Lahra Monica M, George C R Robert, van Hal Sebastiaan, Hogan Tiffany R
World Health Organisation Collaborating Centre for STI and AMR, Sydney and Neisseria Reference Laboratory, Department of Microbiology, NSW Health Pathology, The Prince of Wales Hospital, Randwick, 2031, NSW Australia.
School of Medical Sciences, Faculty of Medicine, The University of New South Wales, NSW, 2052 Australia.
Commun Dis Intell (2018). 2024 Dec 18;48. doi: 10.33321/cdi.2024.48.52.
In Australia, both probable and laboratory-confirmed cases of invasive meningococcal disease (IMD) are reported to the National Notifiable Diseases Surveillance System (NNDSS). When compared to 2022, the number of IMD notifications in 2023 increased by 14% to 143. Laboratory confirmation of IMD occurred in 140/143 (98%) of these cases, with 64% (90/140) diagnosed by bacterial culture and 36% (50/140) by nucleic acid amplification testing. The serogroup was determined for 96% of laboratory-confirmed cases (134/140): serogroup B (MenB) accounted for 84% of infections (112/134); MenW for 8% (11/134); MenY for 8% (11/134). There were no infections attributed to MenC disease. Fine typing was available on 75% of the cases for which the serogroup was determined (100/134). In MenB isolates, 25 types were detected, the most prevalent of which were P1.7-2,4 (32%; 26/82), P1.7,16-26 (16%; 13/82) and P1.22,14 (9%; 7/82). All eight typed MenW infections identified as type P1.5,2, with two different multi-locus sequence types (MLST) present: ST-11 (5) and ST-1287 (3) from the clonal complex 11, the hypervirulent strain reported in outbreaks in Australia and overseas. In MenY, the predominant type was P1.5-1,10-1 (90%; 9/10), ST-1655 and from clonal complex 23. Peaks of IMD occurred in children aged less than 5 years and in those aged 15-24 years, accounting for 21% (30/140) and 26% (37/140) of laboratory-confirmed cases respectively. In children aged under 5 years, 93% of IMD (27/29) was MenB; in those aged 15-24 years, 97% of IMD (36/37) was MenB, with serogroup not determined for one case in each of these age groups. Of note, 14-15% of IMD occurred in each of the older age groups reported: adults 25-44 years (14%, 19/140), 45-64 years (14%, 20/140), and in those aged 65 years and older (15%, 21/140). Whilst MenB predominated in all age groups, the majority of MenY and MenW IMD cases were reported in adults aged 45 years and older. All cultured IMD isolates (n = 90) had antimicrobial susceptibility testing performed. Minimum inhibitory concentration (MIC) values were reported using Clinical Laboratory Standards Institute (CLSI) interpretative criteria: 9% (8/90) were defined as penicillin resistant (MIC value: ≥ 0.5 mg/L); 71% (64/90) had intermediate susceptibility to penicillin (MIC values: 0.125 and 0.25 mg/L) and 20% (18/90) were susceptible to penicillin (MIC values: ≤ 0.064 mg/L). All isolates tested susceptible to ceftriaxone, ciprofloxacin and rifampicin.
在澳大利亚,侵袭性脑膜炎球菌病(IMD)的疑似病例和实验室确诊病例均需上报至国家法定传染病监测系统(NNDSS)。与2022年相比,2023年IMD的上报病例数增加了14%,达到143例。其中140/143(98%)的病例通过实验室确诊为IMD,64%(90/140)的病例通过细菌培养确诊,36%(50/140)的病例通过核酸扩增检测确诊。96%(134/140)的实验室确诊病例确定了血清群:B群脑膜炎球菌(MenB)占感染病例的84%(112/134);W群脑膜炎球菌占8%(11/134);Y群脑膜炎球菌占8%(11/134)。未发现C群脑膜炎球菌病感染病例。在确定血清群的病例中,75%(100/134)的病例进行了精细分型。在MenB分离株中,检测到25种类型,其中最常见的是P1.7-2,4(32%;26/82)、P1.7,16-26(16%;13/82)和P1.22,14(9%;7/82)。所有8例分型的MenW感染均鉴定为P1.5,2型,存在两种不同的多位点序列类型(MLST):来自克隆复合体11的ST-11(5例)和ST-1287(3例),该克隆复合体是在澳大利亚和海外疫情中报告的高毒力菌株。在Y群脑膜炎球菌中,主要类型是P1.5-1,10-1(90%;9/10),ST-1655,来自克隆复合体23。IMD发病高峰出现在5岁以下儿童和15-24岁人群中,分别占实验室确诊病例的21%(30/140)和26%(37/140)。在5岁以下儿童中,93%(27/29)的IMD病例是MenB;在15-24岁人群中,97%(36/37)的IMD病例是MenB,这两个年龄组各有1例病例血清群未确定。值得注意的是,在报告的每个老年组中,14%-15%的IMD病例发生在25-44岁的成年人(14%,19/140)、45-64岁的成年人(14%,20/140)以及65岁及以上的老年人(15%,21/140)中。虽然MenB在所有年龄组中占主导地位,但大多数MenY和MenW IMD病例报告发生在45岁及以上的成年人中。所有培养的IMD分离株(n = 90)均进行了药敏试验。使用临床实验室标准协会(CLSI)的解释标准报告最低抑菌浓度(MIC)值:9%(8/90)被定义为对青霉素耐药(MIC值:≥ 0.5 mg/L);71%(64/90)对青霉素中度敏感(MIC值:0.125和0.25 mg/L),20%(18/90)对青霉素敏感(MIC值:≤ 0.064 mg/L)。所有分离株对头孢曲松钠、环丙沙星和利福平均敏感。