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Lasting Gammaproteobacteria profile changes characterized hematological cancer patients who developed oral mucositis following conditioning therapy.
Mougeot, Jean-Luc C; Beckman, Micaela F; Stevens, Craig B; Almon, Kathryn G; Morton, Darla S; Von Bültzingslöwen, Inger; Brennan, Michael T; Mougeot, Farah Bahrani.
Affiliation
  • Mougeot JC; Department of Oral Medicine, Carolinas Medical Center-Atrium Health, Charlotte, NC, USA.
  • Beckman MF; Department of Oral Medicine, Carolinas Medical Center-Atrium Health, Charlotte, NC, USA.
  • Stevens CB; Department of Oral Medicine, Carolinas Medical Center-Atrium Health, Charlotte, NC, USA.
  • Almon KG; Department of Oral Medicine, Carolinas Medical Center-Atrium Health, Charlotte, NC, USA.
  • Morton DS; Department of Oral Medicine, Carolinas Medical Center-Atrium Health, Charlotte, NC, USA.
  • Von Bültzingslöwen I; Institute of Odontology, Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
  • Brennan MT; Department of Oral Medicine, Carolinas Medical Center-Atrium Health, Charlotte, NC, USA.
  • Mougeot FB; Department of Oral Medicine, Carolinas Medical Center-Atrium Health, Charlotte, NC, USA.
J Oral Microbiol ; 12(1): 1761135, 2020.
Article in En | MEDLINE | ID: mdl-32537095
ABSTRACT

Background:

Oral mucositis (OM) is a common side effect of conditioning therapy implemented before hematopoietic stem cell transplantation (HSCT). The role of oral microbiome in OM is not fully elucidated.

Objective:

To determine oral microbiome profile changes post-conditioning in HSCT patients who developed moderate OM, or mild to no OM.

Design:

Patient groups were Muc0-1 with OM-score = 0-1 (43 paired samples) and Muc2 with WHO OM-score = 2 (36 paired samples). Bacterial DNA was isolated from oral samples (saliva, swabs of buccal mucosa, tongue, and supragingival plaque) at pre-conditioning (T 0 ), post-conditioning mucositis onset (T Muc ), and one-year post-conditioning (T Year ). 16S-rRNA gene next-generation sequencing was used to determine the relative abundance (RA) of >700 oral species. Alpha-diversity, beta-diversity and linear discriminant analyses (LDA) were performed Muc2 versus Muc0-1.

Results:

Muc2 oral microbiome alpha- and beta-diversity differed between T 0 and T Muc . Muc2 alpha-diversity and Muc0-1 beta-diversity did not differ between T 0 and T Year . T 0 to T Muc LDA scores were significant in Muc2 for Gammaproteobacteria. For Muc2 patients, the average RA decreased for Haemophilus parainfluenza, a species known as mucosal surfaces protector, but increased for Escherichia-Shigella genera.

Conclusions:

Post-conditioning OM might contribute to long-term oral microbiome changes affecting Gammaproteobacteria, in HSCT patients.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Oral Microbiol Year: 2020 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Oral Microbiol Year: 2020 Document type: Article Affiliation country: Estados Unidos