85 research outputs found

    Multiple (inverse) binomial sums of arbitrary weight and depth and the all-order epsilon-expansion of generalized hypergeometric functions with one half-integer value of parameter

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    We continue the study of the construction of analytical coefficients of the epsilon-expansion of hypergeometric functions and their connection with Feynman diagrams. In this paper, we show the following results: Theorem A: The multiple (inverse) binomial sums of arbitrary weight and depth (see Eq. (1.1)) are expressible in terms of Remiddi-Vermaseren functions. Theorem B: The epsilon expansion of a hypergeometric function with one half-integer value of parameter (see Eq. (1.2)) is expressible in terms of the harmonic polylogarithms of Remiddi and Vermaseren with coefficients that are ratios of polynomials. Some extra materials are available via the www at this http://theor.jinr.ru/~kalmykov/hypergeom/hyper.htmlComment: 24 pages, latex with amsmath and JHEP3.cls; v2: some typos corrected and a few references added; v3: few references added

    BIOINFORMATION SEARCH AND ANALYSIS OF STRUCTURES OF CRISPR/CAS SYSTEMS IN PHAGE STAPHYLOCOCUS AUREUS GENOME AND ESTIMATION OF PROFILES OF PHAGE DETECTED THROUGH CRISPR-CASSETTE BACTERIA

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    The emergence of resistance among the most important bacterial pathogens is generally recognized as one of the major public health problems. The most important of these organisms are penicillin-resistant Streptococcus pneumoniae, vancomycin-resistant enterococci and methicillin- and vancomycin-resistant Staphylococcus aureus. These antibiotic resistance in common pathogens have made antimicrobial therapy of many infections. Scientists need to look for new ways of treating bacterial infections in the work, using the developed algorithm from the methods of search software in the genomic structure of Staphylococcus aureus subsp. aureus ST228, the CRISPR/Cas locus and the division structures of its CRISPR cassette. The results of the bacteriophage search through the decoded spacer sequences of CRISPR-cassettes of this strain were also obtained using the developed algorithm of the software methods of bioinformatics. It was determined that the CRISPR/Cas system of strain of ST228 of S. aureus was of type IIIA. It is shown that cas-genes are in the immediate vicinity of CRISPR cassettes. The spacer structures in the detected CRISPR cassette are the Staphylococcus, Mycobacterium, Streptococcus, Bacillus, Gordonia, Arthrobacter, Streptomyces. The implementation of the algorithm of program methods for locating CRISPR/Cas-loci can be applied to many other decoded bacterial genomes to return bacteriophage therapy

    BIOINFORMATIC SEARCH OF CRISPR/CAS SYSTEM STRUCTURES IN GENOME OF PCT281 PLASMID OF BACILLUS THURINGIENSIS SUBSP. CHINENSIS STRAIN CT-43

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    Background. CRISPR/Cas systems loci are one of the functionally important patterns in bacterial genome which perform the role of “adaptive immune defense” from foreign nucleic acids. The study of CRISPR/Cas systems structure in genomes of plasmids and phages provide new information about the evolution of this systems in bacterial hosts.Aims. A search of CRISPR/Cas systems structures in pCT281 plasmid from Bacillus thuringiensis subsp. chinensis strain CT-43 using bioinformatic methods.Materials and methods. Search studies using bioinformatics methods were performed with the genome of pCT281 plasmid of B. thuringiensis subsp. chinensis strain CT-43 from the RefSeq database. To search for the CRISPR/Cas system structure MacSyFinder (ver. 1.0.5) and three combined algorithms were used: CRISPRFinder; PILER-CR; CRISPR Recognition Tool (CRT). The consensus repeat sequence was generated in WebLogo 3.Results and discussion. In pCT281 plasmid we detected one locus of CRISPR/Cas system of the type I-C which contains 2 CRISPR-cassettes and 4 cas-genes located between them. The CRISPR-cassette 1 includes 10 spacers from 32 to 35 bp and 11 repeats 32bp in length. 5 spacers (33–35 bp) separated by 6 repeats 32 bp in length were detected in the CRISPR-cassette 2.Conclusions. The bioinformatic methods used in this study enable to conduct a search of CRISPR/Cas systems structures in plasmid genomes. The presence of the CRISPR-Cas locus in pCT281 plasmid confirms a possible transfer of this system from the nucleoid to this plasmid. The detected spacers provide information about phages this bacteria was encountered

    CHARACTERISTICS OF THE BAIKAL SUBTYPE OF TICK-BORNE ENCEPHALITIS VIRUS CIRCULATING IN EASTERN SIBERIA

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    Background. During the study of the genetic variability of the tick-borne encephalitis virus (TBEV) in Eastern Siberia, a group of 22  strains with a unique genetic structure significantly different from all  known TBEV subtypes was identified. This TBEV variant was  tentatively called “group 886”. Therefore, for this original TBEV  variant it was necessary to study the genetic, biological properties of the “group 886” strains, clarify its TBEV taxonomic status, its range, evolutionary history, etc.Aim. The generalization of the currently available data on genetic and biological properties of TBEV “886” group.Materials and methods. The genetic structure of “group 886” strains was studied by the complex of molecular-genetic methods (MHNA, sequencing of fragments or the complete genome).Results. It was shown that “group 886” strains form a separate cluster on phylogenetic tree, and the level of genetic differences  from other genotypes is more than 12 %. It was defined that this  TBEV variant has its own area (Irkutsk region, Republic of Buryatia,  Trans-Baikal region, Northern Mongolia). Its ecological connection  with all links of the transmissive chain (ixodid ticks, small mammals,  human), participation in human pathology, stability and duration of  circulation in the Baikal region, individual evolutionary history  were proved. Some phenotypic characteristics of the “group 886” strains were considered.Conclusion. The presented data testify to the validity of the “886 group” isolation as an independent genetic type. Taking into account  the geographical distribution of this TBEV genotype, we propose to assign it the name “Baikal genotype/subtype”

    In silico сраĐČĐœĐžŃ‚Đ”Đ»ŃŒĐœŃ‹Đč Đ°ĐœĐ°Đ»ĐžĐ· crispr-ŃĐžŃŃ‚Đ”ĐŒ ŃˆŃ‚Đ°ĐŒĐŒĐŸĐČ Yersinia pseudotuberculosis, ĐČŃ‹Đ·Ń‹ĐČающох Ń€Đ°Đ·Đ»ĐžŃ‡ĐœŃ‹Đ” ĐșĐ»ĐžĐœĐžŃ‡Đ”ŃĐșОД ĐżŃ€ĐŸŃĐČĐ»Đ”ĐœĐžŃ псДĐČĐŽĐŸŃ‚ŃƒĐ±Đ”Ń€ĐșŃƒĐ»Ń‘Đ·Đ°

