Different responses to temperature in three closely-related sympatric cereal aphids

Cotesia glomerata L. (Hymenoptera: Braconidae) is a parasitoid of early instar larvae of Pieris brassicae L. (Lepidoptera: Pieridae). Late instars of P. brassicae can more often overcome parasitization by hemocytic encapsulation of C. glomerata eggs. Short-term hemocyte responses to parasitization were examined in third and fourth instar larvae of P. brassicae. Total and differential hemocyte counts did not differ between parasitized and unparasitized host larvae. A rapid, but temporary decrease of total hemocyte as well as plasmatocyte numbers was observed immediately after oviposition. Numbers of hemocytes adhering to tissues were shown to be the same in untreated, wounded and parasitized P. brassicae larvae by tracing hemocytes with monoclonal antibodies as markers. The in vitro spreading ability of hemocytes from unparasitized third and fourth instar larvae was lower than that of the last instar's; parasitization, however, had no influence on hemocyte spreading. We therefore suggest that the higher parasitization success of C. glomerata in earlier instars of P. brassicae is mainly due to the low spreading ability of the hemocytes. Abbreviations: ACS – anticoagulant saline; BSA – bovine serum albumin; DABCO – 1,4-diazabicyclo-[2,2,2]-octane; DHC – differential hemocyte count; FITC – fluorescein isothiocyanate; GR – granular cells; LPS – lipopolysaccharide; mAb – monoclonal antibody; OE – oenocytoids; PL – plasmatocytes; PRO – prohemocytes; PS – Pieris saline; PVP – polyvinylpyrrolidone; TBS – tris-buffered saline; THC – total hemocyte count.     

Morphofunctional characterization of hemocytes in black soldier fly larvae

In insects, the cell-mediated immune response involves an active role of hemocytes in phagocytosis, nodulation, and encapsulation. Although these processes have been well documented in multiple species belonging to different insect orders, information concerning the immune response, particularly the hemocyte types and their specific function in the black soldier fly Hermetia illucens, is still limited. This is a serious gap in knowledge given the high economic relevance of H. illucens larvae in waste management strategies and considering that the saprophagous feeding habits of this dipteran species have likely shaped its immune system to efficiently respond to infections. The present study represents the first detailed characterization of black soldier fly hemocytes and provides new insights into the cell-mediated immune response of this insect. In particular, in addition to prohemocytes, we identified five hemocyte types that mount the immune response in the larva, and analyzed their behavior, role, and morphofunctional changes in response to bacterial infection and injection of chromatographic beads. Our results demonstrate that the circulating phagocytes in black soldier fly larvae are plasmatocytes. These cells also take part in nodulation and encapsulation with granulocytes and lamellocyte-like cells, developing a starting core for nodule/capsule formation to remove/encapsulate large bacterial aggregates/pathogens from the hemolymph, respectively. These processes are supported by the release of melanin precursors from crystal cells and likely by mobilizing nutrient reserves in newly circulating adipohemocytes, which could thus trophically support other hemocytes during the immune response. Finally, the regulation of the cell-mediated immune response by eicosanoids was investigated.     

Purification and binding properties of hemagglutinin from Biomphalaria glabrata.

A hemagglutinin has been purified from Biomphalaria glabrata (PR-B) hemolymph, albumin glands, and egg masses using affinity chromatography with Sephadex gels. The purified material from any of the sources above demonstrated identical immunological properties during immunoelectrophoresis or immunodiffusion, and similar serological specificity for human A₁ erythrocytes and to a lesser extent A₂ erythrocytes. Hemagglutinin was able to bind in vitro to the tegumental surface of cultured Schistosoma mansoni sporocysts, cercariae, and miracidia. Sporocysts dissected from infected snails and shed cercariae were already found to have hemagglutinin on their tegumental surface as demonstrated by immunofluorescence. It is postulated that hemagglutinin binding to the surface of larval helminths may “mask” them from being recognized by the snail host's cellular defense system.     

