Katsutoshi Hori

Prof. Dr. Katsutoshi Hori

Graduate School of Engineering, Nagoya University
orcid

Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

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

Representative Publications

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1 February 2010 in Biochemical Engineering Journal
Verified
Journal Article
Closed access
Katsutoshi HoriKatsutoshi Hori
Katsutoshi Hori
SMShinya Matsumoto
Shinya Matsumoto

1 December 2005 in Applied and Environmental Microbiology
Verified
Journal Article
Closed access
PDF file
SIShun'ichi Ishii
Shun'ichi Ishii
TKTommoyuki Kosaka
Tommoyuki Kosaka
Katsutoshi HoriKatsutoshi Hori
Katsutoshi Hori
YHYasuaki Hotta
Yasuaki Hotta
KWKazuya Watanabe
Kazuya Watanabe
A thermophilic syntrophic bacterium,Pelotomaculum thermopropionicumstrain SI, was grown in a monoculture or coculture with a hydrogenotrophic methanogen,Methanothermobacter thermautotrophicusstrain ΔH. Microscopic observation revealed that cells of each organism were dispersed in a monoculture independent of the growth substrate. In a coculture, however, these organisms coaggregated to different degrees depending on the substrate; namely, a large fraction of the cells coaggregated when they were grown on propionate, but relatively few cells coaggregated when they were grown on ethanol or 1-propanol. Field emission-scanning electron microscopy revealed that flagellum-like filaments of SI cells played a role in making contact with ΔH cells. Microscopic observation of aggregates also showed that extracellular polymeric substance-like structures were present in intercellular spaces. In order to evaluate the importance of coaggregation for syntrophic propionate oxidation, allowable average distances between SI and ΔH cells for accomplishing efficient interspecies hydrogen transfer were calculated by using Fick's diffusion law. The allowable distance for syntrophic propionate oxidation was estimated to be approximately 2 μm, while the allowable distances for ethanol and propanol oxidation were 16 μm and 32 μm, respectively. Considering that the mean cell-to-cell distance in the randomly dispersed culture was approximately 30 μm (at a concentration in the mid-exponential growth phase of the coculture of 5 × 107cells ml−1), it is obvious that close physical contact of these organisms by coaggregation is indispensable for efficient syntrophic propionate oxidation.

1 April 2004 in Applied Microbiology and Biotechnology
Verified
Journal Article
Closed access
PDF file
YTYasunori Tanji
Yasunori Tanji
TST. Shimada
T. Shimada
MYM. Yoichi
M. Yoichi
KMK. Miyanaga
K. Miyanaga
Katsutoshi HoriKatsutoshi Hori
Katsutoshi Hori
HUH. Unno
H. Unno

1 January 2019 in Virulence
Verified
Journal Article
Open access
MWMarko Weidensdorfer
Marko Weidensdorfer
MIMasahito Ishikawa
Masahito Ishikawa
Katsutoshi HoriKatsutoshi Hori
Katsutoshi Hori
DLDirk Linke
Dirk Linke
BDBardya Djahanschiri
Bardya Djahanschiri
SGStephan Göttig
Stephan Göttig
Acinetobacter baumannii is a Gram-negative pathogen that causes a multitude of nosocomial infections. The Acinetobacter trimeric autotransporter adhesin (Ata) belongs to the superfamily of trimeric autotransporter adhesins which are important virulence factors in many Gram-negative species. Phylogenetic profiling revealed that ata is present in 78% of all sequenced A. baumannii isolates but only in 2% of the closely related species A. calcoaceticus and A. pittii. Employing a markerless ata deletion mutant of A. baumannii ATCC 19606 we show that adhesion to and invasion into human endothelial and epithelial cells depend on Ata. Infection of primary human umbilical cord vein endothelial cells (HUVECs) with A. baumannii led to the secretion of interleukin (IL)-6 and IL-8 in a time- and Ata-dependent manner. Furthermore, infection of HUVECs by WT A. baumannii was associated with higher rates of apoptosis via activation of caspases-3 and caspase-7, but not necrosis, in comparison to ∆ata. Ata deletion mutants were furthermore attenuated in their ability to kill larvae of Galleria mellonella and to survive in larvae when injected at sublethal doses. This indicates that Ata is an important multifunctional virulence factor in A. baumannii that mediates adhesion and invasion, induces apoptosis and contributes to pathogenicity in vivo.

14 November 2012 in PLOS ONE
Verified
Journal Article
Open access
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MIMasahito Ishikawa
Masahito Ishikawa
HNHajime Nakatani
Hajime Nakatani
Katsutoshi HoriKatsutoshi Hori
Katsutoshi Hori
Acinetobacter sp. Tol 5 exhibits an autoagglutinating nature and noteworthy adhesiveness to various abiotic surfaces from hydrophobic plastics to hydrophilic glass and stainless steel. Although previous studies have suggested that bacterionanofibers on Tol 5 cells are involved in the adhesive phenotype of Tol 5, the fiber that directly mediates Tol 5 adhesion has remained unknown. Here, we present a new member of trimeric autotransporter adhesins designated AtaA, which we discovered by analyzing a less adhesive mutant of Tol 5, T1, obtained by transposon mutagenesis. AtaA forms thinner and shorter nanofibers than fimbriae on Tol 5 cells. We performed target disruption of ataA by allelic marker exchange, and the resulting ΔataA strain was complemented with ataA on the Escherichia coli-Acinetobacter shuttle vector, which was newly constructed. These results proved that AtaA is essential for Tol 5’s autoagglutinating nature and high adhesiveness to surfaces of various materials. In addition, the adhesiveness to solid surfaces mediated by AtaA is notably higher than that mediated by YadA of Yersinia enterocolitica WA-314. Moreover, and importantly, these characteristics can be conferred to the non-adhesive, non-agglutinating bacterium Acinetobacter sp. ADP1 in trans by transformation with ataA, with expected applications to microbial immobilization.

1 January 2002 in Applied Microbiology and Biotechnology
Verified
Journal Article
Closed access
PDF file
Byoung-In SangByoung-In Sang
Byoung-In Sang
Katsutoshi HoriKatsutoshi Hori
Katsutoshi Hori
YTYasunori Tanji
Yasunori Tanji
HUH. Unno
H. Unno