Phenotypic and genetic alterations of Burkholderia pseudomallei in patients during relapse and persistent infections
Issued Date
2023-02-06
Resource Type
eISSN
1664302X
Scopus ID
2-s2.0-85148510560
Journal Title
Frontiers in Microbiology
Volume
14
Rights Holder(s)
SCOPUS
Bibliographic Citation
Frontiers in Microbiology Vol.14 (2023)
Suggested Citation
Seng R., Phunpang R., Saiprom N., Dulsuk A., Chewapreecha C., Thaipadungpanit J., Batty E.M., Chantratita W., West T.E., Chantratita N. Phenotypic and genetic alterations of Burkholderia pseudomallei in patients during relapse and persistent infections. Frontiers in Microbiology Vol.14 (2023). doi:10.3389/fmicb.2023.1103297 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/81941
Title
Phenotypic and genetic alterations of Burkholderia pseudomallei in patients during relapse and persistent infections
Author's Affiliation
Other Contributor(s)
Abstract
The bacterium Burkholderia pseudomallei is the causative agent of melioidosis, a severe tropical disease associated with high mortality and relapse and persistent infections. Treatment of melioidosis requires prolonged antibiotic therapy; however, little is known about relapse and persistent infections, particularly the phenotypic and genetic alterations of B. pseudomallei in patients. In this study, we performed pulsed-field gel electrophoresis (PFGE) to compare the bacterial genotype between the initial isolate and the subsequent isolate from each of 23 suspected recurrent and persistent melioidosis patients in Northeast Thailand. We used whole-genome sequencing (WGS) to investigate multilocus sequence types and genetic alterations of within-host strain pairs. We also investigated the bacterial phenotypes associated with relapse and persistent infections, including multinucleated giant cell (MNGC) formation efficiency and intracellular multiplication. We first identified 13 (1.2%) relapse, 7 (0.7%) persistent, and 3 (0.3%) reinfection patients from 1,046 survivors. Each of the 20 within-host strain pairs from patients with relapse and persistent infections shared the same genotype, suggesting that the subsequent isolates arise from the infecting isolate. Logistic regression analysis of clinical data revealed regimen and duration of oral antibiotic therapies as risk factors associated with relapse and persistent infections. WGS analysis demonstrated 17 within-host genetic alteration events in 6 of 20 paired isolates, including a relatively large deletion and 16 single-nucleotide polymorphism (stocktickerSNP) mutations distributed across 12 genes. In 1 of 20 paired isolates, we observed significantly increased cell-to-cell fusion and intracellular replication in the second isolate compared with the initial isolate from a patient with persistent infection. WGS analysis suggested that a non-synonymous mutation in the tssB-5 gene, which encoded an essential component of the type VI secretion system, may be associated with the increased intracellular replication and MNGC formation efficiency of the second isolate of the patient. This information provides insights into genetic and phenotypic alterations in B. pseudomallei in human melioidosis, which may represent a bacterial strategy for persistent and relapse infections.