Hossain Md Mer Mosharraf, Farjana Nawshin, Afroz Rukaiya, Saha Pobitra Kumar, Roy Hironmoy Shovon, Rahman Md Anisur, Farid Md Almamun
Department of Fisheries and Marine Bioscience, Jashore University of Science and Technology (JUST), Bangladesh.
PCF Feed Industries Ltd, Bangladesh.
Fish Shellfish Immunol Rep. 2023 Apr 3;4:100092. doi: 10.1016/j.fsirep.2023.100092. eCollection 2023 Dec.
the causative agent of Acute hepatopancreatic necrosis disease (AHPND), was discovered in 2013 as a unique isolate that produces toxins and kills penaeid shrimps in devasting nature in Bangladesh and causes severe economic losses. This research aimed to understand the expressions of immune genes in different stages of the host species, against virulence and toxin genes upon being challenged with . Healthy post-larvae (PL) samples were collected from southwestern of Bangladesh from July 2021 to August 2022. The tryptic soy agar with 1.5% sodium chloride (NaCl) was used to inoculate the cells of and the tryptic soy broth (TSB) with 1.5% NaCl was used to transfer the colonies. The spectrophotometry measured bacteria density. PCR, qPCR, SDS-PAGE, and Western blot measured gene expression and survivability after the immersion challenge. The 1 × 10CFU/mL of was used for 144 h.p.i (hours post-infection) challenge to six stages of post-larvae (PL) of (PL20, PL25, PL30, PL35, PL40, and PL45), PL30 and PL35 showed 100% mortality by day 72 (h.p.i.) after exposure that indicated most vulnerable to . The expression of immune and toxic genes was confirmed by qPCR. The immune genes toll-like receptors (TLR), prophenoloxidase (ProPO), lysozyme (lyso), and penaeidin (PEN) of PL20 and PL25 of were expressed robustly up-trends. PL30 and PL35 showed the lowest gene expression at the end of 72 (h.p.i.). At the end of the 144 (h.p.i.) exposure, the immune genes TLR, ProPO, lyso, and PEN expressed highest in PL45 than other post-larvae stages of . The toxic genes (pirA, ToxR, ToxA, ToxB, tlh, tdh, and trh) in PL30 and PL35 of after exposure of were expressed highest at the end of the 72 (h.p.i.). The lowest toxic genes expressions were revealed in PL20 and PL45 at the end of the 144 (h.p.i.). The SDS-PAGE analysis of proteins from the bacterium revealed identical protein profiles with toxic genes, and those toxins were further confirmed by Western blot. The 20 kDa, 78 kDa (ToxR), 20 kDa, 25 kDa (ToxA), 25 kDa (ToxB), 20 kDa, 27 kDa, 75 kDa (tdh), and 20 kDa, 27 kDa, 75 kDa, and 78 kDa (trh) proteins were strong responses in Western blot, indicating the crucial involvement of these immune-related genes in the defense and recovery of the first-line defense mechanisms during infection to shrimp. The all-toxic genes showed a unique homology and those derived from the common ancestor compared with (NCBI accession no. AP014859.1). All clades were derived with different traits with very low genetic distance, where the overall mean distance was 3.18 and showed a very uniform and homogenous pattern among the lineages. The infection process in different PL stages in revealed novel insights into the immune responses. The responses may lead to the subsequent production of a DNA vaccine, enhancing shrimp health management to minimize the economic losses due to AHPND experiencing an outbreak of early mortality syndrome (EMS) toward sustainable production (shrimp).
急性肝胰腺坏死病(AHPND)的病原体于2013年被发现,是一种独特的分离株,它产生毒素,在孟加拉国以毁灭性的方式杀死对虾,并造成严重的经济损失。本研究旨在了解宿主物种不同阶段免疫基因在受到[病原体名称未明确]攻击时对毒力和毒素基因的表达情况。2021年7月至2022年8月从孟加拉国西南部收集健康的后期幼体(PL)样本。用含1.5%氯化钠(NaCl)的胰蛋白胨大豆琼脂接种[细菌名称未明确]细胞,并用含1.5%NaCl的胰蛋白胨大豆肉汤(TSB)转接菌落。用分光光度法测量细菌密度。PCR、qPCR、SDS - PAGE和蛋白质印迹法测量浸泡攻击后的基因表达和存活率。用1×10CFU/mL的[细菌名称未明确]对凡纳滨对虾后期幼体(PL)的六个阶段(PL20、PL25、PL30、PL35、PL40和PL45)进行144小时感染后(h.p.i)的攻击,PL30和PL35在暴露后第72小时(h.p.i)显示100%死亡率,表明对[病原体名称未明确]最易感。通过qPCR确认免疫和毒性基因的表达。凡纳滨对虾PL20和PL25的免疫基因Toll样受体(TLR)、前酚氧化酶(ProPO)、溶菌酶(lyso)和对虾抗菌肽(PEN)呈强劲上升趋势表达。PL30和PL35在72小时(h.p.i)结束时显示最低的基因表达。在144小时(h.p.i)暴露结束时,免疫基因TLR、ProPO、lyso和PEN在PL45中的表达高于凡纳滨对虾其他后期幼体阶段。凡纳滨对虾PL30和PL35在暴露于[细菌名称未明确]后,毒性基因(pirA、ToxR、ToxA、ToxB、tlh、tdh和trh)在72小时(h.p.i)结束时表达最高。在144小时(h.p.i)结束时,PL20和PL45中的毒性基因表达最低。对该细菌蛋白质的SDS - PAGE分析显示与毒性基因具有相同的蛋白质谱,并且这些毒素通过蛋白质印迹法进一步得到证实。20kDa、78kDa(ToxR)、20kDa、25kDa(ToxA)、25kDa(ToxB)、20kDa、27kDa、75kDa(tdh)以及20kDa、27kDa、75kDa和78kDa(trh)蛋白质在蛋白质印迹中产生强烈反应,表明这些免疫相关基因在凡纳滨对虾感染[病原体名称未明确]期间的一线防御机制的防御和恢复中起关键作用。所有毒性基因显示出独特的同源性,与[比较对象未明确](NCBI登录号AP014859.1)相比源自共同祖先。所有进化枝具有不同特征且遗传距离非常低,总体平均距离为3.18,并且在谱系中显示出非常一致和同质的模式。凡纳滨对虾不同PL阶段的[病原体名称未明确]感染过程揭示了免疫反应的新见解。这些反应可能导致随后生产DNA疫苗,加强对虾健康管理,以尽量减少因AHPND经历早期死亡综合征(EMS)爆发而导致的经济损失,实现对虾的可持续生产。