Nos gustaría agradecer a Michelle Moon (Vanderbilt University) por asistencia con la fotografía. Proporcionado la Universidad de Vanderbilt a PA y SSLB se admiten por DGE-1445197.

<ol>
	<li>Brisson, J. A., Stern, D. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+pea+aphid,+Acyrthosiphon+pisum.:+an+emerging+genomic+model+system+for+ecological,+developmental+and+evolutionary+studies.">The pea aphid, Acyrthosiphon pisum.: an emerging genomic model system for ecological, developmental and evolutionary studies.</a> BioEssays. 28, 747-755 (2006).</li><li>Dixon, A. F. G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Aphid Ecology: An Optimization Approach. , (1985).</li><li>Consortium, T. I. A. 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Los autores no tienen nada que revelar.

Durante mucho tiempo se ha reconocido que la catalogada a. nerii puede proporcionar penetraciones en los patrones y mecanismos de resistencia a las defensas de la planta y secuestro particularmente química18,37. Recientemente ha surgido una serie de recursos genómicos de a. nerii10, ofreciendo nuevas oportunidades para estudios de genómica funcionales y ecológicos que usan a. nerii como modelo. Describiremos ...

Los áfidos son insectos hemimetabolous, pequeño que colonizan en familias de diversas plantas en todo el mundo. Son distintivos para varias características, más en particular sus ciclos de vida complejos con partenogénesis cíclica y polyphenisms discreta y sus simbiosis nutricionales obligados con endosimbionte bacteriano o de levadura que suministrar nutrientes en el la dieta de savia de planta1. Mientras más áfidos son especialistas de planta huésped, algunas especies generalistas son importantes plagas, causando un daño económico considerable en los cultivos ya sea directamente o a través de los agentes patógenos y virus vector2. La publicación del primer genoma del pulgón en el 2010, el áfido de la arveja Acyrthosiphon pisum3, marcó un hito importante en el estudio de la biología de los áfidos porque proporcionó los recursos genomic para abordar preguntas acerca de los insectos adaptaciones al estilo de vida herbívora, los que podrían conducir a un mejor control estrategias4incluidos. Desde entonces, han acumulado más recursos genomic con la publicación de un genoma anotado para la soja pulgón glycines Aphis5y recursos disponibles al público todo el genoma de otra especie de pulgón tres (Myzus Cerasi (cereza negra pulgón), Myzus persicae (pulgón de patatas y melocotón), Rhopalosiphum padi (pulgón de la avena de la cereza de pájaro)6. Valiosa de novo transcriptómicos recursos está disponible, así como para un número de otras especies de áfidos (e.g.,Aphis gossypii (pulgón del algodón)7, Sitobion avenae (áfido grano)8, Cinara pinitabulaeformis (pulgón del pino)9, Aphis nerii (pulgón de la adelfa de algodoncillo)10).
Áfidos también han hecho contribuciones duraderas a nuestro entendimiento de las interacciones planta-insecto y la ecología de la vida en las plantas11. Un área donde los pulgones han hecho contribuciones especialmente importantes es en nuestra comprensión de la ecología química de las interacciones de la planta de host. Adaptaciones expresan diversos insectos herbívoros para superar las defensas de la planta y algunos incluso cooptación las defensas de la planta para su propio benefician de12,13,14. Por ejemplo, el pulgón de la adelfa de algodoncillo, Aphis nerii, es un brillante amarillo, invasor pulgones encontrados en regiones templadas y tropicales en todo el mundo que colonizan en las plantas de la familia del algodoncillo (Apocynaceae). Planta de la familia Apocynaceae ha desarrollado defensas químicas diversas, incluyendo látex lechoso y glucósidos cardíacos conocidos como cardenolides, que se unen el portador de catión Na, K-ATPasa y son eficaces elementos de disuasión a generalistas herbívoros15, 16. especialistas de algodoncillo expresan distintos modos de resistencia a los cardenolides, y selectivamente o pasivamente se acumulan o modificar cardenolides en sus tejidos como medio para disuadir depredadores o para otros beneficios17. A. nerii piensa secuestrar cardenolides de esta manera, aunque los mecanismos y beneficios funcionales siguen siendo claro10,18.
Teniendo en cuenta los recursos genomic a la mano, a. nerii ofrece un excelente modelo experimental para el estudio de los mecanismos moleculares y genéticos involucrados en las interacciones chemo-ecológicas entre las plantas tóxicas acogida y su especialista herbívoros. Cabe señalar que, mientras algunos de los primeros estudios de a. nerii se centró en el secuestro de cardenolides19, desde entonces, los estudios de a. nerii han proporcionado penetraciones en un amplio conjunto de preguntas evolutivas y ecológicas, incluyendo la estructura genética de insectos invasores20 y la interacción entre regulación ascendente y descendente de la densidad de herbívoros21. A. nerii así es un buen candidato como un modelo experimental para un conjunto especialmente amplio de estudios de las interacciones planta insecto. Crítico para el éxito de cualquier estudio con a. nerii es la cultura de cuidado del pulgón las poblaciones, que incluye el cultivo de plantas de las que dependen los pulgones, así como una eficiente generación de datos de alta calidad - omic. Nuestro objetivo es guiar al lector a través de ambos. A continuación figuran los métodos para la generación y mantenimiento de la planta y pulgón en invernadero y laboratorio, DNA y RNA extracciones, análisis de microsatélites, de novo transcriptoma conjunto y anotación, transcriptoma Análisis de expresión diferencial y verificación de la qPCR de diferencialmente expresan genes. Mientras que estos métodos se escriben de a. nerii, los métodos generales de cultivo, la extracción y el análisis se pueden extender a una gran variedad de especies de áfidos.

