Use of Recombinant Escherichia coli Strains in Immunofluorescence Assays for Melioidosis Diagnosis.
Kanoknart LantongJirarat SongsriSueptrakool WisessombatWanida MalaWarinda PrommachoteWilaiwan SenghoiManas KotepuiJedsada KaewrakmukTreenate JiranantasakApichai TuanyokWiyada Kwanhian KlangbudPublished in: Pathogens (Basel, Switzerland) (2021)
Burkholderia pseudomallei is a Gram-negative bacterium and the causative agent of melioidosis in humans and animals in the tropics. The clinical manifestations of melioidosis are diverse, ranging from localized infections to whole-body sepsis. The effective serological method is crucial for the point-of-care diagnosis of melioidosis. The aim of this study was to develop indirect immunofluorescence assay (IFA)-based methods for detecting immunoglobulin G (IgG) antibodies in melioidosis patients. These methods use whole-cell antigens made from recombinant E. coli strains that express major B. pseudomallei antigens, including TssM, OmpH, AhpC, BimA, and Hcp1. A total of 271 serum samples from culture-confirmed melioidosis patients (n = 81), patients with other known infections (n = 70), and healthy donors (n = 120) were tested. Our study showed that the recombinant TssM strain had the highest performance, with 92.6% sensitivity, 100% specificity, 100% positive predictive value, 96.9% negative predictive value, 97.8% efficiency, 97.0% accuracy, and no cross-reactivity. The method agreement analysis based on k efficiency calculations showed that all five IFA methods perfectly agreed with the standard culturing method, while the traditional indirect hemagglutination (IHA) method moderately agreed with the culture. In summary, our investigations showed that the TssM-IFA method could be used for melioidosis diagnosis.
Keyphrases
- escherichia coli
- end stage renal disease
- gram negative
- ejection fraction
- newly diagnosed
- chronic kidney disease
- multidrug resistant
- high throughput
- intensive care unit
- prognostic factors
- acute kidney injury
- peritoneal dialysis
- single cell
- molecular dynamics
- cystic fibrosis
- staphylococcus aureus
- cell therapy
- stem cells
- cell free
- mesenchymal stem cells
- kidney transplantation
- structural basis