Larval Alimentary Canal Research Articles

Defining the mechanisms of action and mosquito larva midgut response to a yeast-encapsulated orange oil larvicide

BackgroundYeast-encapsulated orange oil (YEOO) is a novel, ingestible larvicide that combines the benefits of a low-cost essential oil with yeast, an attractive food source for mosquito larvae. In this work, we investigated the underlying mechanisms of action associated with YEOO ingestion by Aedes aegypti larvae.MethodsAedes aegypti third-stage larvae (L3) were treated with sublethal or lethal concentrations of YEOO. Genes associated with apoptosis, autophagy and innate immune responses were investigated by RT-qPCR in guts and carcasses dissected from treated and control larvae. Differential expression of cytochrome P450 genes in the CYP6 and CYP9 families were also investigated. Confocal and transmission electron microscopy were used to assess damage caused by YEOO throughout the larval alimentary canal. TUNEL was used to assess apoptosis via DNA fragmentation.ResultsThe apoptosis genes IAP1 and IAP2 in larvae displayed opposing effects following exposure to lethal doses of YEOO, with a 26-fold induction of IAP1 at 8 h post YEOO ingestion. The effector caspase CASPS8 displayed a 6.7-fold induction in the gut and concomitant 70-fold induction in the carcass at 8 h post YEOO ingestion. The midgut epithelia regenerator, Vein, had an 11-fold induction in the gut after 4 h and was repressed 7.6-fold in the carcass at 24 h. Sublethal concentrations (< LC50) led to significant differential expression of CYP6 and CYP9 genes. Midgut epithelial damage was highlighted by the destruction of microvilli, vacuolization of midgut cells and damage to cell junctions and basal lamina as early as 30 min. Larval type 2 peritrophic matrix structural integrity and porosity remain unchanged.ConclusionOur results strongly suggest that the robust larvicidal activity of YEOO is due to a generalized broad-acting mechanism combining epithelial damage and apoptosis, with concomitant expression of multiple innate response genes involved in epithelial regeneration and detoxification. YEOO’s amenability for use as part of an integrated vector management program makes this novel larvicide a practical approach for mosquito larval control in the future.Graphical

Knockdown of a nutrient amino acid transporter gene LdNAT1 reduces free neutral amino acid contents and impairs Leptinotarsa decemlineata pupation.

A Leptinotarsa decemlineata SLC6 NAT gene (LdNAT1) was cloned. LdNAT1 was highly expressed in the larval alimentary canal especially midgut. LdNAT1 mRNA levels were high right after the molt and low just before the molt. JH and a JH analog pyriproxyfen activated LdNAT1 expression. RNAi of an allatostatin gene LdAS-C increased JH and upregulated LdNAT1 transcription. Conversely, silencing of a JH biosynthesis gene LdJHAMT decreased JH and reduced LdNAT1 expression. Moreover, 20E and an ecdysteroid agonist halofenozide repressed LdNAT1 expression, whereas a decrease in 20E by RNAi of an ecdysteroidogenesis gene LdSHD and disruption of 20E signaling by knockdown of LdE75 and LdFTZ-F1 activated LdNAT1 expression. Thus, LdNAT1 responded to both 20E and JH. Moreover, knockdown of LdNAT1 reduced the contents of cysteine, histidine, isoleucine, leucine, methionine, phenylalanine and serine in the larval bodies and increased the contents of these amino acids in the larval feces. Furthermore, RNAi of LdNAT1 inhibited insulin/target of rapamycin pathway, lowered 20E and JH titers, reduced 20E and JH signaling, retarded larval growth and impaired pupation. These data showed that LdNAT1 was involved in the absorption of several neutral amino acids critical for larval growth and metamorphosis.

Chironomidae larvae (Diptera) of Neotropical floodplain: overlap niche in different habitats.

The niche overlap between trophic groups of Chironomidae larvae in different habitats was observed between trophic groups and between different environments in Neotropical floodplain. For the evaluation we used the index of niche overlap (CXY) and analysis of trophic networks, both from the types and amount of food items identified in the larval alimentary canal. In all environments, the larvae fed on mainly organic matter such as plants fragments and algae, but there were many omnivore larvae. Species that have high values of food items occurred in diverse environments as generalists with great overlap niche and those with a low amount of food items with less overlap niche were classified as specialists. The largest number of trophic niche overlap was observed among collector-gatherers in connected floodplain lakes. The lower values of index niche overlap were predators. The similarity in the diet of different taxa in the same niche does not necessarily imply competition between them, but coexistence when the food resource is not scarce in the environment even in partially overlapping niches.

