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Modeling Root-Knot Nematode Regulation by the Biocontrol Fungus Pochonia chlamydosporia
Two models of increasing complexity were constructed to simulate the interactions between the root-knot nematode (RKN) Meloidogyne incognita and the biocontrol fungus Pochonia chlamydosporia var. catenulata in a rhizosphere microcosm. The models described discrete population dynamics at hourly rates...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10512345/ https://www.ncbi.nlm.nih.gov/pubmed/37746233 http://dx.doi.org/10.3389/ffunb.2022.900974 |
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author | Ciancio, Aurelio Cabrera, Ileana Miranda Hidalgo-Diáz, Leopoldo Puertas, Ana Duvergel, Yoannia Castillo |
author_facet | Ciancio, Aurelio Cabrera, Ileana Miranda Hidalgo-Diáz, Leopoldo Puertas, Ana Duvergel, Yoannia Castillo |
author_sort | Ciancio, Aurelio |
collection | PubMed |
description | Two models of increasing complexity were constructed to simulate the interactions between the root-knot nematode (RKN) Meloidogyne incognita and the biocontrol fungus Pochonia chlamydosporia var. catenulata in a rhizosphere microcosm. The models described discrete population dynamics at hourly rates over a 6-month period and were validated using real parasitism and nematode or fungus data. A first, general Pochonia–nematode–root model (GPNR) used five functions and 16 biological constants. The variables and constants describing the RKN life cycle included the rates of egg production, hatching, juvenile (J2), and mature female development, including root or nematode self-density-dependent factors. Other constants accounted for egg parasitism, nematode-induced root losses, growth, and mortalities. The relationship between nematodes and fungal propagules showed density dependence and cyclic variations in time, including an attractor on the propagules and J2 phases space. The simulations confirmed a P. chlamydosporia optimal initial density of 5 · 10(3) propagules · cc soil(-1), as usually applied in assays. The constants used in GPNR showed adherence to the nematode biology, with 10(3) eggs per egg mass, a 10-day average lifespan of J2, with 2 days required to enter roots, and adult lifespan lasting 24 days. The fungus propagule lifespan was 25 days, with an average feeder root lifespan lasting around 52 days. A second, more complex Pochonia–nematode–root detailed model (GPNRd) was then constructed using eight functions and 23 constants. It was built as GPNR did not allow the evaluation of host prevalence. GPNRd allowed simulations of all RKN life stages and included non-parasitic and parasitic fungus population fractions. Both GPNR and GPNRd matched real J2 and fungus density data observed in a RKN biocontrol assay. Depending on the starting conditions, simulations showed stability in time, interpreted as effective host regulation. GPNRd showed a fungus cyclic relationship with the J2 numbers, with prevalence data close to those observed (38.3 vs. 39.4%, respectively). This model also showed a further density-independent nematode regulation mechanism based on the P. chlamydosporia switch from a non-parasitic to a parasitic trophic behavior. This mechanism supported the biocontrol of M. incognita, also sustained by a concomitant increase of the root density. |
format | Online Article Text |
id | pubmed-10512345 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105123452023-09-22 Modeling Root-Knot Nematode Regulation by the Biocontrol Fungus Pochonia chlamydosporia Ciancio, Aurelio Cabrera, Ileana Miranda Hidalgo-Diáz, Leopoldo Puertas, Ana Duvergel, Yoannia Castillo Front Fungal Biol Fungal Biology Two models of increasing complexity were constructed to simulate the interactions between the root-knot nematode (RKN) Meloidogyne incognita and the biocontrol fungus Pochonia chlamydosporia var. catenulata in a rhizosphere microcosm. The models described discrete population dynamics at hourly rates over a 6-month period and were validated using real parasitism and nematode or fungus data. A first, general Pochonia–nematode–root model (GPNR) used five functions and 16 biological constants. The variables and constants describing the RKN life cycle included the rates of egg production, hatching, juvenile (J2), and mature female development, including root or nematode self-density-dependent factors. Other constants accounted for egg parasitism, nematode-induced root losses, growth, and mortalities. The relationship between nematodes and fungal propagules showed density dependence and cyclic variations in time, including an attractor on the propagules and J2 phases space. The simulations confirmed a P. chlamydosporia optimal initial density of 5 · 10(3) propagules · cc soil(-1), as usually applied in assays. The constants used in GPNR showed adherence to the nematode biology, with 10(3) eggs per egg mass, a 10-day average lifespan of J2, with 2 days required to enter roots, and adult lifespan lasting 24 days. The fungus propagule lifespan was 25 days, with an average feeder root lifespan lasting around 52 days. A second, more complex Pochonia–nematode–root detailed model (GPNRd) was then constructed using eight functions and 23 constants. It was built as GPNR did not allow the evaluation of host prevalence. GPNRd allowed simulations of all RKN life stages and included non-parasitic and parasitic fungus population fractions. Both GPNR and GPNRd matched real J2 and fungus density data observed in a RKN biocontrol assay. Depending on the starting conditions, simulations showed stability in time, interpreted as effective host regulation. GPNRd showed a fungus cyclic relationship with the J2 numbers, with prevalence data close to those observed (38.3 vs. 39.4%, respectively). This model also showed a further density-independent nematode regulation mechanism based on the P. chlamydosporia switch from a non-parasitic to a parasitic trophic behavior. This mechanism supported the biocontrol of M. incognita, also sustained by a concomitant increase of the root density. Frontiers Media S.A. 2022-07-26 /pmc/articles/PMC10512345/ /pubmed/37746233 http://dx.doi.org/10.3389/ffunb.2022.900974 Text en Copyright © 2022 Ciancio, Cabrera, Hidalgo-Diáz, Puertas and Duvergel https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Fungal Biology Ciancio, Aurelio Cabrera, Ileana Miranda Hidalgo-Diáz, Leopoldo Puertas, Ana Duvergel, Yoannia Castillo Modeling Root-Knot Nematode Regulation by the Biocontrol Fungus Pochonia chlamydosporia |
title | Modeling Root-Knot Nematode Regulation by the Biocontrol Fungus Pochonia chlamydosporia
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title_full | Modeling Root-Knot Nematode Regulation by the Biocontrol Fungus Pochonia chlamydosporia
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title_fullStr | Modeling Root-Knot Nematode Regulation by the Biocontrol Fungus Pochonia chlamydosporia
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title_full_unstemmed | Modeling Root-Knot Nematode Regulation by the Biocontrol Fungus Pochonia chlamydosporia
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title_short | Modeling Root-Knot Nematode Regulation by the Biocontrol Fungus Pochonia chlamydosporia
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title_sort | modeling root-knot nematode regulation by the biocontrol fungus pochonia chlamydosporia |
topic | Fungal Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10512345/ https://www.ncbi.nlm.nih.gov/pubmed/37746233 http://dx.doi.org/10.3389/ffunb.2022.900974 |
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