Moreira_2010_BMC.Genomics_11_238

Reference

Title : Novel insights into the genomic basis of citrus canker based on the genome sequences of two strains of Xanthomonas fuscans subsp. aurantifolii - Moreira_2010_BMC.Genomics_11_238
Author(s) : Moreira LM , Almeida NF, Jr. , Potnis N , Digiampietri LA , Adi SS , Bortolossi JC , da Silva AC , da Silva AM , de Moraes FE , de Oliveira JC , de Souza RF , Facincani AP , Ferraz AL , Ferro MI , Furlan LR , Gimenez DF , Jones JB , Kitajima EW , Laia ML , Leite RP, Jr. , Nishiyama MY , Rodrigues Neto J , Nociti LA , Norman DJ , Ostroski EH , Pereira HA, Jr. , Staskawicz BJ , Tezza RI , Ferro JA , Vinatzer BA , Setubal JC
Ref : BMC Genomics , 11 :238 , 2010
Abstract :

BACKGROUND: Citrus canker is a disease that has severe economic impact on the citrus industry worldwide. There are three types of canker, called A, B, and C. The three types have different phenotypes and affect different citrus species. The causative agent for type A is Xanthomonas citri subsp. citri, whose genome sequence was made available in 2002. Xanthomonas fuscans subsp. aurantifolii strain B causes canker B and Xanthomonas fuscans subsp. aurantifolii strain C causes canker C.
RESULTS: We have sequenced the genomes of strains B and C to draft status. We have compared their genomic content to X. citri subsp. citri and to other Xanthomonas genomes, with special emphasis on type III secreted effector repertoires. In addition to pthA, already known to be present in all three citrus canker strains, two additional effector genes, xopE3 and xopAI, are also present in all three strains and are both located on the same putative genomic island. These two effector genes, along with one other effector-like gene in the same region, are thus good candidates for being pathogenicity factors on citrus. Numerous gene content differences also exist between the three cankers strains, which can be correlated with their different virulence and host range. Particular attention was placed on the analysis of genes involved in biofilm formation and quorum sensing, type IV secretion, flagellum synthesis and motility, lipopolysacharide synthesis, and on the gene xacPNP, which codes for a natriuretic protein. CONCLUSION: We have uncovered numerous commonalities and differences in gene content between the genomes of the pathogenic agents causing citrus canker A, B, and C and other Xanthomonas genomes. Molecular genetics can now be employed to determine the role of these genes in plant-microbe interactions. The gained knowledge will be instrumental for improving citrus canker control.

PubMedSearch : Moreira_2010_BMC.Genomics_11_238
PubMedID: 20388224
Gene_locus related to this paper: xanax-CATD , xanax-ENTF2 , xanax-estA1 , xanax-GAA , xanax-PTRB , xanax-XAC0198 , xanax-XAC0515 , xanax-XAC0591 , xanax-XAC0619 , xanax-XAC0628 , xanax-XAC0736 , xanax-XAC0753 , xanax-XAC0805 , xanax-XAC1213 , xanax-XAC1713 , xanax-XAC1752 , xanax-XAC2393 , xanax-XAC2532 , xanax-XAC2541 , xanax-XAC2987 , xanax-XAC3315 , xanax-XAC3371 , xanax-XAC4046 , xanax-XAC4055 , xanax-XAC4106 , xanax-XYNB , xanc5-q3bqi2 , xanca-impep , xanca-XCC1105 , xanca-XCC2566 , xanca-XCC2722 , xanor-acvB , xanor-metx , 9xant-a0a0g8v5k2

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Moreira LM, Almeida NF, Jr., Potnis N, Digiampietri LA, Adi SS, Bortolossi JC, da Silva AC, da Silva AM, de Moraes FE, de Oliveira JC, de Souza RF, Facincani AP, Ferraz AL, Ferro MI, Furlan LR, Gimenez DF, Jones JB, Kitajima EW, Laia ML, Leite RP, Jr., Nishiyama MY, Rodrigues Neto J, Nociti LA, Norman DJ, Ostroski EH, Pereira HA, Jr., Staskawicz BJ, Tezza RI, Ferro JA, Vinatzer BA, Setubal JC (2010)
Novel insights into the genomic basis of citrus canker based on the genome sequences of two strains of Xanthomonas fuscans subsp. aurantifolii
BMC Genomics 11 :238

Moreira LM, Almeida NF, Jr., Potnis N, Digiampietri LA, Adi SS, Bortolossi JC, da Silva AC, da Silva AM, de Moraes FE, de Oliveira JC, de Souza RF, Facincani AP, Ferraz AL, Ferro MI, Furlan LR, Gimenez DF, Jones JB, Kitajima EW, Laia ML, Leite RP, Jr., Nishiyama MY, Rodrigues Neto J, Nociti LA, Norman DJ, Ostroski EH, Pereira HA, Jr., Staskawicz BJ, Tezza RI, Ferro JA, Vinatzer BA, Setubal JC (2010)
BMC Genomics 11 :238