Kenji Gotoh
Kurume University
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Publication
Featured researches published by Kenji Gotoh.
Journal of Hospital Infection | 2008
Nobuyuki Hamada; Kenji Gotoh; Koyu Hara; Jun Iwahashi; Yoshihiro Imamura; S. Nakamura; C. Taguchi; M. Sugita; Ryoji Yamakawa; Y. Etoh; N. Sera; Tetsuya Ishibashi; K. Chijiwa; Hiroshi Watanabe
An outbreak of acute keratoconjunctivitis involving 27 patients occurred in the Department of Ophthalmology, Kurume University Hospital. Adenoviral DNA was detected in four inpatients, one outpatient and one healthcare worker. Sequence-based typing of adenoviral DNA indicated serotype 3 from one inpatient, the rest being serotype 37. At a later stage of the outbreak adenoviral DNA types 37 and/or 3 were also detected from almost all environmental instruments and commonly used eye drops, despite thorough disinfection of the environment and enforcement of various infection control measures. The detection rate of adenoviral DNA in environmental swabs was 81%. A further second disinfection of the environment reduced the detection rate of adenoviral DNA to 38%. The outbreak ceased after closing the ophthalmology ward and outpatient consulting room, accompanied by enhanced cleaning of environmental instruments and the introduction of disposable eye drops for individual patients.
Journal of Infection and Chemotherapy | 2008
Kenji Gotoh; Liang Qin; Kiwao Watanabe; Dang Duc Anh; Phan Le Thanh Huong; Nguyen Thi Hien Anh; Nguyen Dinh Lien Cat; Luong Linh Ha; Le Thi Thuy Ai; Nguyen Manh Tien; Truong Tan Minh; Kazunori Oishi; Hiroshi Watanabe
Our study was undertaken to investigate the characteristics of Haemophilus influenzae in young children with acute lower respiratory tract infections in Nha Trang, Vietnam. The study population consisted of 116 children less than 5 years of age admitted to Khanh Hoa General Hospital due to acute lower respiratory tract infections between July 2004 and April 2005. Organisms could be detected from nasopharyngeal swabs (NP) in 72 (62.1%) of the 116 children. Haemophilus influenzae was the most common organism, and 39 strains were isolated from 39 children aged 2 to 60 months (mean age, 16 months). We examined 37 of these 39 H. influenzae strains. The serotypes of the 37 isolates were all nontypeable, and 22 strains (59.5%) were β-lactamase producing. Polymerase chain reaction (PCR) analysis to identify resistance genes revealed that 17 strains had the TEM-1-type β-lactamase gene alone, 6 strains had the ftsI gene with the same substitution as that in g low-β-lactamase-negative ampicillin-resistant (g low-BLNAR) strains, and 6 strains had both the TEM-1-type β-lactamase gene and the ftsI gene with the same substitution as that in g β-lactamase-producing amoxicillin clavulanic acid-resistant (g BLPACR I) strains, although no BLNAR strains were found. Molecular typing by pulsed-field gel electrophoresis (PFGE) showed that the 6 g low-BLNAR strains had five PFGE patterns and the 6 g BLPACR I strains had four PFGE patterns. Our results indicate that BLNAR strains are still not prevalent, but that g low-BLNAR and g BLPACR I strains are potentially spreading in Nha Trang, Vietnam.
Journal of Infection and Chemotherapy | 2013
Yusaku Uemura; Liang Qin; Kenji Gotoh; Keisuke Ohta; Kei-ichiro Nakamura; Hiroshi Watanabe
Nontypeable Haemophilus influenzae (NTHi) is an opportunistic pathogen and a common cause of otitis media in children, chronic bronchitis, and pneumonia in patients with chronic obstructive pulmonary disease. Many studies have reported that NTHi is capable of producing biofilms, which may be one of the important factors involved in chronic diseases and accelerating antimicrobial resistance. Unfortunately, there is still no consensus about the elimination of biofilms. In this study, concurrent administrations of levofloxacin (LVFX)-imipenem (IPM) and clarithromycin (CAM)-IPM, as well as the single administration of IPM, LVFX, and CAM, were performed to treat the mature biofilms produced by NTHi, respectively. Biofilm inhibition was quantified using microtiter biofilm assay (MBA), and relative biomass was calculated as the ratio compared to that of untreated control biofilms. The relative biomasses of biofilms treated with IPM, LVFX-IPM, and CAM-IPM against a β-lactamase-negative ampicillin-resistant strain was 1.10, 0.08, and 0.13 at 1× minimum inhibitory concentration (MIC), 0.90, 0.05, and 0.07 at 10× MIC, and 0.80, 0.06, and 0.07 at 100× MIC, respectively. Biofilms were also visually observed by scanning electron microscopy, and a focused ion-beam system showed that high concentrations of combined administration strongly inhibited the biofilms, which was consistent with the results of MBA. Our data demonstrated the antibiofilm effect of concurrent administration against mature NTHi biofilms, which indicated a rationale for the potential use of concurrent administrations in diseases involving chronic NTHi biofilms.