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    The aim of this research was to analyze and compare CRIPSR loci and cas-proteins of Yersinia pseudotuberculosis strains isolated in different territories from patients with various clinical manifestations of pseudotuberculosis.Materials and Methods. Complete genomes of Y. pseudotuberculosis IP329353 (NC_006155) and IP31758 (NC_009708) were obtained from NCBI Nucleotide Database. Strains were isolated from patients with gastroenteritis and systemic infection respectively. Search, identification, and analysis of CRISPR systems were carried out by onlinetools CRISPROne, CRISPRDetect, and CRISPRTarget.Results. Analyzed strains have CRISPR-Cas systems that include one set of cas-genes and arrays situated at the long distances from each other. We defined three CRISPR arrays in Y. pseudotuberculosis IP32953: array YP1 located near cas-genes, arrays YP2 and YP3. CRISPR-Cas system of Y. pseudotuberculosis IP31758 includes two arrays – YP1 and YP3. CRISPR systems do not share similar spacers.Conclusion. CRISPR systems of the analyzed strains differ in CRISPR loci and cas-protein structures that can be used as specific molecular marks of analyzed strains during the study of intra-species variability and evolution of Y. pseudotuberculosis.ĐŠĐ”Đ»ŃŒ: сраĐČĐœĐžŃ‚ŃŒ CRISPR-ŃĐžŃŃ‚Đ”ĐŒŃ‹ ĐŽĐČух ŃˆŃ‚Đ°ĐŒĐŒĐŸĐČ, ĐČŃ‹ĐŽĐ”Đ»Đ”ĐœĐœŃ‹Ń… ĐœĐ° Ń€Đ°Đ·Đ»ĐžŃ‡ĐœŃ‹Ń… Ń‚Đ”Ń€Ń€ĐžŃ‚ĐŸŃ€ĐžŃŃ… ĐŸŃ‚ ĐżĐ°Ń†ĐžĐ”ĐœŃ‚ĐŸĐČ Ń Ń€Đ°Đ·ĐœŃ‹ĐŒĐž ĐșĐ»ĐžĐœĐžŃ‡Đ”ŃĐșĐžĐŒĐž ĐżŃ€ĐŸŃĐČĐ»Đ”ĐœĐžŃĐŒĐž псДĐČĐŽĐŸŃ‚ŃƒĐ±Đ”Ń€ĐșулДза, Đž ĐŸĐżŃ€Đ”ĐŽĐ”Đ»ĐžŃ‚ŃŒ спДцОфОчДсĐșОД Ń€Đ°Đ·Đ»ĐžŃ‡ĐžŃ ĐČ ŃĐżĐ”ĐčŃĐ”Ń€ĐœĐŸĐŒ ŃĐŸŃŃ‚Đ°ĐČĐ” Đž ĐČ ŃŃ‚Ń€ŃƒĐșŃ‚ŃƒŃ€Đ” cas-бДлĐșĐŸĐČ.