Lahra Monica M, Enriquez Rodney P
WHO Collaborating Centre for STD, Microbiology Department, South Eastern Area Laboratory Services, The Prince of Wales Hospital, Sydney, New South Wales; The School of Medical Sciences, The University of New South Wales, Sydney, New South Wales.
WHO Collaborating Centre for STD, Microbiology Department, South Eastern Area Laboratory Services, The Prince of Wales Hospital, Sydney, New South Wales.
Commun Dis Intell Q Rep. 2013 Sep 30;37(3):E224-32.
In 2012, there were 208 laboratory-confirmed cases of invasive meningococcal disease (IMD) analysed by the National Neisseria Network, and 222 cases notified to the National Notifiable Diseases Surveillance System, thus laboratory data were available for 93.7% of cases of IMD in Australia in 2012. Isolates of Neisseria meningitidis from 116 invasive cases of meningococcal disease were available for testing, and the phenotype (serogroup, serotype and serosubtype) and/or genotype, and antibiotic susceptibility were determined. Molecular typing was performed for the 92 cases confirmed by nucleic acid amplification testing (NAAT). Typing information was available for 194 of the 208 laboratory confirmed cases and 83% (161 cases) were serogroup B infections, 5.7% (11 cases) were serogroup C infections, 3.6% (11 cases) were serogroup W135, and 7.7% (15 cases) were serogroup Y meningococci. The number of laboratory confirmed IMD cases in 2012 was the lowest since laboratory surveillance data have been reported. Primary and secondary disease peaks were observed in those aged 4 years or less and in adolescents (15-19 years) and young adults (20-24 years), respectively. Serogroup B cases predominated in all age groups and jurisdictions. In 2012, the most common porA genotype circulating in Australia was P1.7-2,4. Serogroup C, W135 and Y cases were numerically low, similar to previous years. Decreased susceptibility to the penicillin group of antibiotics was observed in 81.9% of isolates, and 1 isolate exhibited resistance to penicillin. All isolates remained susceptible to ceftriaxone, ciprofloxacin and rifampicin.
2012年,国家奈瑟菌网络分析了208例实验室确诊的侵袭性脑膜炎球菌病(IMD)病例,国家法定传染病监测系统通报了222例病例,因此2012年澳大利亚93.7%的IMD病例有实验室数据。从116例侵袭性脑膜炎球菌病病例中分离出的脑膜炎奈瑟菌可供检测,并确定了其表型(血清群、血清型和血清亚型)和/或基因型以及抗生素敏感性。对92例经核酸扩增检测(NAAT)确诊的病例进行了分子分型。在208例实验室确诊病例中,有194例获得了分型信息,其中83%(161例)为B血清群感染,5.7%(11例)为C血清群感染,3.6%(11例)为W135血清群,7.7%(15例)为Y血清群脑膜炎球菌。2012年实验室确诊的IMD病例数是自报告实验室监测数据以来的最低水平。分别在4岁及以下儿童以及青少年(15 - 19岁)和青年成人(20 - 24岁)中观察到原发性和继发性疾病高峰。B血清群病例在所有年龄组和辖区中均占主导地位。2012年,澳大利亚流行的最常见porA基因型是P1.7 - 2,4。C、W135和Y血清群病例数量较少,与前几年相似。在81.9%的分离株中观察到对青霉素类抗生素的敏感性降低,1株分离株对青霉素耐药。所有分离株对头孢曲松、环丙沙星和利福平仍敏感。