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Published on: March 22, 2012
Rapid and sensitive detection of Yersinia pestis by lateral-flow assay in simulated clinical samples
Hui-Ling Hsu1, Chuan-Chang Chuang1, Chung-Chih Liang1
1Institute of Preventive Medicine, National Defense Medical Center, P.O. Box 90048-700, Taipei, Taiwan.
Background:
Yersinia pestis is a contributing agent to the epidemic disease, plague, which killed an estimated 200 million people during historical times. In this study, a rapid, cheap, sensitive, and specific technique, the lateral flow assay (F1 strips), has been successfully developed to detect this pathogen, by using paired monoclonal antibodies (MAbs) against Y. pestis capsule like fraction 1 (F1) protein. Compared with the polyclonal antibody (PAb) based F1 strips, the Mab-based F1 strips have a remarkable increased detection limitation (10 to 100 folds). Furthermore, besides the limitation and specificity evaluation, the application of this F1 strip on simulated clinical samples indicate the LFA can be a good candidate to detect plague.
Methods:
Recombinant F1 antigen was expressed and purified from a series of works. The various anti-F1 monoclonal antibodies generated from hybridoma cells were screened with the ELISA technique. To evaluate the feasibility of this Y. pestis F1 test strip, the F1 protein/Y. pestis was spiked into simulated clinical samples such as human serum, mouse bronchoalveolar lavage fluids, and mouse blood to mimic natural infection status. Additionally, this technique was applied to detect the Y. pestis in the environment-captured rats, to evaluate the practical usefulness of the strips.
Results:
By using this MAb-based-LFA technique, 4 ng/ml of recombinant F1-protein and 103 CFU/ml of Y. pestis could be detected in less than 10 mins, which is at least 10-folds than that of the PAb format. On the other hand, although various Yersinia strains were applied to the strips, only Y. pestis strain showed a positive result; all other Yersinia species did not produce a positive signal, indicating the high efficiency and specificity of the MAb-based F1-strips.
Conclusion:
Based on our findings, we suggest that the MAb-format-LFA will be valuable as a diagnostic tool for the detection of Y. pestis. This report shows that the F1 strip is sufficient to support not only the detection of plague in simulated clinical samples, but also it may be a good candidate to meet the epidemiological surveillance during an outbreak of the biological warfare.
Insights
A new rapid, sensitive, and specific lateral flow assay (F1 strip) using monoclonal antibodies (MAbs) can detect Yersinia pestis, the plague pathogen. This MAb-based F1 strip offers a significant improvement over previous methods for plague detection.
Area of Science:
- Microbiology
- Immunology
- Biotechnology
Background:
- Yersinia pestis causes plague, a historically devastating epidemic disease.
- Current diagnostic methods for Y. pestis may lack the speed, sensitivity, or specificity required for rapid detection.
- The development of an efficient diagnostic tool is crucial for controlling plague outbreaks.
Purpose of the Study:
- To develop a rapid, cost-effective, sensitive, and specific diagnostic assay for Yersinia pestis.
- To create a lateral flow assay (F1 strip) utilizing monoclonal antibodies (MAbs) against the Y. pestis Fraction 1 (F1) protein.
- To evaluate the performance of the MAb-based F1 strip compared to existing polyclonal antibody (PAb) based assays.
Main Methods:
- Expression and purification of recombinant F1 antigen.
- Screening of anti-F1 monoclonal antibodies using ELISA.
- Development of a lateral flow assay (F1 strip) with paired MAbs against Y. pestis F1 protein.
- Spiking experiments with F1 protein and Y. pestis into simulated clinical samples (serum, bronchoalveolar lavage fluid, blood).
- Testing the assay on environmental samples from rats to assess practical utility.
Main Results:
- The MAb-based F1 strip achieved a detection limit of 4 ng/ml for recombinant F1 protein and 10^3 CFU/ml for Y. pestis in under 10 minutes.
- This represents a 10-fold or greater improvement in detection limit compared to PAb-based F1 strips.
- The assay demonstrated high specificity, with positive results only for Y. pestis and no cross-reactivity with other Yersinia species.
Conclusions:
- The MAb-format lateral flow assay (LFA) is a valuable diagnostic tool for Yersinia pestis detection.
- The F1 strip is suitable for detecting plague in simulated clinical samples.
- The assay holds potential for epidemiological surveillance during biological warfare events or outbreaks.
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