Skip directly to site content Skip directly to page options Skip directly to A-Z link Skip directly to A-Z link Skip directly to A-Z link
Volume 21, Number 1—January 2015
Letter

Burkholderia pseudomallei Sequence Type 562 in China and Australia

On This Page
Figures
Article Metrics
12
citations of this article
EID Journal Metrics on Scopus

Cite This Article

To the Editor: Melioidosis is increasingly being recognized in tropical and subtropical areas worldwide; the world’s 2 major endemic foci are Thailand and northern Australia (1,2). Phylogenetic analyses of Burkholderia pseudomallei isolates, performed by using multilocus sequence typing (MLST) (3), have led to phylogeographic associations that can be used to track melioidosis epidemics (4). However, in contrast to the previous separation of B. pseudomallei into 2 phylogenetic groups (Australia and Southeast Asia/rest of the world) (5), we report an MLST sequence type (ST) that seems to be present in northern Australia, Taiwan, and southern China.

In mainland China, melioidosis was first reported in 1990 (6) and is now known to be endemic to several tropical provinces, including Hainan, a southern island province close to Southeast Asia. Since 2008, cases of melioidosis in Hainan have escalated; from July 2008 through July 2012, a total of 110 cases were microbiologically diagnosed at 2 general hospitals (Sanya People’s Hospital and Haikou Municipal Hospital).

We characterized clinical isolates of B. pseudomallei from the 110 cases by using MLST, pulsed-field gel electrophoresis (PFGE), and 4-locus multilocus variable-number tandem-repeat analysis (MLVA-4) (3,7,8). MLST revealed 40 STs, 39 of which were consistent with STs from Southeast Asia, as evident from the global B. pseudomallei MLST database (http://bpseudomallei.mlst.net/). A single ST, ST562, which accounted for 3 cases in Hainan, was previously described on the global database as being from Australia; the 20 isolates from humans and 10 isolates from the environment deposited until September 1, 2014, all from Australia, had been isolated from 2005 through 2012. Although not deposited in the global MLST database, ST562 has also recently been reported from Taiwan (7). Among the 253 isolates of B. pseudomallei collected in Taiwan during 2004–2010, 1 clinical isolate and 9 environmental isolates were described as being ST562. Moreover, these 10 ST562 isolates displayed a unique PFGE pulsotype, distinct from that of other B. pseudomallei strains from Taiwan (7).

Figure

Thumbnail of Pulsed-field gel electrophoresis (PFGE) patterns for 3 sequence type (ST) 562 and 1 ST167 Burkholderia pseudomallei strains isolated during 2008–2012, Hainan, China. The isolate source, isolation time, ST, and 4-locus multilocus variable-number tandem-repeat analysis (4-MLVA) profiles are indicated for each strain. Scale bar indicates percentage similarity.

Figure. Pulsed-field gel electrophoresis (PFGE) patterns for 3 sequence type (ST) 562 and 1 ST167 Burkholderia pseudomallei strains isolated during 2008–2012, Hainan, China. The isolate source, isolation time, ST, and 4-locus multilocus...

Of the 3 patients from Hainan from whom ST562 strains were isolated, 2 resided in the city of Sanya and 1 in the neighboring city of Lingshui (Technical Appendix); all denied a history of foreign travel, they shared no common risk factors, and all survived the infection. Further analysis of ST562, performed by using eBURST-based (http://eburst.mlst.net/) population analysis of the MLST dataset, showed that ST562 is a single-locus variant of ST167, which is represented on the MLST dataset by multiple human and environmental isolates from Thailand and to date by 1 human isolate from Cambodia. ST167 accounted for 1 of the 110 B. pseudomallei strains from Hainan. The narK locus of ST167contains allele 3 instead of allele 29, as seen in ST562; 3 base differences are found in allele 3: C72T (C→T position 72), C126T, and A435G. According to PFGE, the 3 ST562 isolates from Hainan displayed a single pulsotype, and the other 107 isolates from Hainan belonged to distinct and diverse pulsotypes, similar to those observed in Taiwan. The uniformity of PFGE patterns in the Hainan and Taiwan isolates supports the possibility that ST562 might be a recently emerging clone. PFGE patterns of Hainan ST562 exhibited 86% similarity with ST167, differing by 6 bands (Figure).

Hainan ST562 isolates were further analyzed by using MLVA-4 (8), which divided 3 isolates (from patients A, B, and C) into 3 distinct MLVA-4 types (Figure). The 2008 isolate (MLVA-4 profile 11,8,15,7) and one 2012 isolate (profile 11,8,17,7) exhibited close relatedness, whereas another 2012 isolate (profile 10,10,11,5) was divergent from these, indicating that ST562 isolates in Hainan have been present long enough for some divergence into lineages.

Two mutually exclusive gene clusters, B. thailandensis–like flagellar gene cluster (BTFC) and Yersinia-like fimbrial gene cluster (YLF), have been linked to geographic origin and have been suggested for differentiating groups of B. pseudomallei (9). By PCR we found that ST562 isolates of Hainan were all YLF positive. BTFC predominates in Australian B. pseudomallei strains, and YLF predominates in Southeast Asia. Presence of YLF was also observed in strains from Papua New Guinea, possibly reflecting that country’s location, intermediate between major foci of melioidosis (10).

