Cargando…
The microbiota of the bilio-pancreatic system: a cohort, STROBE-compliant study
Background: The gut microbiota play an essential role in protecting the host against pathogenic microorganisms by modulating immunity and regulating metabolic processes. In response to environmental factors, microbes can hugely alter their metabolism. These factors can substantially impact the host...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6578573/ https://www.ncbi.nlm.nih.gov/pubmed/31354308 http://dx.doi.org/10.2147/IDR.S200378 |
_version_ | 1783427857236623360 |
---|---|
author | Di Carlo, Paola Serra, Nicola D'Arpa, Francesco Agrusa, Antonino Gulotta, Gaspare Fasciana, Teresa Rodolico, Vito Giammanco, Anna Sergi, Consolato |
author_facet | Di Carlo, Paola Serra, Nicola D'Arpa, Francesco Agrusa, Antonino Gulotta, Gaspare Fasciana, Teresa Rodolico, Vito Giammanco, Anna Sergi, Consolato |
author_sort | Di Carlo, Paola |
collection | PubMed |
description | Background: The gut microbiota play an essential role in protecting the host against pathogenic microorganisms by modulating immunity and regulating metabolic processes. In response to environmental factors, microbes can hugely alter their metabolism. These factors can substantially impact the host and have potential pathologic implications. Particularly pathogenic microorganisms colonizing pancreas and biliary tract tissues may be involved in chronic inflammation and cancer evolution. Purpose: To evaluate the effect of bile microbiota on survival in patients with pancreas and biliary tract disease (PBD). Patients and Methods: We investigated 152 Italian patients with cholelithiasis (CHL), cholangitis (CHA), cholangiocarcinoma (CCA), gallbladder carcinoma (GBC), pancreas head carcinoma (PHC), ampullary carcinoma (ACA), and chronic pancreatitis (CHP). Demographics, bile cultures, therapy, and survival rates were analyzed in cohorts (T(1) death <6 months; T(2) death <12 months; T(3) death <18 months, T(3S) alive at 18 months). Results: The most common bacteria in T(1) were E. coli, K. pneumoniae, and P. aeruginosa. In T(2), the most common bacteria were E. coli and P. aeruginosa. In T(3), there were no significant bacteria isolated, while in T(3S) the most common bacteria were like those found in T(1). E. coli and K. pneumoniae were positive predictors of survival for PHC and ACA, respectively. E. coli, K. pneumoniae, and P. aeruginosa showed a high percentage of resistant bacteria to 3CGS, aminoglycosides class, and quinolone group especially at T(1) and T(2) in cancer patients. Conclusions: An unprecedented increase of E. coli in bile leads to a decrease in survival. We suggest that some strains isolated in bile samples may be considered within the group of risk factors in carcinogenesis and/or progression of hepato-biliary malignancy. A better understanding of bile microbiota in patients with PBD should lead to a multifaceted approach to rapidly detect and treat pathogens before patients enter the surgical setting in tandem with the implementation of the infection control policy. |
format | Online Article Text |
id | pubmed-6578573 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-65785732019-07-26 The microbiota of the bilio-pancreatic system: a cohort, STROBE-compliant study Di Carlo, Paola Serra, Nicola D'Arpa, Francesco Agrusa, Antonino Gulotta, Gaspare Fasciana, Teresa Rodolico, Vito Giammanco, Anna Sergi, Consolato Infect Drug Resist Original Research Background: The gut microbiota play an essential role in protecting the host against pathogenic microorganisms by modulating immunity and regulating metabolic processes. In response to environmental factors, microbes can hugely alter their metabolism. These factors can substantially impact the host and have potential pathologic implications. Particularly pathogenic microorganisms colonizing pancreas and biliary tract tissues may be involved in chronic inflammation and cancer evolution. Purpose: To evaluate the effect of bile microbiota on survival in patients with pancreas and biliary tract disease (PBD). Patients and Methods: We investigated 152 Italian patients with cholelithiasis (CHL), cholangitis (CHA), cholangiocarcinoma (CCA), gallbladder carcinoma (GBC), pancreas head carcinoma (PHC), ampullary carcinoma (ACA), and chronic pancreatitis (CHP). Demographics, bile cultures, therapy, and survival rates were analyzed in cohorts (T(1) death <6 months; T(2) death <12 months; T(3) death <18 months, T(3S) alive at 18 months). Results: The most common bacteria in T(1) were E. coli, K. pneumoniae, and P. aeruginosa. In T(2), the most common bacteria were E. coli and P. aeruginosa. In T(3), there were no significant bacteria isolated, while in T(3S) the most common bacteria were like those found in T(1). E. coli and K. pneumoniae were positive predictors of survival for PHC and ACA, respectively. E. coli, K. pneumoniae, and P. aeruginosa showed a high percentage of resistant bacteria to 3CGS, aminoglycosides class, and quinolone group especially at T(1) and T(2) in cancer patients. Conclusions: An unprecedented increase of E. coli in bile leads to a decrease in survival. We suggest that some strains isolated in bile samples may be considered within the group of risk factors in carcinogenesis and/or progression of hepato-biliary malignancy. A better understanding of bile microbiota in patients with PBD should lead to a multifaceted approach to rapidly detect and treat pathogens before patients enter the surgical setting in tandem with the implementation of the infection control policy. Dove 2019-06-11 /pmc/articles/PMC6578573/ /pubmed/31354308 http://dx.doi.org/10.2147/IDR.S200378 Text en © 2019 Di Carlo et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Di Carlo, Paola Serra, Nicola D'Arpa, Francesco Agrusa, Antonino Gulotta, Gaspare Fasciana, Teresa Rodolico, Vito Giammanco, Anna Sergi, Consolato The microbiota of the bilio-pancreatic system: a cohort, STROBE-compliant study |
title | The microbiota of the bilio-pancreatic system: a cohort, STROBE-compliant study |
title_full | The microbiota of the bilio-pancreatic system: a cohort, STROBE-compliant study |
title_fullStr | The microbiota of the bilio-pancreatic system: a cohort, STROBE-compliant study |
title_full_unstemmed | The microbiota of the bilio-pancreatic system: a cohort, STROBE-compliant study |
title_short | The microbiota of the bilio-pancreatic system: a cohort, STROBE-compliant study |
title_sort | microbiota of the bilio-pancreatic system: a cohort, strobe-compliant study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6578573/ https://www.ncbi.nlm.nih.gov/pubmed/31354308 http://dx.doi.org/10.2147/IDR.S200378 |
work_keys_str_mv | AT dicarlopaola themicrobiotaofthebiliopancreaticsystemacohortstrobecompliantstudy AT serranicola themicrobiotaofthebiliopancreaticsystemacohortstrobecompliantstudy AT darpafrancesco themicrobiotaofthebiliopancreaticsystemacohortstrobecompliantstudy AT agrusaantonino themicrobiotaofthebiliopancreaticsystemacohortstrobecompliantstudy AT gulottagaspare themicrobiotaofthebiliopancreaticsystemacohortstrobecompliantstudy AT fascianateresa themicrobiotaofthebiliopancreaticsystemacohortstrobecompliantstudy AT rodolicovito themicrobiotaofthebiliopancreaticsystemacohortstrobecompliantstudy AT giammancoanna themicrobiotaofthebiliopancreaticsystemacohortstrobecompliantstudy AT sergiconsolato themicrobiotaofthebiliopancreaticsystemacohortstrobecompliantstudy AT dicarlopaola microbiotaofthebiliopancreaticsystemacohortstrobecompliantstudy AT serranicola microbiotaofthebiliopancreaticsystemacohortstrobecompliantstudy AT darpafrancesco microbiotaofthebiliopancreaticsystemacohortstrobecompliantstudy AT agrusaantonino microbiotaofthebiliopancreaticsystemacohortstrobecompliantstudy AT gulottagaspare microbiotaofthebiliopancreaticsystemacohortstrobecompliantstudy AT fascianateresa microbiotaofthebiliopancreaticsystemacohortstrobecompliantstudy AT rodolicovito microbiotaofthebiliopancreaticsystemacohortstrobecompliantstudy AT giammancoanna microbiotaofthebiliopancreaticsystemacohortstrobecompliantstudy AT sergiconsolato microbiotaofthebiliopancreaticsystemacohortstrobecompliantstudy |