<table><tbody><tr><td>Sun Gro Fafard Germination Mix</td><td>Hummert International</td><td>10-0952-2</td><td></td></tr><tr><td>Sun Gro Fafard 3B/ Metro Mix</td><td>Hummert International</td><td>10-0951-2</td><td></td></tr><tr><td>2&quot; x 4&quot; Round Standard Pot</td><td>Anderson Pots</td><td>1503</td><td></td></tr><tr><td>DreamTaq DNA Polymerase</td><td>ThermoFisher Scientific</td><td>EP0701</td><td></td></tr><tr><td>Trizol</td><td>ThermoFisher Scientific</td><td>15596026</td><td></td></tr><tr><td>SuperScript&amp;reg; III First-Strand Synthesis kit</td><td>ThermoFisher Scientific</td><td>18080051</td><td></td></tr><tr><td>Power SYBR Green PCR Master Mix</td><td>ThermoFisher Scientific</td><td>4367659</td><td></td></tr></tbody></table>

maintaining biological cultures and measuring gene expression in aphis nerii: a non-model system for plant-insect interactions

Áfidos son excelentes modelos experimentales para una variedad de cuestiones biológicas que van desde la evolución de la simbiosis y el desarrollo de polyphenisms a preguntas alrededor de las interacciones de los insectos con sus plantas hospederas. Recursos genómicos están disponibles para varias especies de áfidos, y con los avances en la secuenciación de próxima generación, transcriptómicos estudios se se amplía a organismos no-modelo que carecen de genomas. Además, culturas de pulgón pueden ser recogidas del campo y criadas en el laboratorio para el uso en experimentos moleculares y el brecha entre los estudios ecológicos y genéticos. Por último, muchos pulgones se pueden mantener en el laboratorio en sus plantas del anfitrión favorito en ciclos de vida perpetuos, partenogénesis que permite comparaciones de reproducir asexualmente genotipos. Aphis nerii, el pulgón de la adelfa de algodoncillo, proporciona uno de estos modelos para estudiar interacciones de insectos con plantas tóxicas usando experimentos de organismos y moleculares. Métodos para la generación y mantenimiento de la planta y pulgón en la expresión diferencial del transcriptoma de invernadero y laboratorio, extracciones de DNA y RNA, análisis de microsatélites, de novo transcriptoma montaje y anotación, Análisis y verificación de la qPCR de genes diferencialmente expresados son descritos y discutidos aquí.

Las culturas de la planta: Las semillas llevará aproximadamente de dos a cuatro semanas, dependiendo de la temporada, para crecer lo suficiente como para ser nuevo en maceta (figura 1A). Las plántulas a macetas tendrá otras dos a cuatro semanas para crecer a un tamaño óptimo para los cultivos de pulgón (figura 1B).
<p class="jove_content" fo:keep-together.within-page="1...

