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  1. Article ; Online: Population snapshot of Streptococcus pneumoniae causing invasive disease in South Africa prior to introduction of pneumococcal conjugate vaccines.

    Ndlangisa, Kedibone M / du Plessis, Mignon / Wolter, Nicole / de Gouveia, Linda / Klugman, Keith P / von Gottberg, Anne

    PloS one

    2014  Volume 9, Issue 9, Page(s) e107666

    Abstract: We determined the sequence types of isolates that caused invasive pneumococcal disease (IPD) prior to routine use of pneumococcal conjugate vaccines (PCV) in South Africa. PCV-13 serotypes and 6C isolates collected in 2007 (1 461/2 437, 60%) from ... ...

    Abstract We determined the sequence types of isolates that caused invasive pneumococcal disease (IPD) prior to routine use of pneumococcal conjugate vaccines (PCV) in South Africa. PCV-13 serotypes and 6C isolates collected in 2007 (1 461/2 437, 60%) from patients of all ages as part of on-going, national, laboratory-based surveillance for IPD, were selected for genetic characterization. In addition, all 134 non-PCV isolates from children <2 years were selected for characterization. Sequence type diversity by serotype and age category (children <5 years vs. individuals ≥5 years) was assessed for PCV serotypes using Simpson's index of diversity. Similar genotypes circulated among isolates from children and adults and the majority of serotypes were heterogeneous. While globally disseminated clones were common among some serotypes (e.g., serotype 1 [clonal complex (CC) 217, 98% of all serotype 1] and 14 [CC230, 43%)]), some were represented mainly by clonal complexes rarely reported elsewhere (e.g., serotype 3 [CC458, 60%] and 19A [CC2062, 83%]). In children <2 years, serotype 15B and 8 were the most common serotypes among non-PCV isolates (16% [22/134] and 15% [20/134] isolates, respectively). Sequence type 7052 and 53 were most common among serotypes 15B and 8 isolates and accounted for 58% (7/12) and 64% (9/14) of the isolates, respectively. Serotype 19F, 14, 19A and 15B had the highest proportions of penicillin non-susceptible isolates. Genotypes rarely reported in other parts of the world but common among some of our serotypes highlight the importance of our data as these genotypes may emerge post PCV introduction.
    MeSH term(s) Adolescent ; Adult ; Anti-Bacterial Agents/pharmacology ; Base Sequence ; Child ; Child, Preschool ; DNA, Bacterial/analysis ; DNA, Bacterial/genetics ; Female ; Humans ; Male ; Microbial Sensitivity Tests ; Multilocus Sequence Typing ; Pneumococcal Infections/drug therapy ; Pneumococcal Infections/epidemiology ; Pneumococcal Vaccines/immunology ; Pneumococcal Vaccines/therapeutic use ; Sequence Analysis, DNA ; Serotyping ; South Africa/epidemiology ; Streptococcus pneumoniae/classification ; Streptococcus pneumoniae/genetics ; Streptococcus pneumoniae/isolation & purification ; Vaccines, Conjugate/immunology ; Vaccines, Conjugate/therapeutic use ; Young Adult
    Chemical Substances Anti-Bacterial Agents ; DNA, Bacterial ; Pneumococcal Vaccines ; Vaccines, Conjugate
    Language English
    Publishing date 2014-09-18
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S.
    ISSN 1932-6203
    ISSN (online) 1932-6203
    DOI 10.1371/journal.pone.0107666
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Two cases of serotypeable and non-serotypeable variants of Streptococcus pneumoniae detected simultaneously during invasive disease.

    Ndlangisa, Kedibone M / du Plessis, Mignon / Allam, Mushal / Wolter, Nicole / Mohale, Thabo / de Gouveia, Linda / Birkhead, Monica / Klugman, Keith P / von Gottberg, Anne

    BMC microbiology

    2016  Volume 16, Issue 1, Page(s) 126

    Abstract: Background: More than 94 serotypes of Streptococcus pneumoniae have been described to date, however the majority of disease is caused by approximately 20 serotypes. Some pneumococci do not react with commercially available antisera used for serotyping ... ...

