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1.
Front Microbiol ; 14: 1288585, 2023.
Article in English | MEDLINE | ID: mdl-38260891

ABSTRACT

Introduction: The contamination of Trichoderma species causing green mold in substrates poses a significant obstacle to the global production of Lentinula edodes, adversely impacting both yield and quality of fruiting bodies. However, the diversity of Trichoderma species in the contaminated substrates of L. edodes (CSL) in China is not clear. The purpose of this study was to assess the biodiversity of Trichoderma species in CSL, and their interactions with L. edodes. Methods: A comprehensive two-year investigation of the biodiversity of Trichoderma species in CSL was conducted with 150 samples collected from four provinces of China. Trichoderma strains were isolated and identified based on integrated studies of phenotypic and molecular data. Resistance of L. edodes to the dominant Trichoderma species was evaluated in dual culture in vitro. Results: A total of 90 isolates were obtained and identified as 14 different Trichoderma species, including six new species named as Trichoderma caespitosus, T. macrochlamydospora, T. notatum, T. pingquanense, T. subvermifimicola, and T. tongzhouense, among which, T. atroviride, T. macrochlamydospora and T. subvermifimicola were identified as dominant species in the CSL. Meanwhile, three known species, namely, T. auriculariae, T. paraviridescens and T. subviride were isolated from CSL for the first time in the world, and T. paratroviride was firstly reported to be associated with L. edodes in China. Notebly, the in vitro evaluation of L. edodes resistance to dominant Trichoderma species showed strains of L. edodes generally possess poor resistance to Trichoderma contamination with L. edodes strain SX8 relatively higher resistant. Discussion: This study systematically investigated the diversity of Trichoderma species in the contaminated substrate of L. edodes, and a total of 31 species so far have been reported, indicating that green mold contaminated substrates of edible fungi were undoubtedly a biodiversity hotspot of Trichoderma species. Results in this study will provide deeper insight into the genus Trichoderma and lay a strong foundation for scientific management of the Trichoderma contamination in L. edodes cultivation.

2.
J Fungi (Basel) ; 8(11)2022 Oct 31.
Article in English | MEDLINE | ID: mdl-36354921

ABSTRACT

Trichoderma is known worldwide as biocontrol agents of plant diseases, producers of enzymes and antibiotics, and competitive contaminants of edible fungi. In this investigation of contaminated substrates of edible fungi from North China, 39 strains belonging to 10 Trichoderma species isolated from four kinds of edible fungi were obtained, and three novel species belonging to the Harzianum clade were isolated from the contaminated substrates of Auricularia heimuer and Pholiota adipose. They were recognized based on integrated studies of phenotypic features, culture characteristics, and molecular analyses of RNA polymerase II subunit B and translation elongation factor 1-α genes. Trichoderma auriculariae was strongly supported as a separate lineage and differed from T. vermifimicola due to its larger conidia. Trichoderma miyunense was closely related to T. ganodermatigerum but differed due to its smaller conidia and higher optimum mycelial growth temperature. As a separate lineage, T. pholiotae was distinct from T. guizhouense and T. pseudoasiaticum due to its higher optimum mycelial growth temperature and larger conidia. This study extends the understanding of Trichoderma spp. contaminating substrates of edible fungi and updates knowledge of species diversity in the group.