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Maintaining Biological Cultures and Measuring Gene Expression in Aphis nerii: A Non-model System for Plant-insect Interactions

El pulgón Aphis nerii coloniza plantas muy defendido en la familia del dogbane (Apocyanaceae) y ofrece numerosas oportunidades para el estudio de las interacciones planta-insecto. Aquí, presentamos una serie de protocolos para el mantenimiento de la planta y el pulgón de las culturas y la generación y el análisis molecular y los datos de a. nerii- omic.

Mantenimiento de cultivos biológicos y medir la expresión génica en Aphis nerii: un sistema no-modelo de las interacciones planta-insecto

Aphids are excellent experimental models for a variety of biological questions ranging from the evolution of symbioses and the development of polyphenisms ...

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Maintaining Biological Cultures and Measuring Gene Expression in Aphis nerii: A Non-model System for Plant-insect Interactions

7.5K vistas.  Vanderbilt University. El pulgón Aphis nerii coloniza plantas muy defendido en la familia del dogbane (Apocyanaceae) y ofrece numerosas oportunidades para el estudio de las interacciones planta-insecto. Aquí, presentamos una serie de protocolos para el mantenimiento de la planta y el pulgón de las culturas y la generación y el análisis molecular y los datos de a. nerii- omic.

Video: Maintaining Biological Cultures and Measuring Gene Expression in Aphis nerii: A Non-model System for Plant-insect Interactions

Delivery of Nucleic Acids through Embryo Microinjection in the Worldwide Agricultural Pest Insect, Ceratitis capitata

The Mediterranean fruit fly (medfly) Ceratitis capitata (Wiedemann) (Diptera: Tephritidae) is a pest species with extremely high agricultural relevance. This is due to its reproductive behavior: females damage the external surface of fruits and vegetables when they lay eggs and the hatched larvae feed on their pulp. Wild C. capitata populations are traditionally controlled through insecticide spraying and/or eco-friendly approaches, the most successful being the Sterile Insect Technique (SIT). The SIT relies on mass-rearing, radiation-based sterilization and field release of males that retain their capacity to mate but are not able to generate fertile progeny. The advent and the subsequent rapid development of biotechnological tools, together with the availability of the medfly genome sequence, has greatly boosted our understanding of the biology of this species. This favored the proliferation of new strategies for genome manipulation, which can be applied to population control.
In this context, embryo microinjection plays a dual role in expanding the toolbox for medfly control. The ability to interfere with the function of genes that regulate key biological processes, indeed, expands our understanding of the molecular machinery underlying medfly invasiveness. Furthermore, the ability to achieve germ-line transformation facilitates the production of multiple transgenic strains that can be tested for future field applications in novel SIT settings. Indeed, genetic manipulation can be used to confer desirable traits that can, for example, be used to monitor sterile male performance in the field, or that can result in early life-stage lethality. Here we describe a method to microinject nucleic acids into medfly embryos to achieve these two main goals.

Delivery of Nucleic Acids through Embryo Microinjection in the Worldwide Agricultural Pest Insect, Ceratitis capitata

The Mediterranean fruit fly (medfly) Ceratitis capitata (Diptera: Tephritidae) is a worldwide pest of agriculture. A deeper understanding of its biology is key to control medfly populations and thus reduce economic impact. Embryo microinjection is a fundamental tool allowing both germ-line transformation and reverse genetics studies in this species.

Entrega de ácidos nucleicos mediante microinyección de embriones en el Mundial de la Agricultura de plagas de insectos,<em&gt; Ceratitis capitata</em

The Mediterranean fruit fly (medfly) Ceratitis capitata (Wiedemann) (Diptera: Tephritidae) is a pest species with extremely high agricultural relevance. ...

