nfective nymphal stages of the family Sebekidae Sambon, 1922 are reported from four species of fish in Australian waters for the first time. Infected fish were collected from locations in Western Australia, the Northern Territory and north Queensland. The infective nymphs of Alofia merki Giglioli in Sambon, 1922 and Sebekia purdieae Riley, Spratt et Winch, 1990 are reported and described for the first time. The remaining specimens were identified as belonging to the genus Sebekia Sambon, 1922 based on the combination of buccal cadre shape, shape and size of hooks, and overall body size, but could not be attributed to any of the other species of Sebekia already reported due to missing required morphological features. DNA sequences of members of the family Sebekidae are presented for the first time. The lack of knowledge on the pentastome fauna of wild crocodiles, and any potential intermediate hosts, in northern Australia, is also outlined., Diane P. Barton, Jess A.T. Morgan., and Obsahuje bibliografii
Wallinia mexicana sp. n. is described from the Mexican tetra, Astyanax mexicanus (De Filippi) (Characidae Weitzman), from two localities in northern Mexico. The new species can be distinguished from the two congeneric species, described from small-bodied characids in South and Central America, mainly by the posterior extent of the vitelline follicles (halfway between the posterior testis and the end of the caeca), by having a larger oesophagus, testes that are always oblique, and eye-spot remnants. The distinct status of the new species was confirmed by molecular data (28S rRNA gene sequences). Phylogenetic analysis suggests the new species is the sister species of W. chavarriae Choudhury, Hartvigsen et Brooks, 2002 described from characids in northwestern Costa Rica. Additionally, genetic divergence between these congeners reached 3.3%, a value higher than that observed for closely related species pairs of allocreadiids for that molecular marker. Based on these new findings, recently published records of this new species as Magnivitellinum simplex Kloss, 1966 and Creptotrematina aguirrepequenoi Jiménez-Guzmán, 1973 in Astyanax mexicanus from Durango and San Luis Potosi states, respectively, are corrected., Gerardo Pérez-Ponce de León, Ulises Razo-Mendivil, Berenit Mendoza-Garfias, Miguel Rubio-Godoy, Anindo Choudhury., and Obsahuje bibliografii
The presence of Neospora caninum Dubey, Carpenter, Speer, Topper et Uggla, 1988 in small mammals (i.e. murid rodents, Erinaceomorpha, Eulipotyphla and Scadentia) was explored for first time in South-East Asia. A total of 192 individuals from six localities across Thailand were analysed. A general prevalence of N. caninum of 22% was observed, with some variation among localities (5-36%). Four main types of habitat were included and rodents trapped in dry-land habitat (17 positive among 41 individuals) were more likely to be infected with N. caninum than those from other habitats (forest, rain-fed land and settlement). Rodent species identity and individual rodent weight had no influence on individual infection. Our results provided the first data on the presence of N. caninum in rodents in South-East Asia and first report of N. caninum in the order Scadentia., Ornampai Japa, Serge Morand, Anamika Karnchanabanthoeng, Kittipong Chaisiri, Alexis Ribas., and Obsahuje bibliografii
DNA repair is an active cellular process to respond to constant DNA damage caused by metabolic processes and environmental factors. Since the outcome of DNA damage is generally adverse and long term effects may contribute to oncogenesis, cells have developed a variety of DNA repair mechanisms, which operate depending on the type of DNA damage inflicted. At least 15 Fanconi anemia (FA) proteins interact in a common pathway involved in homologous recombination. Inherited homozygous mutations in any of these FA genes cause a rare disease, Fanconi anemia, characterized by congenit al abnormalities, progressive bone-marrow failure and cancer susceptibility. Heterozygous germline FA mutations predispose to various types of cancer. In addition, somatic FA mutations ha ve been identified in diverse cancer types. Evidence exists that cells deficient in the FA pathway become dependent on alternative pathways for survival. Additional inhibition of such alternative pathways is thus expected to result in cell death, creating a relationship of synthetic lethality. Identifying these relationships can reveal yet unknown mechanisms of DNA repair and new targets for therapy., T. Hucl, E. Gallmeier., and Obsahuje bibliografii a bibliografické odkazy
