Potential ProbioticEscherichia coli16 Harboring theVitreoscillaHemoglobin Gene Improves Gastrointestinal Tract Colonization and Ameliorates Carbon Tetrachloride Induced Hepatotoxicity in Rats
Author(s) -
Prasant Kumar,
Ayush Ranawade,
Naresh Kumar
Publication year - 2014
Publication title -
biomed research international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.772
H-Index - 126
eISSN - 2314-6141
pISSN - 2314-6133
DOI - 10.1155/2014/213574
Subject(s) - colonization , escherichia coli , carbon tetrachloride , probiotic , gastrointestinal tract , microbiology and biotechnology , hemoglobin , gene , escherichia , biology , chemistry , bacteria , biochemistry , genetics , organic chemistry
The present study describes the beneficial effects of potential probiotic E. coli 16 (pUC8:16 gfp ) expressing Vitreoscilla hemoglobin ( vgb ) gene, associated with bacterial respiration under microaerobic condition, on gastrointestinal (GI) colonization and its antioxidant activity on carbon tetrachloride (CCl 4 ) induced toxicity in Charles Foster rats. In vitro , catalase activity in E. coli 16 (pUC8:16 gfp ) was 1.8 times higher compared to E. coli 16 (pUC- gfp ) control. In vivo , E. coli 16 (pUC8:16 gfp ) not only was recovered in the fecal matter after 70 days of oral administration but also retained antibacterial activities, whereas E. coli 16 (pUC- gfp ) was not detected. Oral administration of 200 and 500 μ L/kg body weight of CCl 4 to rats at weekly interval resulted in elevated serum glutamyl pyruvate transaminase (SGPT) and serum glutamyl oxalacetate transaminase (SGOT) levels compared to controls. Rats prefed with E. coli 16 (pUC8:16 gfp ) demonstrated near to normal levels for SGPT and SGOT, whereas the liver homogenate catalase activity was significantly increased compared to CCl 4 treated rats. Thus, pUC8:16 gfp plasmid encoding vgb improved the growth and GI tract colonization of E. coli 16. In addition, it also enhanced catalase activity in rats harboring E. coli 16 (pUC8:16 gfp ), thereby preventing the absorption of CCl 4 to GI tract.
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