Investigación

Genética

Rearing and Double-stranded RNA-mediated Gene Knockdown in the Hide Beetle, Dermestes maculatus

Advances in genomics have raised the possibility of probing biodiversity at an unprecedented scale. However, sequence alone will not be informative without tools to study gene function. The development and sharing of detailed protocols for the establishment of new model systems in laboratories, and for tools to carry out functional studies, is thus crucial for leveraging the power of genomics. Coleoptera (beetles) are the largest clade of insects and occupy virtually all types of habitats on the planet. In addition to providing ideal models for fundamental research, studies of beetles can have impacts on pest control as they are often pests of households, agriculture, and food industries. Detailed protocols for rearing and maintenance of D. maculatus laboratory colonies and for carrying out dsRNA-mediated interference in D. maculatus are presented. Both embryonic and parental RNAi procedures-including apparatus set up, preparation, injection, and post-injection recovery-are described. Methods are also presented for analyzing embryonic phenotypes, including viability, patterning defects in hatched larvae, and cuticle preparations for unhatched larvae. These assays, together with in situ hybridization and immunostaining for molecular markers, make D. maculatus an accessible model system for basic and applied research. They further provide useful information for establishing procedures in other emerging insect model systems.

Rearing and Double-stranded RNA-mediated Gene Knockdown in the Hide Beetle, Dermestes maculatus

Here, we present protocols for rearing an intermediate-germ beetle, Dermestes maculatus (D. maculatus) in the lab. We also share protocols for embryonic and parental RNAi and methods for analyzing embryonic phenotypes to study gene function in this species.

La cría y el doble-stranded RNA mediada gen desmontables en el Hide Escarabajo,<em&gt; Dermestes maculatus</em

Advances in genomics have raised the possibility of probing biodiversity at an unprecedented scale. However, sequence alone will not be informative ...

Identification of Critical Conditions for Immunostaining in the Pea Aphid Embryos: Increasing Tissue Permeability and Decreasing Background Staining

The pea aphid Acyrthosiphon pisum, with a sequenced genome and abundant phenotypic plasticity, has become an emerging model for genomic and developmental studies. Like other aphids, A. pisum propagate rapidly via parthenogenetic viviparous reproduction, where the embryos develop within egg chambers in an assembly-line fashion in the ovariole. Previously we have established a robust platform of whole-mount in situ hybridization allowing detection of mRNA expression in the aphid embryos. For analyzing the expression of protein, though, established protocols for immunostaining the ovarioles of asexual viviparous aphids did not produce satisfactory results. Here we report conditions optimized for increasing tissue permeability and decreasing background staining, both of which were problems when applying established approaches. Optimizations include: (1) incubation of proteinase K (1 &#181;g/ml, 10 min), which was found essential for antibody penetration in mid- and late-stage aphid embryos; (2) replacement of normal goat serum/bovine serum albumin with a blocking reagent supplied by a Digoxigenin (DIG)-based buffer set and (3) application of methanol rather hydrogen peroxide (H2O2) for bleaching endogenous peroxidase; which significantly reduced the background staining in the aphid tissues. These critical conditions optimized for immunostaining will allow effective detection of gene products in the embryos of A. pisum and other aphids.

A protocol of whole-mount immunostaining on aphid embryos is presented, in which critical conditions for decreasing background staining and increasing tissue permeability are addressed. These conditions are specifically developed for effective detection of protein expression in the embryonic tissues of aphids.

Identificación de las condiciones críticas para inmunotinción en el guisante áfido embriones: El aumento del tejido Permeabilidad y disminución de la tinción de fondo

The pea aphid Acyrthosiphon pisum, with a sequenced genome and abundant phenotypic plasticity, has become an emerging model for genomic and developmental ...