    Abstract Background: More than 94 serotypes of Streptococcus pneumoniae have been described to date, however the majority of disease is caused by approximately 20 serotypes. Some pneumococci do not react with commercially available antisera used for serotyping and are thus regarded as non-serotypeable (NT). These pneumococci are commonly isolated during carriage studies and very rarely cause invasive disease. Colonization may occur with more than one serotype however disease with more than one serotype is rarely detected. Thus there are limited data describing cases of pneumococcal disease caused by more than one isolate.
    Results: In two cases of invasive pneumococcal disease in South Africa, a non-serotypeable and a serotypeable isolate were co-detected during routine serotyping. A serotype 1 and 18C isolate were each co-detected with a non-serotypeable isolate in 2009 (case A) and 2010 (case B), from cerebrospinal fluid and blood, respectively. Both patients were 10-14 years old. For case A, the serotypeable isolate could not be obtained due to low representation in the mixed culture. Using electron microscopy we confirmed lack of capsule for the non-serotypeable isolates. Comparison of the case A non-serotypeable isolate with a serotype 1 genome revealed only the presence of the rhamnose biosynthesis genes (rmlA, B, C and D) in the capsular locus, all other capsular genes were absent. Nonetheless it had a multilocus sequence type (ST) associated with serotype 1 (ST217 and ribosomal ST3462) and its core genome clustered with other ST217 isolates. The case B non-serotypeable isolate had all serotype 18C capsular genes except for variation in the wchA and wze genes, compared to the 18C isolate. Both case B isolates were ST9817 and their core genomes were identical.
    Conclusions: The ability of pneumococci to alter capsule production is a potential vaccine escape mechanism and therefore non-serotypeable pneumococci should be monitored as such organisms may increase under vaccine pressure.
    MeSH term(s) Adolescent ; Child ; Humans ; Male ; Pneumococcal Infections/diagnosis ; Pneumococcal Infections/microbiology ; Serotyping ; Streptococcus pneumoniae/classification ; Streptococcus pneumoniae/genetics ; Streptococcus pneumoniae/isolation & purification
    Language English
    Publishing date 2016-06-24
    Publishing country England
    Document type Case Reports ; Journal Article
    ISSN 1471-2180
    ISSN (online) 1471-2180
    DOI 10.1186/s12866-016-0745-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: A

    Ndlangisa, Kedibone M / du Plessis, Mignon / Lo, Stephanie / de Gouveia, Linda / Chaguza, Chrispin / Antonio, Martin / Kwambana-Adams, Brenda / Cornick, Jennifer / Everett, Dean B / Dagan, Ron / Hawkins, Paulina A / Beall, Bernard / Corso, Alejandra / Grassi Almeida, Samanta Cristine / Ochoa, Theresa J / Obaro, Stephen / Shakoor, Sadia / Donkor, Eric S / Gladstone, Rebecca A /
    Ho, Pak Leung / Paragi, Metka / Doiphode, Sanjay / Srifuengfung, Somporn / Ford, Rebecca / Moïsi, Jennifer / Saha, Samir K / Bigogo, Godfrey / Sigauque, Betuel / Eser, Özgen Köseoglu / Elmdaghri, Naima / Titov, Leonid / Turner, Paul / Kumar, K L Ravi / Kandasamy, Rama / Egorova, Ekaterina / Ip, Margaret / Breiman, Robert F / Klugman, Keith P / McGee, Lesley / Bentley, Stephen D / von Gottberg, Anne / The Global Pneumococcal Sequencing Consortium

    Microbial genomics

    2022  Volume 8, Issue 4

    Abstract: Pneumococcal serotype 35B is an important non-conjugate vaccine (non-PCV) serotype. Its continued emergence, post-PCV7 in the USA, was associated with expansion of a pre-existing 35B clone (clonal complex [CC] 558) along with post-PCV13 emergence of a ... ...

    Abstract Pneumococcal serotype 35B is an important non-conjugate vaccine (non-PCV) serotype. Its continued emergence, post-PCV7 in the USA, was associated with expansion of a pre-existing 35B clone (clonal complex [CC] 558) along with post-PCV13 emergence of a non-35B clone previously associated with PCV serotypes (CC156). This study describes lineages circulating among 35B isolates in South Africa before and after PCV introduction. We also compared 35B isolates belonging to a predominant 35B lineage in South Africa (GPSC5), with isolates belonging to the same lineage in other parts of the world. Serotype 35B isolates that caused invasive pneumococcal disease in South Africa in 2005-2014 were characterized by whole-genome sequencing (WGS). Multi-locus sequence types and global pneumococcal sequence clusters (GPSCs) were derived from WGS data of 63 35B isolates obtained in 2005-2014. A total of 262 isolates that belong to GPSC5 (115 isolates from South Africa and 147 from other countries) that were sequenced as part of the global pneumococcal sequencing (GPS) project were included for comparison. Serotype 35B isolates from South Africa were differentiated into seven GPSCs and GPSC5 was most common (49 %, 31/63). While 35B was the most common serotype among GPSC5/CC172 isolates in South Africa during the PCV13 period (66 %, 29/44), 23F was the most common serotype during both the pre-PCV (80 %, 37/46) and PCV7 period (32 %, 8/25). Serotype 35B represented 15 % (40/262) of GPSC5 isolates within the global GPS database and 75 % (31/40) were from South Africa. The predominance of the GPSC5 lineage within non-vaccine serotype 35B, is possibly unique to South Africa and warrants further molecular surveillance of pneumococci.
    MeSH term(s) Humans ; Pneumococcal Infections/epidemiology ; Pneumococcal Infections/prevention & control ; Pneumococcal Vaccines ; Serogroup ; South Africa/epidemiology ; Streptococcus pneumoniae/genetics ; Vaccines, Conjugate
    Chemical Substances Pneumococcal Vaccines ; Vaccines, Conjugate
    Language English
    Publishing date 2022-05-22
    Publishing country England
    Document type Journal Article ; Research Support, U.S. Gov't, Non-P.H.S. ; Research Support, Non-U.S. Gov't
    ZDB-ID 2835258-0
    ISSN 2057-5858 ; 2057-5858
    ISSN (online) 2057-5858
    ISSN 2057-5858
    DOI 10.1099/mgen.0.000746
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: International links between Streptococcus pneumoniae vaccine serotype 4 sequence type (ST) 801 in Northern European shipyard outbreaks of invasive pneumococcal disease

