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1.
Plant Biol (Stuttg) ; 20 Suppl 1: 176-183, 2018 Jan.
Article in English | MEDLINE | ID: mdl-28637086

ABSTRACT

Plant-pollinator network structure is the outcome of ecological and evolutionary processes, and although the importance of environmental factors is beyond doubt, our knowledge of how abiotic factors (e.g. climate) shape plant-pollinator networks remains limited. This knowledge gap is critical, as climate change poses a major threat to ecosystems, especially in the Mediterranean. This study focuses on one of the hottest parts of the Mediterranean Basin, the Aegean Archipelago, Greece, and examines how climate affects species richness and network properties (e.g. nestedness, modularity and specialisation) - either directly or indirectly through species richness. We sampled systematically 39 local plant-pollinator networks on eight islands along a north-south climate gradient in the Aegean. All plant-pollinator material used in the analyses was collected in 2012 and identified to species level. Aspects of climate used in the models were expressed as average conditions (mean temperature and annual precipitation) or as seasonal variability (isothermality and temperature seasonality). Structural properties of plant-pollinator networks were found to be strongly associated with species richness, which was in turn affected by climate, implying that pollination network structure is driven indirectly by climate. In addition, climate had a direct effect on network structure, especially on modularity and specialisation. Different aspects of climate affected network properties in different ways. We highlight that even in a relatively narrow latitudinal gradient, such as within the Aegean Sea region, climate constitutes a significant driver of plant-pollinator interactions.


Subject(s)
Climate , Insecta , Pollination , Animals , Insecta/physiology , Mediterranean Islands , Mediterranean Sea , Plants , Pollination/physiology
2.
Bull Entomol Res ; 107(1): 126-138, 2017 Feb.
Article in English | MEDLINE | ID: mdl-27572819

ABSTRACT

Eumerus is one of the most diverse genera of hoverfly worldwide. Species delimitation within genus is considered to be difficult due to: (a) lack of an efficient key; (b) non-defined taxonomical status of a large number of species; and (c) blurred nomenclature. Here, we present the first molecular study to delimit species of the genus by using a fragment of the mitochondrial cytochrome-c oxidase subunit I gene (COI) gene. We assessed 75 specimens assigned to 28 taxa originating from two biogeographic zones: 22 from the western Palaearctic and six from the Afrotropical region. Two datasets were generated based on different sequence lengths to explore the significance of availability of more polymorphic sites for species delimitation; dataset A with a total length of 647 bp and dataset B with 746 bp. Various tree inference approaches and Poisson tree processes models were applied to evaluate the putative 'taxonomical' vs. 'molecular' taxa clusters. All analyses resulted in high taxonomic resolution and clear species delimitation for both the dataset lengths. Furthermore, we revealed a high number of mitochondrial haplotypes and high intraspecific variability. We report two major monophyletic clades, and seven 'molecular' groups of taxa formed, which are congruent with morphology-based taxonomy. Our results support the use of the mitochondrial COI gene in species diagnosis of Eumerus.


Subject(s)
Diptera/classification , Diptera/genetics , Electron Transport Complex IV/genetics , Genetic Variation , Insect Proteins/genetics , Mitochondrial Proteins/genetics , Africa , Animals , DNA Barcoding, Taxonomic , Europe , Phylogeny , Sequence Analysis, DNA
3.
J Mol Cell Cardiol ; 82: 174-83, 2015 May.
Article in English | MEDLINE | ID: mdl-25784084

ABSTRACT

Differential DNA methylation exists in the epigenome of end-stage failing human hearts but whether it contributes to disease progression is presently unknown. Here, we report that cardiac specific deletion of Dnmt3b, the predominant DNA methyltransferase in adult mouse hearts, leads to an accelerated progression to severe systolic insufficiency and myocardial thinning without a preceding hypertrophic response. This was accompanied by widespread myocardial interstitial fibrosis and myo-sarcomeric disarray. By targeted candidate gene quantitative RT-PCR, we discovered an over-activity of cryptic splice sites in the sarcomeric gene Myh7, resulting in a transcript with 8 exons missing. Moreover, a region of differential methylation overlies the splice site locus in the hearts of the cardiac-specific conditional knockout (CKO) mice. Although abundant and complex forms of alternative splice variants have been reported in diseased hearts and the contribution of each remains to be understood in further detail, our results demonstrate for the first time that a link may exist between alternative splicing and the cardiac epigenome. In particular, this gives the novel evidence whereby the loss of an epigenome modifier promotes the development and progression of heart disease.