Biología del Desarrollo

Rearing and Injection of Manduca sexta Larvae to Assess Bacterial Virulence

Manduca sexta, commonly known as the tobacco hornworm, is considered a significant agricultural pest, feeding on solanaceous plants including tobacco and tomato. The susceptibility of M. sexta larvae to a variety of entomopathogenic bacterial species1-5, as well as the wealth of information available regarding the insect's immune system6-8, and the pending genome sequence9 make it a good model organism for use in studying host-microbe interactions during pathogenesis. In addition, M. sexta larvae are relatively large and easy to manipulate and maintain in the laboratory relative to other susceptible insect species. Their large size also facilitates efficient tissue/hemolymph extraction for analysis of the host response to infection.
The method presented here describes the direct injection of bacteria into the hemocoel (blood cavity) of M. sexta larvae. This approach can be used to analyze and compare the virulence characteristics of various bacterial species, strains, or mutants by simply monitoring the time to insect death after injection. This method was developed to study the pathogenicity of Xenorhabdus and Photorhabdus species, which typically associate with nematode vectors as a means to gain entry into the insect. Entomopathogenic nematodes typically infect larvae via natural digestive or respiratory openings, and release their symbiotic bacterial contents into the insect hemolymph (blood) shortly thereafter10. The injection method described here bypasses the need for a nematode vector, thus uncoupling the effects of bacteria and nematode on the insect. This method allows for accurate enumeration of infectious material (cells or protein) within the inoculum, which is not possible using other existing methods for analyzing entomopathogenesis, including nicking11 and oral toxicity assays12. Also, oral toxicity assays address the virulence of secreted toxins introduced into the digestive system of larvae, whereas the direct injection method addresses the virulence of whole-cell inocula.
The utility of the direct injection method as described here is to analyze bacterial pathogenesis by monitoring insect mortality. However, this method can easily be expanded for use in studying the effects of infection on the M. sexta immune system. The insect responds to infection via both humoral and cellular responses. The humoral response includes recognition of bacterial-associated patterns and subsequent production of various antimicrobial peptides7; the expression of genes encoding these peptides can be monitored subsequent to direct infection via RNA extraction and quantitative PCR13. The cellular response to infection involves nodulation, encapsulation, and phagocytosis of infectious agents by hemocytes6. To analyze these responses, injected insects can be dissected and visualized by microscopy13, 14.

Rearing and Injection of Manduca sexta Larvae to Assess Bacterial Virulence

The method described here utilizes direct injection of entomopathogenic bacteria into the hemocoel of Manduca sexta insect larvae. M. sexta is a commercially available and well-studied insect. Thus, this method represents a simple approach to analyzing host-bacterial interactions from the perspective of one or both partners.

Crianza y la inyección de<em&gt; Manduca sexta</em&gt; Las larvas para evaluar la virulencia bacteriana

Manduca sexta, commonly known as the tobacco hornworm, is considered a significant agricultural pest, feeding on solanaceous plants including tobacco and ...

Inmunología e Infección

Mass-Rearing and Molecular Studies in Tortricidae Pest Insects

Tortricidae (Lepidoptera), commonly known as tortrix or leafroller moths, comprises many agricultural and forestry pests, which cause serious agricultural losses. To understand the biology of such pest moths, fundamental techniques have been in high demand. Here, methods for mass-rearing, observations, and molecular studies are developed using two tea tortrix, Homona magnanima and Adoxophyes honmai (Lepidoptera: Tortricidae). Insects were mass-reared with sliced artificial diet and maintained by inbreeding for over 100 generations by considering their biological characteristics. Insects have various sex dimorphisms; hence it is difficult to distinguish the sex during the developing stages, which have prevented subsequent assays. The present work highlighted that the sex of tortricids larvae could be determined by observing testes or lactic-acetic orcein staining to visualize the female-specific W chromosome. Moreover, using the sex determination methods, the present study enabled nucleic acid extractions from sex determined embryos and application toward high throughput sequencing. These tips are applicable for other pest insects and will facilitate further morphological and genetic studies.

The present protocol describes the rearing method of tortricid pest insects in the laboratories. The procedures to distinguish insects' sex and extract nucleic acids for high throughput sequencing are established using two tortricid pests.

Cría masiva y estudios moleculares en insectos plaga tortricidae

Tortricidae (Lepidoptera), commonly known as tortrix or leafroller moths, comprises many agricultural and forestry pests, which cause serious agricultural ...

Medio ambiente

RNAi-mediated Double Gene Knockdown and Gustatory Perception Measurement in Honey Bees (Apis mellifera)

