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1.
Risk Anal ; 43(8): 1682-1693, 2023 Aug.
Article de Anglais | MEDLINE | ID: mdl-36307375

RÉSUMÉ

Several Japanese companies and the government are recently promoting a plastic ban and imposing a tax levy to curb litter and reduce greenhouse gas emissions. This has led to a rapid rise of nonplastic packaging alternatives. While plastics and litter are pressing concerns, it is paramount to examine environmental risks of other alternatives before wide application and legislative action, to not further the risk of environmental damage. This study aims to quantify and compare plastic products such as polyethylene-terephthalate (PET) bottles and high-density polyethylene (HDPE) bags with widely available alternatives in Japan like glass bottles, aluminum bottles, paper bags, and textile bags, to find a product with the least environmental impact. A life cycle assessment is conducted from a cradle-to-grave environmental impact approach that includes raw material extraction, production, transportation, end-of-life treatment, and disposal. Sixteen impact categories including climate change, acidification, aquatic-toxicity, so forth, and weighing is assessed using the MiLCA software. The functional unit is one piece of each packaging product, and impacts of product-filling, storage, recycling, and reuse are excluded for a consistent comparison. HDPE bags performed better than paper and textile bags in 15 of the 16 analyzed impact categories. Similarly, PET bottles outperformed aluminum and glass bottles in 12 out of the 16 impact categories analyzed. Weighted results also highlight the heightened negative environmental impacts of replacing plastic packaging with widely available alternatives.

2.
BMC Genomics ; 23(1): 765, 2022 Nov 22.
Article de Anglais | MEDLINE | ID: mdl-36418933

RÉSUMÉ

BACKGROUND: The first metazoan genome sequenced, that of Caenorhabditis elegans, has motivated animal genome evolution studies. To date > 50 species from the genus Caenorhabditis have been sequenced, allowing research on genome variation. RESULTS: In the present study, we describe a new gonochoristic species, Caenorhabditis niphades n. sp., previously referred as C. sp. 36, isolated from adult weevils (Niphades variegatus), with whom they appear to be tightly associated during its life cycle. Along with a species description, we sequenced the genome of C. niphades n. sp. and produced a chromosome-level assembly. A genome comparison highlighted that C. niphades n. sp. has the smallest genome (59 Mbp) so far sequenced in the Elegans supergroup, despite being closely related to a species with an exceptionally large genome, C. japonica. CONCLUSIONS: The compact genome of C. niphades n. sp. can serve as a key resource for comparative evolutionary studies of genome and gene number expansions in Caenorhabditis species.


Sujet(s)
Caenorhabditis , Charançons , Animaux , Charançons/génétique , Bois , Génome , Caenorhabditis elegans/génétique
3.
Commun Biol ; 4(1): 649, 2021 05 31.
Article de Anglais | MEDLINE | ID: mdl-34059788

RÉSUMÉ

The cryptic parasite Sparganum proliferum proliferates in humans and invades tissues and organs. Only scattered cases have been reported, but S. proliferum infection is always fatal. However, S. proliferum's phylogeny and life cycle remain enigmatic. To investigate the phylogenetic relationships between S. proliferum and other cestode species, and to examine the mechanisms underlying pathogenicity, we sequenced the entire genomes of S. proliferum and a closely related non-life-threatening tapeworm Spirometra erinaceieuropaei. Additionally, we performed larvae transcriptome analyses of S. proliferum plerocercoid to identify genes involved in asexual reproduction in the host. The genome sequences confirmed that the S. proliferum has experienced a clearly distinct evolutionary history from S. erinaceieuropaei. Moreover, we found that nonordinal extracellular matrix coordination allows asexual reproduction in the host, and loss of sexual maturity in S. proliferum are responsible for its fatal pathogenicity to humans. Our high-quality reference genome sequences should be valuable for future studies of pseudophyllidean tapeworm biology and parasitism.


Sujet(s)
Sparganum/génétique , Animaux , Séquence nucléotidique/génétique , Prolifération cellulaire/génétique , Cestoda/classification , Cestoda/génétique , Infections à cestodes/génétique , Infections à cestodes/parasitologie , Génome/génétique , Humains , Larve/classification , Larve/génétique , Étapes du cycle de vie/génétique , Phylogenèse , Sparganum/classification , Spirometra/classification , Spirometra/génétique
4.
Microbiol Resour Announc ; 9(42)2020 Oct 15.
Article de Anglais | MEDLINE | ID: mdl-33060277

RÉSUMÉ

Bursaphelenchus xylophilus has been destroying pine forests in East Asia and western Europe. Here, we report its nearly complete genomic sequence containing five ∼12-Mb scaffolds and one ∼15-Mb scaffold representing six chromosomes. Large repeat regions that were previously unidentified are now reasonably integrated, particularly in the ∼15-Mb scaffold.

