2015 Fiscal Year Final Research Report
To clarify why the stability of CDT-I prophage is different between Escherichia coli belonging to different O serogroups
Project/Area Number |
25860323
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Bacteriology (including mycology)
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Research Institution | Osaka Prefecture University |
Principal Investigator |
Atsushi Hinenoya 大阪府立大学, 生命環境科学研究科(系), 助教 (20548490)
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Project Period (FY) |
2013-04-01 – 2016-03-31
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Keywords | CDT / 大腸菌 / ファージ / spontaneous induction |
Outline of Final Research Achievements |
Cytolethal distending toxin (CDT-I) produced by Escherichia coli is encoded on lambdoid phage, and its phage induction is associated with the toxin production. We found that the induction level of CDT-I phage is different among the strains, and correlated with O serogroup of host E. coli including O127 and O142. The present study tried to identify the host factor which regulate CDT-I phage induction. Finally although we could not identify it during this research period, new findings could be obtained: (1) CDT-I phage induction is occurred in a RecA dependent pathway, and (2) intra-prophage interaction could be involved in the different CDT-I phage induction between CDT-I-producing E. coli O serogroups O127 and O142.
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Free Research Field |
細菌学
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