3.
Biomed Res Int ; 2021: 6669570, 2021.
Article in English | MEDLINE | ID: mdl-34671679

ABSTRACT

OBJECTIVE: This study is aimed at identifying stemness-related genes in pancreatic ductal adenocarcinoma (PDAC). METHODS: The RNA-seq data of PADC patients were downloaded from The Cancer Genome Atlas (TCGA) and Genotype-Tissue Expression (GTEx) databases. The mRNA expression-based stemness index (mRNAsi) and epigenetically regulated mRNAsi (EREG-mRNAsi) of PADC patients were evaluated. The mRNAsi-related gene sets in PADC were identified by weighted gene coexpression network analysis (WGCNA). The key genes were further analyzed using functional enrichment analysis. The Kaplan-Meier survival analysis and the Cox proportional hazards model were used to evaluate the prognostic value of the key genes. Prognostic hub genes were used to establish nomograms. The receiver operating characteristic (ROC) curves, concordance index (C-index), and calibration curves were used to assess the discrimination and accuracy of the nomogram. Finally, these results were validated in the Gene Expression Omnibus (GEO) database. RESULTS: A total of 36 key genes related to mRNAsi were identified by WGCNA. A prognostic gene signature compromising seven genes (TPX2, ZWINT, UBE2C, CCNB2, CDK1, BUB1, and BIRC5) was established to predict the overall survival (OS) of PADC patients. The Cox regression analysis revealed that the risk score was an independent prognostic factor for PADC. Patients were then divided into the high-risk and low-risk groups. The ROC curves, C-index, and calibration curves indicated good performance of the prognostic signature in the TCGA and GEO datasets. Moreover, the nomogram incorporating clinical parameters showed better sensitivity and specificity for predicting the OS of PADC patients. CONCLUSION: The stemness-related prognostic model successfully predicted the OS of PADC patients and could be used for the treatment of PADC.


Subject(s)
Carcinoma, Pancreatic Ductal/pathology , Neoplastic Stem Cells/pathology , Pancreatic Neoplasms/pathology , Aged , Biomarkers, Tumor/genetics , Carcinoma, Pancreatic Ductal/genetics , Carcinoma, Pancreatic Ductal/metabolism , Databases, Genetic , Female , Humans , Male , Middle Aged , Neoplastic Stem Cells/metabolism , Nomograms , Pancreatic Neoplasms/genetics , Pancreatic Neoplasms/metabolism , ROC Curve , Survival Rate , Transcriptome
4.
Huan Jing Ke Xue ; 40(5): 2368-2374, 2019 May 08.
Article in Chinese | MEDLINE | ID: mdl-31087878

ABSTRACT

Wastewater treatment plants (WWTPs) are important facilities to control water pollution and ensure the sustainable development of cities and humans. As an indispensable part of the activated sludge (AS) system, eukaryotic microbes play important roles in indicating the properties of AS, predicting the quality of the effluent, enhancing the purification effect, and ensuring a stable performance of the system in WWTPs. In this study, 61 AS samples from 14 full-scale WWTPs of Beijing, Shenzhen, and Wuxi were collected. Characteristics and regional heterogeneity of eukaryotic microbial community were elucidated via high-throughput sequencing (HTS) of the 18S rDNA and multi ecological and statistical methods. Results showed that eukaryotic microbial communities in different scales shared similar main members, which were mainly composed of fungi, ciliophora, and metazoa in division level with their total relative abundance up to 86.22%-89.40%. Diversity of eukaryotic microbial community in WWTPs of different cites varied. Richness and Shannon Wiener index of eukaryotic microbial communities in the AS system of Wuxi were the highest, while that of Beijing was the lowest. Diversity of eukaryotic microbes from HTS in this study was higher than that of conventional methods, but lower than the diversity of bacteria in AS systems. Regional heterogeneity of eukaryotic microbial community structure was uncovered by nonmetric multidimensional scaling based on Bray-Curtis distance and dissimilarity analysis. Results of partial mantel test and multiple regression matrix analysis showed that the eukaryotic microbial community was significantly correlated with the temperature of the aeration tank mixture and the total nitrogen concentration of the effluent of the AS system. These results help deepen the understanding of eukaryotic microbes in WWTPs.


Subject(s)
Eukaryotic Cells/classification , Microbiota , Wastewater/microbiology , Beijing , Ciliophora/classification , Fungi/classification
5.
Mol Cell Proteomics ; 18(2): 372-382, 2019 02.
Article in English | MEDLINE | ID: mdl-30482845

