Umasuthan Navaneethaiyer, Xue Xi, Caballero-Solares Albert, Kumar Surendra, Westcott Jillian D, Chen Zhiyu, Fast Mark D, Skugor Stanko, Nowak Barbara F, Taylor Richard G, Rise Matthew L
Department of Ocean Sciences, Memorial University of Newfoundland, St. John's, NL A1C 5S7, Canada.
Fisheries and Marine Institute, Memorial University of Newfoundland, P.O. Box 4920, St. John's, NL A1C 5R3, Canada.
Int J Mol Sci. 2020 Mar 31;21(7):2417. doi: 10.3390/ijms21072417.
Parasitic sea lice (e.g., ) cause costly outbreaks in salmon farming. Molecular insights into parasite-induced host responses will provide the basis for improved management strategies. We investigated the early transcriptomic responses in pelvic fins of Atlantic salmon parasitized with chalimus I stage sea lice. Fin samples collected from non-infected (i.e. pre-infected) control (PRE) and at chalimus-attachment sites (ATT) and adjacent to chalimus-attachment sites (ADJ) from infected fish were used in profiling global gene expression using 44 K microarrays. We identified 6568 differentially expressed probes (DEPs, FDR < 5%) that included 1928 shared DEPs between ATT and ADJ compared to PRE. The ATT versus ADJ comparison revealed 90 DEPs, all of which were upregulated in ATT samples. Gene ontology/pathway term network analyses revealed profound changes in physiological processes, including extracellular matrix (ECM) degradation, tissue repair/remodeling and wound healing, immunity and defense, chemotaxis and signaling, antiviral response, and redox homeostasis in infected fins. The QPCR analysis of 37 microarray-identified transcripts representing these functional themes served to confirm the microarray results with a significant positive correlation ( < 0.0001). Most immune/defense-relevant transcripts were downregulated in both ATT and ADJ sites compared to PRE, suggesting that chalimus exerts immunosuppressive effects in the salmon's fins. The comparison between ATT and ADJ sites demonstrated the upregulation of a suite of immune-relevant transcripts, evidencing the salmon's attempt to mount an anti-lice response. We hypothesize that an imbalance between immunomodulation caused by chalimus during the early phase of infection and weak defense response manifested by Atlantic salmon makes it a susceptible host for .
寄生性海虱(如 )在鲑鱼养殖中引发代价高昂的疫情。对寄生虫诱导的宿主反应的分子洞察将为改进管理策略提供基础。我们研究了感染了无节幼体I期海虱的大西洋鲑鱼臀鳍的早期转录组反应。从未感染(即感染前)的对照鱼(PRE)以及感染鱼的无节幼体附着部位(ATT)和与无节幼体附着部位相邻的部位(ADJ)采集的鳍样本,用于使用44 K微阵列分析全球基因表达。我们鉴定出6568个差异表达探针(DEP,FDR < 5%),其中与PRE相比,ATT和ADJ之间有1928个共享的DEP。ATT与ADJ的比较揭示了90个DEP,所有这些DEP在ATT样本中均上调。基因本体/通路术语网络分析显示生理过程发生了深刻变化,包括细胞外基质(ECM)降解、组织修复/重塑和伤口愈合、免疫和防御、趋化性和信号传导、抗病毒反应以及感染鳍中的氧化还原稳态。对代表这些功能主题的37个微阵列鉴定转录本的QPCR分析用于确认微阵列结果,具有显著正相关(< 0.0001)。与PRE相比,大多数与免疫/防御相关的转录本在ATT和ADJ部位均下调,表明无节幼体在鲑鱼鳍中发挥免疫抑制作用。ATT和ADJ部位之间的比较表明一组与免疫相关的转录本上调,证明鲑鱼试图发起抗海虱反应。我们假设在感染早期无节幼体引起的免疫调节与大西洋鲑鱼表现出的弱防御反应之间的失衡,使其成为 的易感宿主。