This video demonstrates novel techniques of RNA interference (RNAi) which downregulate two genes simultaneously in honey bees using double-stranded RNA (dsRNA) injections. It also presents a protocol of proboscis extension response (PER) assay for measuring gustatory perception.	
	RNAi-mediated gene knockdown is an effective technique downregulating target gene expression. This technique is usually used for single gene manipulation, but it has limitations to detect interactions and joint effects between genes. In the first part of this video, we present two strategies to simultaneously knock down two genes (called double gene knockdown). We show both strategies are able to effectively suppress two genes, vitellogenin (vg) and ultraspiracle (usp), which are in a regulatory feedback loop. This double gene knockdown approach can be used to dissect interrelationships between genes and can be readily applied in different insect species.	
	The second part of this video is a demonstration of proboscis extension response (PER) assay in honey bees after the treatment of double gene knockdown. The PER assay is a standard test for measuring gustatory perception in honey bees, which is a key predictor for how fast a honey bee's behavioral maturation is. Greater gustatory perception of nest bees indicates increased behavioral development which is often associated with an earlier age at onset of foraging and foraging specialization in pollen. In addition, PER assay can be applied to identify metabolic states of satiation or hunger in honey bees. Finally, PER assay combined with pairing different odor stimuli for conditioning the bees is also widely used for learning and memory studies in honey bees.

RNAi-mediated Double Gene Knockdown and Gustatory Perception Measurement in Honey Bees Apis mellifera

In this protocol, we describe two strategies that simultaneously suppress two genes (double gene knockdown) in honey bees. Then we present how to use the proboscis extension response (PER) assay to study the effect of double gene knockdown on honey bee gustatory perception.

RNAi mediada Doble derribo Gene y medición percepción gustativa de las abejas (<em&gt; Apis mellifera</em&gt;)

This video demonstrates novel techniques of RNA  interference (RNAi) which downregulate two genes simultaneously in honey bees  using double-stranded RNA ...

Neurociencias

Culturing and Genetically Manipulating Entomopathogenic Nematodes

Entomopathogenic nematodes in the genera Heterorhabditis and Steinernema are obligate parasites of insects that live in the soil. The main characteristic of their life cycle is the mutualistic association with the bacteria Photorhabdus and Xenorhabdus, respectively. The nematode parasites are able to locate and enter suitable insect hosts, subvert the insect immune response, and multiply efficiently to produce the next generation that will actively hunt new insect prey to infect. Due to the properties of their life cycle, entomopathogenic nematodes are popular biological control agents, which are used in combination with insecticides to control destructive agricultural insect pests. Simultaneously, these parasitic nematodes represent a research tool to analyze nematode pathogenicity and host anti-nematode responses. This research is aided by the recent development of genetic techniques and transcriptomic approaches for understanding the role of nematode secreted molecules during infection. Here, a detailed protocol on maintaining entomopathogenic nematodes and using a gene knockdown procedure is provided. These methodologies further promote the functional characterization of entomopathogenic nematode infection factors.

Entomopathogenic nematodes live in symbiosis with bacteria and together they successfully infect insects by undermining their innate immune system. To promote research on the genetic basis of nematode infection, methods for maintaining and genetically manipulating entomopathogenic nematodes are described.

Cultivo y manipulación genética de nematodos entomopatógenos

Entomopathogenic nematodes in the genera Heterorhabditis and Steinernema are obligate parasites of insects that live in the soil. The main characteristic ...

Transient Expression and Cellular Localization of Recombinant Proteins in Cultured Insect Cells

Heterologous protein expression systems are used for the production of recombinant proteins, the interpretation of cellular trafficking/localization, and the determination of the biochemical function of proteins at the sub-organismal level. Although baculovirus expression systems are increasingly used for protein production in numerous biotechnological, pharmaceutical, and industrial applications, nonlytic systems that do not involve viral infection have clear benefits but are often overlooked and underutilized. Here, we describe a method for generating nonlytic expression vectors and transient recombinant protein expression. This protocol allows for the efficient cellular localization of recombinant proteins and can be used to rapidly discern protein trafficking within the cell. We show the expression of four&#160;recombinant proteins in a commercially available insect cell line, including two aquaporin proteins from the insect Bemisia tabaci, as well as subcellular marker proteins specific for the cell plasma membrane and for intracellular lysosomes. All recombinant proteins were produced as chimeras with fluorescent protein markers at their carboxyl termini, which allows for the direct detection of the recombinant proteins. The double transfection of cells with plasmids harboring constructs for the genes of interest and a known subcellular marker allows for live cell imaging and improved validation of cellular protein localization.

Nonlytic insect cell expression systems are underutilized for production, cellular trafficking/localization, and recombinant protein functional analysis. Here, we describe methods to generate expression vectors and subsequent transient protein expression in commercially available lepidopteran cell lines. The co-localization of Bemisia tabaci aquaporins with subcellular fluorescent marker proteins is also presented.