Ultrastructure of differentiating hemocytes in the embryo of Oncopeltus fasciatus Dallas (Insecta,Heteroptera)

Summary The hemocytes of Oncopeltus differentiate rather early during embryogenesis. They are segregated by the mesoderm soon after its formation (about 50h after egg deposition). Newly segregated hemocytes show the typical features of embryonic cells: many free ribosomes, a few strands of rough ER, the cisternae of which are considerably distended, electron lucent vacuoles around the periphery, and glycogen deposits. A few hours thereafter the hemocytes undergo striking subcellular changes. First, glycogen, electron lucent vacuoles and rough ER disappear and phagocytotic activity can be observed. Golgi complexes become well expressed and give rise to electron dense vesicles which fuse to larger bodies. Then, rough ER develops again and occupies large areas of the cytoplasm. Its cisternae are often considerably distended by proteinaceous secretions. All hemocytes undergo the same steps of differentiation.Embryonic hemocytes obviously play a decisive role in the elimination of waste products, in particular of tissue debris that results from programmed cellular death. The significance of the conspicuous protein secretions is not fully understood. They may participate in the deposition of the acellular connective tissue, or may have some of the other functions ascribed to insect blood cells.Larvae and imagines of Oncopeltus have four types of hemocytes, which agree rather well with those found in Rhodnius (Lai-Fook, 1970). All embryonic hemocytes, aside from the newly segregated ones, represent plasmatocytes but, unlike plasmatocytes of postembryonic stages, they contain no large inclusion bodies. Newly segregated embryonic hemocytes, in addition to their typical embryonic features, have some similarities with larval and adult prohemocytes. Oenocytoids and granulocytophagous cells are absent in the embryo. Some aspects concerning the differentiation and classification of hemocytes are discussed.Supported by research grant Do 163 from the Deutsche ForschungsgemeinschaftThe author is grateful to Ms. K. Schmidtke and Ms. M. Ullmann for technical assistance     

Evasion of encapsulation by parasitoid correlated with the extent of host hemocyte pathology

The egg and larval stages of the generalist endoparasitoid Campoletis sonorensis Carlson (Hymenoptera: Ichneumonidae), which normally avoid the hemocytic reaction of many Lepidopteran host species, are encapsulated in 40% of Spodoptera frugiperda J. E. Smith (Lepidoptera: Noctuidae) larvae. The effect of parasitism on inhibiting the spreading ability of S. frugiperda plasmatocytes in vitro is more pronounced in susceptible larvae which fail to encapsulate the parasitoid than in resistant ones permitting parasitoid development. This suggests that induction of plasmatocyte pathology is relevant to the successful evasion of encapsulation by the parasitoid. Some granular cells disappear from the hemolymph of the parasitized resistant larvae, which implicates their involvement in the encapsulation reaction. Calyx fluid of C. sonorensis injected into host larvae produced effects on host hemocytes identical to natural parasitism. Several mechanism may cooperate to protect the parasitoid from encapsulation. The pathological reactions by the host plasmatocytes is one main manifestation of the immunosuppressive parasitoid effect. Results are discussed in regard to the known effects of C. sonorensis on Heliothis virescens Fabricius (Lepidoptera: Noctuidae) larval hemocytes which are totally unable to respond with a successful cellular defense reaction.