Subject(s)
DNA (Cytosine-5-)-Methyltransferases/metabolism , Epigenesis, Genetic , Gene Expression Regulation , Heart Failure/genetics , Heart Failure/metabolism , Myocytes, Cardiac/metabolism , Alternative Splicing , Animals , DNA (Cytosine-5-)-Methyltransferases/genetics , DNA Methylation , Disease Models, Animal , Fibrosis , Gene Deletion , Heart Failure/pathology , Heart Failure/physiopathology , Heart Failure, Systolic/genetics , Heart Failure, Systolic/metabolism , Heart Failure, Systolic/pathology , Heart Failure, Systolic/physiopathology , Humans , Mice , Mice, Knockout , Myocardium/metabolism , Myocardium/pathology , Myosin Heavy Chains/genetics , Organ Specificity/genetics , Protein Aggregates , Proteolysis , Sarcomeres/genetics , Sarcomeres/metabolism , Sarcomeres/pathology , Ubiquitin/metabolism , DNA Methyltransferase 3B
4.
Environ Monit Assess ; 164(1-4): 337-48, 2010 May.
Article in English | MEDLINE | ID: mdl-19365607

ABSTRACT

The field site network (FSN) plays a central role in conducting joint research within all Assessing Large-scale Risks for biodiversity with tested Methods (ALARM) modules and provides a mechanism for integrating research on different topics in ALARM on the same site for measuring multiple impacts on biodiversity. The network covers most European climates and biogeographic regions, from Mediterranean through central European and boreal to subarctic. The project links databases with the European-wide field site network FSN, including geographic information system (GIS)-based information to characterise the test location for ALARM researchers for joint on-site research. Maps are provided in a standardised way and merged with other site-specific information. The application of GIS for these field sites and the information management promotes the use of the FSN for research and to disseminate the results. We conclude that ALARM FSN sites together with other research sites in Europe jointly could be used as a future backbone for research proposals.


Subject(s)
Biodiversity , Europe , Risk Assessment
5.
Mol Ecol Resour ; 9(6): 1431-8, 2009 Nov.
Article in English | MEDLINE | ID: mdl-21564929

ABSTRACT

DNA barcoding has become a useful system for linking different biological life stages, and for identification of species within a known taxonomic framework. In this study, we generated mitochondrial DNA COI barcodes using adult specimens of all 22 species of the hoverfly genus Merodon (Diptera, Syrphidae) occurring on Lesvos island (Greece). The generated COI barcodes could well discriminate between all Merodon taxa of Lesvos, except for M. loewi and M. papillus that shared the same haplotype, despite their clear morphological differences. In addition, the barcodes revealed two cases of hitherto unknown morphologically cryptic species close to M. avidus and M. nigritarsis, respectively. Because only few successful rearings of immature stages of Merodon hoverflies are available, the larval host plant remains unknown for these phytophagous taxa. The obtained COI barcode library for the Merodon spp. of Lesvos will constitute a tool to link any unknown immature stages with already known species, and thus provide important life-history information and promise for ecological studies.

