Cover image of the article: Review on the Laboratory diagnosis of Q-Fever

Image Credit:Ann Mil Health Sci Res

Review on the Laboratory diagnosis of Q-Fever

Authors

Raziyeh Zabihi1, Keyvan Majidzadeh2, Amir Hossein Mohseni3, Mohammad Soleimani4,*
1Researcher, Department of Microbiology, Qom Branch, Islamic Azad University, Qom, Iran., Andorra
2Assistant Professor, Tasnim Biotechnology of Research Center (TBRC), AJA University of Medical Sciences, Tehran, Iran., Andorra
3Researcher, Tasnim Biotechnology of Research Center (TBRC), AJA University of Medical Sciences, Tehran, Iran., Andorra
4Assistant Professor, Department of Microbiology, Qom Branch, Islamic Azad University, Qom, Iran., Andorra
*Corresponding Author: Corresponding author: Mohammad Soleimani, Assistant Professor, Department of Microbiology, Qom Branch, Islamic Azad University, Qom, Iran., Andorra Email: soleimanidr@yahoo.com

Annals of Military and Health Sciences Research:Vol. 11, issue 4; e64999
Published online:Dec 05, 2013
Article type:Review Article
Received:Jul 29, 2013
Accepted:Nov 05, 2013
How to Cite: Zabihi R, Majidzadeh K, Mohseni AH, Soleimani M. Review on the Laboratory diagnosis of Q-Fever. Ann Mil Health Sci Res. 2013;11(4):e64999. doi:

Abstract

Background: Coxiella burnetii is the etiologicagent of a zoonotic disease which named Q-fever in humans and coxiellosis in animals. This bacterium can survive in the environment out of the specific host. Accordingly, it categorized by the CDC in bioterrorism agents ‘category B. Consequently, rapid detection of the bacteriumadministratesthe treatment of disease. Materials and Methods: A review study on the different researches on laboratory diagnosis field in the world and Iran scientific databases was conducted. This paper includes biological safety, cultivation and detection assays. Results: Detection of Coxiella burnetii can be done byclassical methods (isolation, cultivation in the appropriate cell line such as P388D1, J774, and L929), serologic tests (immunofluorescence, micro immunofluorescence, complement fixation test and ELISA) and molecular biology methods (PCR, Nested PCR and Real Time PCR). Conclusions: While have existed kinds of detection methods for this agent, costly, need to specific laboratory and time consuming are the limitation of the mentioned techniques. Molecular methods due to accuracy and high rapidity in detection can be effective.

Highlights

Fulltext

Full text is available in pdf

References

  • 1.
    References are available in pdf.

Copyright

© 2013, Annals of Military and Health Sciences Research. This open-access article is available under the Creative Commons Attribution-NonCommercial 4.0 (CC BY-NC 4.0) International License (https://creativecommons.org/licenses/by-nc/4.0/), which allows for the copying and redistribution of the material only for noncommercial purposes, provided that the original work is properly cited.

Similar Articles

27
Jun
2015
The Sensitivity of the PCR Method for Detection of Coxiella burnetii in the Milk Samples

The Sensitivity of the PCR Method for Detection of Coxiella burnetii in the Milk Samples

Mohammad Kargar,
Afsaneh Rashidi,
Abbass Doosti,
Akram Najafi,
Sadegh Ghorbani-Dalini

Kargar M, Rashidi A, Doosti A, Najafi A, Ghorbani-Dalini S. The Sensitivity of the PCR Method for Detection of Coxiella burnetii in the Milk Samples. Zahedan J Res Med Sci. 2015;17(6):-. doi: https://doi.org/10.17795/zjrms988

16
Mar
2025
First Report of Coxiella Burnetii Meningitis in Iran

First Report of Coxiella Burnetii Meningitis in Iran

Saeed Soleiman-Meigooni,
Mehdi Sakhabakhsh,
Mousa Ahmadi

Soleiman-Meigooni S, Sakhabakhsh M, Ahmadi M. First Report of Coxiella Burnetii Meningitis in Iran. Ann Mil Health Sci Res. 2025;23(1):e159919. doi: https://doi.org/10.5812/amh-159919

9
Dec
2023
Molecular Detection of Coxiella burnetii by Nested PCR Method in Cattle and Buffalo Raw Milk, Urmia Region, Iran

Molecular Detection of Coxiella burnetii by Nested PCR Method in Cattle and Buffalo Raw Milk, Urmia Region, Iran

Ahmad Enferadi,
Abdolghaffar Ownagh,
Karim Mardani

Enferadi A, Ownagh A, Mardani K. Molecular Detection of Coxiella burnetii by Nested PCR Method in Cattle and Buffalo Raw Milk, Urmia Region, Iran. Jentashapir J Cell Mol Biol. 2023;14(4):e136221. doi: https://doi.org/10.5812/jjcmb-136221

14
Nov
2016
Seroprevalence of Coxiella burnetii in Dairy Cattle and Camel in Sudan

Seroprevalence of Coxiella burnetii in Dairy Cattle and Camel in Sudan

Mohammed Osman Hussien,
Khalid Abdallah Enan,
Shima Hassan Alfaki,
Rana Alhibir Gafar,
Khalid Mohamed Taha,
Abdel Rahim Mohamed El Hussein

Hussien MO, Enan KA, Hassan Alfaki S, Alhibir Gafar R, Mohamed Taha K, et al. Seroprevalence of Coxiella burnetii in Dairy Cattle and Camel in Sudan. Int J Infect. 2017;4(3):e42945. doi: https://doi.org/10.5812/iji.42945

9
Feb
2023
Seroprevalence of Q Fever and Risk Factors Affecting Transmission of Coxiella burnetii in Industrial Slaughterhouse; A Survey from Northeastern Iran

Seroprevalence of Q Fever and Risk Factors Affecting Transmission of Coxiella burnetii in Industrial Slaughterhouse; A Survey from Northeastern Iran

Majid Khadem-Rezaiyan,
Golam Ali Azari Garmjan,
Lida Jarahi,
Kiarash Ghazvini,
Masoud Youssefi

Khadem-Rezaiyan M, Azari Garmjan GA, Jarahi L, Ghazvini K, Youssefi M. Seroprevalence of Q Fever and Risk Factors Affecting Transmission of Coxiella burnetii in Industrial Slaughterhouse; A Survey from Northeastern Iran. Health Scope. 2023;12(1):e132858. doi: https://doi.org/10.5812/jhealthscope-132858

More by these authors

Raziyeh ZabihiPubMedScholar
Keyvan MajidzadehPubMedScholar
Amir Hossein MohseniPubMedScholar
Mohammad SoleimaniPubMedScholar
Share
Cited by
Metrics