TY - JOUR
T1 - Mucosal dysbiosis in patients with gastrointestinal follicular lymphoma
AU - Zeze, Keizo
AU - Hirano, Atsushi
AU - Torisu, Takehiro
AU - Esaki, Motohiro
AU - Shibata, Hiroki
AU - Moriyama, Tomohiko
AU - Umeno, Junji
AU - Fujioka, Shin
AU - Okamoto, Yasuharu
AU - Fuyuno, Yuta
AU - Matsuno, Yuichi
AU - Kitazono, Takanari
N1 - Publisher Copyright:
© 2020 John Wiley & Sons Ltd
PY - 2020/4/1
Y1 - 2020/4/1
N2 - Because the pathogenesis of gastrointestinal follicular lymphoma (GI-FL) remains unclear, no standardized treatment strategy has been established. Of the gastrointestinal lymphomas, gastric mucosa-associated lymphoid tissue lymphomas are strongly associated with Helicobacter pylori; hence, the microbiota may be involved in GI-FL pathogenesis. However, the association between GI-FL and the microbiota remains uninvestigated. Therefore, we compared the mucosal microbiotas of GI-FL patients with those of controls to identify microbiota changes in GI-FL patients. Mucosal biopsy samples were obtained from the second portion of the duodenum from 20 GI-FL patients with duodenal lesions and 20 controls. Subsequent 16S rRNA gene sequencing was performed on these samples. QIIME pipeline and LEfSe software were used to analyze the microbiota. The GI-FL patients had significantly lower alpha diversity (P =.049) than did the controls, with significant differences in the microbial composition (P =.023) evaluated by the beta diversity metrics between the two groups. Comparing the taxonomic compositions indicated that the genera Sporomusa, Rothia, and Prevotella and the family Gemellaceae were significantly less abundant in the GI-FL patients than in the controls. GI-FL patients presented altered duodenal mucosal microbial compositions, suggesting that the microbiota might be involved in the GI-FL pathogenesis.
AB - Because the pathogenesis of gastrointestinal follicular lymphoma (GI-FL) remains unclear, no standardized treatment strategy has been established. Of the gastrointestinal lymphomas, gastric mucosa-associated lymphoid tissue lymphomas are strongly associated with Helicobacter pylori; hence, the microbiota may be involved in GI-FL pathogenesis. However, the association between GI-FL and the microbiota remains uninvestigated. Therefore, we compared the mucosal microbiotas of GI-FL patients with those of controls to identify microbiota changes in GI-FL patients. Mucosal biopsy samples were obtained from the second portion of the duodenum from 20 GI-FL patients with duodenal lesions and 20 controls. Subsequent 16S rRNA gene sequencing was performed on these samples. QIIME pipeline and LEfSe software were used to analyze the microbiota. The GI-FL patients had significantly lower alpha diversity (P =.049) than did the controls, with significant differences in the microbial composition (P =.023) evaluated by the beta diversity metrics between the two groups. Comparing the taxonomic compositions indicated that the genera Sporomusa, Rothia, and Prevotella and the family Gemellaceae were significantly less abundant in the GI-FL patients than in the controls. GI-FL patients presented altered duodenal mucosal microbial compositions, suggesting that the microbiota might be involved in the GI-FL pathogenesis.
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U2 - 10.1002/hon.2717
DO - 10.1002/hon.2717
M3 - Article
C2 - 31990065
AN - SCOPUS:85078914660
SN - 0278-0232
VL - 38
SP - 181
EP - 188
JO - Hematological Oncology
JF - Hematological Oncology
IS - 2
ER -