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Name- Jitendra Chandra Devrari Reg. no- 155/Jan 2015 Gist of the articles: 1. María D. Alcántar-Curiel et. al. Multi-functional analysis of Klebsiella pneumonia fimbrial types in adherence and biofilm formation. Landes Bioscience, 2013, virulence 4:2, p.129–138. Klebsiella pneumonia is one of the emerging opportunistic pathogen which is responsible for the most common hospital acquired infection. The Type 1 and type 3 fimbriae which are encoded by the fimA and mrkA gene respectively mediates the host cell adherence and biofilm formation of klebsiella pneumonia. among E. coli patho groups and adhesive structure that is e coli common pilus (ECP) is being produced however a homolog of the ecpABCDE operon is present in the klebsiella pneumonia genome. The prevalence of mrkA, fimA, ECP fimbrial genes were determine among the clinical and environmental klebsiella pneumonia and correlation was stablished with fimbrial production during cell adherence and biofilm formation. ECP is reqired both in vitro and in vivo for expression of these fimbrial subunits. therefore ecp produced by Klebsiella pnumoniae strain represents a new important adhesive structure of this organism. 2. Magesh H et. al. Identification of plasmid-mediated quinolone resistance genes qnrA1, qnrB1 and aac(6')-1b-cr in a multiple drug-resistant isolate of Klebsiella pneumoniae from Chennai, Indian J Med Microbiol, 2011, vol. 29, p.262-268. Fluoroquinolones were the commonly prescribed antimicrobial for gram positive as well as gram negative microorganism before the emergence of resistance to these antimicrobials. The determinants of PMQR in the clinical isolates were identified in this study. The qnrA and qnrB are the gens which mediates the PMQR in MDR Klebsiella pneuoniae isolates. However high ciprofloxacin rersistance was conferred by the MDR plasmid which was found to carry another mutant gene that is aac(6’)-lb-cr which is another type of PMQR gene. This was the first report submitted from the India. 3. Yamane Kunikazu et. al. New Plasmid-Mediated Fluoroquinolone Efflux Pump, QepA Found in an Escherichia coli Clinical Isolate. Antimicrobial agents and chemotherapy, 2007,vol. 51 (9), p. 3354–3360. A new molecular mechanism responsible for fluoroquinolone resistance have been identified by plasmid mediated qnr and aac(6’)-lb-cr gene. A PCR detection was failed for the detection qnr genes for fluoroquinolones resistance in a variant of E. coli thus suggesting that the novel mechanism for PMQR. However another novel qepA gene was identified for PMQR in E coli C316. Under the AcrB- TolC-deficient conditions and the presence of qep gene in e coli C316 significantly raises the resistance levels of norfloxacin, ciprofloxacin and enrofloxcin. Thus to stop the dissemination of plasmid dependent fluoroquinolone resistance among pathogenic microbe it is important to check periodically qepA harboring clinical isolates. 4. Bendaoud Meriem et. al. Broad-Spectrum Biofilm Inhibition by Kingella kingae Exopolysaccharide. Journal of bacteriology, 2011, p. 3879–3886. Extracted exopolysacharide from the Kingella kingae which inhibited the biofilm formation of Aggregatibacter actinomycetemcomitans, Klebsiella pneumoniae, S. aureus, S. epidermidis, C. albicans and K. kingae. Exopolysaccharide will inhibit the biofilm formation of bacteria due to the certain changes in the chemical structure of the cell wall, matrix and its substrate. Extracted polysaccharide is belonging to the two important polysaccharide which is the major role in inhibition of bifilm formation. One was the linear polysaccharide that is 6α-D-GlcNAcp-(1-5)-βD-OclAp-2 extracted from the Actinobacillus pleuropneumoniae and other was the novel linear PAM galactan. In e.coli for the synthesis of PAM galactan, clusters of 3 genes were used from K. kingae. PAM galactan acts as antibiofilm agent, which inhbits the biofilm production in bacteria. 5. Struve Carsten et. al. Characterization of Klebsiella pneumoniae Type 1 Fimbriae by Detection of Phase Variation during Colonization and Infection and Impact on Virulence. INFECTION AND IMMUNITY, 2008, Vol. 76(9), p. 4055–4065. Klebsiella pneumoniae is one of the most common hospital acquired pathogen, which is also producing the disease in immunocompromised patients. The type 1 fimbrial gene cluster of k.pneumoniae was examined which was not identical to the gene cluster of e.coli although their structural resemblance was quite high. The fimbrial gene in Klebsiella species was named as fimk gene, which belongs to the EAL domain in gene cluster, having main role in the regulation and adhesion property to the host cell. Expression of Type 1 fimbriae of Klebsiella pneumoniae has a significant role in UTIs in comparison with the colonization in the intestine or infection in the lungs. With the help of molecular techniques like PCR, the expression of switching on or off of fimK gene during infections of urinary tract, intestine and lung was determined. It has been found that all the expressions of fimK gene while UTIs were found to be “switched on”, while it was all “switched off” during the infection of intestine and lungs. Therefore the expression of type1 fimbrie of K.pneumoniae in the colonization and infection is dependent on the host environment.