The role of DSPF, the type III secretion chaperone of DspA/E of Erwinia amylovora, in pathogenicity in host and non-host plants

Erwinia amylovora is a Gram-negative enterobacterium that causes a devastating blight disease on rosaceous plants. In this study, the structure of DspF, a type III secretion system (T3SS) chaperone required for virulence of E. amylovora, was investigated in bacterial growth and pathogenesis in host and non-host plants, including apple, strawberry, rose, Arabidopsis and tobacco. DspF genes were mutated through homologous recombination and the result was the arrest of disease development on apple, strawberry and rose, and of the hypersensitivity response in tobacco. In addition, bacterial development of the wild type was compared with that of dspF mutants in leaves of A. thaliana Columbia-5 (Col-5), and the resistant A. thaliana Landsberg erecta (Ler-0). It was concluded that DspF is essential for the bacterium to induce hypersensitive responce (HR) disease on host plants (Rosaceous family plant) and non-host plants (Arabidopsis thaliana).

[1]  Q. Zeng,et al.  HrcU and HrpP are pathogenicity factors in the fire blight pathogen Erwinia amylovora required for the type III secretion of DspA/E , 2016, BMC Microbiology.

[2]  C. Ramos,et al.  The olive knot disease as a model to study the role of interspecies bacterial communities in plant disease , 2015, Front. Plant Sci..

[3]  B. Sabater-Muñoz,et al.  Medfly Ceratitis capitata as Potential Vector for Fire Blight Pathogen Erwinia amylovora: Survival and Transmission , 2015, PloS one.

[4]  N. A. Ashmawy,et al.  Isolation and molecular characterization of the fire blight pathogen, Erwinia amylovora, isolated from apple and pear orchards in Egypt. , 2015 .

[5]  L. Taconnat,et al.  The bacterial effector DspA/E is toxic in Arabidopsis thaliana and is required for multiplication and survival of fire blight pathogen. , 2013, Molecular plant pathology.

[6]  R. R. McNally Identification and characterization of virulence factors via the elucidation of regulatory networks in the fire blight pathogen Erwinia amylovora , 2013 .

[7]  R. Heitefuss Fire Blight, History, Biology, and Management , 2012 .

[8]  H. Vervaeren,et al.  Techniques for transformation of biogas to biomethane , 2011 .

[9]  M. Melotto,et al.  Functional analysis of the N terminus of the Erwinia amylovora secreted effector DspA/E reveals features required for secretion, translocation, and binding to the chaperone DspB/F. , 2009, Molecular plant-microbe interactions : MPMI.

[10]  S. He,et al.  Type III Protein Secretion in Plant Pathogenic Bacteria , 2009, Plant Physiology.

[11]  M. Barny Erwinia amylovora hrpN mutants, blocked in harpin synthesis, express a reduced virulence on host plants and elicit variable hypersensitive reactions on tobacco , 1995, European Journal of Plant Pathology.

[12]  Sheng Yang He,et al.  Type III protein secretion mechanism in mammalian and plant pathogens. , 2004, Biochimica et biophysica acta.

[13]  A. Collmer,et al.  EFFECTOR PROTEINS : Double Agents in Bacterial Disease and Plant Defense , 2004 .

[14]  R. Innes New effects of type III effectors , 2003, Molecular microbiology.

[15]  C. Parsot,et al.  The various and varying roles of specific chaperones in type III secretion systems. , 2003, Current opinion in microbiology.

[16]  Alan Collmer,et al.  Genomic mining type III secretion system effectors in Pseudomonas syringae yields new picks for all TTSS prospectors. , 2002, Trends in microbiology.

[17]  J. Paulin,et al.  The DspB/F protein of Erwinia amylovora is a type III secretion chaperone ensuring efficient intrabacterial production of the Hrp-secreted DspA/E pathogenicity factor. , 2002, Molecular plant pathology.

[18]  Jonathan D. G. Jones,et al.  Plant pathogens and integrated defence responses to infection , 2001, Nature.

[19]  S. He,et al.  Visualization of secreted Hrp and Avr proteins along the Hrp pilus during type III secretion in Erwinia amylovora and Pseudomonas syringae , 2001, Molecular microbiology.

[20]  S. Beer,et al.  Regulation of hrp genes and type III protein secretion in Erwinia amylovora by HrpX/HrpY, a novel two-component system, and HrpS. , 2000, Molecular plant-microbe interactions : MPMI.

[21]  G. Cornelis,et al.  Assembly and function of type III secretory systems. , 2000, Annual review of microbiology.

[22]  J. Vanneste Fire Blight: The Disease and its Causative Agent, Erwinia amylovora , 2000 .

[23]  Jihyun F. Kim,et al.  hrp genes and harpins of Erwinia amylovora: a decade of discovery. , 2000 .

[24]  Jihyun F. Kim,et al.  HrpW of Erwinia amylovora, a New Harpin That Contains a Domain Homologous to Pectate Lyases of a Distinct Class , 1998, Journal of bacteriology.

[25]  S. Gaudriault,et al.  HrpW of Erwinia amylovora, a new Hrp‐secreted protein , 1998, FEBS letters.

[26]  A. Bogdanove,et al.  Erwinia amylovora Secretes DspE, a Pathogenicity Factor and Functional AvrE Homolog, through the Hrp (Type III Secretion) Pathway , 1998, Journal of bacteriology.

[27]  A. Bogdanove,et al.  Homology and functional similarity of an hrp-linked pathogenicity locus, dspEF, of Erwinia amylovora and the avirulence locus avrE of Pseudomonas syringae pathovar tomato. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[28]  J. Paulin,et al.  DspA, an essential pathogenicity factor of Erwinia amylovora showing homology with AvrE of Pseudomonas syringae, is secreted via the Hrp secretion pathway in a DspB‐dependent way , 1997, Molecular microbiology.

[29]  A. Collmer,et al.  The type III (Hrp) secretion pathway of plant pathogenic bacteria: trafficking harpins, Avr proteins, and death , 1997, Journal of bacteriology.

[30]  A. Bogdanove,et al.  Unified nomenclature for broadly conserved hrp genes of phytopathogenic bacteria , 1996, Molecular microbiology.

[31]  Keen Nt,et al.  Characterization of avrE from Pseudomonas syringae pv. tomato: a hrp-linked avirulence locus consisting of at least two transcriptional units. , 1995 .

[32]  N. Keen,et al.  Characterization of avrE from Pseudomonas syringae pv. tomato: a hrp-linked avirulence locus consisting of at least two transcriptional units. , 1995, Molecular plant-microbe interactions : MPMI.

[33]  S. He,et al.  Harpin, elicitor of the hypersensitive response produced by the plant pathogen Erwinia amylovora. , 1992, Science.

[34]  B. Marçais,et al.  Cloning of a large gene cluster involved in Erwinia amylovora CFBP1430 virulence , 1990, Molecular microbiology.

[35]  S. Beer,et al.  Creation and complementation of pathogenicity mutants of Erwinia amylovora , 1988 .

[36]  N. Panopoulos,et al.  Gene cluster of Pseudomonas syringae pv. "phaseolicola" controls pathogenicity of bean plants and hypersensitivity of nonhost plants , 1986, Journal of bacteriology.

[37]  J. Bradbury Guide to plant pathogenic bacteria. , 1986 .

[38]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .