Insights into wing dimorphism in worldwide agricultural pest and host-alternating aphid Aphis gossypii

Background The worldwide pest Aphis gossypii has three-winged morphs in its life cycle, namely, winged parthenogenetic female (WPF), winged gynopara (GP), and winged male, which are all produced by a wingless parthenogenetic female (WLPF). Most studies on A. gossypii have focused on WPF, while few have investigated GP and male. The shared molecular mechanism underlying the wing differentiation in the three wing morphs of A. gossypii remains unknown. The wing differentiation of WPF was explored in a previous study. Herein, GP and male were induced indoors. The characters of the body, internal genitals, wing veins, and fecundity of GP and male were compared with those of WPF or WLPF. Compared with WLPF, the shared and separate differentially expressed genes (DEGs) were identified in these three-wing morphs. Results Newly-born nymphs reared in short photoperiod condition (8 L:16D, 18 °C) exclusively produced gynoparae (GPe) and males in adulthood successively, in which the sex ratio was GP biased. A total of 14 GPe and 9 males were produced by one mother aphid. Compared with WLPF, the three-wing morphs exhibited similar morphology and wing vein patterns but were obviously discriminated in the length of fore- and underwings, reproductive system, and fecundity. A total of 37 090 annotated unigenes were obtained from libraries constructed using the four morphs via RNA sequencing (RNA-Seq). In addition, 10 867 and 19 334 DEGs were identified in the pairwise comparison of GP versus WLPF and male versus WLPF, respectively. Compared with WLPF, the winged morphs demonstrated 2 335 shared DEGs (1 658 upregulated and 677 downregulated). The 1 658 shared upregulated DEGs were enriched in multiple signaling pathways, including insulin, FoxO, MAPK, starch and sucrose metabolism, fatty acid biosynthesis, and degradation, suggesting their key roles in the regulation of wing plasticity in the cotton aphid. Forty-four genes that spanned the range of differential expression were chosen to validate statistical analysis based on RNA-Seq through the reverse transcription quantitative real time polymerase chain reaction (RT-qPCR). The comparison concurred with the expression pattern (either up- or downregulated) and supported the accuracy and reliability of RNA-Seq. Finally, the potential roles of DEGs related to the insulin signaling pathway in wing dimorphism were discussed in the cotton aphid. Conclusions The present study established an efficiently standardized protocol for GP and male induction in cotton aphid by transferring newly-born nymphs to short photoperiod conditions (8 L:16D, 18 °C). The external morphological characters, especially wing vein patterns, were similar among WPFs, GPe, and males. However, their reproductive organs were strikingly different. Compared with WLPF, shared (2 235) and exclusively (1 470 in WLPF, 2 419 in GP, 10 774 male) expressed genes were identified in the three-wing morphs through RNA-Seq, and several signaling pathways that are potentially involved in their wing differentiation were obtained, including insulin signaling, starch and sucrose metabolism.

Insights into wing dimorphism in the worldwide agricultural pest Aphis gossypii, the host-alternating aphid

Background: Three wing morphs exists in the life cycle of the worldwide pest Aphis gossypii, i.e., wing parthenogenetic female (WPF), gynopara (GP) and male, which were produced mostly by crowding and host quality, photoperiod, loss of X chromosome, respectively. However, the shared molecular mechanism underlying their wing differentiation remains an enigma. Here we firstly induced gynoparae and males indoors and compared the characters of these wing morphs in body, internal genitals and fecundity. Then we identified the shared and separate differentially expressed genes (DEGs) and signaling pathways potentially involved in the wing morphs regulation in WPF, GP and male compared to wingless parthenogenetic female (WLPF). Results: Newly-born nymphs reared in short photoperiod condition exclusively produce gynoparae and males in adulthood successively, in which the sex ratio is gynoparae biased. Compared with WLPF, three wing morphs have similar morphology in bodies but is obviously discriminated in the reproductive system and fecundity. Built upon our previous study, 37 090 annotated unigenes were obtained from libraries constructed by the four morphs above through RNA-sequencing, in which 10 867, 19 334 DEGs were identified in pairwise comparison of GP vs. WLPF, Male vs. WLPF, respectively. Furthermore, 2 335 shared DEGs including 1 658 up- and 677 downregulated were obtained in these wing morphs compared to WLPF. The 1 658 shared up-regulated DEGs were enriched in multiple signaling pathways including insulin, FoxO, MAPK, strarch and sucrose metabolism, fatty acid biosynthesis and degradation which hint their key roles in the regulation of wing plasticity in cotton aphid. Gene expression levels were validated by using Pearson’s correlation (r) and potential roles of 15 DEGs related to the insulin signaling pathway in cotton wing dimorphism were discussed. Conclusions: The results of this study establish a solid foundation for deciphering molecular mechanisms underlying the switch between wingless and wing morphs in the cotton aphid and provide valuable resources for future research on the host-alternating aphid species.

