Characterization of invasive Neisseria meningitidis from Atlantic Canada, 2009 to 2013: With special reference to the nonpolysaccharide vaccine targets (PorA, factor H binding protein, Neisseria heparin-binding antigen and Neisseria adhesin A).

IF 2.6 4区 计算机科学 Q2 COMPUTER SCIENCE, INFORMATION SYSTEMS Peer-To-Peer Networking and Applications Pub Date : 2015-11-01 DOI:10.1155/2015/393659
Raymond Sw Tsang, Dennis Ks Law, Rita R Gad, Tim Mailman, Gregory German, Robert Needle
{"title":"Characterization of invasive Neisseria meningitidis from Atlantic Canada, 2009 to 2013: With special reference to the nonpolysaccharide vaccine targets (PorA, factor H binding protein, Neisseria heparin-binding antigen and Neisseria adhesin A).","authors":"Raymond Sw Tsang, Dennis Ks Law, Rita R Gad, Tim Mailman, Gregory German, Robert Needle","doi":"10.1155/2015/393659","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Serogroup B Neisseria meningitidis (MenB) has always been a major cause of invasive meningococcal disease (IMD) in Canada. With the successful implementation of a meningitis C conjugate vaccine, the majority of IMD in Canada is now caused by MenB.</p><p><strong>Objective: </strong>To investigate IMD case isolates in Atlantic Canada from 2009 to 2013. Data were analyzed to determine the potential coverage of the newly licensed MenB vaccine.</p><p><strong>Methods: </strong>Serogroup, serotype and serosubtype antigens were determined from IMD case isolates. Clonal analysis was performed using multilocus sequence typing. The protein-based vaccine antigen genes were sequenced and the predicted peptides were investigated.</p><p><strong>Results: </strong>The majority of the IMD isolates were MenB (82.5%, 33 of 40) and, in particular, sequence type (ST)-154 B:4:P1.4 was responsible for 47.5% (19 of 40) of all IMD case isolates in Atlantic Canada. Isolates of this clone expressed the PorA antigen P1.4 and possessed the nhba genes encoding for Neisseria heparin-binding antigen peptide 2, which together matched exactly with two of the four components of the new four-component meningococcal B vaccine. Nineteen MenB isolates had two antigenic matches, another five MenB and one meningitis Y isolate had one antigenic match. This provided 75.8% (25 of 33) potential coverage for MenB, or a 62.5% (25 of 40) overall potential coverage for IMD.</p><p><strong>Conclusion: </strong>From 2009 to 2013, IMD in Atlantic Canada was mainly caused by MenB and, in particular, the B:4:P1.4 ST-154 clone, which accounted for 47.5% of all IMD case isolates. The new four-component meningococcal B vaccine appeared to offer adequate coverage against MenB in Atlantic Canada.</p>","PeriodicalId":49313,"journal":{"name":"Peer-To-Peer Networking and Applications","volume":"5 1","pages":"299-304"},"PeriodicalIF":2.6000,"publicationDate":"2015-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4692298/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Peer-To-Peer Networking and Applications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2015/393659","RegionNum":4,"RegionCategory":"计算机科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"COMPUTER SCIENCE, INFORMATION SYSTEMS","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Serogroup B Neisseria meningitidis (MenB) has always been a major cause of invasive meningococcal disease (IMD) in Canada. With the successful implementation of a meningitis C conjugate vaccine, the majority of IMD in Canada is now caused by MenB.

Objective: To investigate IMD case isolates in Atlantic Canada from 2009 to 2013. Data were analyzed to determine the potential coverage of the newly licensed MenB vaccine.

Methods: Serogroup, serotype and serosubtype antigens were determined from IMD case isolates. Clonal analysis was performed using multilocus sequence typing. The protein-based vaccine antigen genes were sequenced and the predicted peptides were investigated.

Results: The majority of the IMD isolates were MenB (82.5%, 33 of 40) and, in particular, sequence type (ST)-154 B:4:P1.4 was responsible for 47.5% (19 of 40) of all IMD case isolates in Atlantic Canada. Isolates of this clone expressed the PorA antigen P1.4 and possessed the nhba genes encoding for Neisseria heparin-binding antigen peptide 2, which together matched exactly with two of the four components of the new four-component meningococcal B vaccine. Nineteen MenB isolates had two antigenic matches, another five MenB and one meningitis Y isolate had one antigenic match. This provided 75.8% (25 of 33) potential coverage for MenB, or a 62.5% (25 of 40) overall potential coverage for IMD.

