Moth oviposition shapes the species-specific transcriptional and phytohormonal response of Nicotiana attenuata to larval feeding

AbstractMany plants emit diverse floral scents that mediate plant-environment interactions and attain reproductive success. However, how plants evolve novel adaptive floral volatiles remains unclear. Here, we show that in the wild tobacco, Nicotiana attenuata, a dominant species-specific floral volatile (benzyl acetone, BA) that attracts pollinators and deters florivore is synthesized by phenylalanine ammonia-lyase 4 (NaPAL4), isoflavone reductase 3 (NaIFR3), and chalcone synthase 3 (NaCHAL3). Transient expression of NaFIR3 alone in N. attenuata leaves is sufficient and necessary for ectopic foliar BA emissions, and the BA emission level is increased by co-expressing NaIFR3 with NaPAL4 and NaCHAL3. Independent changes in transcription in all three genes contributed to intraspecific variations of floral BA emission. However, among species, the gain-of-expression in NaIFR3 resulted in the biosynthesis of BA that was only found in N. attenuata. This study suggests that novel metabolic pathways associated with adaptation can arise via re-configurations of gene expression.

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Evolution of a Novel and Adaptive Floral Scent in Wild Tobacco

Molecular Biology and Evolution ◽

10.1093/molbev/msz292 ◽

2019 ◽

Vol 37 (4) ◽

pp. 1090-1099 ◽

Cited By ~ 2

Author(s):

Han Guo ◽

Nathalie D Lackus ◽

Tobias G Köllner ◽

Ran Li ◽

Julia Bing ◽

...

Keyword(s):

Metabolic Pathways ◽

Phenylalanine Ammonia Lyase ◽

Floral Scent ◽

Nicotiana Attenuata ◽

Plant Environment ◽

Intraspecific Variations ◽

In The Wild ◽

Isoflavone Reductase ◽

Floral Volatile ◽

Species Specific

Abstract Many plants emit diverse floral scents that mediate plant–environment interactions and attain reproductive success. However, how plants evolve novel and adaptive biosynthetic pathways for floral volatiles remains unclear. Here, we show that in the wild tobacco, Nicotiana attenuata, a dominant species-specific floral volatile (benzyl acetone, BA) that attracts pollinators and deters florivore is synthesized by phenylalanine ammonia-lyase 4 (NaPAL4), isoflavone reductase 3 (NaIFR3), and chalcone synthase 3 (NaCHAL3). Transient expression of NaFIR3 alone in N. attenuata leaves is sufficient and necessary for ectopic foliar BA emissions, and coexpressing NaIFR3 with NaPAL4 and NaCHAL3 increased the BA emission levels. Independent changes in transcription of NaPAL4 and NaCHAL3 contributed to intraspecific variations of floral BA emission. However, among species, the gain of expression of NaIFR3 resulted in the biosynthesis of BA, which was only found in N. attenuata. This study suggests that novel metabolic pathways associated with adaptation can arise via reconfigurations of gene expression.

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Stylostome of the trombiculid mite larvae Neotrombicula talmiensis (Schluger, 1955) (Acariformes, Trombiculidae) feeding on two host species in the Russian Far East

Acarologia ◽

10.24349/acarologia/20214442 ◽

2021 ◽

Vol 61 (2) ◽

pp. 412-431

Author(s):

Andrey B. Shatrov ◽

Anastasia A. Antonovskaia

Keyword(s):