5.
Article de Anglais | MEDLINE | ID: mdl-31293983

RÉSUMÉ

Soil-transmitted helminths (STHs) are medically important parasites that infect 1. 5 billion humans globally, causing a substantial disease burden. These parasites infect the gastrointestinal tract (GIT) of their host where they co-exist and interact with the host gut bacterial flora, leading to the coevolution of the parasites, microbiota, and host organisms. However, little is known about how these interactions change through time with the progression of infection. Strongyloidiasis is a human parasitic disease caused by the nematode Strongyloides stercoralis infecting 30-100 million people. In this study, we used a closely related rodent parasite Strongyloides venezuelensis and mice as a model of gastrointestinal parasite infection. We conducted a time-course experiment to examine changes in the fecal microbiota from the start of infection to parasite clearance. We found that bacterial taxa in the host intestinal microbiota changed significantly as the infection progressed, with an increase in the genera Bacteroides and Candidatus Arthromitus, and a decrease in Prevotella and Rikenellaceae. However, the microbiota recovered to the pre-infective state after parasite clearance from the host, suggesting that these perturbations are reversible. Microarray analysis revealed that this microbiota transition is likely to correspond with the host immune response. These findings give us an insight into the dynamics of parasite-microbiota interactions in the host gut during parasite infection.


Sujet(s)
Bactéries/classification , Microbiome gastro-intestinal/physiologie , Intestins/microbiologie , Intestins/parasitologie , Strongyloides/physiologie , Strongyloïdose/microbiologie , Strongyloïdose/parasitologie , Animaux , Bactéries/génétique , Biodiversité , Modèles animaux de maladie humaine , Fèces/microbiologie , Interactions hôte-microbes/immunologie , Interactions hôte-microbes/physiologie , Interactions hôte-parasite/immunologie , Interactions hôte-parasite/physiologie , Mâle , Souris , Souris de lignée C57BL , Nematoda , Parasites , ARN ribosomique 16S/génétique , Strongyloides/pathogénicité
6.
Sci Rep ; 9(1): 6080, 2019 04 15.
Article de Anglais | MEDLINE | ID: mdl-30988401

RÉSUMÉ

The pine wood nematode Bursaphelenchus xylophilus is the causal agent of pine wilt disease, one of the most devastating forest diseases in East Asian and West European countries. The lifecycle of B. xylophilus includes four propagative larval stages and gonochoristic adults which are involved in the pathogenicity, and two stages of dispersal larvae involved in the spread of the disease. To elucidate the ecological roles of each developmental stage in the pathogenic life cycle, we performed a comprehensive transcriptome analysis using RNA-seq generated from all developmental stages of B. xylophilus and compared transcriptomes between stages. We found more than 9000 genes are differentially expressed in at least one stage of the life cycle including genes involved in general nematode biology such as reproduction and moulting but also effector genes likely to be involved in parasitism. The dispersal-stage transcriptome revealed its analogy to C. elegans dauer and the distinct roles of the two larval stages from each other regarding survival and transmission. This study provides important insights and resources to understand B. xylophilus parasitic biology.


Sujet(s)
Régulation de l'expression des gènes au cours du développement , Étapes du cycle de vie/génétique , Pinus/parasitologie , Maladies des plantes/parasitologie , Tylenchida/génétique , Répartition des animaux , Animaux , Gènes d'helminthe/génétique , Protéines d'helminthes/génétique , Protéines d'helminthes/métabolisme , RNA-Seq , Tylenchida/pathogénicité
7.
Parasit Vectors ; 12(1): 21, 2019 Jan 09.
Article de Anglais | MEDLINE | ID: mdl-30626426

RÉSUMÉ

BACKGROUND: Parasites excrete and secrete a wide range of molecules that act as the primary interface with their hosts and play critical roles in establishing parasitism during different stages of infection. Strongyloides venezuelensis is a gastrointestinal parasite of rats that is widely used as a laboratory model and is known to produce both soluble and insoluble (adhesive) secretions during its parasitic stages. However, little is known about the constituents of these secretions. RESULTS: Using mass spectrometry, we identified 436 proteins from the infective third-stage larvae (iL3s) and 196 proteins from the parasitic females of S. venezuelensis. The proteins that were secreted by the iL3s were enriched with peptidase activity, embryo development and the oxidation-reduction process, while those of the parasitic females were associated with glycolysis, DNA binding (histones) and other unknown functions. Trypsin inhibitor-like domain-containing proteins were identified as the main component of the adhesive secretion from parasitic females. An absence of secretion signals in many of the proteins indicated that they are secreted via non-classical secretion pathways. CONCLUSIONS: We found that S. venezuelensis secretes a wide range of proteins to establish parasitism. This includes proteins that have previously been identified as being involved in parasitism in other helminths as well as proteins that are unique to this species. These findings provide insights into the molecular mechanisms underlying Strongyloides parasitism.


