Caenorhabditis elegans mutants resistant to attachment of Yersinia biofilms

被引:33
作者
Darby, Creg
Chakraborti, Amrita
Politz, Samuel M.
Daniels, Calvin C.
Tan, Li
Drace, Kevin
机构
[1] Univ Calif San Francisco, Dept Cell & Tissue Biol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Program Microbial Pathogenesis & Host Def, San Francisco, CA 94143 USA
[3] Worcester Polytech Inst, Dept Biol & Biotechnol, Worcester, MA 01609 USA
[4] Univ Alabama, Dept Microbiol, Birmingham, AL 35294 USA
关键词
D O I
10.1534/genetics.106.067496
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The detailed composition and structure of the Caenorhabditis elegans surface are unknown. Previous genetic studies used antibody or lectin binding to identify srf genes that play roles in surface determination. Infection by Microbacterium nematophilum identified bus (bacterially unswollen) genes that also affect Surface characteristics. We report that biofilms produced by Yersinia pestis and Y. pseudotuberculosis, which bind the C. elegans surface predominantly on the head, can be used to identify additional surface-determining genes. A screen for C. elegans mutants with a biofilm absent on the head (Bah) phenotype identified three novel genes: bah-1, bah-2, and bah-3. The bah-1 and bah-2 mutants have slightly fragile cuticles but are neither Srf nor BUS, suggesting that they are specific for surface components involved in biofilm attachment. A bah-3 mutant has normal cuticle integrity, but shows a stage-specific Srf phenotype. The screen produced alleles of five known surface genes: srf-2, srf-3, bus-4, bus-12, and bus-17. For the X-linked bus-17, a paternal effect was observed in biofilm assays.
引用
收藏
页码:221 / 230
页数:10
相关论文
共 36 条
[11]   Identification of gmhA, a Yersinia pestis gene required for flea blockage, by using a Caenorhabditis elegans biofilm system [J].
Darby, C ;
Ananth, SL ;
Tan, L ;
Hinnebusch, BJ .
INFECTION AND IMMUNITY, 2005, 73 (11) :7236-7242
[12]   Caenorhabditis elegans -: Plague bacteria biofilm blocks food intake [J].
Darby, C ;
Hsu, JW ;
Ghori, N ;
Falkow, S .
NATURE, 2002, 417 (6886) :243-244
[13]   Optimization of ENU mutagenesis of Caenorhabditis elegans [J].
De Stasio, EA ;
Dorman, S .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2001, 495 (1-2) :81-88
[14]   An abundantly expressed mucin-like protein from Toxocara canis infective larvae: The precursor of the larval surface coat glycoproteins [J].
Gems, D ;
Maizels, RM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (04) :1665-1670
[15]  
GEMSKI P, 1980, INFECT IMMUN, V28, P1044
[16]   Multiple genes affect sensitivity of Caenorhabditis elegans to the bacterial pathogen Microbacterium nematophilum [J].
Gravato-Nobre, MJ ;
Nicholas, HR ;
Nijland, R ;
O'Rourke, D ;
Whittington, DE ;
Yook, KJ ;
Hodgkin, J .
GENETICS, 2005, 171 (03) :1033-1045
[17]   Environmental induction and genetic control of surface antigen switching in the nematode Caenorhabditis elegans [J].
Grenache, DG ;
Caldicott, I ;
Albert, PS ;
Riddle, DL ;
Politz, SM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (22) :12388-12393
[18]   ALTERED EXPRESSION OF AN L1-SPECIFIC, O-LINKED CUTICLE SURFACE GLYCOPROTEIN IN MUTANTS OF THE NEMATODE CAENORHABDITIS-ELEGANS [J].
HEMMER, RM ;
DONKIN, SG ;
CHIN, KJ ;
GRENACHE, DG ;
BHATT, H ;
POLITZ, SM .
JOURNAL OF CELL BIOLOGY, 1991, 115 (05) :1237-1247
[19]   A SPERM-SUPPLIED PRODUCT ESSENTIAL FOR INITIATION OF NORMAL EMBRYOGENESIS IN CAENORHABDITIS-ELEGANS IS ENCODED BY THE PATERNAL-EFFECT EMBRYONIC-LETHAL GENE, SPE-11 [J].
HILL, DP ;
SHAKES, DC ;
WARD, S ;
STROME, S .
DEVELOPMENTAL BIOLOGY, 1989, 136 (01) :154-166
[20]   CAENORHABDITIS-BRIGGSAE - AGING AND STRUCTURAL TURNOVER OF OUTER CUTICLE SURFACE AND INTESTINE [J].
HIMMELHOCH, S ;
ZUCKERMAN, BM .
EXPERIMENTAL PARASITOLOGY, 1978, 45 (02) :208-214