Hernández-Velázquez Ioreni Margarita, Zamora-Briseño Jesús Alejandro, Pereira-Santana Alejandro, Huchin-Mian Juan Pablo, González-Penagos Carlos Eduardo, Pérez-Vega Juan Antonio, Lozano-Álvarez Enrique, Briones-Fourzán Patricia, Rodríguez-Canul Rossanna
Laboratorio de Inmunología y Biología Molecular, Departamento de Recursos del Mar, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional-Unidad Mérida, Km 6 Antigua Carretera a Progreso, CORDEMEX, Mérida, Yucatán CP 97310, México.
Laboratorio de Inmunología y Biología Molecular, Departamento de Recursos del Mar, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional-Unidad Mérida, Km 6 Antigua Carretera a Progreso, CORDEMEX, Mérida, Yucatán CP 97310, México; Current affiliation: Laboratorio de Entomología Molecular. Red de Estudios Moleculares Avanzados, Clúster Científico y Tecnológico BioMimic®. El Instituto de Ecología, Carretera antigua a Coatepec 351, El Haya, Xalapa, Veracruz CP 91070, México.
Virus Res. 2022 Apr 2;311:198713. doi: 10.1016/j.virusres.2022.198713. Epub 2022 Feb 15.
The Caribbean spiny lobster, Panulirus argus (Latreille, 1804) supports important fisheries in the Caribbean region. This species is affected by a deadly virus, Panulirus argus Virus 1 (PaV1), the only known pathogenic virus for this species. As infection progresses, the effects of PaV1 on its host become systemic, with far reaching impacts on the host's physiology, including structural injuries to its gastrointestinal organs, such as the hepatopancreas and the gut. This last one becomes highly compromised in the last stages of infection. Since the gut is a key organ for the physiological stability of lobsters, we compared the transcriptomic changes in the gut of juvenile individuals of Panulirus argus naturally infected with PaV1. In the RNA-Seq analysis, we obtained a total of 485 × 10 raw reads. After cleaning, reads were de novo assembled into 68,842 transcripts and 50,257 unigenes. The length of unigenes ranged from 201 bp to 28,717 bp, with a N50 length of 2079, and a GC content of 40.61%. In the differential gene expression analysis, we identified a total of 3405 non redundant differential transcripts, of which 1920 were up-regulated and 1485 were down-regulated. We found alterations in transcripts encoding for proteins involved in transcriptional regulation, splicing, postraductional regulation, protein signaling, transmembrane transport, cytoskeletal regulation, and proteolysis, among others. This is the first insight into the transcriptomic regulation of PaV1-P. argus interaction. The information generated can help to unravel the molecular mechanisms that may intervene in the gut during PaV1 infection.
加勒比刺龙虾(Panulirus argus,拉特雷尔,1804年)支撑着加勒比地区重要的渔业。该物种受到一种致命病毒——加勒比刺龙虾病毒1(PaV1)的影响,这是已知的该物种唯一致病病毒。随着感染的进展,PaV1对其宿主的影响会变得全身性,对宿主的生理机能产生深远影响,包括对其消化器官如肝胰腺和肠道造成结构性损伤。在感染的最后阶段,肠道受到的损害尤为严重。由于肠道是龙虾生理稳定性的关键器官,我们比较了自然感染PaV1的幼年加勒比刺龙虾肠道中的转录组变化。在RNA测序分析中,我们总共获得了485×10的原始读数。经过清理后,读数被从头组装成68,842个转录本和50,257个单基因。单基因的长度范围从201碱基对到28,717碱基对,N50长度为2079,GC含量为40.61%。在差异基因表达分析中,我们总共鉴定出3405个非冗余差异转录本,其中1920个上调,1485个下调。我们发现参与转录调控、剪接、转录后调控、蛋白质信号传导、跨膜运输、细胞骨架调控和蛋白水解等过程的蛋白质编码转录本发生了变化。这是对PaV1与加勒比刺龙虾相互作用的转录组调控的首次深入研究。所产生的信息有助于揭示在PaV1感染期间可能在肠道中起作用的分子机制。