Feng-Chia Hsieh

Dr. Feng-Chia Hsieh

Taiwan Agricultural Chemicals and Toxic Substances Research Institute, Taichung, Taiwan
orcid

Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

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

Representative Publications

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1 September 2004 in Current Microbiology
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Feng-Chia HsiehFeng-Chia Hsieh
Feng-Chia Hsieh
MLMei-Chen Li
Mei-Chen Li
TLTsung-Chun Lin
Tsung-Chun Lin
SKSuey-Sheng Kao
Suey-Sheng Kao

20 November 2007 in Current Microbiology
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Feng-Chia HsiehFeng-Chia Hsieh
Feng-Chia Hsieh
TLTsung-Chun Lin
Tsung-Chun Lin
Menghsiao MengMenghsiao Meng
Menghsiao Meng
SKSuey-Sheng Kao
Suey-Sheng Kao

8 September 2016 in Scientific Reports
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Journal Article
Open access
WCWen-Jen Chen
Wen-Jen Chen
TKTzu-Yen Kuo
Tzu-Yen Kuo
Feng-Chia HsiehFeng-Chia Hsieh
Feng-Chia Hsieh
PCPi-Yu Chen
Pi-Yu Chen
CWChang-Sheng Wang
Chang-Sheng Wang
MSMing-Che Shih
Ming-Che Shih
Rice bacterial blight caused by Xanthomonas oryzae pv. oryzae (Xoo) is one of the most destructive rice diseases worldwide. Therefore, in addition to breeding disease-resistant rice cultivars, it is desirable to develop effective biocontrol agents against Xoo. Here, we report that a soil bacterium Pseudomonas taiwanensis displayed strong antagonistic activity against Xoo. Using matrix-assisted laser desorption/ionization imaging mass spectrometry, we identified an iron chelator, pyoverdine, secreted by P. taiwanensis that could inhibit the growth of Xoo. Through Tn5 mutagenesis of P. taiwanensis, we showed that mutations in genes that encode components of the type VI secretion system (T6SS) as well as biosynthesis and maturation of pyoverdine resulted in reduced toxicity against Xoo. Our results indicated that T6SS is involved in the secretion of endogenous pyoverdine. Mutations in T6SS component genes affected the secretion of mature pyoverdine from the periplasmic space into the extracellular medium after pyoverdine precursor is transferred to the periplasm by the inner membrane transporter PvdE. In addition, we also showed that other export systems, i.e., the PvdRT-OpmQ and MexAB-OprM efflux systems (for which there have been previous suggestions of involvement) and the type II secretion system (T2SS), are not involved in pyoverdine secretion.

1 May 2015 in European Journal of Pharmacology
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YCYi-Ching Chung
Yi-Ching Chung
Feng-Chia HsiehFeng-Chia Hsieh
Feng-Chia Hsieh
YLYing-Ju Lin
Ying-Ju Lin
TWTzong-Yuan Wu
Tzong-Yuan Wu
Cheng-Wen LinCheng-Wen Lin
Cheng-Wen Lin
TJTzyy-Rong Jinn
Tzyy-Rong Jinn

3 December 2016 in Molecules
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JLJen-Hung Liao
Jen-Hung Liao
PCPi-Yu Chen
Pi-Yu Chen
YYYu-Liang Yang
Yu-Liang Yang
SKShu-Chen Kan
Shu-Chen Kan
Feng-Chia HsiehFeng-Chia Hsieh
Feng-Chia Hsieh
Yung-Chuan LiuYung-Chuan Liu
Yung-Chuan Liu
This study tried to clarify the antagonistic effect of the lipopeptides secreted by Bacillus amyloliquefaciens strain BPD1 (Ba-BPD1) against Pyricularia oryzae Cavara (PO). To determine the major antifungal lipopeptides effective against PO, single and dual cultures were carried out in solid-state media. The matrix-assisted laser desorption/ionization–time of flight imaging mass spectrometry (MALDI-TOF IMS) was used to identify the most effective lipopeptide in situ. Meanwhile, the morphology of pathogen fungi treated with lipopeptides was observed via the SEM. Of the three lipopeptide families, surfactin, iturin, and fengycin, the last was identified as the most effective for inhibiting mycelium growth and conidial germination of PO. The conidia and hyphae of fengycin-treated PO were shown to become deformed and tumorous under exposure. This study provides insights into the antagonistic effect of Ba-BPD1 against fungal phytopathogens. Such insights are helpful in the development of reagents for biological control applications.

21 August 2014 in PLOS Pathogens
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WCWen-Jen Chen
Wen-Jen Chen
Feng-Chia HsiehFeng-Chia Hsieh
Feng-Chia Hsieh
FHFu-Chiun Hsu
Fu-Chiun Hsu
YTYi-Fang Tasy
Yi-Fang Tasy
JLJe-Ruei Liu
Je-Ruei Liu
MSMing-Che Shih
Ming-Che Shih
Pseudomonas taiwanensis is a broad-host-range entomopathogenic bacterium that exhibits insecticidal activity toward agricultural pests Plutella xylostella, Spodoptera exigua, Spodoptera litura, Trichoplusia ni and Drosophila melanogaster. Oral infection with different concentrations (OD = 0.5 to 2) of wild-type P. taiwanensis resulted in insect mortality rates that were not significantly different (92.7%, 96.4% and 94.5%). The TccC protein, a component of the toxin complex (Tc), plays an essential role in the insecticidal activity of P. taiwanensis. The ΔtccC mutant strain of P. taiwanensis, which has a knockout mutation in the tccC gene, only induced 42.2% mortality in P. xylostella, even at a high bacterial dose (OD = 2.0). TccC protein was cleaved into two fragments, an N-terminal fragment containing an Rhs-like domain and a C-terminal fragment containing a Glt symporter domain and a TraT domain, which might contribute to antioxidative stress activity and defense against macrophagosis, respectively. Interestingly, the primary structure of the C-terminal region of TccC in P. taiwanensis is unique among pathogens. Membrane localization of the C-terminal fragment of TccC was proven by flow cytometry. Sonicated pellets of P. taiwanensis ΔtccC strain had lower toxicity against the Sf9 insect cell line and P. xylostella larvae than the wild type. We also found that infection of Sf9 and LD652Y-5d cell lines with P. taiwanensis induced apoptotic cell death. Further, natural oral infection by P. taiwanensis triggered expression of host programmed cell death-related genes JNK-2 and caspase-3. Most entomopathogenic bacteria can produce toxin proteins and proliferate in the intestines of insects after natural oral ingestion. These bacteria can evade the systemic and local immune responses of insects. Here, we used insect larva of the diamond back moth (Plutella xylostella), a cruciferous crop pest to study the pathogenic mechanism of infection by novel bacterium Psudomonas taiwanensis. We examined how P. taiwanensis colonizes and escapes the immune response in the gut of P. xylostella and the mechanism of pathogenesis after oral ingestion of P. taiwanensis. Oral ingestion of P. taiwanensis induced severe damage in intestinal cells of P. xylostella and disrupted intestinal epithelial integrity. A toxin protein, the C component of insecticidal toxin protein complex (TccC) contributed to the pathogenicity of P. taiwanensis by thwarting oxidative stress and phagocytosis and inducing apoptosis in the gut cells of the host. Taken together our results shed light on the bacterial pathogenic processes in insect hosts, particularly the mechanism of pathogenesis of P. taiwanensis.