Host Species ◽

Russian Far East ◽

Far East ◽

Feeding Tube ◽

Larval Feeding ◽

Trombiculid Mite ◽

Tamias Sibiricus ◽

Species Specific ◽

Myodes Rufocanus ◽

Neutrophil Leukocytes

Stylostome and skin inflammatory reaction during feeding of Neotrombicula talmiensis (Schluger, 1955) (Acariformes, Trombiculidae) larvae on the naturally infected host animals – voles Myodes rufocanus Sundevall, 1846 and Asian chipmunk Tamias sibiricus (Laxmann, 1769) were studied by histological methods. In addition, larvae were studied in scanning electron microscope (SEM). The apical hypostomal portions form a temporal sucker, which applies to the host skin during feeding. Larval feeding on both naturally infected voles and chipmunks causes an epidermal hyperkeratosis and a permanent delayed inflammation with predominance of neutrophil leukocytes, dilation of dermal capillaries and local hemorrhages. Larvae tend to feed in tight groups and may attach themselves to both ‘living’ epidermis and hypertrophic stratum corneum. The stylostome is organized nearly identically in the two host species, which points to the species-specific character of the feeding tube in trombiculid larvae. The stylostome does not penetrate the epidermis through, so it may be classified as belonging to the epidermal type. The stylostome is produced by a solidifying larval secretion and composed of the proximal eosinophil cone and the main stylostome tube, both pale-pink in azure-II-eosin with a greyish peripheral portion more pronounced in voles. No longitudinal and transverse stratification is found in the stylostome composition. In contrast with other trombiculid larvae studied so far, larvae of N. talmiensis also ingest, besides liquefied nutrients, a pure blood that reveals a possibility for trombiculid larvae to be natural bloodsuckers.

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Arabidopsis, tobacco, nightshade and elm take insect eggs as herbivore alarm and show similar transcriptomic alarm responses

Scientific Reports ◽

10.1038/s41598-020-72955-y ◽

2020 ◽

Vol 10 (1) ◽

Cited By ~ 1

Author(s):

Tobias Lortzing ◽

Reinhard Kunze ◽

Anke Steppuhn ◽

Monika Hilker ◽

Vivien Lortzing

Keyword(s):

Plant Species ◽

Insect Species ◽

Nicotiana Attenuata ◽

Larval Feeding ◽

Transcriptomic Response ◽

Insect Eggs ◽

Phenylpropanoid Biosynthesis ◽

Transcriptional Changes ◽

Transcriptomic Responses ◽

Bittersweet Nightshade

Abstract Plants respond to insect eggs with transcriptional changes, resulting in enhanced defence against hatching larvae. However, it is unknown whether phylogenetically distant plant species show conserved transcriptomic responses to insect eggs and subsequent larval feeding. We used Generally Applicable Gene set Enrichment (GAGE) on gene ontology terms to answer this question and analysed transcriptome data from Arabidopsis thaliana, wild tobacco (Nicotiana attenuata), bittersweet nightshade (Solanum dulcamara) and elm trees (Ulmus minor) infested by different insect species. The different plant–insect species combinations showed considerable overlap in their transcriptomic responses to both eggs and larval feeding. Within these conformable responses across the plant–insect combinations, the responses to eggs and feeding were largely analogous, and about one-fifth of these analogous responses were further enhanced when egg deposition preceded larval feeding. This conserved transcriptomic response to eggs and larval feeding comprised gene sets related to several phytohormones and to the phenylpropanoid biosynthesis pathway, of which specific branches were activated in different plant–insect combinations. Since insect eggs and larval feeding activate conserved sets of biological processes in different plant species, we conclude that plants with different lifestyles share common transcriptomic alarm responses to insect eggs, which likely enhance their defence against hatching larvae.

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Electron Microscopy in the Study of Natural Phytoplankton Assemblages

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100119831 ◽

1985 ◽

Vol 43 ◽

pp. 620-623

Author(s):

Linda Sicko-Goad

Keyword(s):

Electron Microscopy ◽

Aquatic Environment ◽

Size Range ◽

Physical Parameters ◽

Specific Information ◽

Phytoplankton Assemblages ◽

Phytoplankton Productivity ◽

Ecosystem Effects ◽

Time Of Year ◽

Species Specific

Although the use of electron microscopy and its varied methodologies is not usually associated with ecological studies, the types of species specific information that can be generated by these techniques are often quite useful in predicting long-term ecosystem effects. The utility of these techniques is especially apparent when one considers both the size range of particles found in the aquatic environment and the complexity of the phytoplankton assemblages.The size range and character of organisms found in the aquatic environment are dependent upon a variety of physical parameters that include sampling depth, location, and time of year. In the winter months, all the Laurentian Great Lakes are uniformly mixed and homothermous in the range of 1.1 to 1.7°C. During this time phytoplankton productivity is quite low.

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