Exogenous functional DNA was introduced into the germline chromosomes of the Mediterranean fruit fly (medfly) Ceratitis capitata with a germline transformation system based on the transposable element Minos from Drosophila hydei. Transformants were identified as phenotypic revertants of a white-eyed mutation carried by the recipient strain. Clusters of transformants were detected among the progeny of 390 individuals screened for germline transformation. Five independent and phenotypically active integration events were identified, in each of which a single copy of the transposon was inserted into a different site of the medfly genome. Molecular analysis indicates that they represent transposase-mediated insertions of the transposon into medfly chromosomes.

Despite the major role of chitin biosynthesis inhibitors such as benzoylureas (BPUs) in the control of pests in agricultural and public health for almost four decades, their molecular mode of action (MoA) has in most cases remained elusive. BPUs interfere with chitin biosynthesis and were thought to interact with sulfonylurea receptors that mediate chitin vesicle transport. Here, we uncover a mutation (I1042M) in the chitin synthase 1 (CHS1) gene of BPU-resistant Plutella xylostella at the same position as the I1017F mutation reported in spider mites that confers etoxazole resistance. Using a genome-editing CRISPR/Cas9 approach coupled with homology-directed repair (HDR) in Drosophila melanogaster, we introduced both substitutions (I1056M/F) in the corresponding fly CHS1 gene (kkv). Homozygous lines bearing either of these mutations were highly resistant to etoxazole and all tested BPUs, as well as buprofezin-an important hemipteran chitin biosynthesis inhibitor. This provides compelling evidence that BPUs, etoxazole, and buprofezin share in fact the same molecular MoA and directly interact with CHS. This finding has immediate effects on resistance management strategies of major agricultural pests but also on mosquito vectors of serious human diseases such as Dengue and Zika, as diflubenzuron, the standard BPU, is one of the few effective larvicides in use. The study elaborates on how genome editing can directly, rapidly, and convincingly elucidate the MoA of bioactive molecules, especially when target sites are complex and hard to reconstitute in vitro

Wolbachia-induced cytoplasmic incompatibility (CI) is expressed when infected males are crossed with either uninfected females or females infected with Wolbachia of different CI specificity. In diploid insects, CI results in embryonic mortality, apparently due to the the loss of the paternal set of chromosomes, usually during the first mitotic division. The molecular basis of CI has not been determined yet; however, several lines of evidence suggest that Wolbachia exhibits two distinct sex-dependent functions: in males, Wolbachia somehow ''imprints'' the paternal chromosomes during spermatogenesis (mod function), whereas in females, the presence of the same Wolbachia strain(s) is able to restore embryonic viability (resc function). On the basis of the ability of Wolbachia to induce the modification and/or rescue functions in a given host, each bacterial strain can be classified as belonging in one of the four following categories:, and mod 1 resc À . A so-called ''suicide'' mod 1 resc À strain has not been found in nature yet. Here, a combination of embryonic cytoplasmic injections and introgression experiments was used to transfer nine evolutionary, distantly related Wolbachia strains (wYak, wTei, wSan, wRi, wMel, wHa, wAu, wNo, and wMa) into the same host background, that of Drosophila simulans (STCP strain), a highly permissive host for CI expression. We initially characterized the modification and rescue properties of the Wolbachia strains wYak, wTei, and wSan, naturally present in the yakuba complex, upon their transfer into D. simulans. Confocal microscopy and multilocus sequencing typing (MLST) analysis were also employed for the evaluation of the CI properties. We also tested the compatibility relationships of wYak, wTei, and wSan with all other Wolbachia infections. So far, the cytoplasmic incompatibility properties of different Wolbachia variants are explained assuming a single pair of modification and rescue factors specific to each variant. This study shows that a given Wolbachia variant can possess multiple rescue determinants corresponding to different CI systems. In addition, our results: (a) suggest that wTei appears to behave in D. simulans as a suicide mod 1 resc À strain, (b) unravel unique CI properties, and (c) provide a framework to understand the diversity and the evolution of new CI-compatibility types. WOLBACHIA is a group of maternally transmitted intracellular bacteria that infect numerous arthropod as well as filarial nematode species (Werren 1997;Bandi et al. 1998;Stouthamer et al. 1999). In arthropod hosts, Wolbachia mainly reside in ovaries and testes. In many cases, they manipulate host reproduction to ensure their own transmission by inducing feminization (Rigaud 1997), thelytokous parthenogenesis (Huigens and Stouthamer 2003), male killing (Hurst et al. 2003) and, most commonly, cytoplasmic incompatibility (CI) . In diploid species, CI is expressed as embryonic lethality of the progeny of a male infected by one (or more) Wolbachia strain(s) and a female that either is u...

