficile colonization status.
KW - Advanced dementia
KW - Clostridium difficile
KW - Colonization
KW - Microbiome
UR - http://www.scopus.com/inward/record.url?scp=85044444834&partnerID=8YFLogxK
U2 - 10.1007/s10620-018-5030-7
DO - 10.1007/s10620-018-5030-7
M3 - Article
AN - SCOPUS:85044444834
SN - 0163-2116
VL - 63
SP - 1
EP - 7
JO - Digestive Diseases and Sciences
JF - Digestive Diseases and Sciences
IS - 6
ER -