bioRxiv Science⌕ Search

Biology subjects

Boland, W.

Publications and source records attributed to Boland, W..

7 recordsLinked to original sources

8-HQA Adjusts the Number and Diversity of Bacteria in the Gut Microbiome of Spodoptera littoralis

Quinolinic carboxylic acids are known for their metal ion chelating properties in insects, plants and bacteria. The larval stages of the lepidopteran pest, Spodoptera littoralis, produce 8-hydroxyquinoline-2-carboxylic acid (8-HQA) in high concentrations from tryptophan in the diet. At the same time, the larval midgut is known to harbor a bacterial population. The motivation behind the work was to investigate whether 8-HQA is controlling the bacterial community in the gut by regulating the concentration of metal ions. Knocking out the gene for kynurenine 3-monooxygenase (KMO) in the insect using CRISPR/Cas9 eliminated production of 8-HQA and significantly increased bacterial numbers and diversity in the larval midgut. Adding 8-HQA to the diet of knockout larvae caused a dose-dependent reduction of bacterial numbers with minimal effects on diversity. Enterococcus mundtii dominates the community in all treatments, probably due to its highly efficient iron uptake system and production of the colicin, mundticin. Thus host factors and bacterial properties interact to determine patterns of diversity and abundance in the insect midgut.

microbiology↗

RNAseq-based gene expression analysis of Melolontha hippocastani hindgut pockets and the surrounding hindgut wall tissue

In this study, the metatranscriptome of newly-discovered structures attached at the distal end of the hindgut of the larvae of a coleopteran (Melolontha hippocastani), is compared with that of the surrounding hindgut wall. Larvae were collected in their natural habitat, RNA was extracted using a commercial kit and sequenced in a Illumina HiSeq2500 platform. 250 bp paired-end reads were used to de novo assemble the transcriptomes. Contig annotation was carried out with BLASTx and Blast2GO PRO and differential expression analysis was performed in edgeR. Contigs aligned mainly to Achromobacter sp. in the pockets and to the Firmicutes phylum in hindgut wall. Host RNAs were expressed in the pockets in higher amounts than in hindgut wall. Gene expression suggest that pocket bacteria undergo aerobic metabolism and are exposed to higher levels of oxidative stress than the population of the hindgut wall. Hypothetical functions for the pocket might be immune-stimulation and regulation of host development, while the hindgut wall appears to be devoted to degradation of dietary polysaccharides and host nitrogenous wastes. Further research is necessary to experimentally prove these suggested roles.

microbiology↗

A partially sex-reversed giant kelp sheds light into the mechanisms of sexual differentiation in a UV sexual system

In UV sexual systems, sex is determined during the haploid phase of the life cycle and males have a V chromosome whereas females have a U chromosome. Previous work in the brown algal model Ectocarpus revealed that the V chromosome has a dominant role in male sex determination and suggested that the female developmental program may occur by default, triggered in the absence of the male master sex determination gene(s). Here, we describe the identification of a genetically male giant kelp strain presenting phenotypic features typical of a female, despite lacking the U-specific region. The conversion to the female developmental program is however incomplete, because gametes of this feminised male are unable to produce the sperm-attracting pheromone lamoxirene. We identify the transcriptomic patterns underlying the male and female specific developmental programs, and reveal the faster evolutionary rates of male-biased genes compared to female-biased and unbiased genes. Moreover, we show that the phenotypic feminisation of the variant strain is associated with both feminisation and de-masculinisation of gene expression patterns. Importantly, the feminisation phenotype was associated with the dramatic downregulation of two V-specific genes including a candidate sex-determining gene on the V-specific region. Our results reveal the transcriptional changes associated with sexual differentiation in a UV system with marked sexual dimorphism, and contribute to disentangling the role of sex-linked genes and autosomal gene expression in the initiation of the male and female developmental programs. Overall, the data presented here imply that the U-specific region in the giant kelp is not required to initiate the female developmental program, but is critical to produce fully functional eggs, arguing against the idea that female is the default sex in this species.

evolutionary biology↗

Survival strategies of Enterococcus mundtii in the gut of Spodoptera littoralis : a live report

The complex interaction between a higher organism and its resident gut flora is a subject of immense interest in the field of symbiosis. Many insects harbor a complex community of microorganisms in their gut. Larvae of Spodoptera littoralis, a lepidopteran pest which is prevalent in tropical and subtropical regions of the world, have a tube-like gut structure containing a simple bacterial community. This community varies both spatially (along the length of the gut) and temporally (during the life cycle of the insect). To monitor the dynamics and rapid adaptation of microbes to the gut conditions, a GFP-tagged reporter E. mundtii was constructed. After feeding to early instar S. littoralis larvae, the tagged-microbes recovered from the fore and hind guts by flow cytometry. The fluorescent reporter confirmed the persistence of E. mundtii in the gut. RNA-sequencing of the sorted bacteria highlighted various strategies that the symbiont employs to survive, including upregulated pathways for tolerating alkaline stress, forming biofilms and two-component signaling systems, resisting oxidative stress and quorum sensing. Although these symbionts depend on the host for amino acid and fatty acids, differential regulation among various metabolic pathways points to an enriched lysine synthesis pathway in the hindgut of the larvae.

