Skip directly to search Skip directly to A to Z list Skip directly to page options Skip directly to site content

Volume 14, Number 8—August 2008

Letter

Plasmodium falciparum in Ancient Egypt

Suggested citation for this article

To the Editor: Malaria is a disease caused by parasites of the genus Plasmodium. The infection is transmitted to humans through the bites of female mosquitoes of the genus Anopheles. Four species of Plasmodium are pathogenic to humans, and each leads to different clinical features: P. falciparum causes severe malaria with undulating high fever (malaria tropica); P. malariae, P. vivax, and P. ovale cause less severe clinical courses of disease with the manifestations of malaria quartana (P. malariae) and malaria tertiana (P. vivax and P. ovale). Literary evidence for malaria infection dates back to the early Greek period when Hippocrates described the typical undulating fever (1), highly suggestive of plasmodial infection. Although it is believed that malaria widely affected early pre-Hippocrates populations, until now only 1 study, which used molecular analysis, clearly identified P. falciparum in a Roman infant dating back to the 5th century AD (2). Two other studies used molecular analysis to identify more recent plasmodial DNA in ancient human remains, i.e., from 100–400 years ago (3,4). A substantial number of nonspecific amplifications in these previous studies raised concerns as to the specificity of current molecular markers for ancient malaria (3,4).

In this report, we describe the unambiguous identification of ancient DNA (aDNA) for P. falciparum in ancient Egyptian mummy tissues from ≈4,000 years ago. We analyzed 91 bone tissue samples from ancient Egyptian mummies and skeletons. The Egyptian material derived from the Predynastic to Early Dynastic site of Abydos (n = 7; 3500–2800 BC), a Middle Kingdom tomb in Thebes West (n = 42; 2050–1650 BC), and various tomb complexes in Thebes West, which were built and used between the Middle and New Kingdom until the Late Period (n = 42; c. 2050–500 BC). All samples were first tested for Plasmodium spp. DNA by using the heminested PCR for the 18S rDNA primer targets usually used for malaria identification (5). Direct sequencing was performed on those with positive amplification products. Thereby, a high number of amplification products of various sizes (including the expected size) were detected. However, on sequencing, all amplicons provided nonspecific products. Consequently, in a second set, all material was tested for the P. falciparum chloroquine-resistance transporter gene (pfcrt gene) (6,7), which was also further characterized by direct sequencing.

Figure

Thumbnail of PCR amplification of a 134-bp fragment of ancient DNA of Plasmodium falciparum in Egyptian mummies. Lane 1, molecular marker; lanes 10 and 11, 2 negative controls. One (lane 6) of 8 samples shows a positive amplification product (arrow). Specificity of the product was verified by sequencing.

Figure. PCR amplification of a 134-bp fragment of ancient DNA of Plasmodium falciparum in Egyptian mummies. Lane 1, molecular marker; lanes 10 and 11, 2 negative controls. One (lane 6) of 8...

In this second set of experiments, 2 of the 91 ancient Egyptian samples tested positive for the 134-bp fragment of the pfcrt region of P. falciparum (Figure). The specificity of the amplification was verified by sequencing, which showed 99% sequence concordance. The result was verified by parallel analysis in 2 independent laboratories; observations were fully concordant. The 2 positive samples originated from 2 different tomb complexes dating from the New Kingdom until Late Period (1500–500 BC). Each sample was obtained from adults who had osteopathologic evidence of chronic anemia. No positive results were found for the earlier samples from the Predynastic to Early Dynastic or Middle Kingdom periods.

Previously, immunologic tests have been used to investigate the presence and incidence of malaria in ancient Egyptian mummies (8,9). Because >40% of all samples and 92% of samples from persons with bone lesions suggestive of chronic anemia tested positive for the P. falciparum histidine-rich protein-2 antigen, doubts as to the specificity of those tests have been raised.

Our study unambiguously identified P. falciparum aDNA in Egyptian mummy samples, thereby proving a specific infection by falciparum malaria in ancient Egypt. With respect to the infection incidence, our molecular analysis suggests a more realistic frequency than had been previously suggested by paleoimmunologic methods. Consequently, the aDNA analysis is superior with respect to the reaction specificity, so that the latter should not further be used for that purpose.