The most latent cladoceran in the Holarctic revealed—sinking Unapertura Sarmaja-Korjonen, Hakojärvi & Korhola, 2000 into the genus Rhynchotalona Norman, 1903 (Branchiopoda: Cladocera: Chydoridae)

The morphology of one of the smallest chydorid cladocerans in the world, Unapertura latens Sarmaja-Korjonen, Hakojärvi & Korhola, 2000 (Branchiopoda: Cladocera: Anomopoda) is studied herein. External features and postabdomen of the adult parthenogenetic female are discussed in detail for the first time, based on an intact specimen from northern Finland. Originally described on Quaternary fossil remains, we investigate the validity of the monotypic genus Unapertura and its position within the Aloninae subfamily, in particular in relation to Rhynchotalona Norman, 1903. As a result, we rename the taxon as Rhynchotalona latens comb. nov., based on morphology. The species, a glacial relict, seems one of the rarest cladocerans in contemporary waters in Finland, yet intact specimens are clearly overlooked and recent remains in surface sediments suggest an Arctic-Alpine distribution in oligotrophic habitats in the Holarctic.

Nematodes from galls on Myrtaceae. XI. Descriptions of five new species of Fergusobia from Australia

Five new species of Fergusobia are described. Fergusobia janetae Davies n. sp. is characterized by the combination of an arcuate to straight, spindle-shaped parthenogenetic female with a relatively small oesophageal gland, an extensile uterus and a conoid tail, an arcuate infective female with a bluntly rounded tail tip, and a C-shaped male with an arcuate to angular spicule and bursa arising at more than 90% of body length. Fergusobia robustae Davies n. sp. is characterized by the combination of a small, C-shaped parthenogenetic female with a short cylindroid tail with a broadly rounded tip; an arcuate to C-shaped, relatively broad, infective female with a tail tip that is almost hemispherical; and an arcuate male with a strong angular spicule and a bursa arising at 30–40% of body length. Fergusobia pruinosae Davies n. sp. is characterized by the combination of a medium sized, open C-shaped, parthenogenetic female in which the cuticle does not swell upon fixation, with a strongly sclerotised stylet, with a more or less narrowly conoid tail with a bluntly or broadly rounded tip; infective female that is arcuate to J-shaped with a notched tail tip; and open C-shaped males with stout, angular spicules and bursa arising near the secretory/excretory pore. Fergusobia pauciflorae Davies n. sp. is characterized by the combination of a medium sized, arcuate, parthenogenetic female with a small stylet, and a conoid tail with a bluntly rounded tip; a small, open C to J-shaped infective female with a broadly rounded to almost hemispherical tail tip; and straight to arcuate males with stout, angular spicules and bursa at ~70% of body length anterior to the cloaca. Fergusobia obliquae Davies n. sp. has a relatively broad, arcuate, parthenogenetic female having a small but strongly sclerotised stylet, and a short conoid tail with a bluntly rounded tip; an arcuate, infective female with an almost hemispherical tail tip; and C-shaped males with arcuate to angular (not heavily sclerotised) spicules and bursa arising 50–80% of body length anterior to tail. Sequencing of the 18S and 28S rDNA domains for F. janetae n. sp. and of mitochondrial DNA cytochrome oxidase subunit I (mtCOI) for F. pauciflorae n. sp. confirm that they are distinct species.

Specific IgG and immune complex responses to parthenogenetic females and eggs of nematode Strongyloides venezuelensis for the diagnosis of immunosuppression in infected rats

In the present study, antigens from parthenogenetic females and eggs of Strongyloides venezuelensis, or anti-parthenogenetic-female and anti-egg antigens were used to detect specific IgG and immune complex responses, respectively. Serum samples from experimentally infected immunocompetent and immunosuppressed rats were analysed on days 5, 8, 13 and 21 post-infection (dpi). An enzyme-linked immunosorbent assay (ELISA) was performed using alkaline parasite extract for specific IgG detection, and anti-parthenogenetic-female or anti-egg antigens for immune complex detection. The data were analysed using analysis of variance (ANOVA), followed by a Bonferroni test. When parthenogenetic female or egg extracts were used as antigens, specific IgGs were not detected in either immunocompetent or immunosuppressed rats. When anti-parthenogenetic-female or anti-S. venezuelensis-eggs were used, immune complexes were detected for the duration of the infection in immunosuppressed animals and were only detected between 5 and 13 dpi in immunocompetent animals. The duration of infection was not significantly different between the immunocompetent and immunosuppressed groups when anti-parthenogenetic-female or anti-S. venezuelensis-eggs were used. Parthenogenetic female extracts yielded significant differences between antibody and immune complex responses in immunocompetent rats from 5 to 13 dpi, but only on day 5 dpi in immunosuppressed rats. Exposure to S. venezuelensis egg extract yielded significant differences in both antibody and immune complex detection between immunocompetent and immunosuppressed rats for the duration of the infection. In conclusion, ELISA using alternative antigens may be a successful strategy for identifying immune complexes in serum samples and diagnosing active strongyloidiasis, particularly under conditions of immunosuppression.

