Hiroyuki Katayama

ORCID: 0000-0002-3429-9069
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About
Contact & Profiles
Research Areas
  • Viral gastroenteritis research and epidemiology
  • SARS-CoV-2 detection and testing
  • Membrane Separation Technologies
  • Coastal and Marine Dynamics
  • Bacteriophages and microbial interactions
  • Viral Infections and Immunology Research
  • Fecal contamination and water quality
  • Animal Virus Infections Studies
  • Respiratory viral infections research
  • Parasitic Infections and Diagnostics
  • Biosensors and Analytical Detection
  • Water Treatment and Disinfection
  • Aquatic Ecosystems and Phytoplankton Dynamics
  • Marine and coastal ecosystems
  • Virus-based gene therapy research
  • Pharmaceutical and Antibiotic Environmental Impacts
  • Biocrusts and Microbial Ecology
  • Earthquake and Tsunami Effects
  • Electrospun Nanofibers in Biomedical Applications
  • Membrane-based Ion Separation Techniques
  • Legionella and Acanthamoeba research
  • Listeria monocytogenes in Food Safety
  • Microbial Community Ecology and Physiology
  • Nanopore and Nanochannel Transport Studies
  • Ocean Waves and Remote Sensing

The University of Tokyo
2016-2025

Penta-Ocean Construction (Japan)
2003-2024

Kyoto University
2023

Bunkyo University
2019

Mitsubishi Heavy Industries (Germany)
2018

IHI Corporation (United States)
2018

Vietnam National University, Hanoi
2018

University of Yamanashi
2010

National Institute of Infectious Diseases
2010

National Archives and Records Administration
2008

ABSTRACT We developed a new procedure for concentration of enteric viruses from water using negatively charged membrane. Rinsing the membrane with 0.5 mM H 2 SO 4 (pH 3.0) in order to elute cations prior viral elution 1 NaOH 10.5) promoted poliovirus recovery yields 33 95% when applied pure and 38 89% natural seawater Tokyo Bay, Japan, respectively. This method showed average spiked 62% ( n = 8) liter artificial seawater. higher (>61%) than that conventional positively (6%) is also free...

10.1128/aem.68.3.1033-1039.2002 article EN Applied and Environmental Microbiology 2002-03-01

ABSTRACT Pepper mild mottle virus (PMMoV) is a plant that has been recently proposed as potential indicator of human fecal contamination environmental waters; however, information on its geographical occurrence in surface water still limited. We aimed to determine the seasonal and geographic PMMoV drinking sources all over Japan. Between July 2008 February 2011, 184 source samples were collected from 30 treatment plants (DWTPs); viruses 1 2 liters each sample concentrated by using an...

10.1128/aem.02354-13 article EN Applied and Environmental Microbiology 2013-09-21

The current situation of COVID-19 measures makes it difficult to accurately assess the prevalence SARS-CoV-2 due a decrease in reporting rates, leading missed initial transmission events and subsequent outbreaks. There is growing recognition that wastewater virus data assist estimating potential infections, including asymptomatic unreported infections. Understanding hidden behind reported cases critical for decision-making when choosing appropriate social intervention measures. However,...

10.1098/rsif.2024.0456 article EN Journal of The Royal Society Interface 2025-01-01

The occurrence of human enteric viruses in surface water the Tamagawa River, Japan, was surveyed for 1 year, from April 2003 to March 2004. Sixty-four samples were collected six sites along river, and 500 ml sample concentrated using cation-coated filter method, which developed our previous study. This method showed recovery yields 56% +/- 32% (n = 37) inoculated with polioviruses. More than one kind tested virus detected 43 (67%) 64 by TaqMan PCR. Noroviruses adenoviruses a high positive...

10.1128/aem.71.5.2403-2411.2005 article EN Applied and Environmental Microbiology 2005-05-01

Photoreactivation of Escherichia coli after inactivation by a low-pressure (LP) UV lamp (254 nm), medium-pressure (MP) (220 to 580 or filtered (MPF) (300 nm) was investigated. An endonuclease sensitive site (ESS) assay used determine the number UV-induced pyrimidine dimers in genomic DNA E. coli, while conventional cultivation investigate colony-forming ability (CFA) coli. In photoreactivation experiments, more than 80% induced LP MPF irradiation were repaired, almost no repair observed MP...

10.1128/aem.68.12.6029-6035.2002 article EN Applied and Environmental Microbiology 2002-11-26

To evaluate and compare the reductions of human viruses F-specific coliphages in a full-scale wastewater treatment plant based on quantitative PCR (qPCR) plate count assays.A total 24 water samples were collected from four locations at plant, relative abundance F-RNA phage genogroups determined by qPCR. Of 10 types tested, enteric adenoviruses most prevalent both influent effluent samples. different steps, activated sludge process was effective reducing microbial loads. Viruses phages showed...

