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Vol. 24. Issue 4.
Pages 349-351 (July - August 2020)
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Vol. 24. Issue 4.
Pages 349-351 (July - August 2020)
Brief communication
Open Access
Trajectory of serogroups causing Invasive Meningococcal Disease in Santa Catarina state, Brazil (2007–2019)
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Ricardo Becker Feijoa,
Corresponding author
rfeijo@hcpa.edu.br

Corresponding author at: Rua Attilio Bilibio 120/23, 91530008 Porto Alegre, RS, Brazil.
, Juarez Cunhab
a Universidade Federal do Rio Grande do Sul, Faculdade de Medicina, Departamento de Pediatria, Porto Alegre, RS, Brazil
b Secretaria Municipal de Saúde, Diretoria Geral de Vigilância em Saúde, Unidade de Vigilância Epidemiológica, Porto Alegre, RS, Brazil
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Table 1. Meningococcal serogroup distribution during the period of 2007-2019.
Abstract

The aim of this study was to compare the trajectory of serogroups causing Invasive Meningococcal Disease (IMD) in the Santa Catarina (SC) state with those of whole Brazil. A retrospective analysis of all IMD cases reported from January 2007 to December 2019 was carried out. During the study period, 26,058 IMD cases were registered in Brazil and 644 and in SC state alone. Overall, Brazil showed progressive reduction in cases since 2010, when the meningococcal C conjugate vaccine was introducted on National Immunization Program, while SC showed an increase in total cases since 2013, particularly from serogroups W and C. Serogroups distribution was significantly different between Brazil and SC. The emergence of serogroup W highlights the improved meningococcal surveillance through increased accuracy in identification methods in SC state. This finding is important for discussing recommendations of quadrivalent (ACWY) conjugate vaccines in different geographical areas of Brazil.

Keywords:
Invasive meningococcal disease
Serogroup W
Santa Catarina state
Brazil
Full Text

Neisseria meningitidis (N. meningitidis) causes extremely severe conditions in humans, especially invasive meningococcal disease (IMD) characterized by one or more clinical syndromes including bacteremia, sepsis, or meningitis, the latter being the most common presentation.1

Capsular groups A, B, C, W, Y, and X cause almost all IMD.2 However, the quality and reliability of the information on IMD are not uniform across the world, due in part to differences in surveillance practices, use of different diagnostic methods and protocols, and application of different meningococcal case definition.3 Since late 1960s capsular group W has become a frequent cause of IMD,4 particularly in Europe, South America, Australia, and some parts of Sub-Saharan Africa.5

The highest incidence rates of IMD are observed in children aged less than one year,6,7 but in some regions other incidence peaks are observed among adolescents (16 through 21 years of age)8,9 and those aged ≥65 years.10,11 In Latin America, the incidence of IMD varies from <0.1 cases per 100,000 in countries including Mexico, Paraguay, Peru, and Bolivia to almost two cases per 100,000 in Brazil.7 In Brazil, N. meningitidis was the primary etiology of acute bacterial meningitis with serogroup C being the most prevalent in the country. In 2010, the National Immunization Program (NIP) included the MenC conjugate vaccine for children under two years old, with no catch-up campaign in older ages groups. Based on the significant IMD reduction observed only in the vaccinated group, the Ministry of Health decided to include MenC vaccine for adolescents aged 11–14 years in 2017.12

The introduction of multiplex real-time PCR (polymerase chain reaction) (RT-PCR) assay testing for S. pneumoniae, N. meningitidis and H. influenzae type B in sentinel hospitals in São Paulo increased the diagnostic yield for bacterial meningitis by 52, 85 and 20%, respectively, over culture-based methods.13 Since then, there has been a progressive increase in the use of PCR assays with improvement in microbiologic confirmation of bacterial meningitis throughout the country.

IMD is associated with substantial morbidity and overall case fatality rates (CFRs) of around 10% (with CFRs as high as 20% reported in some countries).14 Meningococcal disease caused by serogroup W alone has been associated with CFRs of >30%.15

Serogroups B and C are currently dominant in Latin America. Nevertheless, the proportion of IMD cases including outbreaks attributable to other serogroups have been reported in several countries.16 Southern Brazil, Argentina and Chile witnessed the emergence of MenW cc11 strain as a major cause of endemic meningococcal disease after 2003.17 The states of Parana, Santa Catarina and Rio Grande do Sul in the southern region of Brazil borders the southern cone countries of Latin America. In fact, W serogroup represented 17.8% of all invasive strains in 2003–2005 compared to 3.2% in 1995–2002.18

Notifications of IMD in Brazil are routinely collected by the Minister of Health trough the Information System for Notifiable Diseases (SINAN). This study is a retrospective review of all IMD cases reported in Brazil as a whole and in SC in particular, from 1 January 2007 to 31 December 2019, using the SINAN electronic database.19,20

The study variables included the number total cases of IMD and meningococcal serogroups. Pearson’s chi squared test was used to compare total cases and serogroups frequencies. For comparing distributions evolution, stacked bars were used as visualization. Statistical software used was R version 3.5.2.

