Publications by authors named "Yi-Jun Qiu"

Article Synopsis
  • Pine wilt disease (PWD) poses a significant threat to pine trees and results in major economic losses, highlighting the need for better understanding of its molecular mechanisms for effective prevention and treatment.
  • Researchers identified a key virulence effector, BxNMP1, that is expressed early during the infection and interacts with important proteins in pine trees, suggesting it plays a role in disease severity.
  • The study indicates that BxNMP1 not only regulates the pathogenicity of the disease but also interferes with the host's natural defense mechanisms, providing insights that might help in developing strategies for combating PWD.
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Bursaphelenchus xylophilus is the pathogen of pine wilt disease, which can devastate the pine forest ecosystem. Usually, plant cells generate reactive oxygen species (ROS) as a defensive substance or signalling molecules to resist the infection of nematodes. However, little is known about how B.

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Lipase is involved in lipid hydrolysis, which is related to nematodes' energy reserves and stress resistance. However, the role of lipases in Bursaphelenchus xylophilus, a notorious plant-parasitic nematode responsible for severe damage to pine forest ecosystems, remains largely obscure. Here, we characterized a class III lipase as a candidate effector and named it BxLip-3.

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Article Synopsis
  • - Pine wilt disease, caused by a specific pathogen, leads to significant economic losses in conifer production by hindering host immune responses through effector proteins.
  • - The study identifies two new effector proteins, BxKU1 and BxKU2, that employ different strategies to suppress plant immunity; they differ in structure, expression patterns, and their effects on host reproduction and feeding rates when silenced.
  • - Both effectors were found to interact with a specific protein (TLP4) in the host, revealing a complex immune evasion strategy that enhances our understanding of plant-pathogen interactions.
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Article Synopsis
  • The pinewood nematode is one of the top ten plant-parasitic nematodes, causing pine wilt, which negatively impacts both the economy and sustainable development in East Asia.
  • Researchers cloned and studied a pathogenic protein called BxTTR-52 from the nematode, which plays a role in immune evasion by suppressing the host plant's immune response.
  • The study found that BxTTR-52 is mostly produced in the nematode's esophageal glands and affects the infection process, revealing potential targets for managing the disease in pine trees.
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The migratory plant-parasitic nematode is the pathogen of the pine wilt disease (PWD), causing serious damage to pine forests in China. During the process of plant resistance to multiple pathogens, plant immunity plays a key role. In this current study, the pathogen-associated molecular pattern (PAMP) BxCDP1 in has been identified, but the host target protein of BxCDP1 and its key amino acid region inducing the plant immunity have yet to be elucidated.

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is the most economically important species of migratory plant-parasitic nematodes (PPNs) and causes severe damage to forestry in China. The successful infection of relies on the secretion of a repertoire of effector proteins. The effectors, which suppress the host pine immune response, are key to the facilitation of parasitism.

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Background: Bursaphelenchus xylophilus is the causal agent of pine wilt disease (PWD) that has caused enormous ecological and economic losses in China. The mechanism in the interaction between nematodes and pine remains unclear. Plant parasitic nematodes (PPNs) secrete effectors into host plant tissues.

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Background: The pine wilt disease (PWD) caused by Bursaphelenchus xylophilus is a devastating forest disease and its pathogenesis remains unclear. Secreted enzymes and proteins are important pathogenicity determinants and Bx-FAR-1 is an important pathogenic protein involved in the interaction between pine and B. xylophilus.

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Emerging evidence revealed the critical roles of long non-coding RNAs (lncRNAs) in maintaining genomic instability. However, genome instability-associated lncRNAs (GILncRNAs) and their performance in clinical prognostic significance in hepatocellular carcinoma (HCC) are rarely reported. Our study constructed a computational framework integrating somatic mutation information and lncRNA expression profiles of HCC genome and we identified 88 GILncRNAs of HCC.

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The plant-parasitic nematode Bursaphelenchus xylophilus, the causal agent of pine wilt disease (PWD), causes enormous economic loss every year. Currently, little is known about the pathogenic mechanisms of PWD. Several effectors have been identified in B.

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We aimed to explore the crucial miRNA-mRNA axis through bioinformatics analysis and provide evidences for the development of pathophysiological mechanisms and new therapies for HBV-related HCC. MiRNA (GSE76903) and mRNA (GSE77509) dataset were used to screen differentially expressed miRNAs (DE-miRNAs) and differentially expressed mRNAs (DE-mRNAs) using R software. Overlapping genes between DE-mRNAs and target genes of DE-miRNAs were identified as candidate genes.

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Objective: To evaluate the level of serum carbohydrate antigen-125(CA125) and its related factors in patients with bronchiectasis.

Methods: The clinical data of 504 patients with bronchiectasis in Zhejiang Putuo People's Hospital from June 2009 to June 2014 were collected in the study.The patients were divided into CA125 elevated group and CA125 normal group according to serum CA125 level,and the differences of serum CA125,age,gender, white blood cell(WBC),C-reactive protein(CRP), blood glucose and other test indicators were compared between two groups.

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Objective: To evaluate the quality of life in patients with chronic obstructive pulmonary disease (COPD) by COPD Assessment Test (CAT) and Body Mass Index, Airflow Obstruction, Dyspnea, Exercise Capacity Index (BODE).

Methods: One hundred patients with stable COPD admitted in Putuo People's Hospital were recruited in the study. CAT and BODE index were measured for each patient.

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