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Epidemiology

Typhoid in Kenya Is Associated with a Dominant Multidrug-Resistant Salmonellaenterica Serovar Typhi Haplotype That Is Also Widespread in Southeast Asia

Samuel Kariuki, Gunturu Revathi, John Kiiru, Doris M. Mengo, Joyce Mwituria, Jane Muyodi, Agnes Munyalo, Yik Y. Teo, Kathryn E. Holt, Robert A. Kingsley, Gordon Dougan
Samuel Kariuki
1Centre for Microbiology Research, Kenya Medical Research Institute, P.O. Box 43640, Nairobi, Kenya
4The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, United Kingdom
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  • For correspondence: skariuki@kemri.org
Gunturu Revathi
2Aga Khan University Hospital, Nairobi, Kenya
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John Kiiru
1Centre for Microbiology Research, Kenya Medical Research Institute, P.O. Box 43640, Nairobi, Kenya
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Doris M. Mengo
1Centre for Microbiology Research, Kenya Medical Research Institute, P.O. Box 43640, Nairobi, Kenya
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Joyce Mwituria
1Centre for Microbiology Research, Kenya Medical Research Institute, P.O. Box 43640, Nairobi, Kenya
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Jane Muyodi
1Centre for Microbiology Research, Kenya Medical Research Institute, P.O. Box 43640, Nairobi, Kenya
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Agnes Munyalo
1Centre for Microbiology Research, Kenya Medical Research Institute, P.O. Box 43640, Nairobi, Kenya
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Yik Y. Teo
3The Wellcome Trust Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, United Kingdom
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Kathryn E. Holt
4The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, United Kingdom
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Robert A. Kingsley
4The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, United Kingdom
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Gordon Dougan
4The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, United Kingdom
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DOI: 10.1128/JCM.01983-09
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  • FIG. 1.
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    FIG. 1.

    Distribution of S. Typhi haplotypes identified in Kenya. (a) Radial phylogram based on 1,485 SNPs originally detected among 19 whole-genome sequences of S. Typhi (11). Black nodes, sequenced control isolates; colored nodes, 94 Kenyan isolates (colors were randomly assigned to the nodes) scaled to reflect the numbers of isolates found; precise numbers are given in parentheses. (b) Distribution of haplotypes of Kenyan S. Typhi by year of isolation. The colors indicate S. Typhi haplotypes as defined in panel a.

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    FIG. 2.

    Subtypes of Kenyan S. Typhi isolates of haplotype H58. (a) Radial phylogram of the H58 cluster of S. Typhi; the dashed line indicates where this phylogram links back to the broader S. Typhi phylogram shown in Fig. 1. Black nodes, genotyped control isolates, including seven genomes sequenced (labeled with strain names [11]) or previously defined (labeled with H groups [27]); colored nodes, nodes to which Kenyan isolates were mapped by SNP typing (colors were randomly assigned to the nodes), labeled with letters. The oval shading highlights two distinct H58 lineages, I and II. (b) Distribution of H58 subtypes of Kenyan S. Typhi by year of isolation, split by the presence of MDR IncHI1 plasmids (note than no non-H58 isolates contained plasmids). The labels and colors correspond to those defined in panel a.

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  • TABLE 1.

    Distribution of drug resistance phenotypes among S. Typhi isolates from three surveillance periods

    Period of isolationNo. (%) fully susceptibleNo. (%) with single resistanceNo. (%) MDRTotal no. (%)
    1988-199333 (73.3)7 (15.6)5 (11.1)45 (13.9)
    1994-200011 (7.7)46 (32.3)85 (60)142 (44.0)
    2001-200810 (7.4)21 (15.4)105 (77.2)136 (42.1)
  • TABLE 2.

    Trends in resistance to quinolones during the study period

    Period of isolation (n)No. (%) NalraNo. (%) DCSb and Nalr
    1988-1993 (45)2 (4.4)0
    1994-2000 (142)8 (5.6)3 (37.5)
    2001-2008 (136)25 (18.4)16 (64)
    • ↵ a Nalr, nalidixic acid resistant; MIC > 16 μg/ml.

    • ↵ b MIC = 0.1 to 1.0 μg/ml.

Additional Files

  • Figures
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  • Supplemental material

    Files in this Data Supplement:

    • Supplemental file 1 - Table S1 (Chromosomal S. Typhi SNPs analyzed in this study)
      Zipped Microsoft Excel file, 41K.
    • Supplemental file 2 - Fig. S1 (Numbers of sensitive and MDR S. Typhi isolates included in the SNP typing by period of surveillance)
      Zipped EPS file, 171K.
    • Supplemental file 3 - Methods, including details of the SNP typing protocol used for the chromosomal and IncHI1 plasmid loci in S. Typhi, as well as legends for Table S1 and Fig. S1
      Microsoft Word document, 48K.
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Typhoid in Kenya Is Associated with a Dominant Multidrug-Resistant Salmonellaenterica Serovar Typhi Haplotype That Is Also Widespread in Southeast Asia
Samuel Kariuki, Gunturu Revathi, John Kiiru, Doris M. Mengo, Joyce Mwituria, Jane Muyodi, Agnes Munyalo, Yik Y. Teo, Kathryn E. Holt, Robert A. Kingsley, Gordon Dougan
Journal of Clinical Microbiology May 2010, 48 (6) 2171-2176; DOI: 10.1128/JCM.01983-09

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Typhoid in Kenya Is Associated with a Dominant Multidrug-Resistant Salmonellaenterica Serovar Typhi Haplotype That Is Also Widespread in Southeast Asia
Samuel Kariuki, Gunturu Revathi, John Kiiru, Doris M. Mengo, Joyce Mwituria, Jane Muyodi, Agnes Munyalo, Yik Y. Teo, Kathryn E. Holt, Robert A. Kingsley, Gordon Dougan
Journal of Clinical Microbiology May 2010, 48 (6) 2171-2176; DOI: 10.1128/JCM.01983-09
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KEYWORDS

Anti-Bacterial Agents
Bacterial Typing Techniques
Drug Resistance, Multiple, Bacterial
Salmonella typhi
Typhoid Fever

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