Melioidosin is a main virulent factor of Bulkholderia pseudomallei

2014 ◽  
Vol 33 (12) ◽  
pp. 1281-1286
Author(s):  
Guang-qiang MA ◽  
Qian WANG ◽  
Jin-hua ZHU ◽  
He-ping YE ◽  
Zhi-ming YUAN ◽  
...  
Keyword(s):  
Genetika ◽  
2013 ◽  
Vol 45 (2) ◽  
pp. 479-492 ◽  
Author(s):  
Katarina Veljovic ◽  
Amarela Terzic-Vidojevic ◽  
Maja Tolinacki ◽  
Milan Kojic ◽  
Ljubisa Topisirovic

Strain Enterococcus faecalis BGPT1-10P was isolated from artisanal semi-hard homemade cheese from Stara Planina, Serbia. Results showed that BGPT1-10P synthesized a heat labile bacteriocin with a broad spectrum of activity, including Listeria and Candida species. Further analysis revealed that synthesized bacteriocin is enterolysin A. Moreover, the entL gene encoding enterolysin A was found to be located on the chromosome. The entL gene was cloned and sequenced. Analysis of nucleotide sequence showed that the entL gene in natural isolate En. faecalis BGPT1-10P is identical to that of the entL gene described previously in En. faecalis LMG 2333. Within the cloned DNA fragment containing the entL gene, four ORFs were detected. One of them was identified as the scpE gene, which encodes a virulent factor staphopain peptidase. Functional analysis of the entL gene showed that the complete genetic information necessary for the synthesis of enterolysin A were directly linked solely to it. Strain BGPT1-10P also synthesized gelatinase and citolysin, and contained a set of virulent factors. In addition, BGPT1-10P carries the ermB and tetM genes conferring the resistance to erythromycin and tetracycline, respectively.


2011 ◽  
Vol 4 (4) ◽  
pp. 401-403
Author(s):  
Dr. Anvitha Sharath Kumar ◽  
◽  
Dr. Kusuma. N Dr. Kusuma. N

1999 ◽  
Vol 41 (3) ◽  
pp. 117-122 ◽  
Author(s):  
Kuniyasu Ochiai ◽  
Ken Kikuchi ◽  
Kazuo Fukushima ◽  
Tomoko Kurita-Ochiai

2021 ◽  
Vol 12 ◽  
Author(s):  
Tanu Atriwal ◽  
Kashish Azeem ◽  
Fohad Mabood Husain ◽  
Afzal Hussain ◽  
Muhammed Nadeem Khan ◽  
...  

In recent years, the demand for novel antifungal therapies has increased several- folds due to its potential to treat severe biofilm-associated infections. Biofilms are made by the sessile microorganisms attached to the abiotic or biotic surfaces, enclosed in a matrix of exopolymeric substances. This results in new phenotypic characteristics and intrinsic resistance from both host immune response and antimicrobial drugs. Candida albicans biofilm is a complex association of hyphal cells that are associated with both abiotic and animal tissues. It is an invasive fungal infection and acts as an important virulent factor. The challenges linked with biofilm-associated diseases have urged scientists to uncover the factors responsible for the formation and maturation of biofilm. Several strategies have been developed that could be adopted to eradicate biofilm-associated infections. This article presents an overview of the role of C. albicans biofilm in its pathogenicity, challenges it poses and threats associated with its formation. Further, it discusses strategies that are currently available or under development targeting prostaglandins, quorum-sensing, changing surface properties of biomedical devices, natural scaffolds, and small molecule-based chemical approaches to combat the threat of C. albicans biofilm. This review also highlights the recent developments in finding ways to increase the penetration of drugs into the extracellular matrix of biofilm using different nanomaterials against C. albicans.


2014 ◽  
Vol 50 (87) ◽  
pp. 13300-13303 ◽  
Author(s):  
Rishi Sharma ◽  
Naresh Kottari ◽  
Yoann M. Chabre ◽  
Leïla Abbassi ◽  
Tze Chieh Shiao ◽  
...  

Both convergent and divergent strategies for the synthesis of “onion peel” glycodendrimers are reported which resulted in one of the best multivalent ligands known against the virulent factor from a bacterial lectin isolated from Pseudomonas aeruginosa.


2009 ◽  
Vol 34 (9) ◽  
pp. 761-768 ◽  
Author(s):  
Lin Ma ◽  
Lixin Xie ◽  
Xiaoguang Dong ◽  
Weiyun Shi

Sign in / Sign up

Export Citation Format

Share Document