ABSTRACT

Src homology 2 (SH2) domains play an essential role in cellular signal transduction by binding to proteins phosphorylated on Tyr residue. Although Tyr phosphorylation (pY) is a prerequisite for binding for essentially all SH2 domains characterized to date, different SH2 domains prefer specific sequence motifs C-terminal to the pY residue. Because all SH2 domains adopt the same structural fold, it is not well understood how different SH2 domains have acquired the ability to recognize distinct sequence motifs. We have shown previously that the EF and BG loops that connect the secondary structure elements on an SH2 domain dictate its specificity. In this study, we investigated if these surface loops could be engineered to encode diverse specificities. By characterizing a group of SH2 variants selected by different pY peptides from phage-displayed libraries, we show that the EF and BG loops of the Fyn SH2 domain can encode a wide spectrum of specificities, including all three major specificity classes (p + 2, p + 3 and p + 4) of the SH2 domain family. Furthermore, we found that the specificity of a given variant correlates with the sequence feature of the bait peptide used for its isolation, suggesting that an SH2 domain may acquire specificity by co-evolving with its ligand. Intriguingly, we found that the SH2 variants can employ a variety of different mechanisms to confer the same specificity, suggesting the EF and BG loops are highly flexible and adaptable. Our work provides a plausible mechanism for the SH2 domain to acquire the wide spectrum of specificity observed in nature through loop variation with minimal disturbance to the SH2 fold. It is likely that similar mechanisms may have been employed by other modular interaction domains to generate diversity in specificity.


Subject(s)
Proto-Oncogene Proteins c-fyn/chemistry , Animals , Crystallography, X-Ray , Genetic Variation , Humans , Ligands , Models, Molecular , Peptide Library , Protein Structure, Secondary , Proto-Oncogene Proteins c-fyn/genetics , src Homology Domains
6.
Genomics Proteomics Bioinformatics ; 16(6): 451-459, 2018 12.
Article in English | MEDLINE | ID: mdl-30639696

ABSTRACT

As a newly-identified protein post-translational modification, malonylation is involved in a variety of biological functions. Recognizing malonylation sites in substrates represents an initial but crucial step in elucidating the molecular mechanisms underlying protein malonylation. In this study, we constructed a deep learning (DL) network classifier based on long short-term memory (LSTM) with word embedding (LSTMWE) for the prediction of mammalian malonylation sites. LSTMWE performs better than traditional classifiers developed with common pre-defined feature encodings or a DL classifier based on LSTM with a one-hot vector. The performance of LSTMWE is sensitive to the size of the training set, but this limitation can be overcome by integration with a traditional machine learning (ML) classifier. Accordingly, an integrated approach called LEMP was developed, which includes LSTMWE and the random forest classifier with a novel encoding of enhanced amino acid content. LEMP performs not only better than the individual classifiers but also superior to the currently-available malonylation predictors. Additionally, it demonstrates a promising performance with a low false positive rate, which is highly useful in the prediction application. Overall, LEMP is a useful tool for easily identifying malonylation sites with high confidence. LEMP is available at http://www.bioinfogo.org/lemp.


Subject(s)
Deep Learning , Forecasting/methods , Lysine/chemistry , Malonates/chemistry , Protein Processing, Post-Translational/genetics , Amino Acid Sequence/genetics , Amino Acids , Animals , Machine Learning
8.
Sci Rep ; 6: 27074, 2016 06 01.
Article in English | MEDLINE | ID: mdl-27245694

ABSTRACT

More than 200 recent collections of Trichoderma from China were examined and 16 species belonging to the Viride clade were identified based on integrated studies of phenotypic and molecular data. Among them, seven wood-inhabiting new species, T. albofulvopsis, T. densum, T. laevisporum, T. sinokoningii, T. sparsum, T. sphaerosporum and T. subviride, are found. They form trichoderma- to verticillium-like conidiophores, lageniform to subulate phialides and globose to ellipsoidal conidia, but vary greatly in colony features, growth rates, and sizes of phialides and conidia. To explore their taxonomic positions, the phylogenetic tree including all the known species of the Viride clade is constructed based on sequence analyses of the combined RNA polymerase II subunit b and translation elongation factor 1 alpha exon genes. Our results indicated that the seven new species were well-located in the Koningii, Rogersonii and Neorufum subclades as well as a few independent terminal branches. They are clearly distinguishable from any existing species. Morphological distinctions and sequence divergences between the new species and their close relatives were discussed.


Subject(s)
DNA, Fungal/genetics , Fungal Proteins/genetics , Peptide Elongation Factor 1/genetics , Phylogeny , RNA Polymerase II/genetics , Trichoderma/genetics , China , Exons , Gene Expression , Phenotype , Sequence Analysis, DNA , Species Specificity , Spores, Fungal/genetics , Spores, Fungal/growth & development , Spores, Fungal/isolation & purification , Trichoderma/classification , Trichoderma/growth & development , Trichoderma/isolation & purification , Wood/microbiology
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