Expresión transitoria y localización celular de proteínas recombinantes en células cultivadas de insectos

Heterologous protein expression systems are used for the production of recombinant proteins, the interpretation of cellular trafficking/localization, and ...

Biología

Maintaining Aedes aegypti Mosquitoes Infected with Wolbachia

Aedes aegypti mosquitoes experimentally infected with Wolbachia are being utilized in programs to control the spread of arboviruses such as dengue, chikungunya and Zika. Wolbachia-infected mosquitoes can be released into the field to either reduce population sizes through incompatible matings or to transform populations with mosquitoes that are refractory to virus transmission. For these strategies to succeed, the mosquitoes released into the field from the laboratory must be competitive with native mosquitoes. However, maintaining mosquitoes in the laboratory can result in inbreeding, genetic drift and laboratory adaptation which can reduce their fitness in the field and may confound the results of experiments. To test the suitability of different Wolbachia infections for deployment in the field, it is necessary to maintain mosquitoes in a controlled laboratory environment across multiple generations. We describe a simple protocol for maintaining Ae. aegypti mosquitoes in the laboratory, which is suitable for both Wolbachia-infected and wild-type mosquitoes. The methods minimize laboratory adaptation and implement outcrossing to increase the relevance of experiments to field mosquitoes. Additionally, colonies are maintained under optimal conditions to maximize their fitness for open field releases.

Maintaining Aedes aegypti Mosquitoes Infected with Wolbachia

Aedes aegypti mosquitoes infected with Wolbachia are being released into natural populations to suppress the transmission of arboviruses. We describe methods to rear Ae. aegypti with Wolbachia infections in the laboratory for experiments and field release, taking precautions to minimize laboratory adaptation and selection.

Mantener los mosquitos Aedes aegypti infectados con Wolbachia

Aedes aegypti mosquitoes experimentally infected with Wolbachia are being utilized in programs to control the spread of arboviruses such as dengue, ...

Pupal and Adult Injections for RNAi and CRISPR Gene Editing in Nasonia vitripennis

The jewel wasp, Nasonia vitripennis, has become an efficient model system to study epigenetics of haplo-diploid sex determination, B-chromosome biology, host-symbiont interactions, speciation, and venom synthesis. Despite the availability of several molecular tools, including CRISPR/Cas9, functional genetic studies are still limited in this organism. The major limitation of applying CRISPR/Cas9 technology in N. vitripennis stems from the challenges of embryonic microinjections. Injections of embryos are particularly difficult in this organism and in general in many parasitoid wasps, due to small embryo size and the requirement of a host pupa for embryonic development. To address these challenges, Cas9 ribonucleoprotein complex delivery into female&#160;ovaries by adult injection, rather than embryonic microinjection, was optimized, resulting in both somatic and heritable germline edits. The injection procedures were optimized in pupae and female wasps using either ReMOT Control (Receptor-Mediated Ovary Transduction of Cargo) or BAPC (Branched Amphiphilic Peptide Capsules). These methods are shown to be effective alternatives to embryo injection, enabling site-specific and heritable germline mutations.

Pupal and Adult Injections for RNAi and CRISPR Gene Editing in Nasonia vitripennis

Here, we describe methods for efficient pupal and adult injections in Nasonia vitripennis as accessible alternatives to embryo microinjection, enabling functional analysis of genes of interest using either RNA-silencing via RNA interference (RNAi) or gene knockout via CRISPR/Cas9 genome editing.

Inyecciones pupales y para adultos para RNAi y edición de genes CRISPR en Nasonia vitripennis

The jewel wasp, Nasonia vitripennis, has become an efficient model system to study epigenetics of haplo-diploid sex determination, B-chromosome biology, ...

Mantenimiento de cultivos biológicos y medir la expresión génica en Aphis nerii: un sistema no-modelo de las interacciones planta-insecto

Resumen

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Capítulos en este video

Entrega de ácidos nucleicos mediante microinyección de embriones en el Mundial de la Agricultura de plagas de insectos,

La cría y el doble-stranded RNA mediada gen desmontables en el Hide Escarabajo,