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Résumé L'ichneumonide Campoletis sonorensis Carlson, endoparasitoïde larvaire, se développe dans de nombreuses espèces de Lépidoptères. Son statut de généraliste est dû, notamment, à son aptitude à déjouer les défenses immunitaires de ses hôtes, c.a.d. la formation d'une capsule d'hémocytes autour de l'oeuf ou de la larve parasite. Cependant, chez le noctuide Spodoptera frugiperda J.E. Smith, C. sonorensis est encapsulé dans 40% des larves qu'il parasite. Nous avons étudié la population hémocytaire de deux catégories de larves de S. frugiperda, celles qualifiées de résistantes à C. sonorensis, et qui arrêtent son développement, et celles susceptibles où le parasitoïde échappe à l'encapsulation.Cinq types d'hémocytes ont été identifiés: les prohémocytes (PR), les sphérulocytes (SP), les granulocytes (GR), les plasmatocytes (PL) et les oenocytoïdes (OE). Chez les hôtes susceptibles et résistants, le parasite provoque une baisse identique de la concentration totale des hémocytes dans l'hémolymphe (THC). Par contre, les PLs sont davantage affectés chez les hôtes susceptibles que chez ceux résistants au parasitoïde. Les résultats montrent que, chez les hôtes susceptibles, 1) le nombre des PLs dans l'hémolymphe est davantage diminué, et 2) leur aptitude d'adhérence in vitro est davantage inhibée. Il existe donc une corrélation positive entre le degré de pathologies qui affectent les PLs de l'hôte et l'incapacité de celui-ci à encapsuler le parasitoïde. Ceci tend à démontrer le rôle-clé des PLs dans la réaction immunitaire d'encapsulation chez S. frugiperda, comme chez de nombreux insectes. De plus, ce résultat renforce l'hypothèse selon laquelle C. sonorensis éviterait l'encapsulation en agissant sur les hémocytes de l'hôte, et plus particulièrement sur les PLs. Inversement aux PLs, les GRs sont moins abondants dans l'hémolymphe des hôtes qui encapsulent C. sonorensis. Les GRs pourraient donc participer à la formation de la capsule hémocytaire.Il est possible que plusieurs facteurs contribuent à protéger C. sonorensis de l'encapsulation. Néanmoins, les pathologies affectant les hémocytes des hôtes parasités sont probablement une manifestation majeure de l'effet immunosuppresseur du parasitoïde.Les effets de C. sonorensis sur les hémocytes des larves parasitées peuvent être reproduits chez des larves saines, en leur injectant de venin extrait des glandes du calyx des femelles parasitoïdes. Ces sécrétions provenant de la glande du calyx, et normalement injectées dans l'hôte lors de l'oviposition, sont probablment responsable, au moins en partie, de l'effet immunosuppresseur du parasitoïde.Ces résultats peuvent être comparés à ceux obtenus chez l'hôte Heliothis virescens Fabricius (lépidoptère, noctuide) qui n'encapsule jamais C. sonorensis. Bien que le parasitoïde provoque les mêmes effets pathologiques sur les hémocytes des hôtes de S. frugiperda et d'H. virescens, on constate que l'effet apparait quelques heures après l'oviposition chez H. virescens, contre 48 heures post-oviposition chez S. frugiperda. Ce délai pourrait contribuer à la résistance immunitaire de certaines larves de S. frugiperda, résistantes, à C. sonorensis.

     

Plasmatocyte spreading peptide induces spreading of plasmatocytes but represses spreading of granulocytes.

In most Lepidoptera, plasmatocytes and granulocytes are the two hemocyte classes capable of adhering to foreign targets. Previously, we identified plasmatocyte spreading peptide (PSP1) from the moth Pseudoplusia includens and reported that it induced plasmatocytes to rapidly spread on foreign surfaces. Here we examine whether the response of plasmatocytes to PSP1 was influenced by cell density or culture conditions, and whether PSP1 affected the adhesive state of granulocytes. Plasmatocyte spreading rates were clearly affected by cell density in the absence of PSP1 but spreading was density independent in the presence of PSP1. PSP1 also induced plasmatocytes in agarose-coated culture wells to form homotypic aggregations rather than spread on the surface of culture wells. In contrast, granulocytes rapidly spread in a density independent manner in the absence of PSP1, but were dose-dependently inhibited from spreading by the addition of peptide. An anti-PSP1 polyclonal antibody neutralized the spreading activity of synthetic PSP1. This antibody also neutralized the plasmatocyte spreading activity of granulocyte-conditioned medium, and significantly delayed plasmatocyte spreading when cells were cultured at a high density in unconditioned medium. These results suggested that the spreading activity derived from granulocytes is due in part to PSP1. Pretreatment of plasmatocytes with trypsin had no effect on PSP1-induced aggregation but PSP1-induced aggregations were readily dissociated by trypsin. This suggested that PSP1 is not an adhesion factor but induces adhesion by stimulating a change in the cell surface of plasmatocytes. Synthetic PSP1 also induced aggregation of plasmatocytes from other Lepidoptera indicating that regulation of hemocyte activity by PSP1-related peptides may be widespread. Arch.     

