Yu-Hsien Lin

Dr. Yu-Hsien Lin

orcid

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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8 September 2016 in Pest Management Science
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Journal Article
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YLYu-Hsien Lin
Yu-Hsien Lin
JHJia‐Hsin Huang
Jia‐Hsin Huang
YLYun Liu
Yun Liu
XBXavier Belles
Xavier Belles
HLHow‐Jing Lee
How‐Jing Lee

28 April 2020 in Frontiers in Immunology
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Journal Article
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YLYu-Hsien Lin
Yu-Hsien Lin
CTChia-Chi Tai
Chia-Chi Tai
VBVáclav Brož
Václav Brož
CTCheng-Kang Tang
Cheng-Kang Tang
PCPing Chen
Ping Chen
YWYueh-Lung Wu
Yueh-Lung Wu
Although the modulation of host physiology has been interpreted as an essential process supporting baculovirus propagation, the requirement of energy supply for host antivirus reactions could not be ruled out. Our present study showed that metabolic induction upon AcMNPV (budded virus) infection of Bombyx mori stimulated virus clearance and production of the antivirus protein, gloverin. In addition, we demonstrated that adenosine receptor signaling (AdoR) played an important role in regulating such metabolic reprogramming upon baculovirus infection. By using a second lepidopteran model, Spodoptera frugiperda Sf-21 cells, we demonstrated that the glycolytic induction regulated by adenosine signaling was a conservative mechanism modulating the permissiveness of baculovirus infection. Another interesting finding in our present study is that both BmNPV and AcMNPV infection cause metabolic activation, but it appears that BmNPV infection moderates the level of ATP production, which is in contrast to a dramatic increase upon AcMNPV infection. We identified potential AdoR miRNAs induced by BmNPV infection and concluded that BmNPV may attempt to minimize metabolic activation by suppressing adenosine signaling and further decreasing the host's anti-baculovirus response. Our present study shows that activation of energy synthesis by adenosine signaling upon baculovirus infection is a host physiological response that is essential for supporting the innate immune response against infection.

1 December 2021 in Insect Biochemistry and Molecular Biology
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Journal Article
Closed access
PCPing Chen
Ping Chen
YLYun-Heng Lu
Yun-Heng Lu
YLYu-Hsien Lin
Yu-Hsien Lin
CWCarol-P Wu
Carol-P Wu
CTCheng-Kang Tang
Cheng-Kang Tang
YWYueh-Lung Wu
Yueh-Lung Wu

8 January 2021 in Communications Biology
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Journal Article
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CTCheng-Kang Tang
Cheng-Kang Tang
CTChih-Hsuan Tsai
Chih-Hsuan Tsai
CWCarol-P. Wu
Carol-P. Wu
YLYu-Hsien Lin
Yu-Hsien Lin
SWSung-Chan Wei
Sung-Chan Wei
YWYueh-Lung Wu
Yueh-Lung Wu
To avoid inducing immune and physiological responses in insect hosts, parasitoid wasps have developed several mechanisms to inhibit them during parasitism, including the production of venom, specialized wasp cells, and symbioses with polydnaviruses (PDVs). These mechanisms alter the host physiology to give the wasp offspring a greater chance of survival. However, the molecular mechanisms for most of these alterations remain unclear. In the present study, we applied next-generation sequencing analysis and identified several miRNAs that were encoded in the genome of Snellenius manilae bracovirus (SmBV), and expressed in the host larvae, Spodoptera litura, during parasitism. Among these miRNAs, SmBV-miR-199b-5p and SmBV-miR-2989 were found to target domeless and toll-7 in the host, which are involved in the host innate immune responses. Microinjecting the inhibitors of these two miRNAs into parasitized S. litura larvae not only severely decreased the pupation rate of Snellenius manilae, but also restored the phagocytosis and encapsulation activity of the hemocytes. The results demonstrate that these two SmBV-encoded miRNAs play an important role in suppressing the immune responses of parasitized hosts. Overall, our study uncovers the functions of two SmBV-encoded miRNAs in regulating the host innate immune responses upon wasp parasitism.

10 August 2020 in Insects
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Journal Article
Open access
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YLYun-Heng Lu
Yun-Heng Lu
CWCarol-P Wu
Carol-P Wu
CTCheng-Kang Tang
Cheng-Kang Tang
YLYu-Hsien Lin
Yu-Hsien Lin
HMHouda Ouns Maaroufi
Houda Ouns Maaroufi
YWYueh-Lung Wu
Yueh-Lung Wu
Plants and pollinators are mutually beneficial: plants provide nectar as a food source and in return their pollen is disseminated by pollinators such as honeybees. Some plants secrete chemicals to deter herbivores as a protective measure, among which is caffeine, a naturally occurring, bitter tasting, and pharmacologically active secondary compound. It can be found in low concentrations in the nectars of some plants and as such, when pollinators consume nectar, they also take in small amounts of caffeine. Whilst caffeine has been indicated as an antioxidant in both mammals and insects, the effect on insect immunity is unclear. In the present study, honeybees were treated with caffeine and the expression profiles of genes involved in immune responses were measured to evaluate the influence of caffeine on immunity. In addition, honeybees were infected with deformed wing virus (DWV) to study how caffeine affects their response against pathogens. Our results showed that caffeine can increase the expression of genes involved in immunity and reduce virus copy numbers, indicating that it has the potential to help honeybees fight against viral infection. The present study provides a valuable insight into the mechanism by which honeybees react to biotic stress and how caffeine can serve as a positive contributor, thus having a potential application in beekeeping.

1 June 2014 in Journal of Insect Physiology
Verified
Journal Article
Closed access
YLYu-Hsien Lin
Yu-Hsien Lin
CLChi-Mei Lee
Chi-Mei Lee
JHJia-Hsin Huang
Jia-Hsin Huang
HLHow-Jing Lee
How-Jing Lee