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Multinuclei Occurred Under Cryopreservation and Enhanced the Pathogenicity of Melampsora larici-populina

Melampsora larici-populina is a macrocyclic rust, and the haploid stage with two nuclei and the diploid of mononuclear sequentially occur annually. During the preservation of dry urediniospores at −80°C, we found that one isolate, ΔTs(06), was different from the usual wild-type isolate Ts(06) at −20...

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Autores principales: Zheng, Wei, Peng, Zijia, Peng, Shaobing, Yu, Zhongdong, Cao, Zhimin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8270653/
https://www.ncbi.nlm.nih.gov/pubmed/34248868
http://dx.doi.org/10.3389/fmicb.2021.650902
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author Zheng, Wei
Peng, Zijia
Peng, Shaobing
Yu, Zhongdong
Cao, Zhimin
author_facet Zheng, Wei
Peng, Zijia
Peng, Shaobing
Yu, Zhongdong
Cao, Zhimin
author_sort Zheng, Wei
collection PubMed
description Melampsora larici-populina is a macrocyclic rust, and the haploid stage with two nuclei and the diploid of mononuclear sequentially occur annually. During the preservation of dry urediniospores at −80°C, we found that one isolate, ΔTs(06), was different from the usual wild-type isolate Ts(06) at −20°C because it has mixed polykaryotic urediniospores. However, the other spores, including the 0, I, III, and IV stages of a life cycle, were the same as Ts(06). After five generations of successive inoculation and harvest of urediniospores from the compatible host Populus purdomii, the isolate ΔTs(06) steadily maintained more than 20% multiple nucleus spores. To test the pathogenesis variation of ΔTs(06), an assay of host poplars was applied to evaluate the differences between ΔTs(06) and Ts(06). After ΔTs(06) and Ts(06) inoculation, leaves of P. purdomii were used to detect the expression of small secreted proteins (SSPs) and fungal biomasses using quantitative real-time PCR (qRT-PCR) and trypan blue staining. ΔTs(06) displayed stronger expression of five SSPs and had a shorter latent period, a higher density of uredinia, and higher DNA mass. A transcriptomic comparison between ΔTs(06) and Ts(06) revealed that 3,224 were differentially expressed genes (DEGs), 55 of which were related to reactive oxygen species metabolism, the Mitogen-activated protein kinase (MAPK) signaling pathway, and the meiosis pathway. Ten genes in the mitotic and meiotic pathways and another two genes associated with the “response to DNA damage stimulus” all had an upward expression, which were detected by qRT-PCR in ΔTs(06) during cryopreservation. Gas chromatography–mass spectrometry (GC-MS) confirmed that the amounts of hexadecanoic acid and octadecadienoic acid were much more in ΔTs(06) than in Ts(06). In addition, using spectrophotometry, hydrogen peroxide (H(2)O(2)) was also present in greater quantities in ΔTs(06) compared with those found in Ts(06). Increased fatty acids metabolism could prevent damage to urediniospores in super-low temperatures, but oxidant species that involved H(2)O(2) may destroy tube proteins of mitosis and meiosis, which could cause abnormal nuclear division and lead to multinucleation, which has a different genotype. Therefore, the multinuclear isolate is different from the wild-type isolate in terms of phenotype and genotype; this multinucleation phenomenon in urediniospores improves the pathogenesis and environmental fitness of M. larici-populina.
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spelling pubmed-82706532021-07-10 Multinuclei Occurred Under Cryopreservation and Enhanced the Pathogenicity of Melampsora larici-populina Zheng, Wei Peng, Zijia Peng, Shaobing Yu, Zhongdong Cao, Zhimin Front Microbiol Microbiology Melampsora larici-populina is a macrocyclic rust, and the haploid stage with two nuclei and the diploid of mononuclear sequentially occur annually. During the preservation of dry urediniospores at −80°C, we found that one isolate, ΔTs(06), was different from the usual wild-type isolate Ts(06) at −20°C because it has mixed polykaryotic urediniospores. However, the other spores, including the 0, I, III, and IV stages of a life cycle, were the same as Ts(06). After five generations of successive inoculation and harvest of urediniospores from the compatible host Populus purdomii, the isolate ΔTs(06) steadily maintained more than 20% multiple nucleus spores. To test the pathogenesis variation of ΔTs(06), an assay of host poplars was applied to evaluate the differences between ΔTs(06) and Ts(06). After ΔTs(06) and Ts(06) inoculation, leaves of P. purdomii were used to detect the expression of small secreted proteins (SSPs) and fungal biomasses using quantitative real-time PCR (qRT-PCR) and trypan blue staining. ΔTs(06) displayed stronger expression of five SSPs and had a shorter latent period, a higher density of uredinia, and higher DNA mass. A transcriptomic comparison between ΔTs(06) and Ts(06) revealed that 3,224 were differentially expressed genes (DEGs), 55 of which were related to reactive oxygen species metabolism, the Mitogen-activated protein kinase (MAPK) signaling pathway, and the meiosis pathway. Ten genes in the mitotic and meiotic pathways and another two genes associated with the “response to DNA damage stimulus” all had an upward expression, which were detected by qRT-PCR in ΔTs(06) during cryopreservation. Gas chromatography–mass spectrometry (GC-MS) confirmed that the amounts of hexadecanoic acid and octadecadienoic acid were much more in ΔTs(06) than in Ts(06). In addition, using spectrophotometry, hydrogen peroxide (H(2)O(2)) was also present in greater quantities in ΔTs(06) compared with those found in Ts(06). Increased fatty acids metabolism could prevent damage to urediniospores in super-low temperatures, but oxidant species that involved H(2)O(2) may destroy tube proteins of mitosis and meiosis, which could cause abnormal nuclear division and lead to multinucleation, which has a different genotype. Therefore, the multinuclear isolate is different from the wild-type isolate in terms of phenotype and genotype; this multinucleation phenomenon in urediniospores improves the pathogenesis and environmental fitness of M. larici-populina. Frontiers Media S.A. 2021-06-25 /pmc/articles/PMC8270653/ /pubmed/34248868 http://dx.doi.org/10.3389/fmicb.2021.650902 Text en Copyright © 2021 Zheng, Peng, Peng, Yu and Cao. 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 Microbiology
Zheng, Wei
Peng, Zijia
Peng, Shaobing
Yu, Zhongdong
Cao, Zhimin
Multinuclei Occurred Under Cryopreservation and Enhanced the Pathogenicity of Melampsora larici-populina
title Multinuclei Occurred Under Cryopreservation and Enhanced the Pathogenicity of Melampsora larici-populina
title_full Multinuclei Occurred Under Cryopreservation and Enhanced the Pathogenicity of Melampsora larici-populina
title_fullStr Multinuclei Occurred Under Cryopreservation and Enhanced the Pathogenicity of Melampsora larici-populina
title_full_unstemmed Multinuclei Occurred Under Cryopreservation and Enhanced the Pathogenicity of Melampsora larici-populina
title_short Multinuclei Occurred Under Cryopreservation and Enhanced the Pathogenicity of Melampsora larici-populina
title_sort multinuclei occurred under cryopreservation and enhanced the pathogenicity of melampsora larici-populina
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8270653/
https://www.ncbi.nlm.nih.gov/pubmed/34248868
http://dx.doi.org/10.3389/fmicb.2021.650902
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