虾类血细胞的分类与功能研究进展

血细胞在动物的免疫防御体系中扮演了重要的角色,尤其是对缺少适应性免疫的无脊椎动物.在这些动物中,血细胞既参与细胞免疫的吞噬、包囊、结节等作用,还参与体液免疫中许多免疫因子的生成与储存.对不同动物类群的血细胞的不同亚群进行区分,是深入了解其免疫机制与血细胞功能的基础.尽管国内外学者利用不同的方法,针对虾类血细胞的不同亚群...     

Experimental evidence of Wolbachia introgressive acquisition between terrestrial isopod subspecies

Wolbachia are the most widespread endosymbiotic bacteria in animals. In many arthropod host species, they manipulate reproduction via several mechanisms that favor their maternal transmission to offspring. Among them, cytoplasmic incompatibility (CI) promotes the spread of the symbiont by specifically decreasing the fertility of crosses involving infected males and uninfected females, via embryo mortality. These differences in reproductive efficiency may select for the avoidance of incompatible mating, a process called reinforcement, and thus contribute to population divergence. In the terrestrial isopod Porcellio dilatatus, the Wolbachia wPet strain infecting the subspecies P. d. petiti induces unidirectional CI with uninfected individuals of the subspecies P. d. dilatatus. To study the consequences of CI on P. d. dilatatus and P. d. petiti hybridization, mitochondrial haplotypes and Wolbachia infection dynamics, we used population cages seeded with different proportions of the 2 subspecies in which we monitored these genetic parameters 5 and 7 years after the initial setup. Analysis of microsatellite markers allowed evaluating the degree of hybridization between individuals of the 2 subspecies. These markers revealed an increase in P. d. dilatatus nuclear genetic signature in all mixed cages, reflecting an asymmetry in hybridization. Hybridization led to the introgressive acquisition of Wolbachia and mitochondrial haplotype from P. d. petiti into nuclear genomes dominated by alleles of P. d. dilatatus. We discuss these results with regards to Wolbachia effects on their host (CI and putative fitness cost), and to a possible reinforcement that may have led to assortative mating, as possible factors contributing to the observed results.     

Structural features,evolutionary relationships,and transcriptional regulation of C-type lectin-domain proteins in Manduca sexta

C-type lectins (CTLs) are a large family of Ca²⁺-dependent carbohydrate-binding proteins recognizing various glycoconjugates and functioning primarily in immunity and cell adhesion. We have identified 34 CTLDP (for CTL-domain protein) genes in the Manduca sexta genome, which encode proteins with one to three CTL domains. CTL-S1 through S9 (S for simple) have one or three CTL domains; immulectin-1 through 19 have two CTL domains; CTL-X1 through X6 (X for complex) have one or two CTL domains along with other structural modules. Nine simple CTLs and seventeen immulectins have a signal peptide and are likely extracellular. Five complex CTLs have both an N-terminal signal peptide and a C-terminal transmembrane region, indicating that they are membrane anchored. Immulectins exist broadly in Lepidoptera and lineage-specific gene duplications have generated three clusters of fourteen genes in the M. sexta genome, thirteen of which have similar expression patterns. In contrast to the family expansion, CTL-S1∼S6, S8, and X1∼X6 have 1:1 orthologs in at least four lepidopteran/dipteran/coleopteran species, suggestive of conserved functions in a wide range of holometabolous insects. Structural modeling suggests the key residues for Ca²⁺-dependent or independent binding of certain carbohydrates by CTL domains. Promoter analysis identified putative κB motifs in eighteen of the CTL genes, which did not have a strong correlation with immune inducibility in the mRNA or protein levels. Together, the gene identification, sequence comparisons, structure modeling, phylogenetic analysis, and expression profiling establish a solid foundation for future studies of M. sexta CTL-domain proteins.