Australian Meningococcal Surveillance Programme Annual Report, 2022

被引:1
|
作者
Lahra, Monica M. [1 ,2 ,6 ,7 ]
George, Robert [3 ]
Hal, Sebastiaan J. van [4 ,5 ]
机构
[1] World Hlth Org Collaborating Ctr STI & AMR, Sydney, Australia
[2] Univ New South Wales, Fac Med cine, Sch Med Sci, Sydney, NSW 2052, Australia
[3] John Hunter Hosp, NSW Hlth Pathol, Newcastle, NSW 2300, Australia
[4] Royal Prince Alfred Hosp, New South Wales Hlth Pathol, Dept Microbiol & Infect Dis, Sydney, NSW, Australia
[5] Univ Sydney, Sch Med, Sydney, Australia
[6] Prince Wales Hosp, Dept Neisseria Reference Lab, NSW Hlth Pathol, Level 4,Campus Ctr, Randwick, NSW 2031, Australia
[7] Prince Wales Hosp, WHO Collaborating Ctr STI & AMR, Level 4,Campus Ctr, Randwick, NSW 2031, Australia
关键词
antimicrobial resistance; disease surveillance; invasive meningococcal disease; Neisseria meningitidis; DISEASE; COMPLEX;
D O I
10.33321/cdi.2023.47.44
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
In Australia, both probable and laboratory-confirmed cases of invasive meningococcal disease (IMD) are reported to the National Notifiable Diseases Surveillance System (NNDSS). Compared to 2021, the number of IMD notifications in 2022 increased by 81% to 127, alongside the easing of COVID-19 containment measures. Laboratory confirmation occurred in 95% of these cases, with 51% (62/121) diagnosed by bacterial culture and 49% (59/121) by nucleic acid amplification testing. The serogroup was determined for 97% of laboratory-confirmed cases (117/121): serogroup B (MenB) accounted for 83% of infections (100/121); MenW for 4% (5/121); MenY for 10% (12/121); no infections were attributed to MenC disease. Fine typing was available on 67% of the cases for which the serogroup was determined (78/117). In MenB isolates, 27 porA types were detected, the most prevalent of which were P1.7-2,4 (18%;11/62), P1.22,14 (15%; 9/62), P1.18-1,34 (10%; 6/62) and P1.7,16-26 (10%; 6/62). All five MenW infections identified as porA type P1.5,2 with different MLST sequence types (ST): 11, 574, 1287, 12351, 13135 all belonging to clonal complex 11, the hypervirulent strain reported in outbreaks in Australia and overseas. In MenY, the predominant porA type was P1.5-1,10-1 (73%; 8/11), ST 1655 and from clonal complex 23.Children less than 5 years of age and people aged 15-19 years were overrepresented with IMD noti-fications, accounting for 22% (27/121) and 23% (28/121) of laboratory-confirmed cases respectively. Fifteen percent of laboratory-confirmed notifications (18/121) were in persons aged 45-64 years. MenB infections were detected in all age groups but predominated in persons aged 15-19 years (93% of IMD in this age group; 26/28) and comprised 89% (24/27) of infections in children aged less than 5 years. MenW infections were markedly reduced in 2022, accounting for two IMD detections in children 1-4 years (2/16) and sporadic detections in other older age groups. MenY infections were largely detected in adults aged 45-64 years, accounting for 28% of IMD in this age group (5/18).All 62 cultured IMD isolates had antimicrobial susceptibility testing performed. Minimum inhibi-tory concentration (MIC) values were categorised using Clinical Laboratory Standards Institute (CLSI) interpretative criteria: 5% (3/62) were defined as penicillin resistant (MIC value & GE; 0.5 mg/L); 71% (44/62) had intermediate susceptibility to penicillin (MIC values 0.125 and 0.25 mg/L) and 24% (15/62) were susceptible to penicillin. All isolates were susceptible to ceftriaxone, ciprofloxacin and rifampicin.
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