Nagz is required for beta-lactamase expression and full pathogenicity in xanthomonas campestris pv. campestris str. 17

Research in Microbiology

Volumn 165, Issue 8, 2014, Pages 612-619

  Yang, Tsuey Ching ^a   Chen, Tzu Fan ^b   Tsai, Jeffrey J P ^b   Hu, Rouh Mei ^b,c  

^a NATIONAL YANG MING UNIVERSITY   (Taiwan)

^b ASIA UNIVERSITY   (Taiwan)

^c CHINA MEDICAL UNIVERSITY   (Taiwan)

Author keywords

AmpR; Antibiotic resistance; Beta lactamase; Bla; NagZ; Pathogenicity

Indexed keywords

BETA LACTAMASE; MONOMER; NAGZ PROTEIN; PEPTIDOGLYCAN; UNCLASSIFIED DRUG; BACTERIAL PROTEIN; BETA N ACETYLHEXOSAMINIDASE; PATHOGENICITY PROTEIN, XANTHOMONAS;

ARTICLE; BACTERIAL VIRULENCE; BACTERIUM MUTANT; GENE EXPRESSION; NONHUMAN; PLANT DISEASE; PROTEIN EXPRESSION; WILD TYPE; XANTHOMONAS CAMPESTRIS; BIOSYNTHESIS; BRASSICA; ENZYMOLOGY; GENE EXPRESSION REGULATION; GENE INACTIVATION; GENETICS; METABOLISM; MICROBIOLOGY; PATHOGENICITY; PLANT LEAF; VIRULENCE;

BACTERIAL PROTEINS; BETA-LACTAMASES; BETA-N-ACETYLHEXOSAMINIDASES; BRASSICA; GENE EXPRESSION REGULATION, BACTERIAL; GENE KNOCKOUT TECHNIQUES; PLANT DISEASES; PLANT LEAVES; VIRULENCE; XANTHOMONAS CAMPESTRIS;

EID: 84910116220     PISSN: 09232508     EISSN: 17697123     Source Type: Journal    
DOI: 10.1016/j.resmic.2014.08.008     Document Type: Article

References (41)