Epidemiology and Infection | 2014
Nobuyuki Hamada; Koyu Hara; Y. Matsuo; Yoshihiro Imamura; Takahito Kashiwagi; Yoko Nakazono; Kenji Gotoh; Y. Ohtsu; E. Ohtaki; T. Motohiro; Hiroshi Watanabe
Using a newly developed rapid test, an outbreak of human metapneumovirus (HMPV) infection in a long-term care facility was detected within only 2 days after the onset of symptoms in a putative index case. The outbreak was almost under control within 8 days mainly by zoning patients, with the exception of two cases of HMPV that were diagnosed 16 and 17 days after the onset of the outbreak. According to an immunological diagnosis as well as the rapid test, it was eventually proven that 18 patients had HMPV infections. We suspected that even asymptomatic residents, who had not been completely separated from the facility population, were a source of infection. That suggested that all asymptomatic residents should be tested and that the separation of the infected patients should be absolute, if an outbreak of HMPV infection is suspected in such a facility.
Journal of Infection and Chemotherapy | 2016
Yuhei Tanaka; Kenji Gotoh; Mariko Teramachi; Kazuhisa Ishimoto; Naoki Tsumura; Shizuo Shindou; Yushiro Yamashita
Here we report the molecular epidemiology of macrolide-resistant Streptococcus pyogenes (group A streptococci, GAS) isolated from children with pharyngotonsillitis between 2011 and 2013 in Japan. In 299 isolates, 124 (41.5%) isolates were macrolide-resistant. We characterized the isolates by emm typing, multilocus sequence typing (MLST), and pulsed-field gel electrophoresis (PFGE). Of 299 isolates, 124 (41.5%) were macrolide-resistant isolates, 76 (61.3%) possessed mefA and 46 (37.1%) possessed ermB. All 76 isolates with mefA possessed msrD. There were no isolates possessed ermTR in this study. Eight emm/MLST types were observed. The predominant type was emm1/ST28 (57 isolates, 46.0%), which possessed the mefA/msrD complex, presenting as the M phenotype. The second most predominant type was emm12/ST467, which possessed ermB, presenting as the cMLSB phenotype. Of the cMLSB phenotype isolates, types emm28/ST52 and emm12/ST36 had multiple genetic backgrounds. We found high proportions of macrolide-resistant GAS in the southwestern areas of Japan.
Internal Medicine | 2016
Kenichiro Yaita; Shigeru Inoue; Takashi Horinouchi; Masahiro Kinoshita; Mitsuaki Unno; Osuke Iwata; Yuhei Tanaka; Kenji Gotoh; Mikio Ishibashi; Yoshiro Sakai; Kenji Masunaga; Hiroshi Watanabe; Masaki Tominaga
A 27-year-old HIV-infected pregnant Japanese woman was admitted to our hospital at gestational week 14. The patients HIV viral load was 71,000 copies/mL, and her CD4 cell count was 147 cells/mm(3). Zidovudine, lamivudine, and lopinavir/ritonavir were administered at gestational week 18. Because the viral load increased to 222,000 copies/mL at the initiation of antiretroviral therapy, we added raltegravir. The decrease in the viral load was satisfactory, and a caesarean delivery was performed. Although the plasma concentration of raltegravir in the neonate was significantly high (2,482 ng/mL), no adverse event was confirmed. There was no evidence of the mother-to-child transmission of HIV.
Internal Medicine | 2011
Koyu Hara; Koji Yahara; Kenji Gotoh; Yoko Nakazono; Takahito Kashiwagi; Yoshihiro Imamura; Nobuyuki Hamada; Weerayut Khositsakulchai; Tippaya Sanchai; Banyong Khantawa; Prasit Tharavichitkul; Niwat Maneekarn; Thira Sirisanthana; Hiroshi Watanabe
The Journal of the Japanese Association for Infectious Diseases | 2008
Kensuke Nagai; Kenji Gotoh; Shintaro Hirotaki; Hidenobu Hidaka; Hiroyasu Koga; Masaaki Ikenaga; Kenji Masunaga; Naoki Tsumura; Koji Hashimoto
Internal Medicine | 2009
Liang Qin; Hironori Masaki; Kenji Gotoh; Akitsugu Furumoto; Mayumi Terada; Kiwao Watanabe; Hiroshi Watanabe
Diagnostic Microbiology and Infectious Disease | 2008
Masaaki Ikenaga; Klaudia Kosowska-Shick; Kenji Gotoh; Hidenobu Hidaka; Hiroyasu Koga; Kenji Masunaga; Kensuke Nagai; Naoki Tsumura; Peter C. Appelbaum; Toyojiro Matsuishi