Next Article in Journal
Expression Patterns of miR398, miR167, and miR159 in the Interaction between Bread Wheat (Triticum aestivum L.) and Pathogenic Fusarium culmorum and Beneficial Trichoderma Fungi
Previous Article in Journal
Insights into the SARS-CoV-2-Mediated Alteration in the Stress Granule Protein Regulatory Networks in Humans
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Pathogens
Volume 10
Issue 11
10.3390/pathogens10111460
pathogens-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite thumb_up
...
Endorse textsms
...
Comment
Erratum to Pathogens 2021, 10(7), 898.
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Erratum

Erratum: Rybnikov et al. Selection for Plastic, Pathogen-Inducible Recombination in a Red Queen Model with Diploid Antagonists. Pathogens 2021, 10, 898

by
Sviatoslav Rybnikov
1,2,
Zeev Frenkel
1,
Abraham B. Korol
1,2,* and
Tzion Fahima
1,2,*
1
Institute of Evolution, University of Haifa, 199 Abba-Hushi Avenue, Haifa 3498838, Israel
2
Department of Evolutionary and Environmental Biology, University of Haifa, 199 Abba-Hushi Avenue, Haifa 3498838, Israel
*
Authors to whom correspondence should be addressed.
Pathogens 2021, 10(11), 1460; https://doi.org/10.3390/pathogens10111460 (registering DOI)
Submission received: 5 November 2021 / Accepted: 5 November 2021 / Published: 11 November 2021
Browse Figures
Versions Notes
In the original article, there was a mistake published in Figure 3 [1]. Figure 3c,d in the published version are identical: instead of inserting Figure 3d, we by mistake repeated Figure 3c. In the legend to Figure 3 (line 4), change “for the modifier locus” to “the modifier locus”. The correct Figure 3d appears below.
In the titles to Figure 2b and Figure 4b, “Antiphase” changes to ‘anti-phase” (the hyphen is used throughout the text).
The last keyword should be “model” instead of “nodal”.
The authors and editorial office would like to apologize for any inconvenience caused to the readers by these changes and state that the scientific conclusions are unaffected. The original article has been updated.

Reference

  1. Rybnikov, S.; Frenkel, Z.; Korol, A.B.; Fahima, T. Selection for Plastic, Pathogen-Inducible Recombination in a Red Queen Model with Diploid Antagonists. Pathogens 2021, 10, 898. [Google Scholar] [CrossRef] [PubMed]
Pathogens 10 01460 g001a 550Pathogens 10 01460 g001b 550
Figure 3. The system’s dynamics under different regimes favoring plastic recombination. The plots show the last 500 out of 10,000 generations of the competition between the optimal constant recombination and plastic recombination; yet, the pattern is qualitatively similar also for other time windows. The colored curves stand for the host (green) and the parasite (orange). A, B and M denote, respectively, the two interaction-mediating loci and the modifier locus while W denotes the population’s mean fitness. All examples stand for anti-phase dominance and prevention strategy: (a) A regime with strong overall selection: s h ≈ 0.88 , s p ≈ 0.91 . The optimal constant recombination in the host is high: r opt h ≈ 0.25 . The oscillations are fairly regular. The modifier allele for plastic recombination generally increases in frequency, again with fairly regular oscillations; (b) A regime with extremely strong overall selection: s h ≈ 0.98 , s p > 0.99 . The optimal constant recombination in the host is high: r opt h = 0.32 . The oscillations are regular. The modifier allele for plastic recombination generally increases in frequency, again with fairly regular oscillations; (c) A regime with weak overall selection due to weak selection in the host: s h ≈ 0.14 , s p ≈ 0.70 . The optimal constant recombination in the host is very low: r opt h < 0.01 . The oscillations are irregular. Although the modifier allele for plastic recombination generally increases in frequency, its oscillations are substantially irregular; (d) A regime with weak overall selection due to weak selection in the parasite: s h ≈ 0.85 , s p ≈ 0.16 . The optimal constant recombination in the host is very low: r opt h < 0.01 . The oscillations are irregular. Although the modifier allele for plastic recombination generally increases in frequency, its dynamics are considerably irregular; in certain time windows (like here), the decline of the modifier allele for plastic recombination may even temporally prevail.
Figure 3. The system’s dynamics under different regimes favoring plastic recombination. The plots show the last 500 out of 10,000 generations of the competition between the optimal constant recombination and plastic recombination; yet, the pattern is qualitatively similar also for other time windows. The colored curves stand for the host (green) and the parasite (orange). A, B and M denote, respectively, the two interaction-mediating loci and the modifier locus while W denotes the population’s mean fitness. All examples stand for anti-phase dominance and prevention strategy: (a) A regime with strong overall selection: s h ≈ 0.88 , s p ≈ 0.91 . The optimal constant recombination in the host is high: r opt h ≈ 0.25 . The oscillations are fairly regular. The modifier allele for plastic recombination generally increases in frequency, again with fairly regular oscillations; (b) A regime with extremely strong overall selection: s h ≈ 0.98 , s p > 0.99 . The optimal constant recombination in the host is high: r opt h = 0.32 . The oscillations are regular. The modifier allele for plastic recombination generally increases in frequency, again with fairly regular oscillations; (c) A regime with weak overall selection due to weak selection in the host: s h ≈ 0.14 , s p ≈ 0.70 . The optimal constant recombination in the host is very low: r opt h < 0.01 . The oscillations are irregular. Although the modifier allele for plastic recombination generally increases in frequency, its oscillations are substantially irregular; (d) A regime with weak overall selection due to weak selection in the parasite: s h ≈ 0.85 , s p ≈ 0.16 . The optimal constant recombination in the host is very low: r opt h < 0.01 . The oscillations are irregular. Although the modifier allele for plastic recombination generally increases in frequency, its dynamics are considerably irregular; in certain time windows (like here), the decline of the modifier allele for plastic recombination may even temporally prevail.
Pathogens 10 01460 g001aPathogens 10 01460 g001b
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Rybnikov, S.; Frenkel, Z.; Korol, A.B.; Fahima, T. Erratum: Rybnikov et al. Selection for Plastic, Pathogen-Inducible Recombination in a Red Queen Model with Diploid Antagonists. Pathogens 2021, 10, 898. Pathogens 2021, 10, 1460. https://doi.org/10.3390/pathogens10111460

AMA Style

Rybnikov S, Frenkel Z, Korol AB, Fahima T. Erratum: Rybnikov et al. Selection for Plastic, Pathogen-Inducible Recombination in a Red Queen Model with Diploid Antagonists. Pathogens 2021, 10, 898. Pathogens. 2021; 10(11):1460. https://doi.org/10.3390/pathogens10111460

Chicago/Turabian Style

Rybnikov, Sviatoslav, Zeev Frenkel, Abraham B. Korol, and Tzion Fahima. 2021. "Erratum: Rybnikov et al. Selection for Plastic, Pathogen-Inducible Recombination in a Red Queen Model with Diploid Antagonists. Pathogens 2021, 10, 898" Pathogens 10, no. 11: 1460. https://doi.org/10.3390/pathogens10111460

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop