<p style="text-align:justify;"> <span><i><span style="font-family:""><span style="font-family:Verdana;">Citrus </span><span style="font-fa...<p style="text-align:justify;"> <span><i><span style="font-family:""><span style="font-family:Verdana;">Citrus </span><span style="font-family:Verdana;">tristeza</span><span style="font-family:Verdana;"> virus</span></span></i></span><span><span><span style="font-family:""><span style="font-family:Verdana;"> (CTV) outbreaks have been reported in the main citrus growing region of Mexico in the past four years. Recently, in eastern Mexico (the major citrus-growing region in the country), severe CTV isolates have been detected. However, the molecular identity of </span><span style="font-family:Verdana;">observed</span><span style="font-family:Verdana;"> isolates remains unestablished. This research was undertaken to elucidate the molecular characterization of CTV populations spreading in this region and to compare it with </span><span style="font-family:Verdana;">phylogeny</span><span style="font-family:Verdana;"> of existing isolates. Genotyping of 32 collected isolates was performed using reverse-transcription polymerase chain reaction (RT-PCR) with sequence analysis of the coat protein (CP) gene, putatively associated with pathogenicity. This protein is a 25 kDa major capsid protein, which forms a long virion body coating 95% of the particle length. </span><span style="font-family:Verdana;">A comparative</span><span style="font-family:Verdana;"> sequence </span><span style="font-family:Verdana;">analys</span></span></span></span><span style="font-family:Verdana;"><span style="font-family:Verdana;"><span style="font-family:Verdana;">is</span></span></span><span style="font-family:Verdana;"><span style="font-family:Verdana;"><span style="font-family:Verdana;"> was performed using CTV sequences from different geographical origins already published and deposited in the GenBank databases. Phylogenetic analysis showed that the degree of sequence divergence among isolates correlated with their pathogenicity. Based on the sequencing results, the collected isolates were categorizedn as mild or severe phylogenetic clusters, each being genetically distinct. The severe group was associated </span></span></span><span style="font-family:Verdana;"><span style="font-family:Verdana;"><span style="font-family:Verdana;">with</span></span></span><span><span><span style="font-family:""><span style="font-family:Verdana;"> either </span><span style="font-family:Verdana;">a</span></span></span></span><span style="font-family:Verdana;"><span style="font-family:Verdana;"><span style="font-family:Verdana;">-</span></span></span><span style="font-family:Verdana;"><span style="font-family:Verdana;"><span style="font-family:Verdana;">like</span></span></span><span><span><span style="font-family:""><span style="font-family:Verdana;"> or with a T36-like genotype. The latter group matched with the quick decline and stem pitting drastic symptoms observed in the field. This study identified the presence of severe CTV isolates related to the T36-like genotype and to the cause of quick decline and stem pitting in sweet orange propagated on sour orange rootstock. Knowledge derived from these analyses could serve to design management strategies for this disease and to understand the cur</span><span style="font-family:Verdana;">rent epidemic outbreak in scenarios where the most efficient vector is present.</span></span></span></span><span></span><span style="font-family:""></span> </p>展开更多
Huanglongbing (HLB) or citrus greening is currently the most important citrus disease, caused by the bacterium </span><i><span style="font-family:Verdana;">Candidatus</span></i>...Huanglongbing (HLB) or citrus greening is currently the most important citrus disease, caused by the bacterium </span><i><span style="font-family:Verdana;">Candidatus</span></i><span style="font-family:Verdana;"> Liberibacter asiaticus (</span><i><span style="font-family:Verdana;">C</span></i><span style="font-family:Verdana;">Las). The impossibility of isolating it causes understanding its pathogenic mechanisms to be a complicated task. Recent studies identified 16 proteins with the signal peptide needed to be secreted in the plant and cause the disease. The present study aims to perform a bioinformatic analysis of these proteins with the function prediction approach by gene ontology (GO) and the detection of conserved domains. It was observed that of the 16 proteins analyzed not all are found in different infective strains reported in the literature. The GO analysis allowed us to relate different proteins with the biological process of energy and pathogenic activity, especially CLIBASIA_03315 and CLIBASIA_05115, respectively. The domain analysis allowed the observation of a </span></span><i><span style="font-family:Verdana;">β</span></i><span style="font-family:""><span style="font-family:Verdana;">-CA domain, tentatively related to the damage caused to the chloroplast and a PAAR domain associated with the T6SS secretory system. Our results provide information on the possible function of potential pathogenicity effectors in </span><i><span style="font-family:Verdana;">C</span></i><span style="font-family:Verdana;">Las.展开更多
