Literature DB >> 24789787

Extensive recombination-induced disruption of genetic interactions is highly deleterious but can be partially reversed by small numbers of secondary recombination events.

Adérito L Monjane1, Darren P Martin2, Francisco Lakay3, Brejnev M Muhire4, Daniel Pande5, Arvind Varsani6, Gordon Harkins7, Dionne N Shepherd3, Edward P Rybicki1.   

Abstract

Although homologous recombination can potentially provide viruses with vastly more evolutionary options than are available through mutation alone, there are considerable limits on the adaptive potential of this important evolutionary process. Primary among these is the disruption of favorable coevolved genetic interactions that can occur following the transfer of foreign genetic material into a genome. Although the fitness costs of such disruptions can be severe, in some cases they can be rapidly recouped by either compensatory mutations or secondary recombination events. Here, we used a maize streak virus (MSV) experimental model to explore both the extremes of recombination-induced genetic disruption and the capacity of secondary recombination to adaptively reverse almost lethal recombination events. Starting with two naturally occurring parental viruses, we synthesized two of the most extreme conceivable MSV chimeras, each effectively carrying 182 recombination breakpoints and containing thorough reciprocal mixtures of parental polymorphisms. Although both chimeras were severely defective and apparently noninfectious, neither had individual movement-, encapsidation-, or replication-associated genome regions that were on their own "lethally recombinant." Surprisingly, mixed inoculations of the chimeras yielded symptomatic infections with viruses with secondary recombination events. These recombinants had only 2 to 6 breakpoints, had predominantly inherited the least defective of the chimeric parental genome fragments, and were obviously far more fit than their synthetic parents. It is clearly evident, therefore, that even when recombinationally disrupted virus genomes have extremely low fitness and there are no easily accessible routes to full recovery, small numbers of secondary recombination events can still yield tremendous fitness gains. Importance: Recombination between viruses can generate strains with enhanced pathological properties but also runs the risk of producing hybrid genomes with decreased fitness due to the disruption of favorable genetic interactions. Using two synthetic maize streak virus genome chimeras containing alternating genome segments derived from two natural viral strains, we examined both the fitness costs of extreme degrees of recombination (both chimeras had 182 recombination breakpoints) and the capacity of secondary recombination events to recoup these costs. After the severely defective chimeras were introduced together into a suitable host, viruses with between 1 and 3 secondary recombination events arose, which had greatly increased replication and infective capacities. This indicates that even in extreme cases where recombination-induced genetic disruptions are almost lethal, and 91 consecutive secondary recombination events would be required to reconstitute either one of the parental viruses, moderate degrees of fitness recovery can be achieved through relatively small numbers of secondary recombination events.
Copyright © 2014, American Society for Microbiology. All Rights Reserved.

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Year:  2014        PMID: 24789787      PMCID: PMC4097777          DOI: 10.1128/JVI.00709-14

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  50 in total

1.  Magnitude and sign epistasis among deleterious mutations in a positive-sense plant RNA virus.

Authors:  J Lalić; S F Elena
Journal:  Heredity (Edinb)       Date:  2012-04-11       Impact factor: 3.821

2.  Widely conserved recombination patterns among single-stranded DNA viruses.

Authors:  P Lefeuvre; J-M Lett; A Varsani; D P Martin
Journal:  J Virol       Date:  2008-12-30       Impact factor: 5.103

3.  A three-nucleotide mutation altering the Maize streak virus Rep pRBR-interaction motif reduces symptom severity in maize and partially reverts at high frequency without restoring pRBR-Rep binding.

Authors:  Dionne N Shepherd; Darren P Martin; David R McGivern; Margaret I Boulton; Jennifer A Thomson; Edward P Rybicki
Journal:  J Gen Virol       Date:  2005-03       Impact factor: 3.891

4.  Forced recombination between distinct strains of Maize streak virus.

Authors:  W H Schnippenkoetter; D P Martin; J A Willment; E P Rybicki
Journal:  J Gen Virol       Date:  2001-12       Impact factor: 3.891

5.  Analysis of the diversity of African streak mastreviruses using PCR-generated RFLPs and partial sequence data.

Authors:  J A Willment; D P Martin; E P Rybicki
Journal:  J Virol Methods       Date:  2001-04       Impact factor: 2.014

6.  Epistasis among deleterious mutations in the HIV-1 protease.

Authors:  Mariona Parera; Nuria Perez-Alvarez; Bonaventura Clotet; Miguel Angel Martínez
Journal:  J Mol Biol       Date:  2009-07-14       Impact factor: 5.469

7.  Rapid host adaptation by extensive recombination.

Authors:  Eric van der Walt; Edward P Rybicki; Arvind Varsani; J E Polston; Rosalind Billharz; Lara Donaldson; Adérito L Monjane; Darren P Martin
Journal:  J Gen Virol       Date:  2009-03       Impact factor: 3.891

8.  Microcomputer-Based Quantification of Maize Streak Virus Symptoms in Zea mays.

Authors:  D P Martin; E P Rybicki
Journal:  Phytopathology       Date:  1998-05       Impact factor: 4.025

9.  Recombination hotspots and host susceptibility modulate the adaptive value of recombination during maize streak virus evolution.

Authors:  Adérito L Monjane; Eric van der Walt; Arvind Varsani; Edward P Rybicki; Darren P Martin
Journal:  BMC Evol Biol       Date:  2011-12-02       Impact factor: 3.260

10.  Genetic diversity and recombination analysis of sweepoviruses from Brazil.

Authors:  Leonardo C Albuquerque; Alice K Inoue-Nagata; Bruna Pinheiro; Renato O Resende; Enrique Moriones; Jesús Navas-Castillo
Journal:  Virol J       Date:  2012-10-20       Impact factor: 4.099

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Journal:  Arch Virol       Date:  2021-01-27       Impact factor: 2.574

2.  RNA Silencing May Play a Role in but Is Not the Only Determinant of the Multiplicity of Infection.

Authors:  Livia Donaire; József Burgyán; Fernando García-Arenal
Journal:  J Virol       Date:  2015-10-21       Impact factor: 5.103

3.  Multiple layers of chimerism in a single-stranded DNA virus discovered by deep sequencing.

Authors:  Mart Krupovic; Ning Zhi; Jungang Li; Gangqing Hu; Eugene V Koonin; Susan Wong; Sofiya Shevchenko; Keji Zhao; Neal S Young
Journal:  Genome Biol Evol       Date:  2015-04-02       Impact factor: 3.416

4.  Interspecies Recombination Has Driven the Macroevolution of Cassava Mosaic Begomoviruses.

Authors:  Alvin Crespo-Bellido; J Steen Hoyer; Divya Dubey; Ronica B Jeannot; Siobain Duffy
Journal:  J Virol       Date:  2021-08-10       Impact factor: 5.103

5.  Pervasive Chimerism in the Replication-Associated Proteins of Uncultured Single-Stranded DNA Viruses.

Authors:  Darius Kazlauskas; Arvind Varsani; Mart Krupovic
Journal:  Viruses       Date:  2018-04-10       Impact factor: 5.048

6.  Recombination and Positive Selection Differentially Shaped the Diversity of Betacoronavirus Subgenera.

Authors:  Diego Forni; Rachele Cagliani; Manuela Sironi
Journal:  Viruses       Date:  2020-11-16       Impact factor: 5.048

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