ĐœĐ°Ń‚Đ”Ń€ĐžĐ°Đ»Ń‹ Đž ĐŒĐ”Ń‚ĐŸĐŽŃ‹: ĐżŃ€ĐŸĐ°ĐœĐ°Đ»ĐžĐ·ĐžŃ€ĐŸĐČĐ°ĐœŃ‹ ĐżĐŸĐ»ĐœĐŸĐłĐ”ĐœĐŸĐŒĐœŃ‹Đ” ĐżĐŸŃĐ»Đ”ĐŽĐŸĐČĐ°Ń‚Đ”Đ»ŃŒĐœĐŸŃŃ‚Đž ŃˆŃ‚Đ°ĐŒĐŒĐŸĐČ Y. pseudotuberculosis IP329353 (NC_006155) Đž IP31758 (NC_009708) Ń€Đ°Đ·Đ»ĐžŃ‡ĐœĐŸĐłĐŸ ĐłĐ”ĐŸĐłŃ€Đ°Ń„ĐžŃ‡Đ”ŃĐșĐŸĐłĐŸ ĐżŃ€ĐŸĐžŃŃ…ĐŸĐ¶ĐŽĐ”ĐœĐžŃ, ĐČŃ‹ĐŽĐ”Đ»Đ”ĐœĐœŃ‹Đ” ĐŸŃ‚ Đ±ĐŸĐ»ŃŒĐœŃ‹Ń… с псДĐČĐŽĐŸŃ‚ŃƒĐ±Đ”Ń€ĐșŃƒĐ»Đ”Đ·ĐŸĐŒ с ŃĐžĐŒĐżŃ‚ĐŸĐŒĐ°ĐŒĐž ĐłĐ°ŃŃ‚Ń€ĐŸŃĐœŃ‚Đ”Ń€ĐžŃ‚Đ° Đž ŃĐžŃŃ‚Đ”ĐŒĐœŃ‹ĐŒĐž ĐżŃ€ĐŸŃĐČĐ»Đ”ĐœĐžŃĐŒĐž ĐžĐœŃ„Đ”Đșцоо ŃĐŸĐŸŃ‚ĐČДтстĐČĐ”ĐœĐœĐŸ. ĐŸĐŸĐžŃĐș, ĐžĐŽĐ”ĐœŃ‚ĐžŃ„ĐžĐșацоя Đž Đ°ĐœĐ°Đ»ĐžĐ· CRISPR ŃĐžŃŃ‚Đ”ĐŒ ĐČŃ‹ĐżĐŸĐ»ĐœĐ”ĐœŃ‹ с ĐžŃĐżĐŸĐ»ŃŒĐ·ĐŸĐČĐ°ĐœĐžĐ”ĐŒ ĐŸĐœĐ»Đ°ĐčĐœ-ĐżŃ€ĐžĐ»ĐŸĐ¶Đ”ĐœĐžĐč CRISPROne, CRISPRDetect Đž CRISPRTarget.Đ Đ”Đ·ŃƒĐ»ŃŒŃ‚Đ°Ń‚Ń‹: ĐČ ĐłĐ”ĐœĐŸĐŒĐ” ĐžŃŃĐ»Đ”ĐŽŃƒĐ”ĐŒŃ‹Ń… ŃˆŃ‚Đ°ĐŒĐŒĐŸĐČ ĐŸĐ±ĐœĐ°Ń€ŃƒĐ¶Đ”ĐœŃ‹ CRISPR-Cas ŃĐžŃŃ‚Đ”ĐŒŃ‹, ĐČĐșлючающОД ĐŸĐŽĐžĐœ ĐœĐ°Đ±ĐŸŃ€ cas-ĐłĐ”ĐœĐŸĐČ Đž ĐœĐ”ŃĐșĐŸĐ»ŃŒĐșĐŸ CRISPR-Đ»ĐŸĐșŃƒŃĐŸĐČ, Đ·ĐœĐ°Ń‡ĐžŃ‚Đ”Đ»ŃŒĐœĐŸ ŃƒĐŽĐ°Đ»Đ”ĐœĐœŃ‹Ń… Юруг ĐŸŃ‚ Юруга. В ĐłĐ”ĐœĐŸĐŒĐ” ŃˆŃ‚Đ°ĐŒĐŒĐ° Y. pseudotuberculosis IP329353 просутстĐČŃƒĐ”Ń‚ тро Đ»ĐŸĐșуса: YP1, ĐœĐ°Ń…ĐŸĐŽŃŃ‰ĐžĐčся ĐČ ĐœĐ”ĐżĐŸŃŃ€Đ”ĐŽŃŃ‚ĐČĐ”ĐœĐœĐŸĐč Đ±Đ»ĐžĐ·ĐŸŃŃ‚Đž ĐŸŃ‚ cas-ĐłĐ”ĐœĐŸĐČ, YP2 Đž YP3. CRISPR-Cas ŃĐžŃŃ‚Đ”ĐŒĐ° Y. pseudotuberculosis IP31758 прДЎстаĐČĐ»Đ”ĐœĐ° Ń‚ĐŸĐ»ŃŒĐșĐŸ ĐŽĐČŃƒĐŒŃ ĐșĐ°ŃŃĐ”Ń‚Đ°ĐŒĐž: YP1 Đž YP3. CRISPR ŃĐžŃŃ‚Đ”ĐŒŃ‹ ĐžŃŃĐ»Đ”ĐŽŃƒĐ”ĐŒŃ‹Ń… ŃˆŃ‚Đ°ĐŒĐŒĐŸĐČ ĐœĐ” ĐžĐŒĐ”ŃŽŃ‚ ĐŸĐŽĐžĐœĐ°ĐșĐŸĐČых спДĐčŃĐ”Ń€ĐŸĐČ.ЗаĐșĐ»ŃŽŃ‡Đ”ĐœĐžĐ”: CRISPR-Cas ŃĐžŃŃ‚Đ”ĐŒŃ‹ ĐžŃŃĐ»Đ”ĐŽĐŸĐČĐ°ĐœĐœŃ‹Ń… ŃˆŃ‚Đ°ĐŒĐŒĐŸĐČ ĐŸŃ‚Đ»ĐžŃ‡Đ°ŃŽŃ‚ŃŃ ĐșĐŸĐ»ĐžŃ‡Đ”ŃŃ‚ĐČĐŸĐŒ CRISPR-Đ»ĐŸĐșŃƒŃĐŸĐČ, ох спДĐčŃĐ”Ń€ĐœŃ‹ĐŒ ŃĐŸŃŃ‚Đ°ĐČĐŸĐŒ Đž струĐșŃ‚ŃƒŃ€ĐŸĐč cas-бДлĐșĐŸĐČ. ĐŸĐŸĐ»ŃƒŃ‡Đ”ĐœĐœŃ‹Đ” Ń€Đ”Đ·ŃƒĐ»ŃŒŃ‚Đ°Ń‚Ń‹ ĐŸĐżŃ€Đ”ĐŽĐ”Đ»ŃŃŽŃ‚ пДрспДĐșтоĐČу ĐžŃĐżĐŸĐ»ŃŒĐ·ĐŸĐČĐ°ĐœĐžŃ CRISPR-Đ»ĐŸĐșŃƒŃĐŸĐČ ĐČ ĐșачДстĐČĐ” спДцОфОчДсĐșох ĐŒĐŸĐ»Đ”ĐșŃƒĐ»ŃŃ€ĐœŃ‹Ń… ĐŒĐ°Ń€ĐșĐ”Ń€ĐŸĐČ ŃˆŃ‚Đ°ĐŒĐŒĐŸĐČ ĐżŃ€Đž ĐžĐ·ŃƒŃ‡Đ”ĐœĐžĐž ĐČĐœŃƒŃ‚Ń€ĐžĐČĐžĐŽĐŸĐČĐŸĐłĐŸ Ń€Đ°Đ·ĐœĐŸĐŸĐ±Ń€Đ°Đ·ĐžŃ Đž эĐČĐŸĐ»ŃŽŃ†ĐžĐž Y. pseudotuberculosis

