Gene expression analysis identifies hypothetical genes that may be critical during the infection process of Xanthomonas citri subsp. citri
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Keywords

Citrus sinensis
DNA microarrays
Gene expression
Hypothetical genes
Oligonucleotide Array Sequence Analysis
RT-qPCR
Transcriptome
Type III secretion systems
Virulence
Xanthan gum

How to Cite

1.
Luiz de Laia M, Marcio Moreira L, Fernandes Gonçalves J, Tiraboschi Ferro MI, Pinto Rodrigues AC, Naiara dos Santos J, Barbosa Felestrino Érica, Aparecido Ferro J. Gene expression analysis identifies hypothetical genes that may be critical during the infection process of Xanthomonas citri subsp. citri. Electron. J. Biotechnol. [Internet]. 2019 Nov. 28 [cited 2024 Dec. 11];42. Available from: https://www.ejbiotechnology.info/index.php/ejbiotechnology/article/view/2019.10.003

Abstract

Background: Gene expression analysis via microarray is widely used in phytobacteria to validate differential gene expression associated with virulence or to compare biological profiles of wild type and mutant strains. Here, we employed DNA microarrays to study the early stages of the infection process (24, 72 and 120 h post-inoculation) of Xanthomonas citri subsp. citri (Xac) infecting Citrus sinensis to interrogate the expression profiles of hypothetical genes.

Results: Under infective conditions, 446 genes were up- and 306 downregulated. Outstanding among genes upregulated during infection were those involved in synthesizing the Type 3 Secretion System and effectors, xanthan gum and quorum-sensing induction, and flagellum synthesis and regulation. Additionally, 161 hypothetical genes were up- and 100 were downregulated, 49 of which are known to have a significant biological role. To understand hypothetical gene co-regulation or -expression, nine expression profiles including 158 genes were identified during the three infection phases. Of these, 47 hypothetical genes were identified as having expression profiles associated with at least one connected to a gene associated with adaptation and virulence.

Conclusions: Expression patterns of six differentially expressed genes were validated by quantitative reverse transcription polymerase chain reaction, thus demonstrating the effectiveness of this tool in global gene expression analysis in Xac.

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