Sujet(s)
Protéines d'helminthes/analyse , Étapes du cycle de vie/physiologie , Protéome/analyse , Strongyloides/physiologie , Animaux , Femelle , Protéines d'helminthes/composition chimique , Protéines d'helminthes/génétique , Protéines d'helminthes/physiologie , Parasitoses intestinales/parasitologie , Larve/métabolisme , Rats , Voie de sécrétion/physiologie , Solubilité , Strongyloides/composition chimique , Strongyloïdose/parasitologie
8.
Nat Commun ; 9(1): 3216, 2018 08 10.
Article de Anglais | MEDLINE | ID: mdl-30097582

RÉSUMÉ

A 'sibling' species of the model organism Caenorhabditis elegans has long been sought for use in comparative analyses that would enable deep evolutionary interpretations of biological phenomena. Here, we describe the first sibling species of C. elegans, C. inopinata n. sp., isolated from fig syconia in Okinawa, Japan. We investigate the morphology, developmental processes and behaviour of C. inopinata, which differ significantly from those of C. elegans. The 123-Mb C. inopinata genome was sequenced and assembled into six nuclear chromosomes, allowing delineation of Caenorhabditis genome evolution and revealing unique characteristics, such as highly expanded transposable elements that might have contributed to the genome evolution of C. inopinata. In addition, C. inopinata exhibits massive gene losses in chemoreceptor gene families, which could be correlated with its limited habitat area. We have developed genetic and molecular techniques for C. inopinata; thus C. inopinata provides an exciting new platform for comparative evolutionary studies.


Sujet(s)
Caenorhabditis elegans/génétique , Génome , Séquence d'acides aminés , Animaux , Séquence nucléotidique , Caenorhabditis elegans/anatomie et histologie , Cellules chimioréceptrices/métabolisme , Séquence conservée/génétique , Éléments transposables d'ADN/génétique , Évolution moléculaire , Femelle , Variation génétique , Mâle , Famille multigénique , Interférence par ARN , Séquences d'acides nucléiques régulatrices/génétique , Spécificité d'espèce
9.
Mol Biol Evol ; 30(11): 2531-40, 2013 Nov.
Article de Anglais | MEDLINE | ID: mdl-23955518

RÉSUMÉ

Mitofish is a database of fish mitochondrial genomes (mitogenomes) that includes powerful and precise de novo annotations for mitogenome sequences. Fish occupy an important position in the evolution of vertebrates and the ecology of the hydrosphere, and mitogenomic sequence data have served as a rich source of information for resolving fish phylogenies and identifying new fish species. The importance of a mitogenomic database continues to grow at a rapid pace as massive amounts of mitogenomic data are generated with the advent of new sequencing technologies. A severe bottleneck seems likely to occur with regard to mitogenome annotation because of the overwhelming pace of data accumulation and the intrinsic difficulties in annotating sequences with degenerating transfer RNA structures, divergent start/stop codons of the coding elements, and the overlapping of adjacent elements. To ease this data backlog, we developed an annotation pipeline named MitoAnnotator. MitoAnnotator automatically annotates a fish mitogenome with a high degree of accuracy in approximately 5 min; thus, it is readily applicable to data sets of dozens of sequences. MitoFish also contains re-annotations of previously sequenced fish mitogenomes, enabling researchers to refer to them when they find annotations that are likely to be erroneous or while conducting comparative mitogenomic analyses. For users who need more information on the taxonomy, habitats, phenotypes, or life cycles of fish, MitoFish provides links to related databases. MitoFish and MitoAnnotator are freely available at http://mitofish.aori.u-tokyo.ac.jp/ (last accessed August 28, 2013); all of the data can be batch downloaded, and the annotation pipeline can be used via a web interface.


Sujet(s)
Bases de données génétiques , Poissons/génétique , Génome mitochondrial , Annotation de séquence moléculaire/méthodes , Animaux , Évolution moléculaire , Génomique , Séquençage nucléotidique à haut débit , Phylogenèse , ARN de transfert/génétique , Logiciel
10.
Risk Anal ; 23(2): 303-10, 2003 Apr.
Article de Anglais | MEDLINE | ID: mdl-12731815

RÉSUMÉ

The causal structure of the determinants of trust in industry, government, and citizen's groups in Japan was investigated on the basis of Peters et al. (1997). A preliminary survey of the adequacy of the hypotheses proposed by Peters et al. in Japan was made. A set of hypothesized determinants of trust in Japan was proposed based on results of the preliminary survey. Questionnaires concerning perceptions of trust in the organizations and the proposed determinants were sent by mail to residents in the area where environmental risk problems had emerged. The data were analyzed by covariance structure analysis to construct models of trust in industry, government, and citizen's groups. As a result, "openness and honesty," "concern and care," "competence," "people's concern with risks," and "consensual values" were found to be factors directly determining trust. Suggested in particular is that "openness" of an organization is not attained merely by information disclosure, but also by bi-directional communication with the people. Moreover, these models include "consensual values," which do not appear in the model proposed by Peters et al.

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