Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0097912
DC FieldValue
dc.titleNovel clones of Streptococcus pneumoniae causing invasive disease in Malaysia
dc.contributor.authorJefferies J.M.
dc.contributor.authorYusof M.Y.M.
dc.contributor.authorSekaran S.D.
dc.contributor.authorClarke S.C.
dc.date.accessioned2019-11-05T00:36:08Z
dc.date.available2019-11-05T00:36:08Z
dc.date.issued2014
dc.identifier.citationJefferies J.M., Yusof M.Y.M., Sekaran S.D., Clarke S.C. (2014). Novel clones of Streptococcus pneumoniae causing invasive disease in Malaysia. PLoS ONE 9 (6) : e97912. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0097912
dc.identifier.issn1932-6203
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/161404
dc.description.abstractAlthough Streptococcus pneumoniae is a leading cause of childhood disease in South East Asia, little has previously been reported regarding the epidemiology of invasive pneumococcal disease in Malaysia and very few studies have explored pneumococcal epidemiology using multilocus sequence typing (MLST). Here we describe serotype, multilocus sequence type (ST), and penicillin susceptibility of thirty pneumococcal invasive disease isolates received by the University of Malaya Medical Centre between February 2000 and January 2007 and relate this to the serotypes included in current pneumococcal conjugate vaccines. A high level of diversity was observed; fourteen serotypes and 26 sequence types (ST), (11 of which were not previously described) were detected from 30 isolates. Penicillin non-susceptible pneumococci accounted for 33% of isolates. The extent of molecular heterogeneity within carried and disease-causing Malaysian pneumococci remains unknown. Larger surveillance and epidemiological studies are now required in this region to provide robust evidence on which to base future vaccine policy. © 2014 Jefferies et al.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20191101
dc.subjectpenicillin derivative
dc.subjectPneumococcus vaccine
dc.subjectantiinfective agent
dc.subjectpenicillin derivative
dc.subjectPneumococcus vaccine
dc.subjectvaccine
dc.subjectadolescent
dc.subjectadult
dc.subjectantibiotic sensitivity
dc.subjectarticle
dc.subjectbacterium isolate
dc.subjectblood
dc.subjectcerebrospinal fluid
dc.subjectchild
dc.subjectcontrolled study
dc.subjecthuman
dc.subjectMalaysia
dc.subjectmicrobial diversity
dc.subjectminimum inhibitory concentration
dc.subjectmultilocus sequence typing
dc.subjectpleura fluid
dc.subjectpneumococcal infection
dc.subjectserotype
dc.subjectStreptococcus pneumoniae
dc.subjectaged
dc.subjectantibiotic resistance
dc.subjectcell clone
dc.subjectchemistry
dc.subjectclassification
dc.subjectgenetics
dc.subjectinfant
dc.subjectisolation and purification
dc.subjectmicrobiology
dc.subjectmiddle aged
dc.subjectnewborn
dc.subjectPneumococcal Infections
dc.subjectpreschool child
dc.subjectserotyping
dc.subjectStreptococcus pneumoniae
dc.subjectvery elderly
dc.subjectAdolescent
dc.subjectAdult
dc.subjectAged
dc.subjectAged, 80 and over
dc.subjectAnti-Bacterial Agents
dc.subjectbeta-Lactam Resistance
dc.subjectChild
dc.subjectChild, Preschool
dc.subjectClone Cells
dc.subjectHumans
dc.subjectInfant
dc.subjectInfant, Newborn
dc.subjectMalaysia
dc.subjectMiddle Aged
dc.subjectMultilocus Sequence Typing
dc.subjectPenicillins
dc.subjectPneumococcal Infections
dc.subjectPneumococcal Vaccines
dc.subjectSerotyping
dc.subjectStreptococcus pneumoniae
dc.subjectVaccines, Conjugate
dc.typeArticle
dc.contributor.departmentMICROBIOLOGY AND IMMUNOLOGY
dc.description.doi10.1371/journal.pone.0097912
dc.description.sourcetitlePLoS ONE
dc.description.volume9
dc.description.issue6
dc.description.pagee97912
dc.published.statePublished
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