The larval alimentary canal of the Antarctic insect, Belgica antarctica

On the Antarctica continent the wingless midge, Belgica antarctica (Diptera, Chironomidae) occurs further south than any other insect. The digestive tract of the larval stage of Belgica that inhabits this extreme environment and feeds in detritus of penguin rookeries has been described for the first time. Ingested food passes through a foregut lumen and into a stomodeal valve representing an intussusception of the foregut into the midgut. A sharp discontinuity in microvillar length occurs at an interface separating relatively long microvilli of the stomodeal midgut region, the site where peritrophic membrane originates, from the midgut epithelium lying posterior to this stomodeal region. Although shapes of cells along the length of this non-stomodeal midgut epithelium are similar, the lengths of their microvilli increase over two orders of magnitude from anterior midgut to posterior midgut. Infoldings of the basal membranes also account for a greatly expanded interface between midgut cells and the hemocoel. The epithelial cells of the hindgut seem to be specialized for exchange of water with their environment, with the anterior two-thirds of the hindgut showing highly convoluted luminal membranes and the posterior third having a highly convoluted basal surface. The lumen of the middle third of the hindgut has a dense population of resident bacteria. Regenerative cells are scattered throughout the larval midgut epithelium. These presumably represent stem cells for the adult midgut, while a ring of cells, marked by a discontinuity in nuclear size at the midgut-hindgut interface, presumably represents stem cells for the adult hindgut.

The invertebrate B 0 system transporter, D. melanogaster NAT1, has unique d-amino acid affinity and mediates gut and brain functions

The CG3252 gene product, DmNAT1, represents the first Nutrient Amino acid Transporter cloned from Drosophila. It absorbs a broader set of neutral amino acids versus earlier characterized insect NATs and mammalian NATs-B 0 system transporters from the Sodium Neurotransmitter symporter Family (SNF, a.k.a. solute carrier family 6, SLC6). In addition to B 0-specific l-substrates, DmNAT1 equally or more effectively transports d-amino acids with sub-millimolar affinities and 1:1 sodium:amino acid transport stoichiometry. DmNAT1 is strongly transcribed in the absorptive and secretory regions of the larval alimentary canal and larval brain, revealing its roles in the primary absorption and redistribution of large neutral l-amino acids as well as corresponding d-isomers. The absorption of d-amino acids via DmNAT1 may benefit the acquisition of fermented and symbiotic products, and may support the unique capacity of fruit fly larvae to utilize a diet with substitution of essential amino acids by d-isomers. It also suggests a remarkable adaptive plasticity of NAT-SLC6 mechanisms via alterations of a few identifiable sites in the substrate-binding pocket. The strong transcription in the brain suggests roles for DmNAT1 in neuronal nutrition and clearance of l-neutral amino acids from the fly brain. In addition, neuronal DmNAT1 may absorb synaptic d-serine and modulate NMDA receptor-coupled signal transduction. The characterization of the first invertebrate B 0-like transporter extends the biological roles of the SLC6 family, revealing adaptations for the absorption of d-isomers of the essential amino acids. These findings suggest that some members of the NAT-SLC6 subfamily are evolving specific properties which contribute to nutrient symbiotic relationships and neuronal functions.

Synergy and specificity of two Na+–aromatic amino acid symporters in the model alimentary canal of mosquito larvae

The nutrient amino acid transporter (NAT) subfamily is the largest subdivision of the sodium neurotransmitter symporter family (SNF; also known as SLC6; HUGO). There are seven members of the NAT population in the African malaria mosquito Anopheles gambiae, two of which, AgNAT6 and AgNAT8, preferably transport indole- and phenyl-branched substrates, respectively. The relative expression and distribution of these aromatic NATs were examined with transporter-specific antibodies in Xenopus oocytes and mosquito larval alimentary canal, representing heterologous and tissue expression systems, respectively. NAT-specific aromatic-substrate-induced currents strongly corresponded with specific accumulation of both transporters in the plasma membrane of oocytes. Immunolabeling revealed elevated expressions of both transporters in specific regions of the larval alimentary canal, including salivary glands, cardia, gastric caeca, posterior midgut and Malpighian tubules. Differences in relative expression densities and spatial distribution of the transporters were prominent in virtually all of these regions, suggesting unique profiles of the aromatic amino acid absorption. For the first time reversal of the location of a transporter between apical and basal membranes was identified in posterior and anterior epithelial domains corresponding with secretory and absorptive epithelial functions, respectively. Both aromatic NATs formed putative homodimers in the larval gut whereas functional monomers were over-expressed heterologously in Xenopus oocytes. The results unequivocally suggest functional synergy between substrate-specific AgNAT6 and AgNAT8 in intracellular absorption of aromatic amino acids. More broadly, they suggest that the specific selectivity, regional expression and polarized membrane docking of NATs represent key adaptive traits shaping functional patterns of essential amino acid absorption in the metazoan alimentary canal and other tissues.

Molecular characterization of the first aromatic nutrient transporter from the sodium neurotransmitter symporter family

Nutrient amino acid transporters (NATs, subfamily of sodium neurotransmitter symporter family SNF, a.k.a. SLC6) represent a set of phylogenetically and functionally related transport proteins, which perform intracellular absorption of neutral, predominantly essential amino acids. Functions of NATs appear to be critical for the development and survival in organisms. However, mechanisms of specific and synergetic action of various NAT members in the amino acid transport network are virtually unexplored. A new transporter, agNAT8, was cloned from the malaria vector mosquito Anopheles gambiae (SS). Upon heterologous expression in Xenopus oocytes it performs high-capacity, sodium-coupled (2:1) uptake of nutrients with a strong preference for aromatic catechol-branched substrates, especially phenylalanine and its derivatives tyrosine and L-DOPA, but not catecholamines. It represents a previously unknown SNF phenotype, and also appears to be the first sodium-dependent B(0) type transporter with a narrow selectivity for essential precursors of catecholamine synthesis pathways. It is strongly and specifically transcribed in absorptive and secretory parts of the larval alimentary canal and specific populations of central and peripheral neurons of visual-, chemo- and mechano-sensory afferents. We have identified a new SNF transporter with previously unknown phenotype and showed its important role in the accumulation and redistribution of aromatic substrates. Our results strongly suggest that agNAT8 is an important, if not the major, provider of an essential catechol group in the synthesis of catecholamines for neurochemical signaling as well as ecdysozoan melanization and sclerotization pathways, which may include cuticle hardening/coloring, wound curing, oogenesis, immune responses and melanization of pathogens.

From the anther to the proctodeum: Pear ( Pyrus communis) pollen digestion in Osmia cornuta larvae

Modifications of the pollen grains of Pyrus communis Linneaus that occur during the digestion by Osmia cornuta (Latreille) larvae were studied histochemically. We compared the features of the pollen grains found in the anthers, in the larval cell provisions and in the alimentary canal of the 5th instar larvae. Modifications were already evident in the provisions and consisted of protoplast protrusions through the apertures and a decrease in the number of starch-containing pollen grains. After pollen grains were ingested by the larvae, the protoplast appeared retracted from the pollen wall. Pollen digestion began in the anterior part of the midgut, where we observed: (1) disorganised intine at the apertures; (2) disappearance of DAPI staining of nuclear pollen DNA; (3) fewer pollen grains containing starch than in the anthers; (4) some empty pollen grains. Pollen grains in the proctodeum appeared extremely compressed and crushed. Some grains appeared to be unaffected by the digestive process. We hypothesise that the protrusion of the intine and of the protoplast from the apertures in bee provisions could be considered a kind of pre-treatment necessary to initiate the digestion process in the larval alimentary canal.

Nuclear and Cytoplasmic Changes in the &lt;I&gt;Culex pipiens&lt;/I&gt; (Diptera: Culicidae) Alimentary Canal During Metamorphosis and Their Relationship to Programmed Cell Death

The metamorphic programmed death of Culex pipiens (L.) alimentary canal cells was studied. Hoechst DNA, Acridine Orange, and TUNEL (terminal deoxynucleotidyl transferase mediated dUTP nick end labeling) staining of larval alimentary canal whole mounts showed that programmed death of polytene cells started during the 4th stadium. The cell death program was initiated in anterior stomach polytene cells and progressed to posterior stomach and gastric caeca polytene cells. Agarose gel electrophoresis confirmed that fragmentation of alimentary canal DNA into nucleosome size fragments occurred. Diploid nuclei of the anterior and posterior stomach increased in number during the time in which programmed death of polytene cells occurred. However, TUNEL staining showed that just before pupation there was also degradation of some diploid nuclear DNA in both the anterior and posterior stomach, which suggested that some of these cells also underwent programmed cell death. MTT (3-[4,5-Dimethylthiazol-2-yl]-2,5 diphenyltetrazolium bromide) staining of the alimentary canal indicated that mitochondrial activity persisted while polytene nuclei were degraded. In addition, histological examination of serial thick sections showed that prepupal midgut cells had vacuoles which suggested that cytoplasmic cell death occurred during metamorphosis.

