Antimycobacterial activity in vitro of pigments isolated from Antarctic bacteria

被引:48
作者
Mojib, Nazia [1 ]
Philpott, Rachel [1 ,2 ]
Huang, Jonathan P. [1 ]
Niederweis, Michael [2 ]
Bej, Asim K. [1 ]
机构
[1] Univ Alabama Birmingham, Dept Biol, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Microbiol, Sch Med, Birmingham, AL 35294 USA
来源
ANTONIE VAN LEEUWENHOEK INTERNATIONAL JOURNAL OF GENERAL AND MOLECULAR MICROBIOLOGY | 2010年 / 98卷 / 04期
关键词
Mycobacterium; Tuberculosis; Antarctica; Antimicrobial; Bacterial pigment; Alamar Blue Assay (MABA); Nitrate Reductase Assay (NRA); Janthinobacterium; Flavobacterium; MYCOBACTERIUM-TUBERCULOSIS; MIC DETERMINATION; XDR TUBERCULOSIS; SOUTH-AFRICA; VIOLACEIN; MICROORGANISMS; CIPROFLOXACIN; BIOSYNTHESIS; INHIBITORS; OFLOXACIN;
D O I
10.1007/s10482-010-9470-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
In this study, we describe the antimycobacterial activity of two pigments, violacein, a purple violet pigment from Janthinobacterium sp. Ant5-2 (J-PVP), and flexirubin, a yellow-orange pigment from Flavobacterium sp. Ant342 (F-YOP). These pigments were isolated from bacterial strains found in the land-locked freshwater lakes of Schirmacher Oasis, East Antarctica. The minimum inhibitory concentrations (MICs) of these pigments for avirulent and virulent mycobacteria were determined by the microplate Alamar Blue Assay (MABA) and Nitrate Reductase Assay (NRA). Results indicated that the MICs of J-PVP and F-YOP were 8.6 and 3.6 mu g/ml for avirulent Mycobacterium smegmatis mc(2)155; 5 and 2.6 mu g/ml for avirulent Mycobacterium tuberculosis mc(2)6230; and 34.4 and 10.8 mu g/ml for virulent M. tuberculosis H(37)Rv, respectively. J-PVP exhibited a similar to 15 times lower MIC for Mycobacterium sp. than previously reported for violacein pigment from Chromobacterium violaceum, while the antimycobacterial effect of F-YOP remains undocumented. Our results indicate these pigments isolated from Antarctic bacteria might be valuable lead compounds for new antimycobacterial drugs used for chemotherapy of tuberculosis.
引用
收藏
页码:531 / 540
页数:10
相关论文
共 50 条
[1]   INVESTIGATIONS ON METABOLITES OF MICROORGANISMS .16. INVESTIGATION OF PIGMENTS FROM CYTOPHAGA-JOHNSONAE-CY-JL - NEW FLEXIRUBIN-TYPE PIGMENTS [J].
ACHENBACH, H ;
KOHL, W ;
WACHTER, W ;
REICHENBACH, H .
ARCHIVES OF MICROBIOLOGY, 1978, 117 (03) :253-257
[2]   Demethoxycurcumin and its Semisynthetic Analogues as Antitubercular Agents [J].
Agrawal, Dinesh Kumar ;
Saikia, Dharmendra ;
Tivvari, Richa ;
Ojha, Shweta ;
Shanker, Karuna ;
Kumar, Jonnala Kotesh ;
Gupta, Anil Kumar ;
Tandon, Sudeep ;
Negi, Arvind Singh ;
Khanuja, Suman Preet Singh .
PLANTA MEDICA, 2008, 74 (15) :1828-1831
[3]   Mycolic acids: Structure, biosynthesis and physiological functions [J].
Barry, CE ;
Lee, RE ;
Mdluli, K ;
Sampson, AE ;
Schroeder, BG ;
Slayden, RA ;
Yuan, Y .
PROGRESS IN LIPID RESEARCH, 1998, 37 (2-3) :143-179
[4]  
Bernardet JF, 2002, INT J SYST EVOL MICR, V52, P1049, DOI [10.1099/ijs.0.02136-0, 10.1099/00207713-52-3-1049]
[5]   THE ENVELOPE OF MYCOBACTERIA [J].
BRENNAN, PJ ;
NIKAIDO, H .
ANNUAL REVIEW OF BIOCHEMISTRY, 1995, 64 :29-63
[6]   Low-temperature extremophiles and their applications [J].
Cavicchioli, R ;
Siddiqui, KS ;
Andrews, D ;
Sowers, KR .
CURRENT OPINION IN BIOTECHNOLOGY, 2002, 13 (03) :253-261
[7]   Intracellular growth and drug susceptibility of Mycobacterium tuberculosis in macrophages [J].
Chanwong, Sakarin ;
Maneekarn, Niwat ;
Makonkawkeyoon, Luksana ;
Makonkawkeyoon, Sanit .
TUBERCULOSIS, 2007, 87 (02) :130-133
[8]  
de Souza Ana Olivia, 1999, Revista do Instituto Adolfo Lutz, V58, P59
[9]   Chromobacterium violaceum:: A review of pharmacological and industiral perspectives [J].
Durán, N ;
Menck, CFM .
CRITICAL REVIEWS IN MICROBIOLOGY, 2001, 27 (03) :201-222
[10]  
Fattorini Lanfranco, 2007, Ann Ist Super Sanita, V43, P317