文摘<p style="text-align:justify;"> <span><i><span style="font-family:""><span style="font-family:Verdana;">Citrus </span><span style="font-family:Verdana;">tristeza</span><span style="font-family:Verdana;"> virus</span></span></i></span><span><span><span style="font-family:""><span style="font-family:Verdana;"> (CTV) outbreaks have been reported in the main citrus growing region of Mexico in the past four years. Recently, in eastern Mexico (the major citrus-growing region in the country), severe CTV isolates have been detected. However, the molecular identity of </span><span style="font-family:Verdana;">observed</span><span style="font-family:Verdana;"> isolates remains unestablished. This research was undertaken to elucidate the molecular characterization of CTV populations spreading in this region and to compare it with </span><span style="font-family:Verdana;">phylogeny</span><span style="font-family:Verdana;"> of existing isolates. Genotyping of 32 collected isolates was performed using reverse-transcription polymerase chain reaction (RT-PCR) with sequence analysis of the coat protein (CP) gene, putatively associated with pathogenicity. This protein is a 25 kDa major capsid protein, which forms a long virion body coating 95% of the particle length. </span><span style="font-family:Verdana;">A comparative</span><span style="font-family:Verdana;"> sequence </span><span style="font-family:Verdana;">analys</span></span></span></span><span style="font-family:Verdana;"><span style="font-family:Verdana;"><span style="font-family:Verdana;">is</span></span></span><span style="font-family:Verdana;"><span style="font-family:Verdana;"><span style="font-family:Verdana;"> was performed using CTV sequences from different geographical origins already published and deposited in the GenBank databases. Phylogenetic analysis showed that the degree of sequence divergence among isolates correlated with their pathogenicity. Based on the sequencing results, the collected isolates were categorizedn as mild or severe phylogenetic clusters, each being genetically distinct. The severe group was associated </span></span></span><span style="font-family:Verdana;"><span style="font-family:Verdana;"><span style="font-family:Verdana;">with</span></span></span><span><span><span style="font-family:""><span style="font-family:Verdana;"> either </span><span style="font-family:Verdana;">a</span></span></span></span><span style="font-family:Verdana;"><span style="font-family:Verdana;"><span style="font-family:Verdana;">-</span></span></span><span style="font-family:Verdana;"><span style="font-family:Verdana;"><span style="font-family:Verdana;">like</span></span></span><span><span><span style="font-family:""><span style="font-family:Verdana;"> or with a T36-like genotype. The latter group matched with the quick decline and stem pitting drastic symptoms observed in the field. This study identified the presence of severe CTV isolates related to the T36-like genotype and to the cause of quick decline and stem pitting in sweet orange propagated on sour orange rootstock. Knowledge derived from these analyses could serve to design management strategies for this disease and to understand the cur</span><span style="font-family:Verdana;">rent epidemic outbreak in scenarios where the most efficient vector is present.</span></span></span></span><span></span><span style="font-family:""></span> </p>
文摘Huanglongbing (HLB) or citrus greening is currently the most important citrus disease, caused by the bacterium </span><i><span style="font-family:Verdana;">Candidatus</span></i><span style="font-family:Verdana;"> Liberibacter asiaticus (</span><i><span style="font-family:Verdana;">C</span></i><span style="font-family:Verdana;">Las). The impossibility of isolating it causes understanding its pathogenic mechanisms to be a complicated task. Recent studies identified 16 proteins with the signal peptide needed to be secreted in the plant and cause the disease. The present study aims to perform a bioinformatic analysis of these proteins with the function prediction approach by gene ontology (GO) and the detection of conserved domains. It was observed that of the 16 proteins analyzed not all are found in different infective strains reported in the literature. The GO analysis allowed us to relate different proteins with the biological process of energy and pathogenic activity, especially CLIBASIA_03315 and CLIBASIA_05115, respectively. The domain analysis allowed the observation of a </span></span><i><span style="font-family:Verdana;">β</span></i><span style="font-family:""><span style="font-family:Verdana;">-CA domain, tentatively related to the damage caused to the chloroplast and a PAAR domain associated with the T6SS secretory system. Our results provide information on the possible function of potential pathogenicity effectors in </span><i><span style="font-family:Verdana;">C</span></i><span style="font-family:Verdana;">Las.