microbiology↗

A cytochrome P450 from juvenile mustard leaf beetles hydroxylates geraniol, a key step in iridoid biosynthesis

Juveniles of the leaf beetle Phaedon cochleariae synthesize iridoid via the mevalonate pathway to repel predators. The normal terpenoid biosynthesis is integrated into the dedicated defensive pathway by the {omega}-hydroxylation of geraniol to 8-hydroxygeraniol. Here we identify and characterize the geraniol 8-hydroxylase as a P450 monooxygenase using integrated transcriptomic and proteomic analyses. In the fat body, 73 individual cytochrome P450s were identified. The double stranded RNA (dsRNA)-mediated knock down of CYP6BH5 led to a significant reduction of 8-hydroxygeraniol-glucoside in the hemolymph and, later, of the chrysomelidial in the defensive secretion. Heterologously expressed CYP6BH5 converted geraniol to 8-hydroxygeraniol. In addition to geraniol, CYP6BH5 also catalyzes other monoterpenols, such as nerol and citronellol, into the corresponding , {omega}-dihydroxy compounds.\n\nHighlightsO_LIThe geraniol 8-hydroxylase in Phaedon cochleariae was identified as a cytochrome P450 CYP6BH5.\nC_LIO_LIRNA interference emphasized the importance of CYP6BH5 in iridoid biosynthesis.\nC_LIO_LIIn vitro enzyme assays showed that recombinant CYP6BH5 is a substrate promiscuous enzyme, converting the {omega}-hydroxylation of geraniol, nerol, citronellol but not linalool.\nC_LIO_LIHomology modeling suggested the -OH group of the substrate plays an important role in coordinating the substrates with the enzymes catalytic cavity.\nC_LI

biochemistry↗

SpitWorm, an herbivorous robot: Mechanical leaf wounding with simultaneous application of salivary components

Induction of plant defense against insect herbivory is initiated by a combination of both, mechanical wounding and chemical factors. In order to study both effects independently on plant defense induction, SpitWorm, a computer controlled device which mimics the damage pattern of feeding insect larvae on leaves and can additionally apply oral secretions (OS) or other solutions to the biting site during feeding, was developed and evaluated. The amount of OS left by a Spodoptera littoralis larva during feeding on Phaseolus lunatus (lima bean) leaves was estimated by combining larval foregut volume, biting rate, and quantification of a fluorescent dye injected into the larvaes foregut prior to feeding. For providing OS amounts by SpitWorm equivalent to larval feeding, dilution and delivery rate were optimized. The effectiveness of SpitWorm was tested by comparing volatile organic compounds (VOC) emissions of P. lunatus leaves treated with either SpitWorm, MecWorm or S. littoralis larvae. Identification and quantification of emitted VOCs revealed that SpitWorm induced a volatile bouquet that is qualitatively and quantitatively similar to herbivory. Additionally, RT-qPCR of four jasmonic acid responsive genes showed that SpitWorm, in contrast to MecWorm, induces the same regulation pattern as insect feeding. Thus, SpitWorm mimics insect herbivory almost identical to real larvae feeding.

ecology↗

Silencing cuticular pigmentation genes enables RNA FISH in intact chemosensory appendages

Optical imaging of gene expression by RNA-fluorescent in situ hybridisation (FISH) in whole-mount sensory appendages of insects is often impeded by their highly pigmented cuticle. Since most chemical bleaching agents are incompatible with imaging fluorescent-labelled nucleotides, we developed a RNA interference-based method for clearing cuticular pigmentation that allows imaging of fluorescent mRNA in whole-mount appendages of insects. Silencing key genes of the tyrosine-derived pigmentation pathway by injecting dsRNA of laccase2 or tyrosine hydroxylase in two leaf beetles species (Chrysomela populi, Phaedon cochleariae) resulted in clearance of the highly pigmented cuticle and in significant decreased light absorbance. Intact chemosensory appendages (palps, antennae and legs) from RNAi-cleared individuals were used to image expression and spatial distribution of antisense mRNA of two chemosensory genes (gustatory receptor, odorant-binding protein) via RNA FISH and confocal laser scanning microscopy. Imaging of these genes did neither work for RNAi-controls (dsGfp) due to retained pigmentation, nor for FISH-controls using sense mRNA. Furthermore, we show that several chemical bleaching agents are not feasible with FISH, either due to significant degradation of polynucleotides, lack of clearing efficacy or long incubation times. Overall, silencing pigmentation genes is a significant improvement over bleaching agents allowing fluorescence imaging in whole-mount appendages and organs.

molecular biology↗