This report adds another infectious disease to the spectrum of paleomicrobiology in ancient Egypt, thereby further explaining the previously postulated influence of infectious diseases on the low life expectancy for ancient Egyptian populations (10). Molecular detection of pathogen aDNA can be used not only to identify a certain disease, but it may also provide information on disease frequency, evolutionary origin, and pathways.

Andreas G. Nerlich*Comments to Author , Bettina Schraut*, Sabine Dittrich†, Thomas Jelinek‡, and Albert R. Zink*1
Author affiliations: *Academic Teaching Hospital München-Bogenhausen, Munich, Germany; †University of Manchester, Manchester, UK; ‡Institute of Tropical Medicine, Berlin, Germany;

References

  1. Hippocrates . Of the epidemics 1.6,7,24–26; Aphorisms 3.21,22;4.59,63; on airs, waters and places c. 10. In: Bogdonoff MD, Crellin JK, Good RA, McGovern JP, Nuland SB, Saffon, MH, et al., editors. The genuine works of Hippocrates. Birmingham (AL): Classics of Medicine Library; 1985.
  2. Sallares R, Gomzi S. Biomolecular archaeology of malaria. Anc Biomol. 2001;3:196213.
  3. Taylor GM, Rutland P, Molleson T. A sensitive polymerase chain reaction method for the detection of Plasmodium species DNA in ancient human remains. Anc Biomol. 1997;1:193203.
  4. Zink A, Haas CJ, Herberth K, Nerlich AG. PCR amplification of Plasmodium DNA in ancient human remains. Anc Biomol. 2001;3:293.
  5. Snounou G, Viriyakosal S, Zhu XP, Jarra W, Pinheiro L, do-Rosario VE, High sensitivity of detection of human malaria parasites by the use of nested polymerase chain reaction. Mol Biochem Parasitol. 1993;61:31520. DOIPubMed
  6. Djimde A, Doumbo OK, Cortese JF, Kayebtao K, Doumbo S, Diourte Y, A molecular marker for chloroquine-resistant falciparum malaria. N Engl J Med. 2001;344:25763. DOIPubMed
  7. Dittrich S, Alifrangis M, Stohrer JM, Thongpaseuth V, Vanisaveth V, Phetsouvanh R, Falciparum malaria in the north of Laos: the occurrence and implications of the Plasmodium falciparum chloroquine resistance transporter (pfcrt) gene haplotype SVMNT. Trop Med Int Health. 2005;10:126770. DOIPubMed
  8. Miller RL, Ikram S, Armelagos GJ, Walker R, Harer WB, Schiff CJ, Diagnosis of Plasmodium falciparum infections in mummies using the rapid manual ParaSight-F test. Trans R Soc Trop Med Hyg. 1994;88:312. DOIPubMed
  9. Rabino Massa E, Cerutti N, Savoia D. Malaria in ancient Egypt: paleoimmunological investigations in predynastic mummified remains. Chungara. 2000;32:79.
  10. Nerlich A, Zink A, Hagedorn HG, Szeimies U, Weyss C. Anthropological and palaeopathological analysis of the human remains from three “Tombs of the Nobles” of the necropolis of Thebes-west, upper Egypt. Anthropol Anz. 2000;58:32143.PubMed

Figure

Suggested citation for this article: Nerlich AG, Schraut B, Dittrich S, Jelinek T, Zink AR. Plasmodium falciparum in ancient Egypt. [letter]. Emerg Infect Dis [serial on the Internet]. 2008 Aug [date cited]. Available from http://wwwnc.cdc.gov/eid/article/14/8/08-0235

DOI: 10.3201/eid1408.080235

1Current affiliation: Eurac, Bolzano, Italy.

Related Links

Table of Contents – Volume 14, Number 8—August 2008

Comments to the Authors

Please use the form below to submit correspondence to the authors or contact them at the following address:

Andreas G. Nerlich, Division of Paleopathology, Institute of Pathology, Academic-Teaching Hospital München-Bogenhausen, Englschalkingerstr 77 D-81925, Munich, Germany;

character(s) remaining.

Comment submitted successfully, thank you for your feedback.

Comments to the EID Editors

Please contact the EID Editors via our Contact Form.

TOP