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2018 ◽  
Vol 293 (10) ◽  
pp. 3651-3662 ◽  
Author(s):  
Christopher M. Goins ◽  
Steven Dajnowicz ◽  
Micholas D. Smith ◽  
Jerry M. Parks ◽  
Donald R. Ronning
Keyword(s):  

2016 ◽  
Vol 306 (4) ◽  
pp. 212-221 ◽  
Author(s):  
Anna S. Świerzko ◽  
Marcin A. Bartłomiejczyk ◽  
Anna Brzostek ◽  
Jolanta Łukasiewicz ◽  
Mateusz Michalski ◽  
...  

2016 ◽  
Vol 84 (8) ◽  
pp. 2264-2273 ◽  
Author(s):  
Shinya Watanabe ◽  
Kazunori Matsumura ◽  
Hiroki Iwai ◽  
Keiji Funatogawa ◽  
Yuji Haishima ◽  
...  

Mycobacterium tuberculosiscontains a single rRNA operon that encodes targets for antituberculosis agents, including kanamycin. To date, only four mutations in the kanamycin binding sites of 16S rRNA have been reported in kanamycin-resistant clinical isolates. We hypothesized that another mutation(s) in the region may dramatically decreaseM. tuberculosisviability and virulence. Here, we describe an rRNA mutation, U1406A, which was generatedin vitroand confers resistance to kanamycin while highly attenuatingM. tuberculosisvirulence. The mutant showed decreased expression of 20% (n= 361) of mycobacterial proteins, including central metabolic enzymes, mycolic acid biosynthesis enzymes, and virulence factors such as antigen 85 complexes and ESAT-6. The mutation also induced three proteins, including KsgA (Rv1010; 16S rRNA adenine dimethyltransferase), which closely bind to the U1406A mutation site on the ribosome; these proteins were associated with ribosome maturation and translation initiation processes. The mutant showed an increase in 17S rRNA (precursor 16S rRNA) and a decrease in the ratio of 30S subunits to the 70S ribosomes, suggesting that the U1406A mutation in 16S rRNA attenuatedM. tuberculosisvirulence by affecting these processes.


2014 ◽  
Vol 78 (3) ◽  
pp. 242-248 ◽  
Author(s):  
Ponrut Phunpae ◽  
Sakarin Chanwong ◽  
Chatchai Tayapiwatana ◽  
Napaporn Apiratmateekul ◽  
Anupong Makeudom ◽  
...  

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