1. Asgarali A., Stubbs K.A., Oliver A., Vocadlo D.J., Mark B.L. Inactivation of the glycoside hydrolase NagZ attenuates antipseudomonal beta-lactam resistance in Pseudomonas aeruginosa. Antimicrob Agents Chemother 2009, 53:2274-2282.
2. Caparros M., Pittenauer E., Schmid E.R., de Pedro M.A., Allmaier G. Molecular weight-determination of biosynthetically modified monomeric and oligomeric muropeptides from Escherichia coli by plasma desorption-mass spectrometry. FEBS Lett 1993, 316:181-185.
3. Cavallari J.F., Lamers R.P., Scheurwater E.M., Matos A.L., Burrows L.L. Changes to its peptidoglycan-remodeling enzyme repertoire modulate beta-lactam resistance in Pseudomonas aeruginosa. Antimicrob Agents Chemother 2013, 57:3078-3084.
4. Cheng Q., Li H., Merdek K., Park J.T. Molecular characterization of the beta-N-acetylglucosaminidase of Escherichia coli and its role in cell wall recycling. J Bacteriol 2000, 182:4836-4840.
5. Cheng Q., Park J.T. Substrate specificity of the AmpG permease required for recycling of cell wall anhydro-muropeptides. J Bacteriol 2002, 184:6434-6436.
6. Chitlaru E., Roseman S. Molecular cloning and characterization of a novel beta-N-acetyl-D-glucosaminidase from Vibrio furnissii. J Biol Chem 1996, 271:33433-33439.
7. Clinical and Laboratory Standards Istitute Performance standards for antimicrobial susceptibility testing of bacteria 2006, 14th Informational Supplement, Clinical and Laboratory Standards Institute, Wayne, PA.
8. Erbs G., Silipo A., Aslam S., De Castro C., Liparoti V., Flagiello A., et al. Peptidoglycan and muropeptides from pathogens Agrobacterium and Xanthomonas elicit plant innate immunity: structure and activity. Chem Biol 2008, 15:438-448.
9. Folkesson A., Eriksson S., Andersson M., Park J.T., Normark S. Components of the peptidoglycan-recycling pathway modulate invasion and intracellular survival of Salmonella enterica serovar Typhimurium. Cell Microbiol 2005, 7:147-155.
10. Goodell E.W. Recycling of murein by Escherichia coli. J Bacteriol 1985, 163:305-310.
11. Hanson N.D., Sanders C.C. Regulation of inducible AmpC beta-lactamase expression among Enterobacteriaceae. Curr Pharm Des 1999, 5:881-894.
12. Harz H., Burgdorf K., Holtje J.V. Isolation and separation of the glycan strands from murein of Escherichia coli by reversed-phase high-performance liquid chromatography. Anal Biochem 1990, 190:120-128.
13. Huang Y.W., Hu R.M., Lin C.W., Chung T.C., Yang T.C. NagZ-dependent and NagZ-independent mechanisms for beta-lactamase expression in Stenotrophomonas maltophilia. Antimicrob Agents Chemother 2012, 56:1936-1941.
14. Jacobs C., Huang L.J., Bartowsky E., Normark S., Park J.T. Bacterial cell wall recycling provides cytosolic muropeptides as effectors for beta-lactamase induction. EMBO J 1994, 13:4684-4694.
15. Jacobs C., Joris B., Jamin M., Klarsov K., Van Beeumen J., Mengin-Lecreulx D., et al. AmpD, essential for both beta-lactamase regulation and cell wall recycling, is a novel cytosolic N-acetylmuramyl-L-alanine amidase. Mol Microbiol 1995, 15:553-559.
16. Johnson J.W., Fisher J.F., Mobashery S. Bacterial cell-wall recycling. Ann N Y Acad Sci 2013, 1277:54-75.
17. Kong K.F., Aguila A., Schneper L., Mathee K., Zamorano L., Reeve T.M., et al. Pseudomonas aeruginosa beta-lactamase induction requires two permeases, AmpG and AmpP. BMC Microbiol 2010, 10:328.
18. Lee M., Zhang W., Hesek D., Noll B.C., Boggess B., Mobashery S. Bacterial AmpD at the crossroads of peptidoglycan recycling and manifestation of antibiotic resistance. J Am Chem Soc 2009, 131:8742-8743.
19. Melly M.A., McGee Z.A., Rosenthal R.S. Ability of monomeric peptidoglycan fragments from Neisseria gonorrhoeae to damage human fallopian-tube mucosa. J Infect Dis 1984, 149:378-386.
20. Minami S., Yotsuji A., Inoue M., Mitsuhashi S. Induction of beta-lactamase by various beta-lactam antibiotics in Enterobacter cloacae. Antimicrob Agents Chemother 1980, 18:382-385.
21. Nigro G., Fazio L.L., Martino M.C., Rossi G., Tattoli I., Liparoti V., et al. Muramylpeptide shedding modulates cell sensing of Shigella flexneri. Cell Microbiol 2008, 10:682-695.
22. Park J.K., Keyhani N.O., Roseman S. Chitin catabolism in the marine bacterium Vibrio furnissii. Identification, molecular cloning, and characterization of A N, N'-diacetylchitobiose phosphorylase. J Biol Chem 2000, 275:33077-33083.
23. Park J.T., Uehara T. How bacteria consume their own exoskeletons (turnover and recycling of cell wall peptidoglycan). Microbiol Mol Biol Rev 2008, 72:211-227.
24. Quintela J.C., Caparros M., de Pedro M.A. Variability of peptidoglycan structural parameters in gram-negative bacteria. FEMS Microbiol Lett 1995, 125:95-100.
25. Rosenthal R.S., Nogami W., Cookson B.T., Goldman W.E., Folkening W.J. Major fragment of soluble peptidoglycan released from growing Bordetella pertussis is tracheal cytotoxin. Infect Immun 1987, 55:2117-2120.
26. Schimpl M., Schuttelkopf A.W., Borodkin V.S., van Aalten D.M. Human OGA binds substrates in a conserved peptide recognition groove. Biochem J 2010, 432:1-7.
27. Sukhithasri V., Nisha N., Biswas L., Anil Kumar V., Biswas R. Innate immune recognition of microbial cell wall components and microbial strategies to evade such recognitions. Microbiol Res 2013, 168:396-406.
28. Tans-Kersten J., Gay J., Allen C. Ralstonia solanacearum AmpD is required for wild-type bacterial wilt virulence. Mol Plant Pathol 2000, 1:179-185.
29. Viala J., Chaput C., Boneca I.G., Cardona A., Girardin S.E., Moran A.P., et al. Nod1 responds to peptidoglycan delivered by the Helicobacter pylori cag pathogenicity island. Nat Immunol 2004, 5:1166-1174.
30. Vollmer W. Structural variation in the glycan strands of bacterial peptidoglycan. FEMS Microbiol Rev 2008, 32:287-306.
31. Votsch W., Templin M.F. Characterization of a beta-N-acetylglucosaminidase of Escherichia coli and elucidation of its role in muropeptide recycling and beta -lactamase induction. J Biol Chem 2000, 275:39032-39038.
32. Williams P.H. Black rot: a continuing threat to world crucifers. Plant Dis 1980, 64:736-742.
33. Woodhams K.L., Chan J.M., Lenz J.D., Hackett K.T., Dillard J.P. Peptidoglycan fragment release from Neisseria meningitidis. Infect Immun 2013, 81:3490-3498.
34. Wyckoff T.J., Taylor J.A., Salama N.R. Beyond growth: novel functions for bacterial cell wall hydrolases. Trends Microbiol 2012, 20:540-547.
35. xc beta-lactamase expression in Xanthomonas campestris pv. campestris str. 17. FEMS Microbiol Lett 2013, 340:101-108.
36. Yang T.C., Leu Y.W., Chang-Chien H.C., Hu R.M. Flagellar biogenesis of Xanthomonas campestris requires the alternative sigma factors RpoN2 and FliA and is temporally regulated by FlhA, FlhB, and FlgM. J Bacteriol 2009, 191:2266-2275.
37. Yang T.C., Tsai M.J., Tsai J.J., Hu R.M. Induction of a secretable beta-lactamase requires a long lag time in Xanthomonas campestris pv. campestris str. 17. Res Microbiol 2011, 162:999-1005.
38. Zamorano L., Reeve T.M., Deng L., Juan C., Moya B., Cabot G., et al. NagZ inactivation prevents and reverts beta-lactam resistance, driven by AmpD and PBP 4 mutations, in Pseudomonas aeruginosa. Antimicrob Agents Chemother 2010, 54:3557-3563.
39. Zamorano L., Reeve T.M., Juan C., Moya B., Cabot G., Vocadlo D.J., et al. AmpG inactivation restores susceptibility of pan-beta-lactam-resistant Pseudomonas aeruginosa clinical strains. Antimicrob Agents Chemother 2011, 55:1990-1996.
40. Zeng X., Lin J. Beta-lactamase induction and cell wall metabolism in Gram-negative bacteria. Front Microbiol 2013, 4:128.
41. Zhao Y., Blumer S.E., Sundin G.W. Identification of Erwinia amylovora genes induced during infection of immature pear tissue. J Bacteriol 2005, 187:8088-8103.