细菌生物被膜耐药及形成相关基因调控机制的研究
[Abstract]:objective
To study the Pathogenic Distribution of bacterial biofilm in tracheal tube of patients with mechanical ventilation, and compare the antibiotic susceptibility test of biofilm bacteria and corresponding plankton bacteria cultured in vitro to explore the antibiotic resistance of bacterial biofilm. Objectives: To investigate the distribution of genes related to biofilm formation of Staphylococcus epidermidis (operon-icaA gene, transcription regulator sigB gene, operon regulator-icaR gene, virulence factor regulator-agrA gene) and their relationship with biofilm formation.
Method
(1) 110 patients with artificial airway (tracheal intubation and tracheotomy) and mechanical ventilation were studied. Biofilm strains and corresponding plankton strains were screened by Congo red medium. Semi-quantitative detection of biofilm bacteria was carried out. Drug susceptibility test showed that biofilm strains and corresponding plankton bacteria were cultured in MH. The difference of drug resistance in culture medium and the difference of drug resistance of biofilm-positive bacteria in Poloxamer (F-127) medium and MH medium were analyzed.
(2) Staphylococcus epidermidis isolated from tracheal cannula was divided into two groups according to biofilm-positive Staphylococcus epidermidis and corresponding planktonic bacteria. The expression of icaA, sigB, icaR and agrA genes in S. epidermidis and S. epidermidis was quantified by 2-delta CT. The correlation between the transcription levels of icaA, sigB, icaR and agrA genes and the biofilm formation of S. epidermidis was analyzed.
Result
(1) 61 strains of biofilm-positive bacteria were screened out from 110 patients with mechanical ventilation, and the positive rate was 55.45%. Staphylococcus, Enterococcus faecalis and Pseudomonas aeruginosa were the most common strains. The drug sensitivity of biofilm-positive bacteria was similar to that of corresponding planktonic bacteria on the common MH medium, but the difference was not statistically significant (P 0.05). The results of susceptibility test on MH medium and Poloxamer medium were significantly different (P 0.05), and the latter was more resistant.
(2) Statistical analysis of the luminosity of icaA, sigB, icaR, agrA genes in RT-PCR showed that there was no significant difference between the two groups (P 0.05), but the average rank and rank of icaA, sigB gene biofilm group were significantly higher than those of plankton group. The average rank and rank of the membranous bacteria group were significantly lower than that of the planktonic bacteria group.
(3) Real-time PCR showed that the expression levels of icaA and sigB genes in S. epidermidis biofilm group were 418.8 and 81 times higher than those in plankton group, while the expression levels of icaR and agrA genes in biofilm group were only 1/145 and 1/270 of that in plankton group.
conclusion
(1) Staphylococcus, Enterococcus faecalis and Pseudomonas aeruginosa were the main pathogens of tracheal tube biofilm in patients with mechanical ventilation in our hospital. There was no significant difference in drug resistance between biofilm bacteria and plankton bacteria on ordinary MH medium. The drug resistance of biofilm bacteria on Poloxamer medium and MH medium was significantly different. Poloxamer medium may reflect the true tolerance of biofilm bacteria to drugs, and it is more tolerant.
(2) icaA, sigB, icaR and agrA genes are closely related to the biofilm formation of S. epidermidis. icaA and sigB genes can promote the biofilm formation of S. epidermidis, while icaR and agrA genes can inhibit the biofilm formation of S. epidermidis. It suggests that AGR system can regulate the expression of icaA, sigB and icaR genes, and agr system can inhibit the formation of icaA and si. GB expression of these two genes promotes icaR gene expression.
【学位授予单位】:中南大学
【学位级别】:硕士
【学位授予年份】:2011
【分类号】:R378
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