» Articles » PMID: 35837060

Applications of Polymerase Chain Reaction-based Methods for the Diagnosis of Plague (Review)

Overview
Journal Exp Ther Med
Specialty Pathology
Date 2022 Jul 15
PMID 35837060
Authors
Affiliations
Soon will be listed here.
Abstract

Plague is an acute bacterial infection caused by . The three major clinical forms of plague are bubonic, pneumonic and septicemic, which have high case-mortality rates. Therefore, rapid and reliable diagnostic tools are crucial. Currently, bacteriological means and traditional serological assays are used for detecting infection with . However, such methods have their limitations. Polymerase chain reaction (PCR) is one of the most useful tools for rapid diagnosis of plague. The present review introduced the main PCR techniques and their applications for detecting and confirmation of . The advantages and disadvantages of the different PCR methods were also summarized.

Citing Articles

Nanotechnology-Enabled PCR with Tunable Energy Dynamics.

Zhao X, Peng H, Hu J, Wang L, Zhang F JACS Au. 2024; 4(9):3370-3382.

PMID: 39328766 PMC: 11423310. DOI: 10.1021/jacsau.4c00570.


Development and evaluation of a multi-target droplet digital PCR assay for highly sensitive and specific detection of Yersinia pestis.

Zhao Y, Yan Z, Song K, Li Y, Shen L, Cui Y PLoS Negl Trop Dis. 2024; 18(5):e0012167.

PMID: 38701065 PMC: 11095742. DOI: 10.1371/journal.pntd.0012167.

References
1.
Thomas M, Janzen T, Huscyzynsky G, Mathews A, Amoako K . Development of a novel multiplexed qPCR and Pyrosequencing method for the detection of human pathogenic yersiniae. Int J Food Microbiol. 2017; 257:247-253. DOI: 10.1016/j.ijfoodmicro.2017.06.019. View

2.
Hennebique A, Gas F, Batina H, De Araujo C, Bizet K, Maurin M . Evaluation of the Biotoxis qPCR Detection Kit for Francisella tularensis Detection in Clinical and Environmental Samples. J Clin Microbiol. 2020; 59(1). PMC: 7771460. DOI: 10.1128/JCM.01434-20. View

3.
Nyirenda S, Hangombe B, Mulenga E, Kilonzo B . Serological and PCR investigation of Yersinia pestis in potential reservoir hosts from a plague outbreak focus in Zambia. BMC Res Notes. 2017; 10(1):345. PMC: 5534097. DOI: 10.1186/s13104-017-2667-9. View

4.
Mayboroda O, Gonzalez Benito A, Sabate Del Rio J, Svobodova M, Julich S, Tomaso H . Isothermal solid-phase amplification system for detection of Yersinia pestis. Anal Bioanal Chem. 2015; 408(3):671-6. DOI: 10.1007/s00216-015-9177-1. View

5.
Wake A . [Pathogenicity of Yersinia pestis: microbiological and molecular aspect]. Nihon Saikingaku Zasshi. 1995; 50(3):651-69. DOI: 10.3412/jsb.50.651. View