Total number of cases and cases according to serogroups were different between Brazil and Santa Catarina state along the reported years (Fig. 1). Analysis of total number of cases by year from 2007 through 2019 showed statistically significant differences between Brazil and SC state (p < 0.001) (Table 1).

Fig. 1.

Meningococcal Disease in Brazil compared to Santa Catarina State.

NT, nontypeable; OTHER, Other serogroups.

(0.12MB).
Table 1.

Meningococcal serogroup distribution during the period of 2007-2019.

SerogroupsTotal
NTa  OTHERb 
Brazil  13,589 (52.1%)  2608 (10.0%)  8728 (33.5%)  802 (3.1%)  331 (1.3%)  26,058 (100%) 
SCc  291 (45.2%)  106 (16.5%)  136 (21.1%)  101 (15.7%)  10 (1.6%)  644 (100%) 
a

Nontypeable.

b

Other serogroups.

c

Santa Catarina State.

A progressive decline of total cases and its respective serogroups occurred after introduction of meningococcal C vaccination in 2010 in Brazil. In contrast, there was a diminishing number of cases in SC state from 2007 to 2013, with a reversal of trends from 2014 to 2018, with a reduction of the number of the cases in 2019.

Serogroup distribution showed specific changes in SC state. Meningococcal disease by serogroup W increased between 2016–2018, with a reduction in 2019. Unlike Brazil, serogroup C showed an increment of cases after 2013 in SC state.

In general, non-identified cases showed decreasing trends in both regions even though they have occurred in different proportions.

Differences between the number of cases and distribution of serogroups cannot be clearly explained. There are several variables that can explain the changes in the prevalence of individual serogroups, one of them could be the naturally occurring periodic changes and another the impact of immunization programs. Another possibility, considering that SC is a region with high affluence of tourism (mainly from Argentina), is that these differences could be influenced by tourism carriage.

The notification of SC state presented a cut point at December 2nd, 2019, which might affect the analysis of the following months of the analyzed period.

The observed number of cases and serogroup distribution along time for SC state compared to Brazil, could imply that health authorities need to review current policies in order to cope with existing epidemiology, especially since the W serogroup is associated directly with increased mortality and morbidity rates.15,16

The emergence of serogroup W in SC highlights the difference in how health authorities have been dealing with meningococcal surveillance as the identification methods increased in accuracy. Moreover, it shows that geographical features should be considered as an important variable when recommending quadrivalent (ACWY) conjugate vaccines exceptionally considering the emergency of a strain that used to be underrepresented.

In summary, we showed that the total number of cases and serogroup distribution in the time period of 2007 through 2019 in SC state was significantly different compared to Brazil.

Funding

Sponsorship of this study and article processing charges were funded by Pfizer Inc.

Conflict of interest

The authors are consultant and speaker Pfizer, Sanofi, GlaxoSmithKline and Merck Sharp & Dohme.

Acknowledgments

Sponsorship of this study and article processing charges were funded by Pfizer Inc. All named authors meet the International Committee of Medical Journal Editors criteria for authorship for this article, take responsibility for the integrity of the work as a whole, and have given their approval for this version to be published. The statistical analysis was conducted by Content Medicine in Buenos Aires, Argentina; funding was provided by Pfizer Inc. This article is based on previously conducted studies and does not contain any studies with human participants or animals performed by any of the authors.

