Australian Meningococcal Surveillance Programme Annual Report, 2022

Authors

  • Monica M Lahra 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
  • CR Robert George NSW Health Pathology, John Hunter Hospital, Newcastle, 2300, NSW Australia
  • Sebastiaan van Hal New South Wales Health Pathology, Microbiology, Royal Prince Alfred Hospital Camperdown, NSW, Australia; School of Medicine, University of Sydney
  • Tiffany R Hogan 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

DOI:

https://doi.org/10.33321/cdi.2023.47.44

Keywords:

antimicrobial resistance, disease surveillance, invasive meningococcal disease, Neisseria meningitidis

Abstract

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 notifications, 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 inhibitory concentration (MIC) values were categorised using Clinical Laboratory Standards Institute (CLSI) interpretative criteria: 5% (3/62) were defined as penicillin resistant (MIC value ≥ 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.

Downloads

Download data is not yet available.

References

National Neisseria Network. Meningococcal Isolate Surveillance Australia 1994. Commun Dis Intell. 1995;19(12):286–9.

Australian Government Department of Health and Aged Care. National Notifiable Diseases Surveillance System (NNDSS) data visualisation tool. [Webpage.] Canberra: Australian Government Department of Health and Aged Care; 14 December 2022. [Accessed on 10 May 2023.] Available from: https://www.health.gov.au/resources/apps-and-tools/national-notifiable-diseases-surveillance-system-nndss-data-visualisation-tool.

National Notifiable Diseases Surveillance System (NNDSS). Number of notifications of Meningococcal disease (invasive), received from State and Territory health authorities in the period of 1991 to 2012 and year-to-date notifications for 2014–2021. Available from: http://www9.health.gov.au/cda/source/rpt_4_sel.cfm.

Australian Government Department of Health and Aged Care. Invasive meningococcal disease. [Internet.] Canberra: Australian Government Department of Health and Aged Care; 12 July 2022. Available from: https://www.health.gov.au/internet/main/publishing.nsf/Content/ohp-meningococcal-W.htm.

Australian Government Department of Health and Aged Care, Communicable Diseases Network Australia (CDNA). Invasive Meningococcal Disease: CDNA National Guidelines for Public Health Units. Canberra: Australian Government Department of Health and Aged Care; 4 July 2017. Available from: https://www.health.gov.au/sites/default/files/documents/2020/02/invasive-meningococcal-disease-cdna-national-guidelines-for-public-health-units.pdf.

George CRR, Smith HV, Lahra MM. Neisseria meningitidis. In de Filippis I, ed. Molecular Typing in Bacterial Infections, Volume I. London: Springer International Publishing, Springer Cham, 2022;85–99.

Clinical and Laboratory Standards Institute (CLSI). Performance standards for antimicrobial susceptibility testing. 32nd ed. CLSI supplement M100. Wayne, PA: CLSI; 2022.

Lahra MM, George CRR, Hogan TR for the National Neisseria Network. Australian Meningococcal Surveillance Programme Annual Report, 2021. Commun Dis Intell (2018). 2022;46. doi: https://doi.org/10.33321/cdi.2022.46.46.

Abad R, López EL, Debbag R, Vázquez JA. Serogroup W meningococcal disease: global spread and current affect on the Southern Cone in Latin America. Epidemiol Infect. 2014;142(12):2461–70. doi: https://doi.org/10.1017/S0950268814001149.

Ladhani SN, Beebeejaun K, Lucidarme J, Campbell H, Gray S, Kaczmarski E et al. Increase in endemic Neisseria meningitidis capsular group W sequence type 11 complex associated with severe invasive disease in England and Wales. Clin Infect Dis. 2015;60(4):578–85. doi: https://doi.org/10.1093/cid/ciu881.

George CR, Booy R, Nissen MD, Lahra MM. The decline of invasive meningococcal disease and influenza in the time of COVID-19: the silver linings of the pandemic playbook. Med J Aust. 2022. doi: https://doi.org/10.5694/mja2.51463.

Chiu C, Dey A, Wang H, Menzies R, Deeks S, Mahajan D et al. Vaccine preventable diseases in Australia, 2005 to 2007. Commun Dis Intell Q Rep. 2010;34(Suppl):S1–167.

Australian Government Department of Health and Aged Care. Immunise Australia Program. Meningococcal Disease. [Internet.] Canberra: Australian Government Department of Health and Aged Care; 20 April 2015. Available from: https://www.health.gov.au/internet/immunise/publishing.nsf/Content/immunise-meningococcal.

Araya P, Fernández J, Del Canto F, Seoane M, Ibarz-Pavón AB, Barra G et al. Neisseria meningitidis ST-11 clonal complex, Chile 2012. Emerg Infect Dis. 2015;21(2):339–41. doi: https://doi.org/10.3201/eid2102.140746.

Bröker M, Jacobsson S, Kuusi M, Pace D, Simões MJ, Skoczynska A et al. Meningococcal serogroup Y emergence in Europe: update 2011. Hum Vaccin Immunother. 2012;8(12):1907–11. doi: https://doi.org/10.4161/hv.21794.

a Source: National Notifiable Diseases Surveillance System. Data extracted 10 May 2023.

Downloads

Published

24/08/23

How to Cite

Lahra , Monica M, CR Robert George, Sebastiaan van Hal, and Tiffany R Hogan. 2023. “Australian Meningococcal Surveillance Programme Annual Report, 2022 ”. Communicable Diseases Intelligence 47 (August). https://doi.org/10.33321/cdi.2023.47.44.

Most read articles by the same author(s)

1 2 3 4 5 6 7 8 9 10 > >>