    Gladstone, R.A. / Siira, L. / Brynildsrud, O.B. / Vestrheim, D.F. / Turner, P. / Clarke, S.C. / Srifuengfung, S. / Ford, R. / Lehmann, D. / Egorova, E. / Voropaeva, E. / Haraldsson, G. / Kristinsson, K.G. / McGee, L. / Breiman, R.F. / Bentley, S.D. / Sheppard, C.L. / Fry, N.K. / Corander, J. /
    Toropainen, M / Steens, A. / Akpaka, Patrick E / Ampofo, Krow / Antonio, Martin / Balaji, Veeraraghavan / Beall, Bernard W. / Belabbès, Houria / Benisty, Rachel / Bigogo, Godfrey / Brooks, Abdullah W / Carter, Philip E. / Cornick, Jennifer E. / Corso, Alejandra / Cristina de Cunto Brandileone, Maria / Cristine Grassi Almeida, Samanta / Croucher, Nicholas J. / Dagan, Ron / Davydov, Alexander / Diawara, Idrissa / Doiphode, Sanjay / du Plessis, Mignon / Elmdaghri, Naima / Köseoglu Eser, Özgen / Everett, Dean B. / Faccone, Diego / Gagetti, Paula / Givon-Lavi, Noga / Hasanuzzaman, Md / Hawkins, Paulina A. / Hryniewicz, Waleria / Hulten, Kristina G. / Ip, Margaret / Kapusta, Aurelie / Kandasamy, Rama / Kastrin, Tamara / Keenan, Jeremy / Klugman, Keith P. / Kwambana-Adams, Brenda / Law, Pierra Y. / Lees, John A / Leung Ho, Pak / Li, Yuan / Lo, Stephanie W. / Ochoa, Theresa J. / Madhi, Shabir A. / Metcalf, Benjamin J / Moïsi, Jennifer / Mucavele Fundação Manhiça, Helio / Ndlangisa, Kedibone M. / Nurse-Lucas, Michele / Nzenze, Susan A. / Obaro, Stephen K / Paragi, Metka / Pollard, Andrew J / Ravikumar, KL. / Sadowy, Ewa / Saha, Samir K. / Sampane-Donkor, Eric / Devi Sekaran, Shamala / Shakoor, Sadia / Shrestha, Shrijana / Sigauque, Betuel / Skoczynska, Anna / Soo ko, Kwan / Tientcheu, Peggy-Estelle / Titov, Leonid / Urban, Yulia / Verani, Jennifer / van Tonder, Andries J. / von Gottberg, Anne / Wolter, Nicole

    Vaccine. 2022 Feb. 11, v. 40, no. 7

    2022  

    Abstract: Pneumococcal disease outbreaks of vaccine preventable serotype 4 sequence type (ST)801 in shipyards have been reported in several countries. We aimed to use genomics to establish any international links between them. Sequence data from ST801-related ... ...

    Institution The Global Pneumococcal Sequencing Consortium
    Abstract Pneumococcal disease outbreaks of vaccine preventable serotype 4 sequence type (ST)801 in shipyards have been reported in several countries. We aimed to use genomics to establish any international links between them. Sequence data from ST801-related outbreak isolates from Norway (n = 17), Finland (n = 11) and Northern Ireland (n = 2) were combined with invasive pneumococcal disease surveillance from the respective countries, and ST801-related genomes from an international collection (n = 41 of > 40,000), totalling 106 genomes. Raw data were mapped and recombination excluded before phylogenetic dating. Outbreak isolates were relatively diverse, with up to 100 SNPs (single nucleotide polymorphisms) and a common ancestor estimated around the year 2000. However, 19 Norwegian and Finnish isolates were nearly indistinguishable (0–2 SNPs) with the common ancestor dated around 2017. The total diversity of ST801 within the outbreaks could not be explained by recent transmission alone, suggesting that harsh environmental and associated living conditions reported in the shipyards may facilitate invasion of colonising pneumococci. However, near identical strains in the Norwegian and Finnish outbreaks does suggest that transmission between international shipyards also contributed to those outbreaks. This indicates the need for improved preventative measures in this working population including pneumococcal vaccination.
    Keywords Northern Ireland ; Streptococcus pneumoniae ; ancestry ; disease surveillance ; genome ; genomics ; phylogeny ; serotypes ; vaccination ; vaccines ; Finland ; Norway
    Language English
    Dates of publication 2022-0211
    Size p. 1054-1060.
    Publishing place Elsevier Ltd
    Document type Article
    ZDB-ID 605674-x
    ISSN 1873-2518 ; 0264-410X
    ISSN (online) 1873-2518
    ISSN 0264-410X
    DOI 10.1016/j.vaccine.2021.10.046
    Database NAL-Catalogue (AGRICOLA)

