Journal of Southern Medical University ›› 2014, Vol. 34 ›› Issue (09): 1241-.
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Abstract: Objective To explore the relationship between Helicobacter pylori (H. pylori) infection and lower esophageal diseasesin light of the changes of the bacterial flora in the lower esophagus. Methods Thirty BALB/C mice were randomized intonegative control group and H. pylori infection group, and in the latter group, the mice were subjected to intragastricadministration of solution containing H. pylori. After 4 weeks of administration, all the mice were sacrificed, and the V6 areasin 16S rDNA were amplified from the bacterial DNA extracted from the lower esophagus using polymerase chainreaction-denaturing gradient gel electrophoresis. The bacterial floras were analyzed on DGGE atlas with Quantity-One 1-Danalysis software, and the differential bands between the two groups were amplified using a 16S rDNA v6 area primerfollowed by DNA sequencing and BLAST analysis. Results DGGE finger-prints showed a significantly greater number of DNAbands in the infection group than in the negative control group (P<0.01). The diversity index and richness index were alsosignificantly higher in the infection group (0.01<P<0.05). Bacterium cluster class analysis well separated the dendrogram in theinfection group. Principal component analysis showed that different groups of bacteria gathered in different locations, andBLAST analysis revealed the presence of special bacteria in the infection group. Conclusions In normal mice, Lactobacillus andthe Bacteroides are the predominant bacterial flora colonizing in the lower esophagus, and Staphylococcus, Acinetobacter andBacteridium become the predominant bacteria after H. pylori infection.
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https://www.j-smu.com/EN/Y2014/V34/I09/1241