Tarimo Brian B, Law Henry Chun Hin, Tao Dingyin, Pastrana-Mena Rebecca, Kanzok Stefan M, Buza Joram J, Dinglasan Rhoel R
School of Life Science and Bioengineering, Nelson Mandela-African Institution of Science and Technology, Tengeru, Arusha 23302, Tanzania.
W. Harry Feinstone Department of Molecular Microbiology & Immunology & the Malaria Research Institute, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA.
Proteomes. 2018 Nov 12;6(4):47. doi: 10.3390/proteomes6040047.
Paraquat is a potent superoxide (O₂)-inducing agent that is capable of inducing an oxidative imbalance in the mosquito midgut. This oxidative imbalance can super-stress the malaria parasite, leading to arrested development in the mosquito midgut and reduced transmission. While several studies have explored the effect of paraquat on malaria parasites, a fundamental understanding of the mosquito response to this compound remains unknown. Here, we quantified the mosquito midgut proteomic response to a paraquat-laced sugar meal, and found that midguts were enriched in proteins that are indicative of cells under endoplasmic reticulum (ER) stress. We also carried out qRT-PCR analyses for nine prominent thioredoxin (Trx) and glutathione (GSH)-dependent genes in mosquito midguts post blood meal ingestion to evaluate the concordance between transcripts and proteins under different oxidative stress conditions. Our data revealed an absence of significant upregulation in the Trx and GSH-dependent genes following infected blood meal ingestion. These data suggest that the intrinsic tolerance of the mosquito midgut to paraquat-mediated oxidative stress is through an ER stress response. These data indicate that mosquitoes have at least two divergent pathways of managing the oxidative stress that is induced by exogenous compounds, and outline the potential application of paraquat-like drugs to act selectively against malaria parasite development in mosquito midguts, thereby blocking mosquito-to-human transmission.
百草枯是一种强效的超氧化物(O₂)诱导剂,能够在蚊子中肠诱导氧化失衡。这种氧化失衡会给疟原虫带来极大压力,导致其在蚊子中肠发育停滞并减少传播。虽然已有多项研究探讨了百草枯对疟原虫的影响,但蚊子对这种化合物的反应的基本情况仍不清楚。在这里,我们对摄入含百草枯糖餐的蚊子中肠蛋白质组反应进行了定量分析,发现中肠中富含指示内质网(ER)应激下细胞的蛋白质。我们还对蚊子在摄入血餐后中肠中九个突出的硫氧还蛋白(Trx)和谷胱甘肽(GSH)依赖性基因进行了qRT-PCR分析,以评估不同氧化应激条件下转录本和蛋白质之间的一致性。我们的数据显示,摄入感染血餐后,Trx和GSH依赖性基因没有明显上调。这些数据表明,蚊子中肠对百草枯介导的氧化应激的内在耐受性是通过内质网应激反应实现的。这些数据表明,蚊子至少有两条不同的途径来应对由外源化合物诱导的氧化应激,并概述了类似百草枯的药物在选择性对抗蚊子中肠疟原虫发育从而阻断蚊子向人类传播方面的潜在应用。