TY - JOUR
T1 - Unusual oral mucosal microbiota after hematopoietic cell transplantation with glycopeptide antibiotics
T2 - potential association with pathophysiology of oral mucositis
AU - Muro, Misato
AU - Soga, Yoshihiko
AU - Higuchi, Tomoko
AU - Kataoka, Kota
AU - Ekuni, Daisuke
AU - Maeda, Yoshinobu
AU - Morita, Manabu
N1 - Funding Information:
Funding This study was partly supported by a Grant-in-Aid from JSPS KAKENHI Grant Number JP26462881 (to Y.S.), a Grant-in-Aid for the COE projects by MEXT, Japan, entitled BCenter of excellence for molecular and gene targeting therapies with micro-dose molecular imaging modalities^ (to Y.S.), and a Grant-in-Aid for the COE projects by Ministry of Health, Labour and Welfare, Japan, entitled BDesignated regional hub hospital promoting hematopoietic stem cell transplantation^ (to M.M.).
Publisher Copyright:
© 2018, Institute of Microbiology, Academy of Sciences of the Czech Republic, v.v.i.
PY - 2018/9/1
Y1 - 2018/9/1
N2 - Severe oral mucositis occurs frequently in patients receiving hematopoietic stem cell transplantation (HCT). Oral mucosal bacteria can be associated with progression of oral mucositis, and systemic infection may occur via ulcerative oral mucositis. However, little information is available regarding the oral microbiota after HCT. Here, PCR-denaturing gradient gel electrophoresis (DGGE) was performed to characterize the oral mucosal microbiota, which can be affected by antibiotics, before and after HCT. Sixty reduced-intensity HCT patients were enrolled. Three patients with the least antibiotic use (quinolone prophylaxis and/or β-lactam monotherapy group) and three patients with the most antibiotic use (β-lactam-glycopeptide combination therapy group) were selected. Bacterial DNA samples obtained from the oral mucosa before and after HCT were subjected to PCR-DGGE. The trajectory of oral mucositis was evaluated. The oral mucosal microbiota in the β-lactam-glycopeptide combination therapy group was different from that in the quinolone prophylaxis and/or β-lactam monotherapy group, and Staphylococcus spp. and Enterococcus spp. were identified. Lautropia mirabilis was dominant in one patient. Ulcerative oral mucositis was observed only in the β-lactam-glycopeptide combination therapy group. In conclusion, especially with the use of strong antibiotics, such as glycopeptides, the oral mucosal microbiota differed completely from that under normal conditions and consisted of Staphylococcus spp., Enterococcus spp., and unexpectedly L. mirabilis. The normal oral microbiota consists not only of bacteria, but these unexpected bacteria could be involved in the pathophysiology as well as systemic infection via oral mucositis. Our results can be used as the basis for future studies in larger patient populations.
AB - Severe oral mucositis occurs frequently in patients receiving hematopoietic stem cell transplantation (HCT). Oral mucosal bacteria can be associated with progression of oral mucositis, and systemic infection may occur via ulcerative oral mucositis. However, little information is available regarding the oral microbiota after HCT. Here, PCR-denaturing gradient gel electrophoresis (DGGE) was performed to characterize the oral mucosal microbiota, which can be affected by antibiotics, before and after HCT. Sixty reduced-intensity HCT patients were enrolled. Three patients with the least antibiotic use (quinolone prophylaxis and/or β-lactam monotherapy group) and three patients with the most antibiotic use (β-lactam-glycopeptide combination therapy group) were selected. Bacterial DNA samples obtained from the oral mucosa before and after HCT were subjected to PCR-DGGE. The trajectory of oral mucositis was evaluated. The oral mucosal microbiota in the β-lactam-glycopeptide combination therapy group was different from that in the quinolone prophylaxis and/or β-lactam monotherapy group, and Staphylococcus spp. and Enterococcus spp. were identified. Lautropia mirabilis was dominant in one patient. Ulcerative oral mucositis was observed only in the β-lactam-glycopeptide combination therapy group. In conclusion, especially with the use of strong antibiotics, such as glycopeptides, the oral mucosal microbiota differed completely from that under normal conditions and consisted of Staphylococcus spp., Enterococcus spp., and unexpectedly L. mirabilis. The normal oral microbiota consists not only of bacteria, but these unexpected bacteria could be involved in the pathophysiology as well as systemic infection via oral mucositis. Our results can be used as the basis for future studies in larger patient populations.
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U2 - 10.1007/s12223-018-0596-1
DO - 10.1007/s12223-018-0596-1
M3 - Article
C2 - 29532421
AN - SCOPUS:85043514475
SN - 0015-5632
VL - 63
SP - 587
EP - 597
JO - Folia Microbiologica
JF - Folia Microbiologica
IS - 5
ER -