| Literature DB >> 29233459 |
Yu Kawasaki1, Kousaku Matsubara2, Hideyuki Takahashi3, Masatomo Morita3, Makoto Ohnishi3, Masayuki Hori2, Kenichi Isome2, Aya Iwata2, Hiroyuki Nigami2, Mami Ikemachi4, Go Yamamoto4, Kiyofumi Ohkusu5.
Abstract
We present a 4-year-old girl who developed invasive meningococcal disease (IMD) caused by Neisseria meningitidis serogroup C sequence type (ST)-4821. She was hospitalized due to fever, vomiting, rash and altered consciousness. Serogroup C N. meningitidis was isolated from blood culture taken on admission and was confirmed by matrix-assisted laser desorption ionization time-of-flight mass spectrometry, a biochemical test, and molecular microbiological analysis. The patient was successfully treated with 50 mg/kg ceftriaxone every 12 hours for 7 days without any complications. The isolate was susceptible to a wide variety of β-lactams and rifampin but was resistant to ciprofloxacin. The isolate harbored gyrA T91I and parC S87I mutations at the quinolone-resistance-determining regions. Multi-locus sequence typing revealed the isolates as ST-4821, which was identical to an endemic clone frequently detected in China. However, neither the patient nor her family members had traveled abroad. To our knowledge, this report is the first to describe an IMD patient caused by ciprofloxacin-resistant N. meningitidis ST-4821 in Japan, and is the first community-acquired IMD case due to this strain outside of China. The high proportion of ciprofloxacin resistance and hypervirulent features of this ST-4821 strain raise special public health concerns. We still consider ciprofloxacin is still appropriate drug for post-exposure chemoprophylaxis in Japan. However, nationwide surveillance for susceptibility of IMD isolates is necessary to establish the regional antibiogram, and thereby to avoid chemoprophylaxis failure.Entities:
Keywords: Endemic strain; Invasive meningococcal disease; Neisseria meningitidis; Quinolone resistance; Sequence type 4821; Serogroup C
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Year: 2017 PMID: 29233459 DOI: 10.1016/j.jiac.2017.11.001
Source DB: PubMed Journal: J Infect Chemother ISSN: 1341-321X Impact factor: 2.211