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      Recombination in viruses: Mechanisms, methods of study, and evolutionary consequences

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          Highlights

          • Recombination is very relevant in generating genetic variability in viral populations.

          • Viral recombination has important consequences for different areas of research. These include molecular biology, virology and evolutionary biology. It also impacts the daily practice of clinicians and public health officials.

          • Here we review three important aspects of viral recombination: (i) molecular mechanisms of model DNA- and RNA-viruses, (ii) methods for detection, characterization and quantification in viral populations, (iii) its impact on the evolutionary analysis of viral populations.

          Abstract

          Recombination is a pervasive process generating diversity in most viruses. It joins variants that arise independently within the same molecule, creating new opportunities for viruses to overcome selective pressures and to adapt to new environments and hosts. Consequently, the analysis of viral recombination attracts the interest of clinicians, epidemiologists, molecular biologists and evolutionary biologists. In this review we present an overview of three major areas related to viral recombination: (i) the molecular mechanisms that underlie recombination in model viruses, including DNA-viruses (Herpesvirus) and RNA-viruses (Human Influenza Virus and Human Immunodeficiency Virus), (ii) the analytical procedures to detect recombination in viral sequences and to determine the recombination breakpoints, along with the conceptual and methodological tools currently used and a brief overview of the impact of new sequencing technologies on the detection of recombination, and (iii) the major areas in the evolutionary analysis of viral populations on which recombination has an impact. These include the evaluation of selective pressures acting on viral populations, the application of evolutionary reconstructions in the characterization of centralized genes for vaccine design, and the evaluation of linkage disequilibrium and population structure.

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          Most cited references122

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          The fine-scale structure of recombination rate variation in the human genome.

          The nature and scale of recombination rate variation are largely unknown for most species. In humans, pedigree analysis has documented variation at the chromosomal level, and sperm studies have identified specific hotspots in which crossing-over events cluster. To address whether this picture is representative of the genome as a whole, we have developed and validated a method for estimating recombination rates from patterns of genetic variation. From extensive single-nucleotide polymorphism surveys in European and African populations, we find evidence for extreme local rate variation spanning four orders in magnitude, in which 50% of all recombination events take place in less than 10% of the sequence. We demonstrate that recombination hotspots are a ubiquitous feature of the human genome, occurring on average every 200 kilobases or less, but recombination occurs preferentially outside genes.
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            Analyzing the mosaic structure of genes.

            Some genes in prokaryotes consist of a mosaic of regions derived from different ancestors by horizontal gene transfer. A method is described for demonstrating the statistical significance of such mosaic structure and for locating the crossover points separating different regions.
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              Approximate Bayesian Computation in Evolution and Ecology

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                Author and article information

                Contributors
                Journal
                Infect Genet Evol
                Infect. Genet. Evol
                Infection, Genetics and Evolution
                Elsevier B.V.
                1567-1348
                1567-7257
                23 December 2014
                March 2015
                23 December 2014
                : 30
                : 296-307
                Affiliations
                [a ]CIBIO, Centro de Investigação em Biodiversidade e Recursos Genéticos, Universidade do Porto, Campus Agrário de Vairão, Portugal
                [b ]Computational Biology Institute, George Washington University, Ashburn, VA 20147, USA
                [c ]Centre for Molecular Biology “Severo Ochoa”, Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain
                [d ]Servicio de Microbiología, Hospital Ramón y Cajal and Instituto Ramón y Cajal de Investigación Sanitaria (IRYCIS), Madrid, Spain
                [e ]CIBER en Epidemiología y Salud Pública, Spain
                [f ]Unidad Mixta Infección y Salud Pública, FISABIO-Universitat de València, Valencia, Spain
                Author notes
                [* ]Corresponding author at: Unidad Mixta Infección y Salud Pública, FISABIO-Universitat de València, C/Catedrático José Beltrán, 2, E-46980 Paterna, Valencia, Spain. Tel.: +34 963543653, +34 961925961; fax: +34 963543670. fernando.gonzalez@ 123456uv.es
                Article
                S1567-1348(14)00478-X
                10.1016/j.meegid.2014.12.022
                7106159
                25541518
                2a62e056-5a2f-44ae-b7f1-f80988a67dd3
                Copyright © 2014 Elsevier B.V. All rights reserved.

                Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.

                History
                : 23 November 2014
                : 15 December 2014
                : 17 December 2014
                Categories
                Article

                Genetics
                recombination,reassortment,linkage disequilibrium,population structure,recombination rate,mutation rate

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