7.
J Neurol Neurosurg Psychiatry ; 76(8): 1099-102, 2005 Aug.
Article in English | MEDLINE | ID: mdl-16024887

ABSTRACT

OBJECTIVES: To determine if myasthenia gravis (MG) with antibodies to MuSK is a distinct subgroup of seronegative MG. METHODS: We assayed antibodies to muscle specific tyrosine kinase (MuSK) in 55 MG patients who had no antibodies to acetylcholine receptors and looked for the specific phenotype, comparing clinical features of anti-MuSK positive and anti-MuSK negative MG patients. RESULTS: MG with anti-MuSK antibodies was characterised by a striking prevalence of female patients (15 women, two men). Age at onset ranged from 22 to 52 years, with 70.6% of patients presenting at < 40 years of age. The majority of patients (82.4%) had prevalent involvement of facial and bulbar muscles. One third of them did not respond well to anticholinesterase drugs. Steroid immunosuppression was effective in eight patients (44.4%). Nine patients underwent thymectomy; six of these had no thymus pathology, while three had a hyperplastic thymus. At the end of the observation period, six (35.3%) patients were in remission, five (29.4%) improved, four (23.6%) did not change, and two (11.7%) had died. CONCLUSIONS: MG patients with antibodies to MuSK have characteristic clinical features that are different from features of the remaining seronegative MG patients. This emphasises the predictive value of anti-MuSK antibody analysis in seronegative MG patients.


Subject(s)
Autoantibodies/immunology , Myasthenia Gravis/immunology , Receptor Protein-Tyrosine Kinases/immunology , Receptors, Cholinergic/immunology , Adult , Age Distribution , Age of Onset , Electromyography , Female , Humans , Hyperplasia/pathology , Hyperplasia/surgery , Male , Middle Aged , Muscle, Skeletal/immunology , Muscle, Skeletal/physiopathology , Myasthenia Gravis/epidemiology , Myasthenia Gravis/physiopathology , Predictive Value of Tests , Prevalence , Sex Distribution , Thymectomy/statistics & numerical data , Thymus Gland/pathology , Thymus Gland/surgery
8.
Acta Neurol Scand ; 111(4): 247-52, 2005 Apr.
Article in English | MEDLINE | ID: mdl-15740576

ABSTRACT

Cyclosporine A (CsA) treatment was evaluated in 52 patients with severe generalized myasthenia gravis (MG) whose illness was not controlled by anticholinesterase drugs, thymectomy, corticosteroids, and azathioprine. The efficacy of CsA treatment was expressed by mean disability score quotient (MDSQ), which was obtained by comparing mean disability score (MDS) at the beginning of the treatment with the MDS at the end of the follow-up period. For the entire group of patients MDSQ was 53.3%, indicating moderate improvement. Analyzing individual cases, eight patients (15%) did not improve, 17 (33%) showed moderate improvement, 20 (38%) showed remarkable improvement, and seven patients (14%) achieved complete remission. The most common side effects were rise of serum creatinine (seven), hypertension (two), gingival hyperplasia (two), hypertrichosis (six), myalgia (10), and 'flu-like' symptoms (10 patients). The results of this study suggest that CsA is efficacious and safe treatment in severe and resistant forms of MG.


Subject(s)
Cyclosporine/therapeutic use , Immunosuppressive Agents/therapeutic use , Myasthenia Gravis/drug therapy , Adult , Cyclosporine/adverse effects , Disabled Persons , Female , Humans , Immunosuppressive Agents/adverse effects , Male , Middle Aged , Myasthenia Gravis/pathology , Severity of Illness Index , Treatment Outcome
9.
Article in English | MEDLINE | ID: mdl-2351816

ABSTRACT

An estimated number of HIV infected individuals in Yugoslavia might be about 3000. I.v. drug users are by far the most affected population group. Prevalence of HIV seropositivity among imprisoned drug users in Belgrade approaches 50%. An effective control of unvoluntary homosexual contacts in prisons is not feasible. Having in mind a moral obligation of the society to preserve the health of its confined members, we advocate the right of (voluntary or on request screened) HIV seronegative individuals to chose to share the cell with inmates shown to be HIV seronegative as well.


Subject(s)
HIV Seropositivity/epidemiology , Prisoners , Enzyme-Linked Immunosorbent Assay , Humans , Prevalence , Substance-Related Disorders/epidemiology , Yugoslavia/epidemiology
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