Serogroup W135 meningococcal meningitis, Northern Cameroon, 2007-2008.
|Publication:||Name: Emerging Infectious Diseases Publisher: U.S. National Center for Infectious Diseases Audience: Academic; Professional Format: Magazine/Journal Subject: Health Copyright: COPYRIGHT 2009 U.S. National Center for Infectious Diseases ISSN: 1080-6040|
|Issue:||Date: Feb, 2009 Source Volume: 15 Source Issue: 2|
|Geographic:||Geographic Scope: Cameroon Geographic Code: 6CAME Cameroon|
We analyzed results of recent microbiologic surveillance of
meningitis in northern Cameroon. During the 2007 and 2008 meningitis
seasons, all 57 identified meningococcal isolates were serogroup W135.
This situation might indicate that the area is experiencing a period
between epidemic waves due to 2 different clones of serogroup A
The 3 provinces constituting the Septentrion, in North Cameroon, belong to the so-called African meningitis belt (1). Until now, in these provinces, the diagnosis of meningitis was made essentially on the basis of clinical signs, and biologic confirmation was uncommon. The rare data that documented meningococci circulating in recent years in this area refer mostly to the early 1990s (2,3), when serogroup A was by far the most frequently identified serogroup in Cameroon, with strains having the antigenic formula A:4:P1.9 and belonging to the sequence type 5 (ST-5) complex (4). From 1999 through 2001, a few cases of meningitis were attributed to serogroup W135 (W135:2a:P1.5,2; ST-11), but these data were from Yaounde, in the southern part of the country (5).
In 2007, microbiologic surveillance of bacterial meningitis was reintroduced in northern Cameroon to monitor the changing epidemiology of meningococci, with particular attention to uncommon serogroups, such as W135 or X, which have been unusually frequent in Sahelian Africa since 2000 (6-10). Health authorities decided that an aliquot of every cerebrospinal fluid (CSF) specimen collected in this area would be sent to the Centre Pasteur du Cameroun in Garoua (CPCAG) for testing. Laboratory procedures included assessment of CSF turbidity, Gram staining, search for soluble capsular antigens by using the Pastorex (Bio-Rad, Hercules, CA, USA) latex agglutination kit and dipstick rapid diagnostic test for Neisseria meningitidis serogroups A, C, W135, and Y (kindly provided by the Centre de Recherche Medicale et Sanitaire, Niamey, Niger) (11). CSF specimens were cultured on blood agar and chocolate agar, supplemented with Polyvitex (bioMerieux, Marcy-l'Etoile, France), with incubation at 37[degrees]C with 5% C[O.sub.2]. Susceptibility to [beta]3-1actam antimicrobial drugs and chloramphenicol was tested according to the recommendations of the Antibiogram Committee of the French Society for Microbiology. The isolates of N. meningitidis were sent to the World Health Organization Collaborating Centre (WHOCC) for Reference and Research on Meningococci in Marseilles, France.
Overall, 409 CSF specimens were tested at CPCAG microbiology laboratory from January 1, 2007, through June 30, 2008, of which 144 (35.2%) had a leukocyte count evocative of bacterial meningitis. Online Appendix Figure 1 (available from www.cdc.gov/EID/content/15/2/340appFl.htm) shows the monthly distribution of CSF specimens tested at CPCAG.
The number of CSF specimens tested at CPCAG increased greatly after 2006 as the number of health facilities sending specimens for testing increased (Table). This rise was not related to any epidemic, but showed the interest of healthcare workers in microbiologic surveillance of meningitis. The number of tested CSF specimens peaked in March and April, during the dry season, and was low during the rainy season (August and September). Overall, 24 Streptococcus pneumoniae, 23 Haemophilus influenzae, and 57 N. meningitidis isolates were identified, either from culture or by soluble antigens identification.
S. pneumoniae and H. influenzae were identified throughout the year, but N. meningitidis was observed only during the dry season, considered the classical meningitis season in the African meningitis belt (1). The median ages of 11 patients with confirmed S. pneumoniae infection and 11 patients with confirmed H. influenzae infection were 14 and 0.6 years, respectively. Neither S. pneumoniae (12) nor H. influenzae isolates (8) were serotyped. The median age of 43 patients with confirmed meningococcal meningitis was 8 years (25th percentile 4.8 years, 75th percentile 15.5 years).
Fifteen N. meningitidis isolates were recovered from culture, representing 28.3% of CSF specimens testing positive for soluble antigens. The frequent implementation of early presumptive treatment with antimicrobial drugs, as well as the unsuitable conditions for CSF specimens transport from health facilities, might account for this low rate of positive cultures. The implementation of PCR for the diagnosis of N. meningitidis, S. pneumoniae, and H. influenzae in CPCAG in Garoua in 2009 will enable further enhancement of the surveillance.
All diagnosed meningococci belonged to serogroup W135, although serogroup A has been classically the most prevalent in this Sahelian region, according to surveys carried out in Garoua (2,3). N. meningitidis serogroup A seems to have completely disappeared since the renewal of the microbiologic surveillance of meningitis in northern Cameroon began in February 2007. To our knowledge, there was no previous report in the literature of such a predominance of serogroup W 135 in countries of the meningitis belt.
