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Whole-genome comparison between reference sequences and oyster Vibrio vulnificus C-genotype strains

CARLOS ABRAHAM GUERRERO RUIZ (2019, [Artículo])

Whole-genome sequences of Vibrio vulnificus clinical genotype (C-genotype) from the CICESE Culture Collection, isolated from oysters, were compared with reference sequences of CMCP6 and YJ016 V. vulnificus C-genotype strains of clinical origin. The RAST web server estimated the whole genome to be ~4.8 Mb in CICESE strain 316 and ~4.7 Mb in CICESE strain 325. No plasmids were detected in the CICESE strains. Based on a phylogenetic tree that was constructed with the whole-genome results, we observed high similarity between the reference sequences and oyster C-genotype isolates and a sharp contrast with environmental genotype (E-genotype) reference sequences, indicating that the differences between the C- and E-genotypes do not necessarily correspond to their isolation origin. The CICESE strains share 3488 genes (63.2%) with the YJ016 strain and 3500 genes (63.9%) with the CMCP6 strain. A total of 237 pathogenicity associated genes were selected from reference clinical strains, where—92 genes were from CMCP6, 126 genes from YJ016, and 19 from MO6-24/ O; the presence or absence of these genes was recorded for the CICESE strains. Of the 92 genes that were selected for CMCP6, 67 were present in both CICESE strains, as were as 86 of the 126 YJ016 genes and 13 of the 19 MO6-24/O genes. The detection of elements that are related to virulence in CICESE strains—such as the RTX gene cluster, vvhA and vvpE, the type IV pili cluster, the XII genomic island, and the viuB genes, suggests that environmental isolates with the C-genotype, have significant potential for infection. © 2019 Guerrero et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Article, bacterial gene, bacterial strain, bacterial virulence, comparative study, controlled study, gene cluster, gene identification, genomic island, genotype, nonhuman, phylogenetic tree, sequence analysis, strain identification, Vibrio vulnificus BIOLOGÍA Y QUÍMICA CIENCIAS DE LA VIDA GENÉTICA GENÉTICA

Evaluación del acondicionamiento reproductivo del ostión japonés (Magallana gigas) en dos sistemas de recirculación con prevalencia de polidóridos mediante la expresión de genes

Evaluation of Japanese oyster (Magallana gigas) broodstock conditioning in two recirculating systems with the prevalence of Polidorids through gene expression

Adrián Andrés Morales Guadarrama (2024, [Tesis de maestría])

El ostión Magallana gigas es ampliamente cultivado a nivel mundial. En Baja California, México, los laboratorios de reproducción deben acondicionar ostiones para su maduración y producción de gametos, y abastecer de semilla a los productores. En nuestro laboratorio, Sistemas de Recirculación Acuícola (SRA), con control del sistema CO2-Carbonatos (SRA-R) o sin control (SRA-C), han permitido madurar ostiones M. gigas y M. sikamea. Recientemente, los ostiones M. gigas acondicionados en nuestros SRA no maduraron, y algunos presentaron prevalencia de polidóridos (PP), poliquetos parásitos excavadores de concha. Para comprender la condición de los ostiones, evaluamos el efecto del SRA y de la PP sobre la expresión relativa de ocho genes asociados a biomineralización (VpATP y Tyr), inmunidad innata (P38, PGRP-L y TLR2) y reproducción (GnRH-RI, Vasa-like y SP1b) de M. gigas en dos etapas del acondicionamiento, 18 °C y 24 °C. La PP se determinó por la presencia de ampollas en la concha. Mediante RT-qPCR se determinó la expresión de VpATP, Tyr, P38, PGRP-L y TLR2 en el manto, y de GnRH-RI, Vasa-like y SP1b en la gónada. La expresión relativa se evaluó con un enfoque estadístico basado en un análisis Bayesiano de dos vías y comparaciones múltiples, p-valor significativo < 0.05 y corrección de Bonferroni. En 18 °C, la expresión de VpATP, Tyr, TLR2 y P38 fue mayor en ostiones con PP (CPP) que sin PP (SPP). En contraste, la expresión de GnRH-RI, Vasa-like y SP1b fue menor CPP que SPP. Dentro del SRA-C, en los ostiones CPP hubo mayor expresión de Tyr y menor expresión de Vasa-like y SP1b, respecto a los ostiones SPP. Esto sugiere que la PP induce la reparación de la concha y las respuestas inmune e inflamatoria en el manto mientras que en la gónada reduce el desarrollo de las células germinales. En 24 °C, en el SRA-R hubo menor expresión de SP1b respecto del SRA-C y sugiere menor división celular en la gónada. En conclusión, el SRA-R y la PP afectaron el balance energético del ostión japonés, limitando la energía y reflejando menor esfuerzo reproductivo en los ostiones del SRA-R al final del acondicionamiento reproductivo.