Androgenesis is a maternal trait in the invasive ant Wasmannia auropunctata

Androgenesis is the production of an offspring containing exclusively the nuclear genome of the fathering male via the maternal eggs. This unusual mating system is generally considered a male trait, giving to androgenetic males a substantial fitness advantage over their sexually reproducing relatives. We here provide the first empirical study of the evolutionary outcomes of androgenesis in a haplo-diploid organism: the invasive ant Wasmannia auropunctata . Some of the populations of this species have a classical haplo-diploid sexual mating system. In other populations, females and males are produced through parthenogenesis and androgenesis, respectively, whereas workers are produced sexually. We conducted laboratory reciprocal-cross experiments with reproductive individuals from both types of populations and analysed their progenies with genetic markers, to determine the respective contribution of males and females to the production of androgenetic males. We found that androgenesis was a parthenogenetic female trait. A population genetic study conducted in natura confirmed the parthenogenetic female origin of androgenesis, with the identification of introgression events of sexual male genotypes into androgenetic/parthenogenetic lineages. We argue that by producing males via androgenesis, parthenogenetic queen lineages may increase and/or maintain their adaptive potential, while maintaining the integrity of their own genome, by occasionally acquiring new male genetic material and avoiding inbreeding depression within the sexually produced worker cast.

Nematodes from galls on Myrtaceae. III. Fergusobia from flower bud and stigma galls on Eucalyptus, with descriptions of four new species

Four new species of Fergusobia from flower bud galls and a stigma gall on Eucalyptus spp. in Australia are described. Fer-gusobia eugenioidae Davies n. sp. is characterised by having an arcuate, open C or C-shaped parthenogenetic female witha conoid tail, an arcuate to open C-shaped infective female with a hooked tail region and a broadly rounded tail tip, andarcuate or open C-shaped males with angular spicules and short bursa. Fergusobia fasciculosae Davies n. sp. is character-ised by the combination of an arcuate parthenogenetic female with a short, broadly conoid tail, an open C-shaped infectivefemale with a hemispherical tail tip, and J-shaped males with angular spicules and short peloderan bursa. This is the firstFergusobia/Fergusonina association to be described from flower stigma galls. Fergusobia juliae Davies n. sp. is character-ised by the combination of an arcuate to C-shaped parthenogenetic female with a short, broadly conoid tail, a J-shaped in-fective female with a hooked tail region, a cuticular plate around the vulva, and a broadly rounded tail tip, and J-shapedmales with angular spicules and short peloderan bursa. Fergusobia morrisae Davies n. sp. has a C-shaped parthenogeneticfemale with a narrowly conoid tail, an arcuate or J-shaped infective female with most curvature behind the vulva and a shorttail with an almost hemispherical tip, and arcuate or J-shaped males with strongly sclerotised, angular spicules and a longpeloderan bursa. Other known similar forms of Fergusobia/Fergusonina flower bud galls from Eucalyptus spp. are outlinedand the larval shield morphology of their associated mutualistic fly species is discussed where known. An inventory of allknown Fergusobia/Fergusonina associations from flower bud galls from Eucalyptus spp. is presented. Molecular analysisof Fergusobia nematodes was inferred from DNA sequencing of 28S rDNA D2/D3 domains and a portion of mitochondrial DNA cytochrome oxidase subunit I (mtCOI). Possible evolutionary relationships are discussed.

Nematodes from galls on Myrtaceae. II. Fergusobia/Fergusonina from small axillary bud ('stem') and leaf ('pea') galls in Australia, with descriptions of two new species

Two new species of Fergusobia, collected from small multilocular axillary vegetative bud ('stem') and unilocular leaf 'pea' galls on, respectively, Eucalyptus camaldulensis from South Australia, and an unknown species of Corymbia growing in sub-coastal north-eastern NSW, Australia, are described. Fergusobia camaldulensae n. sp. Davies is characterized morphologically by an almost straight to open-C shaped parthenogenetic female with a broadly conoid tail, an arcuate infective female with a hemispherical tail tip, and males of varying shape with weakly sclerotised angular spicules and bursa arising at mid-body length. Fergusobia rileyi n. sp. Davies is characterized morphologically by the combination of an almost straight to arcuate parthenogenetic female with a broadly conoid tail, an arcuate infective female with relatively narrow tail with a pointed tip, and arcuate males with arcuate spicules, a relatively slender tail, and long peloderan bursa. These species are associated with larvae of undescribed fly species having dorsal shields of the 'transverse bars' form or lacking. Other apparently related forms of Fergusobia/Fergusonina associations from small 'stem' and 'shoot' galls and unilocular leaf 'pea' galls are reported, the larval shield morphology of their associated mutualistic fly species is discussed where known, and their possible relationships are outlined. DNA sequence analyses of the domain 2 and 3 segments of the large subunit rDNA gene (D2/D3) and mitochondrial DNA cytochrome oxidase subunit 1 (mtCOI) supported the new species status and their phylogenetic relationships with other sequenced species in Fergusobia.