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      A new millipede-parasitizing horsehair worm, Gordius chiashanus sp. nov., at medium altitudes in Taiwan (Nematomorpha, Gordiida)

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          Abstract

          Gordius chiashanus sp. nov., a newly described horsehair worm that parasitizes the Spirobolus millipede, is one of the three described horsehair worm species in Taiwan. It is morphologically similar to G. helveticus Schmidt-Rhaesa, 2010 because of the progressively broadening distribution of bristles concentrated on the male tail lobes, but it is distinguishable from G. helveticus because of the stout bristles on the mid-body. In addition, a vertical white stripe on the anterior ventral side and areoles on the inside wall of the cloacal opening are rarely mentioned in other Gordius species. Free-living adults emerged and mated on wet soil under the forest canopy in the winter (late November to early February) at medium altitudes (1100–1700 m). Mucus-like structure covering on the body surface, which creates a rainbow-like reflection, might endow the worm with high tolerance to dehydration. Although Gordius chiashanus sp. nov. seems to be more adaptive to the terrestrial environment than other horsehair worm species, cysts putatively identified as belonging to this hairworm species found in the aquatic paratenic host, Ephemera orientalis McLachlan, 1875, suggest the life cycle of Gordius chiashanus sp. nov. could involve water and land. The free-living adults emerged from the definitive hosts might reproduce in the terrestrial environment or enter an aquatic habitat by moving or being washed away by heavy rain instead of manipulating the behavior of their terrestrial definitive hosts.

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          Use of ITS2 Region as the Universal DNA Barcode for Plants and Animals

          Background The internal transcribed spacer 2 (ITS2) region of nuclear ribosomal DNA is regarded as one of the candidate DNA barcodes because it possesses a number of valuable characteristics, such as the availability of conserved regions for designing universal primers, the ease of its amplification, and sufficient variability to distinguish even closely related species. However, a general analysis of its ability to discriminate species in a comprehensive sample set is lacking. Methodology/Principal Findings In the current study, 50,790 plant and 12,221 animal ITS2 sequences downloaded from GenBank were evaluated according to sequence length, GC content, intra- and inter-specific divergence, and efficiency of identification. The results show that the inter-specific divergence of congeneric species in plants and animals was greater than its corresponding intra-specific variations. The success rates for using the ITS2 region to identify dicotyledons, monocotyledons, gymnosperms, ferns, mosses, and animals were 76.1%, 74.2%, 67.1%, 88.1%, 77.4%, and 91.7% at the species level, respectively. The ITS2 region unveiled a different ability to identify closely related species within different families and genera. The secondary structure of the ITS2 region could provide useful information for species identification and could be considered as a molecular morphological characteristic. Conclusions/Significance As one of the most popular phylogenetic markers for eukaryota, we propose that the ITS2 locus should be used as a universal DNA barcode for identifying plant species and as a complementary locus for CO1 to identify animal species. We have also developed a web application to facilitate ITS2-based cross-kingdom species identification (http://its2-plantidit.dnsalias.org).
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            Do hairworms (Nematomorpha) manipulate the water seeking behaviour of their terrestrial hosts?

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              Water-seeking behavior in worm-infected crickets and reversibility of parasitic manipulation

              One of the most fascinating examples of parasite-induced host manipulation is that of hairworms, first, because they induce a spectacular “suicide” water-seeking behavior in their terrestrial insect hosts and, second, because the emergence of the parasite is not lethal per se for the host that can live several months following parasite release. The mechanisms hairworms use to increase the encounter rate between their host and water remain, however, poorly understood. Considering the selective landscape in which nematomorph manipulation has evolved as well as previously obtained proteomics data, we predicted that crickets harboring mature hairworms would display a modified behavioral response to light. Since following parasite emergence in water, the cricket host and parasitic worm do not interact physiologically anymore, we also predicted that the host would recover from the modified behaviors. We examined the effect of hairworm infection on different behavioral responses of the host when stimulated by light to record responses from uninfected, infected, and ex-infected crickets. We showed that hairworm infection fundamentally modifies cricket behavior by inducing directed responses to light, a condition from which they mostly recover once the parasite is released. This study supports the idea that host manipulation by parasites is subtle, complex, and multidimensional.
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                Author and article information

                Contributors
                Journal
                Zookeys
                Zookeys
                2
                urn:lsid:arphahub.com:pub:45048D35-BB1D-5CE8-9668-537E44BD4C7E
                urn:lsid:zoobank.org:pub:91BD42D4-90F1-4B45-9350-EEF175B1727A
                ZooKeys
                Pensoft Publishers
                1313-2989
                1313-2970
                2020
                16 June 2020
                : 941
                : 25-48
                Affiliations
                [1 ] Department of Biology, Kobe University, Kobe 657-8501, Japan Kobe University Kobe Japan
                [2 ] Current address: Department of Biology, National Changhua University of Education, Changhua City 55007, Taiwan National Changhua University of Education Changhua Taiwan
                [3 ] National Mosquito-Borne Diseases Control Research Center, National Health Research Institutes, Tainan City 704, Taiwan National Health Research Institutes Tainan Taiwan
                [4 ] Department of Earth and Life Science, University of Taipei, Taipei 100, Taiwan University of Taipei Taipei Taiwan
                [5 ] Department of Entomology, National Taiwan University, Taipei 106, Taiwan National Taiwan University Taipei Taiwan
                [6 ] Department of Biological Resources, National Chiayi University, Chiayi 300, Taiwan National Chiayi University Chiayi Taiwan
                Author notes
                Corresponding author: Shiuh-Feng Shiao ( sfshiao@ 123456ntu.edu.tw )

                Academic editor: A. Schmidt-Rhaesa

                Article
                49100
                10.3897/zookeys.941.49100
                7311483
                32595406
                3aedd874-f1cc-4430-8df2-071c425cfc7c
                Ming-Chung Chiu, Chin-Gi Huang, Wen-Jer Wu, Zhao-Hui Lin, Hsuan-Wien Chen, Shiuh-Feng Shiao

                This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 18 February 2020
                : 08 April 2020
                Funding
                Bureau of Animal and Plant Health Inspection and Quarantine, Council of Agriculture, Taiwan
                Categories
                Research Article
                Gordiidae
                Gordioida
                Gordioidea
                Nematomorpha
                Molecular Systematics
                Phylogeny
                Taxonomy
                Cenozoic
                Asia
                Far East
                Taiwan

                Animal science & Zoology
                definitive host,immature stage,parasitic life cycle,terrestrial adaptation,animalia,gordea,gordiidae

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