A transposon based on the transposable element Minos from Drosophila hydei was introduced into the genome of Drosophila melanogaster using transformation mediated by the Minos transposase. The transposon carries a wild-type version of the white gene (w) of Orosophila inserted into the second exon of Minos. Transformation was obtained by injecting the transposon into preblastoderm embryos that were expressing transposase either from a Hsp7O-Minos fusion inserted into the genome via P-element-mediated transformation or from a coinjected plasmid carrying the Hsp7O-Minos fusion. Between 1% and 6% of the fertile injected individuals gave transformed progeny. Four of the insertions were cloned and the DNA sequences flanking the transposon ends were determined. The "empty" sites corresponding to three ofthe insertions were amplified from the recipient strain by PCR, cloned, and sequenced. In all cases, the transposon has inserted into a TA dinucleotide and has created the characteristic TA target site duplication. In the absence of transposase, the insertions were stable in the soma and the germ line. However, in the presence of the Hsp7O-Minos gene the Minos-w transposon excises, resulting in mosaic eyes and germ-line reversion to the white phenotype. Minos could be utilized as an alternative to existing systems for transposon tagging and enhancer trapping in Drosophila; it might also be of use as a germ-line transformation vector for non-Drosophila insects.Transposable elements have been used as vectors for stable germ-line transformation in Drosophila melanogaster. The mobile element P, present in some D. melanogaster populations, was the first element shown to insert into germ-line chromosomes in embryos (1). Typically, P-element-mediated transformation is achieved by coinjecting into preblastoderm embryos a mixture of two plasmids: one expressing transposase but unable to transpose and one carrying a gene (or genes) of interest flanked by the inverted terminal repeats of the element. Transformants are detected among the progeny of the injected individuals through the expression of dominant phenotypes. Germ-line transformation has revolutionized Drosophila research through the introduction of powerful methodologies such as analysis of in vitro mutagenized genes, gene cloning by transposon tagging, and enhancer trapping.Two other elements unrelated to P, hobo and mariner, have been shown to be able to transpose in the genome of D.melanogaster. hobo is found in some but not all D. melanogaster populations and causes hybrid dysgenesis (2, 3). Defective hobo elements containing foreign DNA can transpose into germline chromosomes from plasmids if coinjected into preblastoderm embryos along with a full-length element that can provide transposase (4). mariner, an element found in Drosophila mauritiana but not in D. melanogaster, has been introduced into D. melanogaster and shown to induce in trans mobilization of a nonautonomous mariner element (5, 6). Efforts to transfer the Drosophila germ-line transformation me...

Wolbachia are obligatory intracellular and maternally inherited bacteria that infect and spread through natural arthropod populations by inducing male‐killing, feminization, parthenogenesis, and, most commonly, unidirectional and bidirectional cytoplasmic incompatibility (CI). Cytoplasmic incompatibility can be used to control natural populations of insect pests, in a way analogous to the Sterile Insect Technique (SIT), namely through the Incompatible Insect Technique (IIT). For the successful application of the IIT (based on a unidirectional CI approach) against a target species, it is essential that only males are released, as the release of females would lead to fertile matings between the released males and the released females and the establishment of a Wolbachia‐carrying field population. In the present study, we describe a Wolbachia‐infected line of the VIENNA 8 genetic sexing strain of the Mediterranean fruit fly, Ceratitis capitata (Wiedemann) (Diptera: Tephritidae), that carries the selectable marker temperature sensitive lethal (tsl). We show that (1) transferred Wolbachia induce high levels of CI even after the temperature treatment required for the male‐only production, and (2) the Wolbachia‐infected genetic sexing C. capitata line can be used in cage population suppression experiments analogous to the SIT. We also discuss our results in a comparison between IIT and SIT, investigating whether irradiation and cytoplasmic factors can be combined toward the development of novel strategies for insect pest control.