Minimally Age-Dependent Gut Microbial Signatures in Pancreatic Neoplasia Identified by qPCR Targeting the but Gene
Tadashi Fujii *
Department of Gastroenterology and Hepatology, Fujita Health University School of Medicine, Toyoake, Aichi 470-1192, Japan, Department of Medical Research on Prebiotics and Probiotics, Fujita Health University, Toyoake, Aichi, Japan and BIOSIS Lab. Co., Ltd., Toyoake, Aichi, Japan.
Eizaburo Ohno
Department of Gastroenterology and Hepatology, Fujita Health University School of Medicine, Toyoake, Aichi 470-1192, Japan.
Yoshiki Hirooka
Department of Gastroenterology and Hepatology, Fujita Health University School of Medicine, Toyoake, Aichi 470-1192, Japan, Department of Medical Research on Prebiotics and Probiotics, Fujita Health University, Toyoake, Aichi, Japan and BIOSIS Lab. Co., Ltd., Toyoake, Aichi, Japan.
Takumi Tochio
Department of Gastroenterology and Hepatology, Fujita Health University School of Medicine, Toyoake, Aichi 470-1192, Japan, Department of Medical Research on Prebiotics and Probiotics, Fujita Health University, Toyoake, Aichi, Japan and BIOSIS Lab. Co., Ltd., Toyoake, Aichi, Japan.
*Author to whom correspondence should be addressed.
Abstract
Background & Aims: Age-related variation in the gut microbiota complicates biomarker discovery for pancreatic cancer. This study aimed to identify microbial taxa with minimal age dependence that are associated with pancreatic neoplasia and to develop a practical quantitative PCR (qPCR)-based assay targeting a shared gene involved in butyrate production.
Study design: Cross-sectional study.
Place and Duration of Study: Department of Gastroenterology and Hepatology, Fujita Health University, Toyoake, Japan, between October 2022 and July 2025.
Methodology: Fecal samples from 64 individuals with precursor lesions considered to be at high risk for pancreatic cancer (HR) and 22 patients with pancreatic cancer (PC) were compared with those from healthy controls aged <50 years (Young; n = 71) and ≥50 years (Old; n = 65). Microbiota composition was analyzed by 16S rRNA gene sequencing. A qPCR primer set targeting the but gene, which encodes butyryl-CoA:acetate CoA-transferase, was designed to evaluate the shared genetic potential of the identified minimally age-dependent taxa, namely the Anaerostipes hadrus group and Agathobacter rectalis.
Results: The A. hadrus group and A. rectalis showed disease-associated depletion with minimal age dependency. The qPCR assay showed no difference in but gene levels between the Young and Old groups (P = 0.3301). but gene levels in the HR group were comparable to those in the Old group (P > 0.9999), whereas levels in the PC group were significantly lower than those in the Old group (P = 0.0020) and the HR group (P = 0.0136).
Conclusion: Targeting the but gene provides a practical approach to assessing the shared butyrate-producing potential of this minimally age-dependent microbial cluster. Within this cross-sectional cohort, but gene levels were preserved in HR individuals, whereas levels in the PC group were reduced, suggesting its potential utility as a non-invasive adjunct for future evaluation in longitudinal monitoring or risk assessment after prospective validation.
Keywords: Ageing, but gene, butyrate, gut microbiota, IPMN, microbial gene marker, pancreatic cancer, quantitative PCR