    The COMPASS Experiment at CERN

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    The COMPASS experiment makes use of the CERN SPS high-intensitymuon and hadron beams for the investigation of the nucleon spin structure and the spectroscopy of hadrons. One or more outgoing particles are detected in coincidence with the incoming muon or hadron. A large polarized target inside a superconducting solenoid is used for the measurements with the muon beam. Outgoing particles are detected by a two-stage, large angle and large momentum range spectrometer. The setup is built using several types of tracking detectors, according to the expected incident rate, required space resolution and the solid angle to be covered. Particle identification is achieved using a RICH counter and both hadron and electromagnetic calorimeters. The setup has been successfully operated from 2002 onwards using a muon beam. Data with a hadron beam were also collected in 2004. This article describes the main features and performances of the spectrometer in 2004; a short summary of the 2006 upgrade is also given.Comment: 84 papes, 74 figure

    Muon Collider Forum report

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    A multi-TeV muon collider offers a spectacular opportunity in the direct exploration of the energy frontier. Offering a combination of unprecedented energy collisions in a comparatively clean leptonic environment, a high energy muon collider has the unique potential to provide both precision measurements and the highest energy reach in one machine that cannot be paralleled by any currently available technology. The topic generated a lot of excitement in Snowmass meetings and continues to attract a large number of supporters, including many from the early career community. In light of this very strong interest within the US particle physics community, Snowmass Energy, Theory and Accelerator Frontiers created a cross-frontier Muon Collider Forum in November of 2020. The Forum has been meeting on a monthly basis and organized several topical workshops dedicated to physics, accelerator technology, and detector R&D. Findings of the Forum are summarized in this report

    HE-LHC: The High-Energy Large Hadron Collider – Future Circular Collider Conceptual Design Report Volume 4

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    In response to the 2013 Update of the European Strategy for Particle Physics (EPPSU), the Future Circular Collider (FCC) study was launched as a world-wide international collaboration hosted by CERN. The FCC study covered an energy-frontier hadron collider (FCC-hh), a highest-luminosity high-energy lepton collider (FCC-ee), the corresponding 100 km tunnel infrastructure, as well as the physics opportunities of these two colliders, and a high-energy LHC, based on FCC-hh technology. This document constitutes the third volume of the FCC Conceptual Design Report, devoted to the hadron collider FCC-hh. It summarizes the FCC-hh physics discovery opportunities, presents the FCC-hh accelerator design, performance reach, and staged operation plan, discusses the underlying technologies, the civil engineering and technical infrastructure, and also sketches a possible implementation. Combining ingredients from the Large Hadron Collider (LHC), the high-luminosity LHC upgrade and adding novel technologies and approaches, the FCC-hh design aims at significantly extending the energy frontier to 100 TeV. Its unprecedented centre-of-mass collision energy will make the FCC-hh a unique instrument to explore physics beyond the Standard Model, offering great direct sensitivity to new physics and discoveries
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