Damage induced in DNA by numerous chemical and physical factors as well as spontaneously formed imperfections in DNA structure pose a threat to all organisms. To counteract this threat, living cells have evolved a series of DNA repair pathways to correct DNA lesions affecting base pairings or the structure of DNA. Today we understand, in a large part, the molecular mechanisms of these pathways in detail due to the pioneering studies by Tomas LIndahl, Paul Modrich and Aziz Sancar, which opened up this field of research. Tomas Lindahl discovered the molecular machinery of base excision repair - the main cell defence against endogeneous DNA damage. Aziz Sancar characterised, at the molecular level, details of the mechanisms of nucleotide excision repair - the major repair system of DNA damage caused by environmental factors such as UV-irradiation and various genotoxic chemicals including chemotherapeutic agents. Paul Modrich uncovered a mismatch repair - the way how cells resolve errors which occur during DNA replication. Therefore, the Royal Swedish Academy of Sciences awarded jointly Lindahl, Modrich, and Sancar the Nobel Prize in Chemistry 2015 for their "Mechanistic studies of DNA repair". In this paper, we briefly summarise the results of their work., Miroslav Piršel., and Obsahuje seznam literatury
The mitochondrial DNA (mtDNA) amount in cells as the basis for mitochondrial energy generating system, which produces ATP, plays an important role in the fetal development and postnatal morbidity. Isolated human cord blood leukocytes (HCBL) contribute very little to the overall metabolic turnover, but they may serve as easily available marker cells for the study of the mtDNA amount changes in cord blood during fetal development. The aim of our study was to analyze the mtDNA amount in HCBL. HCBL were isolated from cord blood samples of 107 neonates born between the 25th and 41st week of gestation. The mtDNA amount was analyzed by the real-time PCR method. The significant negative correlations were found between the relative mtDNA amount in HCBL and gestational age (r = -0.54, p<0.01) and birth weight (r = -0.43, p<0.01), respectively. The results revealed that the mtDNA content per cell decreases in HCBL with progressing fetal development. This may be explained by gradual shift of the hematopoiesis from fetal liver to bone marrow during the second half of pregnancy presumably accompanied by decreasing cell volume of HCBL as it was shown similarly in red blood cells., M. Pejznochová, M. Tesařová, T. Honzík, H. Hansíková, M. Magner, J. Zeman., and Obsahuje bibliografii a bibliografické odkazy
a1_Three new species of acanthocephalans are described from marine fishes collected in Sodwana Bay, South Africa: Rhadinorhynchus gerberi n. sp. from Trachinotus botla (Shaw), Pararhadinorhynchus sodwanensis n. sp. from Pomadasys furcatus (Bloch et Schneider) and Transvena pichelinae n. sp. from Thalassoma purpureum (Forsskål). Transvena pichelinae n. sp. differs from the single existing species of the genus Transvena annulospinosa Pichelin et Cribb, 2001, by the lower number of longitudinal rows of hooks (10-12 vs 12-14, respectively) and fewer hooks in a row (5 vs 6-8), shorter blades of anterior hooks (55-63 vs 98), more posterior location of the ganglion (close to the posterior margin of the proboscis receptacle vs mid-level of the proboscis receptacle) and smaller eggs (50-58 × 13 µm vs 62-66 × 13-19 µm). Pararhadinorhynchus sodwanensis n. sp. differs from all known species of the genus by a combination of characters. It closely resembles unidentified species Pararhadinorhynchus sp. sensu Weaver and Smales (2014) in the presence of a similar number of longitudinal rows of hooks on the proboscis (16-18 vs 18) and hooks in a row (11-13 vs 13-14), but differs in the position of the lemnisci (extend to the level of the posterior end of the proboscis receptacle or slightly posterior vs extend to the mid-level of the receptacle), length of the proboscis receptacle (910-1180 µm vs 1,460 µm) and cement glands (870-880 µm vs 335-350 µm). Rhadinorhynchus gerberi n. sp. is distinguishable from all its congeners by a single field of 19-26 irregular circular rows of the tegumental spines on the anterior part of the trunk, 10 longitudinal rows of hooks on the proboscis with 29-32 hooks in each row, subterminal genital pore in both sexes, and distinct separation of the opening of the genital pore from the posterior edge of the trunk (240-480 μm) in females., a2_Sequences for the 18S rDNA, 28S rDNA and cox1 genes were generated to molecularly characterise the species and assess their phylogenetic position. This study provides the first report based on molecular evidence for the presence of species of Transvena Pichelin et Cribb, 2001 and Pararhadinorhynchus Johnston et Edmonds, 1947 in African coastal fishes., Olga I. Lisitsyna, Olena Kudlai, Thomas H. Cribb, Nico J. Smit., and Obsahuje bibliografii
Medical genetic research achieved in last decade many efforts leading to better understanding of inherited basis of human diseases. This will not be possible without the participation of patients and controls. However, the general understanding of the background and possibilities of genetic association studies is very low. It was confirmed by study of university of students. Because of the fair of misuses of the individual genetic information, significant part of participants refused the use of already donated blood samples for genetic testing but agreed with using of buccal swabs for the same analysis. To enhance the general knowledge’s of the population, leading to realistic expectations not just about genetic predictive power but also about the eventual risks in behind will be the major mission in the next years., V. Adámková ... [et al.]., and Obsahuje seznam literatury