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Absence of a pancreatic microbiome in intraductal papillary mucinous neoplasm.
Pust, Marie-Madlen; Rocha Castellanos, Darío Missael; Rzasa, Kara; Dame, Andrea; Pishchany, Gleb; Assawasirisin, Charnwit; Liss, Andrew; Fernandez-Del Castillo, Carlos; Xavier, Ramnik J.
Afiliação
  • Pust MM; Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA xavier@molbio.mgh.harvard.edu mpust@mgh.harvard.edu cfernandez@mgh.harvard.edu.
  • Rocha Castellanos DM; Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.
  • Rzasa K; Center for Computational and Integrative Biology, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Dame A; Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Pishchany G; Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.
  • Assawasirisin C; Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.
  • Liss A; Broad Institute of MIT and Harvard, Cambridge, Massachusetts, USA.
  • Fernandez-Del Castillo C; Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, Massachusetts, USA.
  • Xavier RJ; Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Gut ; 73(7): 1131-1141, 2024 Jun 06.
Article em En | MEDLINE | ID: mdl-38429112
ABSTRACT

OBJECTIVE:

This study aims to validate the existence of a microbiome within intraductal papillary mucinous neoplasm (IPMN) that can be differentiated from the taxonomically diverse DNA background of next-generation sequencing procedures.

DESIGN:

We generated 16S rRNA amplicon sequencing data to analyse 338 cyst fluid samples from 190 patients and 19 negative controls, the latter collected directly from sterile syringes in the operating room. A subset of samples (n=20) and blanks (n=5) were spiked with known concentrations of bacterial cells alien to the human microbiome to infer absolute abundances of microbial traces. All cyst fluid samples were obtained intraoperatively and included IPMNs with various degrees of dysplasia as well as other cystic neoplasms. Follow-up culturing experiments were conducted to assess bacterial growth for microbiologically significant signals.

RESULTS:

Microbiome signatures of cyst fluid samples were inseparable from those of negative controls, with no difference in taxonomic diversity, and microbial community composition. In a patient subgroup that had recently undergone invasive procedures, a bacterial signal was evident. This outlier signal was not characterised by higher taxonomic diversity but by an increased dominance index of a gut-associated microbe, leading to lower taxonomic evenness compared with the background signal.

CONCLUSION:

The 'microbiome' of IPMNs and other pancreatic cystic neoplasms does not deviate from the background signature of negative controls, supporting the concept of a sterile environment. Outlier signals may appear in a small fraction of patients following recent invasive endoscopic procedures. No associations between microbial patterns and clinical or cyst parameters were apparent.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / RNA Ribossômico 16S / Microbiota / Neoplasias Intraductais Pancreáticas Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Pancreáticas / RNA Ribossômico 16S / Microbiota / Neoplasias Intraductais Pancreáticas Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article