Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2012 Jan 26:5:72.
doi: 10.1186/1756-0500-5-72.

Evidence of Yersinia pestis DNA from fleas in an endemic plague area of Zambia

Affiliations

Evidence of Yersinia pestis DNA from fleas in an endemic plague area of Zambia

Bernard M Hang'ombe et al. BMC Res Notes. .

Abstract

Background: Yersinia pestis is a bacterium that causes plague which infects a variety of mammals throughout the world. The disease is usually transmitted among wild rodents through a flea vector. The sources and routes of transmission of plague are poorly researched in Africa, yet remains a concern in several sub-Saharan countries. In Zambia, the disease has been reported on annual basis with up to 20 cases per year, without investigating animal reservoirs or vectors that may be responsible in the maintenance and propagation of the bacterium. In this study, we undertook plague surveillance by using PCR amplification of the plasminogen activator gene in fleas.

Findings: Xenopsylla species of fleas were collected from 83 rodents trapped in a plague endemic area of Zambia. Of these rodents 5 had fleas positive (6.02%) for Y. pestis plasminogen activator gene. All the Y. pestis positive rodents were gerbils.

Conclusions: We conclude that fleas may be responsible in the transmission of Y. pestis and that PCR may provide means of plague surveillance in the endemic areas of Zambia.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Map of Zambia, showing the two provinces of Zambia that had reports of plague. The study area, Namwala district in Southern province is highlighted.
Figure 2
Figure 2
Detection of Y. pestis plasminogen activator gene in fleas by PCR that were collected from rodents. Lanes1 to 5, results of the positive fleas from the gerbils. Lane 6 is the negative control from fleas trapped in a non endemic area, while Lane 7 is the negative control of using brain-heart infusion broth as template.

References

    1. Hinnebusch J, Schwan TG. New method for plague surveillance using polymerase chain reaction to detect Yersinia pestis in fleas. J Clin Microbiol. 1993;31:1511–1514. - PMC - PubMed
    1. Stenseth NC, Atshabar BB, Begon M, Belmain SR, Bertherat E, Carniel E, Gage KL, Leirs H, Rahalison L. Plague: Past, present and future. PLoS Med. 2008;5:e3. doi:10.1371/journal.pmed.005003. - PMC - PubMed
    1. World Health Organization. Human plague in 1998 and 1999. Weekly Epidemiol Rec. 2000;75:338–343. - PubMed
    1. Ngulube TJ, Mwanza K, Njobvu CA, Muula AS. Knowledge, attitudes and public health response towards plague in Petauke, Zambia. Trop Doct. 2006;36:223–225. doi: 10.1258/004947506778604779. - DOI - PubMed
    1. Mwase ET, Mwansa JC, Musonda MM. Plague outbreaks in Zambia: an overview. Zambian J Med Health Sci. 1999;3:50–54.

LinkOut - more resources