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Fecal Microbiota of Toxigenic -Associated Diarrhea

Overview
Journal Front Microbiol
Specialty Microbiology
Date 2019 Jan 31
PMID 30697203
Citations 21
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Abstract

infection (CDI) is currently one of the most important causes of infectious diarrhea in developed countries and the main cause in healthcare settings. Here, we characterized the gut microbiota from the feces of 57 patients with diarrhea from nosocomial and community-acquired CDI. We performed an ecological analysis by high-throughput sequencing of the V3-V4 region of 16S rRNA amplicons and evaluated the association of the various ecological profiles with CDI risk factors. Among all samples 31.01%, 9.82%, 9.33%, 6,16%, and 5.64%, were the most abundant families. A reduced abundance of was associated with a poor CDI prognosis, with severe diarrhea and a high incidence of recurrence. This reduction was associated with a weakened host immune system and previous aggressive antibiotherapy. family was 1.56% overall and within the family the only identified member was the genus , positively correlated with the presence of that may be predictive of the presence of a CDI. Finally, a relevant aspect that must be considered in clinical practice is the misdiagnosis of CDI, as patients with a stool sample that tests positive for are usually diagnosed with CDI and subsequently treated as such. However, co-infection with other pathogenic agents often plays an important role in the development of diarrhea, and must be considered when prescribing antibiotic treatment.

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References
1.
Callahan B, McMurdie P, Holmes S . Exact sequence variants should replace operational taxonomic units in marker-gene data analysis. ISME J. 2017; 11(12):2639-2643. PMC: 5702726. DOI: 10.1038/ismej.2017.119. View

2.
Pruesse E, Quast C, Knittel K, Fuchs B, Ludwig W, Peplies J . SILVA: a comprehensive online resource for quality checked and aligned ribosomal RNA sequence data compatible with ARB. Nucleic Acids Res. 2007; 35(21):7188-96. PMC: 2175337. DOI: 10.1093/nar/gkm864. View

3.
Lagier J, Million M, Hugon P, Armougom F, Raoult D . Human gut microbiota: repertoire and variations. Front Cell Infect Microbiol. 2012; 2:136. PMC: 3487222. DOI: 10.3389/fcimb.2012.00136. View

4.
Juul F, Garborg K, Bretthauer M, Skudal H, Oines M, Wiig H . Fecal Microbiota Transplantation for Primary Clostridium difficile Infection. N Engl J Med. 2018; 378(26):2535-2536. DOI: 10.1056/NEJMc1803103. View

5.
Smits W, Lyras D, Lacy D, Wilcox M, Kuijper E . Clostridium difficile infection. Nat Rev Dis Primers. 2016; 2:16020. PMC: 5453186. DOI: 10.1038/nrdp.2016.20. View