Emergence of W135 meningococcal meningitis in Ghana

Summary Neisseria meningitidis serogroup W135, well known for a long time as a cause of isolated cases of meningococcal meningitis, has recently increasingly been associated with disease outbreaks of considerable magnitude. Burkina Faso was hit by W135 epidemics in the dry seasons of 2002–2004, but...

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Veröffentlicht in:Tropical medicine & international health 2005-12, Vol.10 (12), p.1229-1234
Hauptverfasser: Forgor, Abudulai Adams, Leimkugel, Julia, Hodgson, Abraham, Bugri, Akalifa, Dangy, Jean‐Pierre, Gagneux, Sébastien, Smith, Tom, Pluschke, Gerd
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container_end_page 1234
container_issue 12
container_start_page 1229
container_title Tropical medicine & international health
container_volume 10
creator Forgor, Abudulai Adams
Leimkugel, Julia
Hodgson, Abraham
Bugri, Akalifa
Dangy, Jean‐Pierre
Gagneux, Sébastien
Smith, Tom
Pluschke, Gerd
description Summary Neisseria meningitidis serogroup W135, well known for a long time as a cause of isolated cases of meningococcal meningitis, has recently increasingly been associated with disease outbreaks of considerable magnitude. Burkina Faso was hit by W135 epidemics in the dry seasons of 2002–2004, but only four W135 meningitis cases were recorded between February 2003 and March 2004 in adjoining Ghana. This reconfirms previous findings that bottlenecks exist in the spreading of new epidemic N. meningitidis clones within the meningitis belt of sub‐Saharan Africa. Of the four Ghanaian W135 meningitis patients one died and three survived, of whom one had profound neurosensory hearing loss and speech impairment. All four disease isolates were sensitive to penicillin G, chloramphenicol, ciprofloxacin and cefotaxime and had the multi‐locus sequence type (ST) 11, which is the major ST of the ET‐37 clonal complex. Pulsed‐field gel electrophoresis (PFGE) profiles of the Ghanaian disease isolates and recent epidemic isolates from Burkina Faso were largely identical. We conducted meningococcal colonization surveys in the home communities of three of the patients and in the Kassena Nankana District located at the border to Burkina Faso. W135 carriage rates ranged between 0% and 17.5%. When three consecutive surveys were conducted in the patient community with the highest carrier rate, persistence of W135 colonization over a period of 1 year was observed. Differences in PFGE profiles of carrier isolates taken at different times in the same patient community were indicative of rapid microevolution of the W135 bacteria, emphasizing the need for innovative fine typing methods to reveal the relationship between W135 isolates.
doi_str_mv 10.1111/j.1365-3156.2005.01520.x
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Burkina Faso was hit by W135 epidemics in the dry seasons of 2002–2004, but only four W135 meningitis cases were recorded between February 2003 and March 2004 in adjoining Ghana. This reconfirms previous findings that bottlenecks exist in the spreading of new epidemic N. meningitidis clones within the meningitis belt of sub‐Saharan Africa. Of the four Ghanaian W135 meningitis patients one died and three survived, of whom one had profound neurosensory hearing loss and speech impairment. All four disease isolates were sensitive to penicillin G, chloramphenicol, ciprofloxacin and cefotaxime and had the multi‐locus sequence type (ST) 11, which is the major ST of the ET‐37 clonal complex. Pulsed‐field gel electrophoresis (PFGE) profiles of the Ghanaian disease isolates and recent epidemic isolates from Burkina Faso were largely identical. We conducted meningococcal colonization surveys in the home communities of three of the patients and in the Kassena Nankana District located at the border to Burkina Faso. W135 carriage rates ranged between 0% and 17.5%. When three consecutive surveys were conducted in the patient community with the highest carrier rate, persistence of W135 colonization over a period of 1 year was observed. 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Burkina Faso was hit by W135 epidemics in the dry seasons of 2002–2004, but only four W135 meningitis cases were recorded between February 2003 and March 2004 in adjoining Ghana. This reconfirms previous findings that bottlenecks exist in the spreading of new epidemic N. meningitidis clones within the meningitis belt of sub‐Saharan Africa. Of the four Ghanaian W135 meningitis patients one died and three survived, of whom one had profound neurosensory hearing loss and speech impairment. All four disease isolates were sensitive to penicillin G, chloramphenicol, ciprofloxacin and cefotaxime and had the multi‐locus sequence type (ST) 11, which is the major ST of the ET‐37 clonal complex. Pulsed‐field gel electrophoresis (PFGE) profiles of the Ghanaian disease isolates and recent epidemic isolates from Burkina Faso were largely identical. We conducted meningococcal colonization surveys in the home communities of three of the patients and in the Kassena Nankana District located at the border to Burkina Faso. W135 carriage rates ranged between 0% and 17.5%. When three consecutive surveys were conducted in the patient community with the highest carrier rate, persistence of W135 colonization over a period of 1 year was observed. 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Burkina Faso was hit by W135 epidemics in the dry seasons of 2002–2004, but only four W135 meningitis cases were recorded between February 2003 and March 2004 in adjoining Ghana. This reconfirms previous findings that bottlenecks exist in the spreading of new epidemic N. meningitidis clones within the meningitis belt of sub‐Saharan Africa. Of the four Ghanaian W135 meningitis patients one died and three survived, of whom one had profound neurosensory hearing loss and speech impairment. All four disease isolates were sensitive to penicillin G, chloramphenicol, ciprofloxacin and cefotaxime and had the multi‐locus sequence type (ST) 11, which is the major ST of the ET‐37 clonal complex. Pulsed‐field gel electrophoresis (PFGE) profiles of the Ghanaian disease isolates and recent epidemic isolates from Burkina Faso were largely identical. 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source MEDLINE; Access via Wiley Online Library; IngentaConnect Free/Open Access Journals; EZB-FREE-00999 freely available EZB journals; Wiley Online Library (Open Access Collection)
subjects Adolescent
Age Distribution
Anti-Bacterial Agents - therapeutic use
Biodiversity
Child
Child, Preschool
Disease Outbreaks
Electrophoresis, Gel, Pulsed-Field - methods
epidemic meningococcal meningitis
Epidemics
Female
Ghana
Ghana - epidemiology
Humans
Male
Meningitis
Meningitis, Meningococcal - drug therapy
Meningitis, Meningococcal - epidemiology
Meningitis, Meningococcal - microbiology
Neisseria meningitidis
Neisseria meningitidis W135
Neisseria meningitidis, Serogroup W-135 - drug effects
Neisseria meningitidis, Serogroup W-135 - genetics
Neisseria meningitidis, Serogroup W-135 - isolation & purification
Prevalence
Sahel
title Emergence of W135 meningococcal meningitis in Ghana
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