Conclusion: From 2009 to 2013, IMD in Atlantic Canada was mainly caused by MenB and, in particular, the B:4:P1.4 ST-154 clone, which accounted for 47.5% of all IMD case isolates. The new four-component meningococcal B vaccine appeared to offer adequate coverage against MenB in Atlantic Canada.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
2009 年至 2013 年加拿大大西洋地区侵袭性脑膜炎奈瑟菌的特征:特别关注非多糖疫苗目标(PorA、H因子结合蛋白、奈瑟氏肝素结合抗原和奈瑟氏粘附素A)。
背景:血清 B 群奈瑟氏脑膜炎球菌 (MenB) 一直是加拿大侵袭性脑膜炎球菌疾病 (IMD) 的主要病因。随着 C 型脑膜炎结合疫苗的成功接种,加拿大大多数侵袭性脑膜炎球菌病现在都是由 MenB 引起的:调查 2009 年至 2013 年加拿大大西洋地区的侵袭性脑膜炎病例分离物。分析数据以确定新许可的 MenB 疫苗的潜在覆盖范围:从 IMD 病例分离株中确定血清群、血清型和血清亚型抗原。使用多焦点序列分型进行克隆分析。对基于蛋白质的疫苗抗原基因进行了测序,并对预测的肽进行了研究:大多数 IMD 分离物为 MenB(占 82.5%,40 例中的 33 例),尤其是序列类型 (ST)-154 B:4:P1.4 在加拿大大西洋地区所有 IMD 病例分离物中占 47.5%(40 例中的 19 例)。该克隆的分离株表达了 PorA 抗原 P1.4,并拥有编码奈瑟氏菌肝素结合抗原肽 2 的 nhba 基因,这些基因与新型四联脑膜炎球菌 B 疫苗四种成分中的两种完全吻合。有 19 个 B 型脑膜炎球菌分离物有两个抗原相匹配,另有 5 个 B 型脑膜炎球菌分离物和 1 个 Y 型脑膜炎球菌分离物有一个抗原相匹配。这为 MenB 提供了 75.8% 的潜在覆盖率(33 例中的 25 例),或为 IMD 提供了 62.5% 的总体潜在覆盖率(40 例中的 25 例):2009年至2013年期间,加拿大大西洋地区的IMD主要由MenB引起,尤其是B:4:P1.4 ST-154克隆,占所有IMD病例分离株的47.5%。在加拿大大西洋地区,新的四联脑膜炎球菌B疫苗似乎对MenB有足够的覆盖率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Peer-To-Peer Networking and Applications
Peer-To-Peer Networking and Applications COMPUTER SCIENCE, INFORMATION SYSTEMS-TELECOMMUNICATIONS
CiteScore
8.00
自引率
7.10%
发文量
145
审稿时长
12 months
期刊介绍: The aim of the Peer-to-Peer Networking and Applications journal is to disseminate state-of-the-art research and development results in this rapidly growing research area, to facilitate the deployment of P2P networking and applications, and to bring together the academic and industry communities, with the goal of fostering interaction to promote further research interests and activities, thus enabling new P2P applications and services. The journal not only addresses research topics related to networking and communications theory, but also considers the standardization, economic, and engineering aspects of P2P technologies, and their impacts on software engineering, computer engineering, networked communication, and security. The journal serves as a forum for tackling the technical problems arising from both file sharing and media streaming applications. It also includes state-of-the-art technologies in the P2P security domain. Peer-to-Peer Networking and Applications publishes regular papers, tutorials and review papers, case studies, and correspondence from the research, development, and standardization communities. Papers addressing system, application, and service issues are encouraged.
期刊最新文献
Privacy preservation in blockchain-based healthcare data sharing: A systematic review. Are neck pain, disability, and deep neck flexor performance the same for the different types of temporomandibular disorders? Enhancing cloud network security with a trust-based service mechanism using k-anonymity and statistical machine learning approach Towards real-time non-preemptive multicast scheduling in reconfigurable data center networks Homomorphic multi-party computation for Internet of Medical Things
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1