The Japanese oyster (Magallana gigas) is highly cultured worldwide. In Baja California, Mexico, the reproduction laboratories must condition oysters to maturity and have gametes to supply oyster seeds to producers. In our laboratory, recirculating aquaculture systems (RAS), with control of the CO2-Carbonate system (RAS-R) and without this control (RAS-C), have allowed oysters M. gigas and M. sikamea to mature. Recently, the M. gigas oysters conditioned in our RAS did not mature, and some have the prevalence of Polidorids (PP), shell-boring polychaete parasites. To understand the oysters' condition, we evaluated the effect of RAS and the PP on the relative expression of eight genes associated with biomineralization (VpATP and Tyr), innate immunity (P38, PGRP-L, and TLR2), and reproduction (GnRH-RI, Vasa-like, and SP1b) of M. gigas at two phases of broodstock conditioning, 18 °C and 24 °C. The PP was determined by mud blisters at the inner oyster shell. RT-qPCR determined the expression of VpATP, Tyr, p38, PGRP-L, and TLR2 in the mantle tissue and GnRH-RI, Vasa-like, and SP1b in the gonad tissue. The relative gene expression was evaluated by a Bayesian statistics frame based on a two-way and multiple comparison analysis, with significant p-value < 0.05 and Bonferroni correction. At 18 °C, there was higher expression of VpATP, Tyr, TLR2, and P38 in oysters with PP (WPP) than without PP (WOPP). In contrast, the expression of GnRH-RI, Vasa-like, and SP1b was less WPP than WOPP. It suggests that the PP induces shell repair and immune and inflammatory responses in mantle tissue, while in gonad tissue, it reduces the development of germinal cells. At 24 °C, in RAS-R, there was less expression of SP1b respect RAS-C, and it suggests less cellular division in the gonad. In conclusion, the RAS-R and the PP affect the energetic balance of the Japanese oyster, limiting the energy and reflecting less reproduction effort in oysters from RAS-R at the end of broodstock conditioning.

SRA, biomineralización, Vasa-like, Tyr, ostión RAS, biomineralization, Vasa-like, Tyr, oyster BIOLOGÍA Y QUÍMICA CIENCIAS DE LA VIDA GENÉTICA CITOGENÉTICA ANIMAL CITOGENÉTICA ANIMAL

The Banana MaWRKY18, MaWRKY45, MaWRKY60 and MaWRKY70 Genes Encode Functional Transcription Factors and Display Differential Expression in Response to Defense Phytohormones

SERGIO GARCIA LAYNES VIRGINIA AURORA HERRERA VALENCIA Lilia Guadalupe Tamayo Torres VERONICA LIMONES BRIONES FELIPE ALONSO BARREDO POOL FRAY MARTIN BAAS ESPINOLA Ángel Gabriel Alpuche Solís CARLOS ALBERTO PUCH HAU SANTY PERAZA ECHEVERRIA (2022, [Artículo])

"WRKY transcription factors (TFs) play key roles in plant defense responses through phytohormone signaling pathways. However, their functions in tropical fruit crops, especially in banana, remain largely unknown. Several WRKY genes from the model plants rice (OsWRKY45) and Arabidopsis (AtWRKY18, AtWRKY60, AtWRKY70) have shown to be attractive TFs for engineering disease resistance. In this study, we isolated four banana cDNAs (MaWRKY18, MaWRKY45, MaWRKY60, and MaWRKY70) with homology to these rice and Arabidopsis WRKY genes. The MaWRKY cDNAs were isolated from the wild banana Musa acuminata ssp. malaccensis, which is resistant to several diseases of this crop and is a progenitor of most banana cultivars. The deduced amino acid sequences of the four MaWRKY cDNAs revealed the presence of the conserved WRKY domain of ~60 amino acids and a zinc-finger motif at the N-terminus. Based on the number of WRKY repeats and the structure of the zinc-finger motif, MaWRKY18 and MaWRKY60 belong to group II of WRKY TFs, while MaWRKY45 and MaWRKY70 are members of group III. Their corresponding proteins were located in the nuclei of onion epidermal cells and were shown to be functional TFs in yeast cells. Moreover, expression analyses revealed that the majority of these MaWRKY genes were upregulated by salicylic acid (SA) or methyl jasmonate (MeJA) phytohormones, although the expression levels were relatively higher with MeJA treatment. The fact that most of these banana WRKY genes were upregulated by SA or MeJA, which are involved in systemic acquired resistance (SAR) or induced systemic resistance (ISR), respectively, make them interesting candidates for bioengineering broad-spectrum resistance in this crop."

Banana Transcription factor WRKY Defense phytohormones Salicylic acid Methyl jasmonate SAR ISR Broad-spectrum resistance BIOLOGÍA Y QUÍMICA CIENCIAS DE LA VIDA GENÉTICA GENÉTICA