Digestion of Pollen Components by Larvae of the Flower-Specialist Bee Chelostoma florisomne (Hymenoptera: Megachilidae)

Pollen digestion in larvae of the solitary bee Chelostoma florisomne (Megachilidae), a pollen-specialist (oligolectic) species on Ranunculus spp. (Ranunculaceae), was investigated using histological techniques. Serial sections from the anterior-, median-, and posterior-midgut/hindgut regions of the larval alimentary canal were selectively stained and examined for disappearance of lipids, proteins, and carbohydrates from ingested Ranunculus pollen grains. During digestion, pollen contents were observed to gradually extrude through the grain apertures. Most of the digestion of lipids and proteins occurred in the anterior- and median-midgut, whereas carbohydrates disappeared more slowly and mainly in the median- and posterior-midgut. In the hindgut, pollen comprised mainly empty exine shells, which were crushed and often broken, suggesting that some components of the wall are degraded during digestion, causing collapse of the outer, chemically resistant wall layer (exine). Lipids were completely digested, but small quantities of proteins and carbohydrates were often still present in grains in the posterior midgut/hindgut. The pollenkitt appeared to be completely absorbed, with none evident in the posterior midgut or in larval feces. The findings indicate that this oligolectic bee has the digestive equipment necessary to effectively remove and absorb the nutrients present in the pollen of its restricted food source. Comparison with similar studies in adult honey bees suggests that differing digestive abilities might be an underlying factor in pollen specialization in bees.

Inter-specific analysis of Drosophila alcohol dehydrogenase by an immunoenzymatic assay using monoclonal antibodies

Three Drosophila alcohol dehydrogenase monoclonal antibodies have been prepared and characterized. These antibodies cross-react with alcohol dehydrogenase from different species as revealed by immunoblotting assay. An enzyme-linked immunosorbent assay has been devised to quantify alcohol dehydrogenase in several species, different strains and individual larval organs. The assay detects alcohol dehydrogenase via a double-antibody sandwich assay technique giving strictly proportional values for antigen concentration and optical densities in the range of 3–30 ng of antigen per 100 μl of sample. When alcohol dehydrogenase specific activity is compared in different larval organs a remarkable similarity is observed, whereas protein distribution varies substantially. Larval fat body and larval alimentary canal contribute 63% and 26% respectively to recovered alcohol dehydrogenase.

The timing of changes in several internal organs during metamorphosis of anadromous larval lamprey Petromyzon marinus L.

A current scheme for identification of stages in metamorphosis of sea lamprey Petromyzon marinus makes use of external features (Manion and Stauffer 1970). Of 13 larvae (ammocoetes) of anadromous sea lamprey sacrificed before they exhibited the earliest (stage 1) features of metamorphosis, 11 showed differentiation of the adult kidneys, and the beginnings of regression of the larval alimentary canal and endostyle. These changes are initiated not more than 1 month nor less than 1 week before known external signs are evident. There is a need for a reexamination and a further description of the early phases pf lamprey metamorphosis. Metamorphosis in anadromous sea lamprey provides excellent potential as an experimental system in comparative developmental biology.

Larvae and Larval Development of Monogeneans

Publisher Summary This chapter focusses on a group of parasitic platyhelminths generally referred to as monogenetic trematodes. A few monogeneans are viviparous and the newly-born young resemble the parents, but most are oviparous, and the newly hatched young is a larva and called an oncomiracidium. Most oncomiracidia are partly covered externally with cilia, but some are without cilia. At its posterior end, the oncomiracidium invariably bears an adhesive organ or haptor in the form of a ventrally-directed disc or cup. A gut is present in all of the oncomiracidia. The osmo-regulatory system of larval monogeneans has flame cells and efferent ducts. The larval alimentary canal and nervous system foreshadow the adult condition, but the patterns of external ciliation and of the osmo-regulatory system may reflect phylogenetic development. The study of development of haptor yielded useful clues to evolutionary trends in monogeneans. Further development now took one of two main directions––that is, to elaborate the hamuli and abandon the marginal hooks and to replace some of the marginal hooks with new muscular adhesive organs that are essentially adult features, leaving the hamuli as largely postoncomiracidial, preadult organs. The elaboration of the hamulus apparatus took place by doubling the number of hooks, by incorporating accessory sclerites, or both. The replacement of marginal hooks by adult muscular organs took place in a variety of definite patterns, and if the parasites are arranged according to these patterns, there is a conspicuous correlation between these groupings and groups arranged according to hosts.