References
[1]
R. Dwilow, S. Fanella.
Invasive meningococcal disease in the 21st century—an update for the clinician.
Curr Neurol Neurosci Rep., 15 (2015), pp. 2
[2]
O.B. Harrison, H. Claus, Y. Jiang, J.S. Bennett, H.B. Bratcher, K.A. Jolley, et al.
Description and nomenclature of Neisseria meningitidis capsule locus.
Emerg Infect Dis., 19 (2013), pp. 566-573
[3]
M.A.P. Sáfadi, E.D.G. McIntosh.
Epidemiology and prevention of meningococcal disease: a critical appraisal of vaccine policies.
Expert Rev Vaccines., 10 (2011), pp. 1717-1730
[4]
P. Araya, J. Fernández, F. Del Canto, M. Seoane, A.B. Ibarz-Pavón, G. Barra, et al.
Neisseria meningitidis ST-11 clonal complex, Chile 2012.
Emerg Infect Dis., 21 (2015), pp. 339-341
[5]
L.H. Harrison.
Epidemiological profile of meningococcal disease in the United States.
Clin Infect Dis Off Publ Infect Dis Soc Am., 50 (2010), pp. S37-44
[6]
L.H. Harrison, S.I. Pelton, A. Wilder-Smith, J. Holst, M.A.P. Safadi, J.A. Vazquez, et al.
The Global Meningococcal Initiative: recommendations for reducing the global burden of meningococcal disease.
Vaccine., 29 (2011), pp. 3363-3371
[7]
M.A.P. Sáfadi, O.A.L. Cintra.
Epidemiology of meningococcal disease in Latin America: current situation and opportunities for prevention.
Neurol Res., 32 (2010), pp. 263-271
[8]
National Advisory Committee on Immunization (NACI).
An update on the invasive meningococcal disease and meningococcal vaccine conjugate recommendations. An Advisory Committee Statement (ACS).
Can Commun Dis Rep Releve Mal Transm Au Can., 35 (2009), pp. 1-40
[9]
A.C. Cohn, J.R. MacNeil, L.H. Harrison, C. Hatcher, J. Theodore, M. Schmidt, et al.
Changes in Neisseria meningitidis disease epidemiology in the United States, 1998-2007: implications for prevention of meningococcal disease.
Clin Infect Dis Off Publ Infect Dis Soc Am., 50 (2010), pp. 184-191
[10]
R. Abad, C.I. Agudelo, M.C. Brandileone, G. Chanto, J.M. Gabastou, J.C. Hormazabal, et al.
Molecular characterization of invasive serogroup Y Neisseria meningitidis strains isolated in the Latin America region.
J Infect., 59 (2009), pp. 104-114
[11]
A.C. Cohn, J.R. MacNeil, T.A. Clark, I.R. Ortega-Sanchez, E.Z. Briere, H.C. Meissner, et al.
Prevention and control of meningococcal disease: recommendations of the Advisory Committee on Immunization Practices (ACIP).
MMWR Recomm Rep Morb Mortal Wkly Rep Recomm Rep., 62 (2013), pp. 1-28
[12]
M.A.P. Safadi, S. Gonzalez-Ayala, A. Jakel, H. Wieffer, C. Moreno, A. Vyse.
The epidemiology of meningococcal disease in Latin America 1945–2010: an unpredictable and changing landscape.
Epidemiol Infect., 141 (2013), pp. 447-458
[13]
C.T. Sacchi, L.O. Fukasawa, M.G. Gonçalves, M.M. Salgado, K.A. Shutt, T.R. Carvalhanas, et al.
Incorporation of Real-Time PCR into Routine Public Health Surveillance of Culture Negative Bacterial Meningitis in São Paulo, Brazil.
[14]
L. Erickson, P. De Wals.
Complications and sequelae of meningococcal disease in Quebec, Canada, 1990-1994.
Clin Infect Dis Off Publ Infect Dis Soc Am., 26 (1998), pp. 1159-1164
[15]
G. Moreno, D. López, N. Vergara, D. Gallegos, M.F. Advis, S. Loayza.
Clinical characterization of cases with meningococcal disease by W135 group in Chile, 2012.
Rev Chil Infectol., 30 (2013), pp. 346-349
[16]
M.T. Valenzuela, G. Moreno, A. Vaquero, M. Seoane, J.C. Hormazábal, M.P. Bertoglia, et al.
[Emergence of W135 meningococcal serogroup in Chile during 2012].
Rev Med Chil., 141 (2013), pp. 959-967
[17]
R. Abad, E.L. López, R. Debbag, J.A. Vázquez.
Serogroup W meningococcal disease: global spread and current affect on the Southern Cone in Latin America.
Epidemiol Infect., 142 (2014), pp. 2461-2470
[18]
L. Weidlich, L.F. Baethgen, L.W. Mayer, C. Moraes, C.C. Klein, L.S. Nunes, et al.
High prevalence of Neisseria meningitidis hypervirulent lineages and emergence of W135:P1.5,2:ST-11 clone in Southern Brazil.
J Infect., 57 (2008), pp. 324-331
[19]
DATASUS [Internet]. [cited 2020 Mar 9]. Available from: http://www2.datasus.gov.br/DATASUS/index.php?area=0203&id=29892234&VObj.
[20]
DIVE - Boletim Epidemiológico Mensal – Vigilância da Doença Meningocócica [Internet]. [cited 2020 Mar 9]. Available from: http://www.dive.sc.gov.br/index.php/arquivo-noticias/805-boletim-epidemiologico-mensal-n-10-2018-vigilancia-da-doenca-meningococica-atualizado-em-04-de-janeiro-de-2019.
Copyright © 2020. Sociedade Brasileira de Infectologia
The Brazilian Journal of Infectious Diseases
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