生物防治真菌厚垣孢子虫对根结线虫的调控模型。

IF 2.1 Q3 MYCOLOGY Frontiers in fungal biology Pub Date : 2022-07-26 eCollection Date: 2022-01-01 DOI:10.3389/ffunb.2022.900974
Aurelio Ciancio, Ileana Miranda Cabrera, Leopoldo Hidalgo-Diáz, Ana Puertas, Yoannia Castillo Duvergel
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引用次数: 0

摘要

构建了两个复杂度递增的模型,模拟根结线虫(RKN)根结线虫与生防菌Poconia chlamydosporia var.catenulata在根际微宇宙中的相互作用。这些模型描述了6个月内每小时的离散种群动态,并使用真实的寄生和线虫或真菌数据进行了验证。第一个,通用的Pochonia线虫根模型(GPNR)使用了五个函数和16个生物常数。描述RKN生命周期的变量和常数包括卵子产生率、孵化率、幼体(J2)和成熟雌性发育率,包括根或线虫自身密度依赖因素。其他常数解释了卵寄生、线虫引起的根系损失、生长和死亡。线虫和真菌繁殖体之间的关系表现出密度依赖性和随时间的循环变化,包括繁殖体上的吸引子和J2相空间。模拟结果证实,厚垣孢子虫的最佳初始密度为5103繁殖体·cc土壤-1,通常用于测定。GPNR中使用的常数显示出对线虫生物学的坚持,每卵103个,J2的平均寿命为10天,进入根需要2天,成虫寿命为24天。真菌繁殖体的寿命为25天,饲养根的平均寿命约为52天。然后使用8个函数和23个常数构建了第二个更复杂的Pochonia线虫根详细模型(GPNRd)。它是由于GPNR不允许评估宿主患病率而建立的。GPNRd允许模拟RKN的所有生命阶段,并包括非寄生和寄生真菌种群部分。GPNR和GPNRd都与RKN生物控制测定中观察到的真实J2和真菌密度数据相匹配。根据启动条件的不同,模拟显示了时间上的稳定性,被解释为有效的宿主调节。GPNRd显示出与J2数量的真菌循环关系,患病率数据与观察到的数据接近(分别为38.3%和39.4%)。该模型还显示了基于厚垣孢子虫从非寄生营养行为转变为寄生营养行为的进一步密度独立的线虫调节机制。这一机制支持了M.incognita的生物防治,同时也通过增加根密度来维持。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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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 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 · 103 propagules · cc soil-1, as usually applied in assays. The constants used in GPNR showed adherence to the nematode biology, with 103 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.

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