| Project/Area Number |
21592271
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (C)
|
| Allocation Type | Single-year Grants |
|---|
| Section | 一般 |
|---|
| Research Field |
Pediatric surgery
|
|---|
| Research Institution | Hokkaido University |
|---|
Principal Investigator |
OKADA Tadao 北海道大学, 北海道大学病院, 講師 (30344469)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
SASAKI Fumiaki 北海道大学, 大学院・医学研究科, 教授 (40178661)
OZAKI Michitaka 北海道大学, 大学院・医学研究科, 特任教授 (80256510)
|
|---|
| Project Period (FY) |
2009 – 2011
|
| Project Status |
Completed (Fiscal Year 2011)
|
| Budget Amount *help |
¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Fiscal Year 2011: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2010: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2009: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
|
|---|
| Keywords | 迅速遺伝子解析 / 細菌プロファイル / T-RFLP法 / 16S-rRNA / 胆道閉鎖症 / 胆管炎 / 糞便 / バイオロジカル・マーカー / 細菌プロファイリング / バイオロジカルマーカー |
|---|
| Research Abstract |
Molecular methods utilizing broad-range primers for 16S rDNA(ribosomal RNA gene) PCR and sequencing have been evaluated for their utility in diagnostic bacteriology. First, microbiota in fecal content from BA individual with recurrent cholangitis was compared using 16S rRNA gene libraries and terminal restriction fragment length polymorphism(T-RFLP). Second, microbiota in fecal content from choledochal cyst(CC) and biliary atresia(BA) individuals at the operation were compared using 16S rRNA gene libraries and T-RFLP As the results, any bile microbiota(bacterial DNA) was not detected using PCR in CC and BA patients. Bacterial DNA showed marked differences in the composition of fecal microbiota in a BA infant with recurrent cholangitis. Molecular analysis of colonic microbiota using 16S rRNA gene libraries and T-RFLP might be useful to detect BA cholangitis more earlier. Bacterial DNA showed marked differences in the composition of fecal microbiota in CC and BA infants. The microbiota consisted of microbial communities of Bifidobacterium, Lactobacillales, Bacteroides, Prevotella, Clostridium clusters IV, XI, and XVIII, and Clostridium subcluster XIVa. The Bifidobacterium, Bacteroides, and Clostridium clusters were detected predominatly in CC than BA group. Lactobacillales was most predominat group in BA feces. Molecular analysis of colonic microbiota using 16S rRNA gene libraries and T-RFLP might be useful to differentiate CC from BA.
|
