Masashi Nakamatsu
University of the Ryukyus
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International Journal of Infectious Diseases | 2017
Tatsuya Tada; Kohei Uechi; Isamu Nakasone; Kayo Shimada; Masashi Nakamatsu; Teruo Kirikae; Jiro Fujita
The mcr-1 is a gene encoding a phosphoethanolamine transferase, which confers resistance to colistin by transferring phosphoethanolamine to lipid A. We describe here the emergence of a colistin-resistant Escherichia coli clinical isolate harboring plasmid-mediated mcr-1 in Japan. The isolate belonged to ST5702 and is suspected to come from livestock and transmitted to human. This is the first report of a clinical isolate harboring mcr-1 in Japan.
Journal of Medical Virology | 2017
Daijiro Nabeya; Takeshi Kinjo; Gretchen Parrott; Ayako Uehara; Daisuke Motooka; Shota Nakamura; Saifun Nahar; Sawako Nakachi; Masashi Nakamatsu; Sakuko Maeshiro; Shusaku Haranaga; Masao Tateyama; Takeaki Tomoyose; Hiroaki Masuzaki; Toshihiro Horii; Jiro Fujita
Although many reports have already shown RSV outbreaks among hemato‐oncology patients, genomic studies detecting similar RSV strains prior to an outbreak in the hospital are rare. In 2014, the University of the Ryukyus hospital hemato‐oncology unit experienced, and successfully managed, a respiratory syncytial virus (RSV) nosocomial outbreak. During the outbreak investigation, genotyping and phylogenetic analysis was used to identify a potential source for the outbreak. Nasopharyngeal swabs were tested for RSV using three tests: (1) rapid antigen test (RAT); (2) reverse transcriptase polymerase chain reaction (PCR); or (3) quantitative PCR (RT‐qPCR); a positive PCR reaction was considered a confirmed case of RSV. Phylogenetic analysis of the G protein was performed for outbreak and reference samples from non‐outbreak periods of the same year. In total, 12 confirmed cases were identified, including 8 hemato‐oncology patients. Patient samples were collected weekly, until all confirmed RSV cases returned RSV negative test results. Median time of suspected viral shedding was 16 days (n = 5, range: 8‐37 days). Sensitivity and specificity of the RAT compared with RT‐qPCR were 30% and 91% (n = 42). Phylogenetic analysis revealed nine genetically identical strains; eight occurring during the outbreak time period and one strain was detected 1 month prior. A genetically similar RSV detected 1 month before is considered one potential source of this outbreak. As such, healthcare providers should always enforce standard precautions, especially in the hemato‐oncology unit.
International Journal of Infectious Diseases | 2018
Tatsuya Tada; Kohei Uechi; Isamu Nakasone; Masashi Nakamatsu; Kazuhito Satou; Takashi Hirano; Teruo Kirikae; Jiro Fujita
The mcr-1 gene encodes a phosphoethanolamine transferase that confers resistance to colistin by transferring phosphoethanolamine to lipid A. A 33-kb IncX4 plasmid harboring mcr-1 was detected in a Klebsiella pneumoniae isolate and two Escherichia coli isolates, and a 66-kb IncI2 plasmid was detected in three E. coli isolates in hospitals in Okinawa, Japan.
Journal of General and Family Medicine | 2015
Satoko Sunagawa; Jiro Fujita; Miyuki Tomishima; Sakiko Mukatake; Masashi Nakamatsu; Futoshi Higa; Masao Tateyama; Tomoko Owan
Influenza virus infection in hospitals is a very important clinical issue. The objective of this study was to describe the effect of oseltamivir in controlling a nosocomial influenza virus infection with an observational study and case report. Intervention was carried out in a ward of the University of the Ryukyus Hospital. Symptomatic staff members were sent home for one week, and the infected inpatients were isolated. In addition, in an episode of influenza infection among the staff members and inpatients, oseltamivir (75 mg once a day for 7 days) was administered to all staff members as well as inpatients who had had close contact with the influenza patients. In the hospital ward, eight staff members (nurses and doctors) and ten hospitalized patients were definitively diagnosed with influenza A viral infection based on results of a rapid diagnostic test. Although a relatively large number of the staff members and inpatients had an influenza virus infection, it was possible that the use of oseltamivir efficiently minimized a nosocomial outbreak. It was very difficult to diagnose influenza A virus infection based on clinical symptoms. It was possible to minimize and end the outbreak immediately by using oseltamivir prophylaxis. With a review of the literature, it is considered that prophylaxis with anti‐influenza drugs are highly recommended in hospital settings.
Microbes and Infection | 2007
Masashi Nakamatsu; Natsuo Yamamoto; Masumitsu Hatta; Chikara Nakasone; Takeshi Kinjo; Kazuya Miyagi; Kaori Uezu; Kiwamu Nakamura; Toshinori Nakayama; Masaru Taniguchi; Yoichiro Iwakura; Mitsuo Kaku; Jiro Fujita; Kazuyoshi Kawakami
Microbes and Infection | 2007
Chikara Nakasone; Natsuo Yamamoto; Masashi Nakamatsu; Takeshi Kinjo; Kazuya Miyagi; Kaori Uezu; Kiwamu Nakamura; Futoshi Higa; Hiromichi Ishikawa; Rebecca L. O'Brien; Koichi Ikuta; Mitsuo Kaku; Jiro Fujita; Kazuyoshi Kawakami
Microbes and Infection | 2004
Natsuo Yamamoto; Kazuyoshi Kawakami; Yuki Kinjo; Kazuya Miyagi; Takeshi Kinjo; Kaori Uezu; Chikara Nakasone; Masashi Nakamatsu; Atsushi Saito
Microbes and Infection | 2006
Takeshi Kinjo; Masashi Nakamatsu; Chikara Nakasone; Natsuo Yamamoto; Yuki Kinjo; Kazuya Miyagi; Kaori Uezu; Kiwamu Nakamura; Futoshi Higa; Masao Tateyama; Kazuyoshi Takeda; Toshinori Nakayama; Masaru Taniguchi; Mitsuo Kaku; Jiro Fujita; Kazuyoshi Kawakami
International Journal of Infectious Diseases | 2016
Jun Hirai; Takeshi Kinjo; T. Tome; Kohei Uechi; Masashi Nakamatsu; Shusaku Haranaga; Jiro Fujita
Journal of Immunology | 2007
Masumitsu Hatta; Masashi Nakamatsu; Chikara Nakasone; Jiro Fujita; Mitsuo Kaku; Kazuyoshi Kawakami