Hawkesbury Institute for the Environment, Western Sydney University, Locked Bag 1797, Penrith, NSW 2751, Australia.
Evolution & Ecology Research Centre, The University of New South Wales, Kensington, NSW 2052, Australia.
J Invertebr Pathol. 2021 Nov;186:107569. doi: 10.1016/j.jip.2021.107569. Epub 2021 Mar 13.
Tephritid fruit flies are amongst the most devastating pests of horticulture, and Sterile Insect Technique (SIT) programs have been developed for their control. Their interactions with viruses are still mostly unexplored, yet, viruses may negatively affect tephritid health and performance in SIT programs, and, conversely, constitute potential biological control agents. Here we analysed ten transcriptome libraries obtained from laboratory populations of nine tephritid species from Australia (six species of Bactrocera, and Zeugodacus cucumis), Asia (Bactrocera dorsalis) and Europe (Ceratitis capitata). We detected new viral diversity, including near-complete (>99%) and partially complete (>80%) genomes of 34 putative viruses belonging to eight RNA virus families. On average, transcriptome libraries included 3.7 viruses, ranging from 0 (Z. cucumis) to 9 (B. dorsalis). Most viruses belonged to the Picornavirales, represented by fourteen Dicistroviridae (DV), nine Iflaviridae (IV) and two picorna-like viruses. Others were a virus from Rhabdoviridae (RV), one from Xinmoviridae (both Mononegavirales), several unclassified Negev- and toti-like viruses, and one from Metaviridae (Ortervirales). Using diagnostic PCR primers for four viruses found in the transcriptome of the Bactrocera tryoni strain bent wings (BtDV1, BtDV2, BtIV1, and BtRV1), we tested nine Australian laboratory populations of five species (B. tryoni, Bactrocera neohumeralis, Bactrocera jarvisi, Bactrocera cacuminata, C. capitata), and one field population each of B. tryoni, B. cacuminata and Dirioxa pornia. Viruses were present in most laboratory and field populations yet their incidence differed for each virus. Prevalence and co-occurrence of viruses in B. tryoni and B. cacuminata were higher in laboratory than field populations. This raises concerns about the potential accumulation of viruses and their potential health effects in laboratory and mass-rearing environments which might affect flies used in research and control programs such as SIT.
实蝇是园艺业中最具破坏性的害虫之一,为此已经开发了不育昆虫技术(SIT)项目来对其进行防治。然而,实蝇与病毒的相互作用在很大程度上仍未得到探索,病毒可能会对实蝇的健康和 SIT 项目中的表现产生负面影响,反之,病毒也可能成为潜在的生物防治剂。在这里,我们分析了来自澳大利亚(6 种 Bactrocera 和 Zeugodacus cucumis)、亚洲(Bactrocera dorsalis)和欧洲(Ceratitis capitata)的 9 种实蝇实验室种群的 10 个转录组文库。我们检测到了新的病毒多样性,包括 34 种假定病毒的近完整(>99%)和部分完整(>80%)基因组,这些病毒属于 8 种 RNA 病毒科。平均而言,转录组文库包含 3.7 种病毒,范围从 0(Z. cucumis)到 9(B. dorsalis)。大多数病毒属于小核糖核酸病毒目,其中包括 14 种双顺反子病毒科(DV)、9 种杆状病毒科(IV)和 2 种类微小核糖核酸病毒。其他病毒分别来自呼肠孤病毒科(RV)、辛诺病毒科(Mononegavirales)各 1 种、几种未分类的 Negev 和 totivirus 样病毒以及有尾病毒科(Ortervirales)1 种。使用在 Bactrocera tryoni 弯翅品系转录组中发现的四种病毒(BtDV1、BtDV2、BtIV1 和 BtRV1)的诊断 PCR 引物,我们测试了澳大利亚五个物种(B. tryoni、Bactrocera neohumeralis、Bactrocera jarvisi、Bactrocera cacuminata、C. capitata)的 9 个实验室种群和每个物种的一个野外种群(B. tryoni、B. cacuminata 和 Dirioxa pornia)。病毒存在于大多数实验室和野外种群中,但每种病毒的发生率不同。在实验室种群中,B. tryoni 和 B. cacuminata 中病毒的流行率和共存率高于野外种群。这引起了人们对实验室和大规模繁殖环境中病毒积累及其对健康影响的担忧,这可能会影响用于研究和控制计划(如 SIT)的苍蝇。