Nine of our 15 N. meningitidis isolates were genotyped by using multilocus sequence typing by the WHOCC in Marseille. Eight were identified as ST-2881 and 1 as ST-11. These findings are consistent with the presence of only sporadic cases of serogroup W135 meningococcal meningitis. Until now, ST-2881 has only been associated with sporadic cases or small epidemics, contrary to the findings for ST- 11, which was involved in a large epidemic in Burkina Faso in 2002 (10,12).
We did not observe any resistance of N. meningitidis to [beta]-1actam antimicrobial agents and chloramphenicol. These findings did not question probabilistic treatment of suspected cases of meningococcal meningitis based on ceftriaxone or oily chloramphenicol in epidemic situations (13).
Laboratory-confirmed cases of serogroup W 135 meningococcal meningitis were from Garoua and 9 other health facilities (online Appendix Figure 2, available from www. cdc.gov/EID/content/15/2/340-appF2.htm). Most cases were from the North and Extreme North Provinces. Adamaoua Province seemed to be less affected, likely because of climate and lower population density.
Our results differ clearly from those observed in Yaounde, the capital, which has a subequatorial climate. In 1999-2000, S. pneumoniae was the main causative bacterial agent identified in meningitis (109/194, 56%), followed by H. influenzae (36/194, 18.6%) and N. meningitidis (26/194, 13.4%) (14).
WHO does not recommend systematic preventive vaccination with the bivalent A + C polysaccharide vaccine, but does recommend reactive mass immunizations of at risk populations when the epidemic threshold is crossed. This policy was applied in northern Cameroon in 1992, 1993, 1996, and 1998, when >400,000 doses of vaccine were administered each year for epidemic control. After this period, 30,000-40,000 persons received preventive immunization against N. meningitidis serogroups A and C each year. However, the vaccination coverage is too low in this population of [approximately equal to]6 million inhabitants to explain by itself the current absence of serogroup A meningococci in this area.
The renewal of microbiologic surveillance of meningitis highlighted the fact that serogroup W135 was the only serogroup of N. meningitidis involved in endemic meningitis cases in northern Cameroon in 2007 and 2008. Serogroup A meningococci seemed to be completely absent during this period. This finding might reflect the transitory period separating 2 epidemic waves caused by 2 different clones of serogroup A meningococci (15); the emergence of the next epidemic clone is thus possible at any moment. In the meantime, this situation has been considered by WHO, and vaccines that include protection against serogroup W135, such as trivalent vaccine (ACW135), are available for immunization campaigns to control epidemics. This vaccine is available in small quantities and can be delivered only by the International Coordinating Group (created in 1997 by WHO to distribute vaccine ACW135). WHO does not recommend this vaccine when meningococcal meningitis is endemic. Unless an epidemiologic upheaval occurs, future large epidemics of meningococcal meningitis will likely be caused by serogroup A, and the serogroup A conjugate vaccine (which will soon be introduced in the meningitis belt) will be a major advance. However, its successful implementation might create a favorable climate for other serogroups such as W135. In the future, a low-cost conjugate vaccine that includes W135 and perhaps X and Y serogroups can be anticipated.
In the early 2000s, scientists and WHO expressed fear of epidemics caused by serogroup W 135 in countries of the African meningitis belt, but the epidemic in Burkina Faso remained isolated. Because the W135 serogroup ST-2881 is known to be less epidemic than W135 ST-11, ST-2881 could have replaced it in the ecologic niche and also have resulted in immunologic protection against ST-11. The observations made in northern Cameroon confirm that we must continue to take into account serogroup W135 and that laboratories should be able to identify it routinely.
We gratefully acknowledge the province authorities and health district staff for their invaluable collaboration. We thank Pascal Boisier for assistance in preparing the manuscript.
This work was supported by the French Ministry of Foreign Affairs (FSP).
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Author affiliations: Centre Pasteur du Cameroun, Garoua, Cameroon (D. Massenet); Delegation de la Sante du Nord, Garoua (J. Inrombe); Delegation de la Sante de l'Extreme-Nord, Maroua, Cameroon (D.-E. Mevoula); and Institut de Medecine Tropicale du Service de Sante des Armees, Marseilles, France (P. Nicolas)
Address for correspondence: Denis Massenet, Centre Pasteur du Cameroun, Annexe de Garoua, BP 921, Garoua, Cameroon; email: denis. email@example.com
Dr Massenet is a medical biologist who directs the annex of the Centre Pasteur du Cameroun in Garoua. His research interests include strengthening laboratory capacities in sub-Saharan Africa toward a better control of infectious diseases such as bacterial meningitis.
Table. CSF specimens from Cameroon tested at CPCAG laboratory in 2007 and 2008 and number of health facilities that sent specimens, compared with 2006 efforts * Characteristic 2006 2007 2008 ([dagger]) No. tested CSF specimens 60 202 207 Health Garoua Hospital Garoua Garoua facilities Hospital plus Hospital plus involved 8 other health 17 other facilities health facilities Specimens not collected in Garoua 0 27 79 * CSF, cerebrospinal fluid; CPCAG, Centre Pasteur du Cameroun in Garoua. ([dagger]) Through June 30.
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