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Campo DCValorIdioma
dc.creatorBarbosa C.S.
dc.creatorda Fonseca R.R.
dc.creatorBatista T.M.
dc.creatorBarreto M.A.
dc.creatorArgolo C.S.
dc.creatorde Carvalho M.R.
dc.creatordo Amaral D.O.J.
dc.creatorSilva E.M.A.
dc.creatorArévalo-Gardini E.
dc.creatorHidalgo K.S.
dc.creatorFranco G.R.
dc.creatorPirovani C.P.
dc.creatorMicheli F.
dc.creatorGramacho K.P.
dc.date.accessioned2019-05-31T16:16:39Z-
dc.date.available2019-05-31T16:16:39Z-
dc.date.issued2018
dc.identifier.issn14712164
dc.identifier.urihttps://hdl.handle.net/10216/120518-
dc.description.abstractBackground: The hemibiotrophic pathogens Moniliophthora perniciosa (witches' broom disease) and Moniliophthora roreri (frosty pod rot disease) are among the most important pathogens of cacao. Moniliophthora perniciosa has a broad host range and infects a variety of meristematic tissues in cacao plants, whereas M. roreri infects only pods of Theobroma and Herrania genera. Comparative pathogenomics of these fungi is essential to understand Moniliophthora infection strategies, therefore the detection and in silico functional characterization of effector candidates are important steps to gain insight on their pathogenicity. Results: Candidate secreted effector proteins repertoire were predicted using the genomes of five representative isolates of M. perniciosa subpopulations (three from cacao and two from solanaceous hosts), and one representative isolate of M. roreri from Peru. Many putative effectors candidates were identified in M. perniciosa: 157 and 134 in cacao isolates from Bahia, Brazil; 109 in cacao isolate from Ecuador, 92 and 80 in wild solanaceous isolates from Minas Gerais (Lobeira) and Bahia (Caiçara), Brazil; respectively. Moniliophthora roreri showed the highest number of effector candidates, a total of 243. A set of eight core effectors were shared among all Moniliophthora isolates, while others were shared either between the wild solanaceous isolates or among cacao isolates. Mostly, candidate effectors of M. perniciosa were shared among the isolates, whereas in M. roreri nearly 50% were exclusive to the specie. In addition, a large number of cell wall-degrading enzymes characteristic of hemibiotrophic fungi were found. From these, we highlighted the proteins involved in cell wall modification, an enzymatic arsenal that allows the plant pathogens to inhabit environments with oxidative stress, which promotes degradation of plant compounds and facilitates infection. Conclusions: The present work reports six genomes and provides a database of the putative effectorome of Moniliophthora, a first step towards the understanding of the functional basis of fungal pathogenicity. © 2018 The Author(s).
dc.description.sponsorshipThis work was done in the frame of the International Consortium in Advanced Biology (CIBA; https://www.ciba-network.org). The authors thank the Molecular Plant Pathology Laboratory and the Plant Pathology Laboratory at INIAP personnel for their assistance in obtaining the DNAs, Dr Carmen Suarez Capello for her kind assistance in Ecuador, and the Núcleo de Biologia Computacional e Gestão de Informações Biotecnológicas - UESC (NBCGIB), and Copenhague University for providing bioinformatics facility. Data sets were processed in sagarana HPC cluster, CPAD-ICB-UFMG. The authors would also like to thank Dr. Claudia Fortes Ferreira (Embrapa CNPMF, Brazil) and Dr. Raul Renné Valle (CEPLAC/CEPEC, Brazil) for English language revision. We are also grateful to Ivanna Michelle Meraz Pérez for helping translating an early version of this manuscript and to the anonymous reviewers who provided helpful comments to our work. KPG, FM and CPP were supported by research fellowship Pq-1 from CNPq. National Council for Scientific Development (CNPq) n° 311759/2014–9. CSB acknowledges FAPESB (Foundation for Research Support of the State of Bahia) for supporting her with a research assistantship during her Master’s Programme.
dc.language.isoeng
dc.publisherBMC
dc.relation.ispartofBMC Genomics, vol. 19(1):509
dc.rightsopenAccess
dc.subjecteffectorome
dc.subjectproteome
dc.subjectunclassified drug
dc.subjectfungal DNA
dc.subjectfungal protein
dc.subjectArticle
dc.subjectBrazil
dc.subjectcacao
dc.subjectcontrolled study
dc.subjectEcuador
dc.subjectfungal cell wall
dc.subjectfungal genome
dc.subjectfungal virulence
dc.subjectgene sequence
dc.subjectMoniliophthora
dc.subjectMoniliophthora perniciosa
dc.subjectMoniliophthora roreri
dc.subjectnonhuman
dc.subjectoxidative stress
dc.subjectPeru
dc.subjectSolanaceae
dc.subjectAgaricales
dc.subjectchemistry
dc.subjectclassification
dc.subjectgenetics
dc.subjectisolation and purification
dc.subjectmetabolism
dc.subjectmicrobiology
dc.subjectphylogeny
dc.subjectplant disease
dc.subjectwhole genome sequencing
dc.subjectAgaricales
dc.subjectBrazil
dc.subjectCacao
dc.subjectDNA, Fungal
dc.subjectFungal Proteins
dc.subjectGenome, Fungal
dc.subjectPhylogeny
dc.subjectPlant Diseases
dc.subjectWhole Genome Sequencing
dc.titleGenome sequence and effectorome of Moniliophthora perniciosa and Moniliophthora roreri subpopulations
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoCIIMAR - Centro Interdisciplinar de Investigação Marinha e Ambiental
dc.identifier.doi10.1186/s12864-018-4875-7
dc.relation.publisherversionhttp://dx.doi.org/10.1186/s12864-018-4875-7
Aparece nas coleções:CIIMAR - Artigo em Revista Científica Internacional

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