10.1111/jam.12051 article EN Journal of Applied Microbiology 2012-11-22

The primary concentration and molecular process are critical to implement wastewater-based epidemiology for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). However, the previously developed methods were optimized nonenveloped viruses. Few studies evaluated if applicable efficient recovery of enveloped viruses from various types raw sewage. This study aims (1) compare whole Pseudomonas phage φ6, a surrogate viruses, among combinations [ultrafiltration (UF), electronegative...

10.1016/j.scitotenv.2020.143067 article EN cc-by-nc-nd The Science of The Total Environment 2020-10-17

Polyethylene glycol (PEG) precipitation is one of the conventional methods for virus concentration. This technique has been used to detect severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) RNA in wastewater. The procedures and seeded surrogate viruses were different among implementers; thus, reported whole process recovery efficiencies considerably varied studies. present study compared five PEG procedures, with operational parameters, RT-qPCR-based efficiency murine hepatitis...

10.1016/j.scitotenv.2021.150722 article EN cc-by-nc-nd The Science of The Total Environment 2021-10-04

ABSTRACT UV inactivation, photoreactivation, and dark repair of Escherichia coli Cryptosporidium parvum were investigated with the endonuclease sensitive site (ESS) assay, which can determine UV-induced pyrimidine dimers in genomic DNA microorganisms. In a 99.9% inactivation E. , high correlation was observed between dose irradiation number induced . The colony-forming ability also correlated highly DNA, indicating that ESS assay is comparable to method conventionally used measure ability....

10.1128/aem.67.10.4630-4637.2001 article EN Applied and Environmental Microbiology 2001-10-01

ABSTRACT A virus concentration method using a cation-coated filter was developed for large-volume freshwater applications. Poliovirus type 1 (LSc 2ab Sabin strain) inoculated into 40 ml of MilliQ (ultrapure) water adsorbed effectively to negatively charged (Millipore HA, 0.45-μm pore size) coated with aluminum ions, 99% (range, 81 114%) which were recovered by elution 1.0 mM NaOH (pH 10.8) following an acid rinse 0.5 H 2 SO 4 3.0). More than 80% poliovirus recovery yields obtained from...

10.1128/aem.70.4.2154-2160.2004 article EN Applied and Environmental Microbiology 2004-04-01

The seasonal profiles of microorganisms in raw sewage, secondary-treated and final effluent at a wastewater treatment plant Tokyo, Japan, were quantitatively determined each month for one year, from July 2003 to June 2004. Human noroviruses, which by real-time PCR, sewage varied 0.17–260 copies/mL genotype 1 2.4–1900 2, showing much higher values winter, the epidemic season. concentration total coliforms, Escherichia coli, or F-specific phages was almost constant throughout year. noroviruses...

10.2166/wst.2006.888 article EN Water Science & Technology 2006-09-08

Aims: The aim of this study was to determine human adenoviruses (HuAdVs) in aquatic environments by real‐time polymerase chain reaction (PCR). Methods and Results: In order describe the ratio enteric serotypes total HuAdVs, primer set specific for 40 41 used parallel with universal all 51 HuAdVs. HuAdVs were detected at concentration 7·3–1500 PCR‐detection units (PDU) per ml raw sewage (n = 17), 0·00060–4·1 PDU ml−1 secondary‐treated before chlorination 0·0018–7·0 river water 36), 0·032–6·1...

10.1111/j.1365-2672.2007.03453.x article EN Journal of Applied Microbiology 2007-08-30

Inhibitors that reduce viral nucleic acid extraction efficiency and interfere with cDNA synthesis and/or polymerase activity affect the molecular detection of viruses in aquatic environments. To overcome these significant problems, we developed a methodology for assessing yields DNA amplification efficiencies environmental water samples. This involved adding particles adenovirus type 5 murine norovirus newly primer-sharing controls, which are amplified same primer pairs result amplicon sizes...

10.1128/aem.00077-11 article EN Applied and Environmental Microbiology 2011-05-21

ABSTRACT Aichi viruses (AiVs) have been proposed as a causative agent of human gastroenteritis potentially transmitted by fecal-oral routes through contaminated food or water. In the present study, we developed TaqMan minor groove binder (MGB)-based reverse transcription-quantitative PCR (RT-qPCR) system that is able to quantify AiVs and differentiate between genotypes A B. This consists two assays, an AiV universal assay utilizing primer pair probe duplex genotype-specific same probes. The...

10.1128/aem.00820-13 article EN Applied and Environmental Microbiology 2013-04-20

ABSTRACT To evaluate the effectiveness of UV irradiation in inactivating Cryptosporidium parvum oocysts, animal infectivities and excystation abilities oocysts that had been exposed to various doses were determined. Infectivity decreased exponentially as dose increased, required for a 2-log 10 reduction infectivity (99% inactivation) was approximately 1.0 mWs/cm 2 at 20°C. However, C. exhibited high resistance irradiation, requiring an extremely 230 excystation, which used assess viability....

10.1128/aem.68.11.5387-5393.2002 article EN Applied and Environmental Microbiology 2002-11-01
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