In conclusion, by using MLST and the online MLST database, we revealed that B. pseudomallei ST562 is present in southern China as well as in Australia and Taiwan. The intercontinental character of this ST raises new questions about the epidemiology and control of melioidosis. Given the usual geographic separation of B. pseudomallei STs, we suggest that this wide-ranging presence of ST562 might result from more recent spread caused by transmission between regions. Increasing farming exchanges and trade of agricultural products between melioidosis-endemic regions might facilitate breaking of the geographic barrier; clonal introduction of B. pseudomallei could potentially occur in new locations. Improved and cooperative surveillance is required for elucidating the current and future global dispersion range of B. pseudomallei and for monitoring the consequent melioidosis infections.

Top

Acknowledgments

We thank Bart Currie for assistance with preparation of the manuscript.

This work was supported by grants from the National Science and Technology Mega-Projects of China (nos. 2012ZX10004-215 and 2008ZX10004-008), the Natural Science Foundation of Hainan Province (no. 814389) from the Science and Technology Department of Hainan Province, and the Scientific Research Project Fund (no. QW2010-65) from the Health Department of Hainan Province.

Top

Hai Chen, Lianxu Xia, Xiong Zhu, Wei Li, Xiaoli Du, Duorong Wu, Rong Hai, Xiaona Shen, Ying Liang, Hong Cai, and Xiao ZhengComments to Author 

Author affiliations: Sanya People’s Hospital, Sanya, China (H. Chen, X. Zhu); State Key Laboratory for Infectious Disease Prevention and Control, Beiiing, China (L. Xia, W. Li, , X. Du, R. Hai, X. Shen, Y. Liang, X. Zheng); National Institute for Communicable Disease Control and Prevention, Beijing (L. Xia, W. Li, R. Hai, X. Du, X. Shen, Y. Liang, H. Cai, X. Zheng); Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Hangzhou, China ( L. Xia, W. Li, X. Zheng); Haikou Municipal Hospital, Haikou, China (D. Wu)

Top

References

  1. Cheng  AC, Currie  BJ. Melioidosis: epidemiology, pathophysiology, and management. Clin Microbiol Rev. 2005;18:383416. DOIPubMed
  2. Wiersinga  WJ, Currie  BJ, Peacock  SJ. Melioidosis. N Engl J Med. 2012;367:103544.PubMed
  3. Godoy  D, Randle  G, Simpson  AJ, Aanensen  DM, Pitt  TL, Kinoshita  R, Multilocus sequence typing and evolutionary relationships among the causative agents of melioidosis and glanders, Burkholderia pseudomallei and Burkholderia mallei. J Clin Microbiol. 2003;41:206879. DOIPubMed
  4. Dale  J, Price  EP, Hornstra  H, Busch  JD, Mayo  M, Godoy  D, Epidemiological tracking and population assignment of the non-clonal bacterium, Burkholderia pseudomallei. PLoS Negl Trop Dis. 2011;5:e1381. DOIPubMed
  5. Pearson  T, Giffard  P, Beckstrom-Sternberg  S, Auerbach  R, Hornstra  H, Tuanyok  A, Phylogeographic reconstruction of a bacterial species with high levels of lateral gene transfer. BMC Biol. 2009;7:78.PubMed
  6. Yang  S. Melioidosis research in China. Acta Trop. 2000;77:15765 and.PubMed
  7. Chen  YL, Lin  YC, Chen  YS, Chen  SC, Liu  YM, Tseng  IL, Characterisation of predominant molecular patterns of Burkholderia pseudomallei in Taiwan. Trans R Soc Trop Med Hyg. 2013;107:1659. DOIPubMed
  8. Currie  BJ, Haslem  A, Pearson  T, Hornstra  H, Leadem  B, Mayo  M, Identification of melioidosis outbreak by multilocus variable number tandem repeat analysis. Emerg Infect Dis. 2009;15:16974.PubMed
  9. Tuanyok  A, Auerbach  RK, Brettin  TS, Bruce  DC, Munk  AC, Detter  JC, A horizontal gene transfer event defines two distinct groups within Burkholderia pseudomallei that have dissimilar geographic distributions. J Bacteriol. 2007;189:90449.PubMed
  10. Baker  A, Pearson  T, Price  EP, Dale  J, Keim  P, Hornstra  H, Molecular phylogeny of Burkholderia pseudomallei from a remote region of Papua New Guinea. PLoS ONE. 2011;6:e18343. DOIPubMed

Top

Figure

Top

Cite This Article

DOI: 10.3201/eid2101.140156

Related Links

Top

Table of Contents – Volume 21, Number 1—January 2015

Comments

Please use the form below to submit correspondence to the authors or contact them at the following address:

Xiao Zheng, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, PO Box 5, Changping, Beijing 102206, People’s Republic of China

Send To

character(s) remaining.

Comment submitted successfully, thank you for your feedback.

Top

Page created: December 19, 2014
Page updated: December 19, 2014
Page reviewed: December 19, 2014
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
file_external