Funk Anna, Uadiale Kennedy, Kamau Charity, Caugant Dominique A, Ango Umar, Greig Jane
Médecins sans Frontières, Sokoto, Nigeria.
Nigeria Emergency Response Unit (NERU), Médecins sans Frontières, Sokoto, Nigeria.
PLoS Curr. 2014 Dec 29;6:ecurrents.outbreaks.b50c2aaf1032b3ccade0fca0b63ee518. doi: 10.1371/currents.outbreaks.b50c2aaf1032b3ccade0fca0b63ee518.
Background Neisseria meningitidis serogroup C (NmC) outbreaks occur infrequently in the African meningitis belt; the most recent report of an outbreak of this serogroup was in Burkina Faso, 1979. Médecins sans Frontières (MSF) has been responding to outbreaks of meningitis in northwest Nigeria since 2007 with no reported cases of serogroup C from 2007-2012. MenAfrivac®, a serogroup A conjugate vaccine, was first used for mass vaccination in northwest Nigeria in late 2012. Reactive vaccination using polysaccharide ACYW135 vaccine was done by MSF in parts of the region in 2008 and 2009; no other vaccination campaigns are known to have occurred in the area during this period. We describe the general characteristics of an outbreak due to a novel strain of NmC in Sokoto State, Nigeria, in 2013, and a smaller outbreak in 2014 in the adjacent state, Kebbi. Methods Information on cases and deaths was collected using a standard line-list during each week of each meningitis outbreak in 2013 and 2014 in northwest Nigeria. Initial serogroup confirmation was by rapid Pastorex agglutination tests. Cerebrospinal fluid (CSF) samples from suspected meningitis patients were sent to the WHO Reference Laboratory in Oslo, where bacterial isolates, serogrouping, antimicrobial sensitivity testing, genotype characterisation and real-time PCR analysis were performed. Results In the most highly affected outbreak areas, all of the 856 and 333 clinically suspected meningitis cases were treated in 2013 and 2014, respectively. Overall attack (AR) and case fatality (CFR) rates were 673/100,000 population and 6.8% in 2013, and 165/100,000 and 10.5% in 2014. Both outbreaks affected small geographical areas of less than 150km2 and populations of less than 210,000, and occurred in neighbouring regions in two adjacent states in the successive years. Initial rapid testing identified NmC as the causative agent. Of the 21 and 17 CSF samples analysed in Oslo, NmC alone was confirmed in 11 and 10 samples in 2013 and 2014, respectively. Samples confirmed as NmC through bacterial culture had sequence type (ST)-10217. Conclusions These are the first recorded outbreaks of NmC in the region since 1979, and the sequence (ST)-10217 has not been identified anywhere else in the world. The outbreaks had similar characteristics to previously recorded NmC outbreaks. Outbreaks of NmC in 2 consecutive years in northern Nigeria indicate a possible emergence of this serogroup. Increased surveillance for multiple serogroups in the region is needed, along with consideration of vaccination with conjugate vaccines rather than for NmA alone.
C群脑膜炎奈瑟菌(NmC)疫情在非洲脑膜炎带很少发生;该血清群最近一次疫情报告发生在1979年的布基纳法索。无国界医生组织(MSF)自2007年以来一直在应对尼日利亚西北部的脑膜炎疫情,2007 - 2012年期间没有C群病例报告。A群结合疫苗MenAfrivac®于2012年末首次在尼日利亚西北部用于大规模疫苗接种。无国界医生组织在2008年和2009年对该地区部分地区使用多糖ACYW135疫苗进行了应急接种;在此期间该地区没有其他已知的疫苗接种活动。我们描述了2013年尼日利亚索科托州由一种新型NmC菌株引起的疫情的一般特征,以及2014年在相邻的凯比州发生的一次规模较小的疫情。
在2013年和2014年尼日利亚西北部每次脑膜炎疫情的每周期间,使用标准病例一览表收集病例和死亡信息。最初通过快速Pastorex凝集试验进行血清群确认。疑似脑膜炎患者的脑脊液(CSF)样本被送往奥斯陆的世卫组织参考实验室,在那里进行细菌分离、血清群鉴定、抗菌药物敏感性测试、基因型特征分析和实时PCR分析。
在受影响最严重的疫情地区,2013年和2014年分别对所有856例和333例临床疑似脑膜炎病例进行了治疗。2013年的总体发病率(AR)和病死率(CFR)分别为673/10万人口和6.8%,2014年为165/10万和10.5%。两次疫情都影响了面积小于150平方公里、人口少于21万的小地理区域,且连续两年发生在相邻两个州的相邻地区。最初的快速检测确定NmC为病原体。在奥斯陆分析的21份和17份CSF样本中,2013年和2014年分别有11份和10份样本仅确诊为NmC感染。通过细菌培养确诊为NmC的样本具有序列型(ST)-10217。
这是该地区自1979年以来首次有记录的NmC疫情,序列型(ST)-10217在世界其他任何地方都未被发现。这些疫情具有与先前记录的NmC疫情相似的特征。尼日利亚北部连续两年发生NmC疫情表明该血清群可能出现。该地区需要加强对多个血清群的监测,同时考虑使用结合疫苗而非仅针对A群进行疫苗接种。