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  5. Article ; Online: Visualizing variation within Global Pneumococcal Sequence Clusters (GPSCs) and country population snapshots to contextualize pneumococcal isolates.

    Gladstone, Rebecca A / Lo, Stephanie W / Goater, Richard / Yeats, Corin / Taylor, Ben / Hadfield, James / Lees, John A / Croucher, Nicholas J / van Tonder, Andries J / Bentley, Leon J / Quah, Fu Xiang / Blaschke, Anne J / Pershing, Nicole L / Byington, Carrie L / Balaji, Veeraraghavan / Hryniewicz, Waleria / Sigauque, Betuel / Ravikumar, K L / Almeida, Samanta Cristine Grassi /
    Ochoa, Theresa J / Ho, Pak Leung / du Plessis, Mignon / Ndlangisa, Kedibone M / Cornick, Jennifer E / Kwambana-Adams, Brenda / Benisty, Rachel / Nzenze, Susan A / Madhi, Shabir A / Hawkins, Paulina A / Pollard, Andrew J / Everett, Dean B / Antonio, Martin / Dagan, Ron / Klugman, Keith P / von Gottberg, Anne / Metcalf, Benjamin J / Li, Yuan / Beall, Bernard W / McGee, Lesley / Breiman, Robert F / Aanensen, David M / Bentley, Stephen D / The Global Pneumococcal Sequencing Consortium

    Microbial genomics

    2020  Volume 6, Issue 5

    Abstract: Knowledge of pneumococcal lineages, their geographic distribution and antibiotic resistance patterns, can give insights into global pneumococcal disease. We provide interactive bioinformatic outputs to explore such topics, aiming to increase ... ...

    Abstract Knowledge of pneumococcal lineages, their geographic distribution and antibiotic resistance patterns, can give insights into global pneumococcal disease. We provide interactive bioinformatic outputs to explore such topics, aiming to increase dissemination of genomic insights to the wider community, without the need for specialist training. We prepared 12 country-specific phylogenetic snapshots, and international phylogenetic snapshots of 73 common Global Pneumococcal Sequence Clusters (GPSCs) previously defined using PopPUNK, and present them in Microreact. Gene presence and absence defined using Roary, and recombination profiles derived from Gubbins are presented in Phandango for each GPSC. Temporal phylogenetic signal was assessed for each GPSC using BactDating. We provide examples of how such resources can be used. In our example use of a country-specific phylogenetic snapshot we determined that serotype 14 was observed in nine unrelated genetic backgrounds in South Africa. The international phylogenetic snapshot of GPSC9, in which most serotype 14 isolates from South Africa were observed, highlights that there were three independent sub-clusters represented by South African serotype 14 isolates. We estimated from the GPSC9-dated tree that the sub-clusters were each established in South Africa during the 1980s. We show how recombination plots allowed the identification of a 20 kb recombination spanning the capsular polysaccharide locus within GPSC97. This was consistent with a switch from serotype 6A to 19A estimated to have occured in the 1990s from the GPSC97-dated tree. Plots of gene presence/absence of resistance genes (
    MeSH term(s) DNA Transposable Elements ; Databases, Genetic ; Drug Resistance, Bacterial ; Evolution, Molecular ; High-Throughput Nucleotide Sequencing ; Phylogeny ; Phylogeography ; Poland ; Polysaccharides, Bacterial/genetics ; Sequence Analysis, DNA/methods ; Serogroup ; South Africa ; Streptococcus pneumoniae/classification ; Streptococcus pneumoniae/genetics ; Streptococcus pneumoniae/isolation & purification ; Utah
    Chemical Substances DNA Transposable Elements ; Polysaccharides, Bacterial
    Language English
    Publishing date 2020-04-29
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 2835258-0
    ISSN 2057-5858 ; 2057-5858
    ISSN (online) 2057-5858
    ISSN 2057-5858
    DOI 10.1099/mgen.0.000357
    Database MEDical Literature Analysis and Retrieval System OnLINE

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