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      Species‐complex diversification and host‐plant associations in Bemisia tabaci: A plant‐defence, detoxification perspective revealed by RNA‐Seq analyses

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          Abstract

          Insect–plant associations and their role in diversification are mostly studied in specialists. Here, we aimed to identify macroevolution patterns in the relationships between generalists and their host plants that have the potential to promote diversification. We focused on the Bemisia tabaci species complex containing more than 35 cryptic species. Mechanisms for explaining this impressive diversification have focused so far on allopatric forces that assume a common, broad, host range. We conducted a literature survey which indicated that species in the complex differ in their host range, with only few showing a truly broad one. We then selected six species, representing different phylogenetic groups and documented host ranges. We tested whether differences in the species expression profiles of detoxification genes are shaped more by their phylogenetic relationships or by their ability to successfully utilize multiple hosts, including novel ones. Performance assays divided the six species into two groups of three, one showing higher performance on various hosts than the other (the lower performance group). The same grouping pattern appeared when the species were clustered according to their expression profiles. Only species placed in the lower performance group showed a tendency to lower the expression of multiple genes. Taken together, these findings bring evidence for the existence of a common detoxification “machinery,” shared between species that can perform well on multiple hosts. We raise the possibility that this “machinery” might have played a passive role in the diversification of the complex, by allowing successful migration to new/novel environments, leading, in some cases, to fragmentation and speciation.

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          Cryptic species as a window on diversity and conservation.

          The taxonomic challenge posed by cryptic species (two or more distinct species classified as a single species) has been recognized for nearly 300 years, but the advent of relatively inexpensive and rapid DNA sequencing has given biologists a new tool for detecting and differentiating morphologically similar species. Here, we synthesize the literature on cryptic and sibling species and discuss trends in their discovery. However, a lack of systematic studies leaves many questions open, such as whether cryptic species are more common in particular habitats, latitudes or taxonomic groups. The discovery of cryptic species is likely to be non-random with regard to taxon and biome and, hence, could have profound implications for evolutionary theory, biogeography and conservation planning.
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            Heat-shock proteins, molecular chaperones, and the stress response: evolutionary and ecological physiology.

            Molecular chaperones, including the heat-shock proteins (Hsps), are a ubiquitous feature of cells in which these proteins cope with stress-induced denaturation of other proteins. Hsps have received the most attention in model organisms undergoing experimental stress in the laboratory, and the function of Hsps at the molecular and cellular level is becoming well understood in this context. A complementary focus is now emerging on the Hsps of both model and nonmodel organisms undergoing stress in nature, on the roles of Hsps in the stress physiology of whole multicellular eukaryotes and the tissues and organs they comprise, and on the ecological and evolutionary correlates of variation in Hsps and the genes that encode them. This focus discloses that (a) expression of Hsps can occur in nature, (b) all species have hsp genes but they vary in the patterns of their expression, (c) Hsp expression can be correlated with resistance to stress, and (d) species' thresholds for Hsp expression are correlated with levels of stress that they naturally undergo. These conclusions are now well established and may require little additional confirmation; many significant questions remain unanswered concerning both the mechanisms of Hsp-mediated stress tolerance at the organismal level and the evolutionary mechanisms that have diversified the hsp genes.
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              The evolutionary ecology of insect resistance to plant chemicals.

              Understanding the diversity of insect responses to chemical pressures (e.g. plant allelochemicals and pesticides) in their local ecological context represents a key challenge in developing durable pest control strategies. To what extent do the resistance mechanisms evolved by insects to deal with the chemical defences of plants differ from those that have evolved to resist insecticides? Here, we review recent advances in our understanding of insect resistance to plant chemicals, with a special emphasis on their underlying molecular basis, evaluate costs associated with each resistance trait, and discuss the ecological and evolutionary significance of these findings.
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                Author and article information

                Contributors
                shai.morin@mail.huji.ac.il
                Journal
                Mol Ecol
                Mol. Ecol
                10.1111/(ISSN)1365-294X
                MEC
                Molecular Ecology
                John Wiley and Sons Inc. (Hoboken )
                0962-1083
                1365-294X
                10 October 2018
                November 2018
                : 27
                : 21 ( doiID: 10.1111/mec.2018.27.issue-21 )
                : 4241-4256
                Affiliations
                [ 1 ] Department of Entomology The Hebrew University of Jerusalem Rehovot Israel
                [ 2 ] Department of Biological Services Weizmann Institute of Science Rehovot Israel
                [ 3 ] Department of Plant Protection School of Agriculture São Paulo State University Botucatu Brazil
                [ 4 ] CIRAD‐UMR PVBMT Saint Pierre, La Réunion France
                [ 5 ] Natural Resources Institute University of Greenwich Kent UK
                [ 6 ] School of Biological Sciences The University of Queensland Brisbane Queensland Australia
                Author notes
                [*] [* ] Correspondence

                Shai Morin, Department of Entomology, The Hebrew University of Jerusalem, Rehovot, Israel.

                Email: shai.morin@ 123456mail.huji.ac.il

                Author information
                http://orcid.org/0000-0003-2157-1999
                Article
                MEC14865
                10.1111/mec.14865
                6334513
                30222226
                73074654-f209-46c3-82ce-cee2e64ecf1c
                © 2018 The Authors. Molecular Ecology Published by John Wiley & Sons Ltd

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 28 August 2017
                : 30 August 2018
                : 04 September 2018
                Page count
                Figures: 6, Tables: 0, Pages: 16, Words: 11393
                Funding
                Funded by: Israel Science Foundation
                Award ID: 1039/12
                Funded by: Natural Resources Institute, University of Greenwich
                Funded by: Bill & Melinda Gates Foundation
                Award ID: OPP1058938
                Categories
                Original Article
                ORIGINAL ARTICLES
                Ecological Genomics
                Custom metadata
                2.0
                mec14865
                November 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.5.4 mode:remove_FC converted:16.01.2019

                Ecology
                bemisia tabaci,diet breadth,diversification,host adaptation,insect–plant interactions,species complex

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