Uniquely insidious:: Yersinia pestis biofilms

被引:32
作者
Darby, Creg [1 ]
机构
[1] Univ Calif San Francisco, Dept Cell & Tissue Biol, San Francisco, CA 94143 USA
关键词
D O I
10.1016/j.tim.2008.01.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bubonic plague, one of history's deadliest infections, is transmitted by fleas infected with Yersinia pestis. The bacteria can starve fleas by blocking their digestive tracts, which stimulates the insects to bite repeatedly and thereby infect new hosts. Direct examination of infected fleas, aided by in vitro studies and experiments with the nematode Caenorhabditis elegans, have established that Y. pestis forms a biofilm in the insect. The extracellular matrix of the biofilm seems to contain a homopolymer of N-acetyl-D-glucosamine, which is a constituent of many bacterial biofilms. A regulatory mechanism involved in Y. pestis biofilm formation, cyclic-di-GMP signaling, is also widespread in bacteria; yet only Y. pestis forms biofilms in fleas. Here, the historical background of bubonic plague is briefly described and recent studies investigating the mechanisms by which these unique and deadly biofilms are formed re discussed.
引用
收藏
页码:158 / 164
页数:7
相关论文
共 65 条
[1]   Yersinia pestis, the cause of plague, is a recently emerged clone of Yersinia pseudotuberculosis [J].
Achtman, M ;
Zurth, K ;
Morelli, C ;
Torrea, G ;
Guiyoule, A ;
Carniel, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (24) :14043-14048
[2]   Initiation and spread of traveling waves of plague, Yersinia pestis, in the western United States [J].
Adjemian, Jennifer Zipser ;
Foley, Patrick ;
Gage, Kenneth L. ;
Foley, Janet E. .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2007, 76 (02) :365-375
[3]  
Bacot A W, 1914, J Hyg (Lond), V13, P423
[4]  
Barondes S H, 1978, Methods Enzymol, V50, P302
[5]   Genetic organization of the yersiniabactin biosynthetic region and construction of avirulent mutants in Yersinia pestis [J].
Bearden, SW ;
Fetherston, JD ;
Perry, RD .
INFECTION AND IMMUNITY, 1997, 65 (05) :1659-1668
[6]   Regulation of rugosity and biofilm formation in Vibrio cholerae:: Comparison of VpsT and VpsR regulons and epistasis analysis of vpsT, vpsR, and hapR [J].
Beyhan, Sinem ;
Bilecen, Kivanc ;
Salama, Sofie R. ;
Casper-Lindley, Catharina ;
Yildiz, Fitnat H. .
JOURNAL OF BACTERIOLOGY, 2007, 189 (02) :388-402
[7]   The phosphodiesterase activity of the HmsP EAL domain is required for negative regulation of biofilm formation in Yersinia pestis [J].
Bobrov, AG ;
Kirillina, O ;
Perry, RD .
FEMS MICROBIOLOGY LETTERS, 2005, 247 (02) :123-130
[8]  
Bobrov AG, 2007, ADV EXP MED BIOL, V603, P178
[9]   FACTORS PROMOTING ACUTE AND CHRONIC DISEASES CAUSED BY YERSINIAE [J].
BRUBAKER, RR .
CLINICAL MICROBIOLOGY REVIEWS, 1991, 4 (03) :309-324
[10]   Insights into the evolution of Yersinia pestis through whole-genome comparison with Yersinia pseudotuberculosis [J].
Chain, PSG ;
Carniel, E ;
Larimer, FW ;
Lamerdin, J ;
Stoutland, PO ;
Regala, WM ;
Georgescu, AM ;
Vergez, LM ;
Land, ML ;
Motin, VL ;
Brubaker, RR ;
Fowler, J ;
Hinnebusch, J ;
Marceau, M ;
Medigue, C ;
Simonet, M ;
Chenal-Francisque, V ;
Souza, B ;
Dacheux, D ;
Elliott, JM ;
Derbise, A ;
Hauser, LJ ;
Garcia, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (38) :13826-13831