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

Volume 13, Number 9—September 2007

Dispatch

Malaria Reemergence in Northern Afghanistan

Michael K. Faulde*Comments to Author , Ralf Hoffmann*, Khair M. Fazilat†, and Achim Hoerauf‡
Author affiliations: *Central Institute of the Bundeswehr Medical Service, Koblenz, Germany; †Provincial Malaria Unit, Kundoz, Afghanistan; ‡University Clinic Bonn, Bonn, Germany;

Suggested citation for this article

Abstract

Field investigations were conducted in Kundoz Province, an Afghan high-risk area, to determine factors responsible for the rapid reemergence of malaria in that country, where 3 million cases were estimated to have occurred during 2002. Results indicate the presence of nonrice-field–dependent Plasmodium falciparum and rice-field–associated P. vivax malaria.

In 2002, the total malaria incidence in Afghanistan was estimated to be 3 million cases per year, most of them in Kundoz Province. Field investigations from 2001 through 2005 showed a rapid reemergence of malaria caused by Plasmodium falciparum and P. vivax, with annual incidence rates from 0.0088 to 4.39 and from 3.58 to 13.37 episodes per 1,000 person-years, respectively. Both diseases peaked during 2002 and then declined independently. Although control campaigns against falciparum malaria, transmitted by the freshwater breeder Anopheles superpictus, have been successful, P. vivax malaria remains highly endemic and is associated with rice-growing areas, where it is transmitted by the endophilic and exophilic rice-field breeders, A. pulcherrimus and A. hyrcanus. P. vivax polymorph VK 247 prevailed in 90% of infected mosquito pools. Field data showed anthropogenically induced increases in rice-field vivax malaria in northern Afghanistan and the need for further control strategies, including large-scale larval mosquito eradication, in rice-growing areas.

Malaria is endemic to large areas of Afghanistan that are <2,000 meters above sea level, but high-altitude epidemic P. falciparum malaria may occur in areas >2,400 meters above sea level (1). From the 1950s through 1979, malaria control in Afghanistan was implemented by the government (2,3). During the 1970s, the number of recorded cases of malaria varied from 40,000 to 80,000 annually (4). At that time, vivax malaria chiefly occurred in the irrigated zones of northeastern Afghanistan (3). Rice fields were located >5 km away from villages to exceed the flight range of vector-competent, widely DDT-resistant anopheline mosquitoes, and larvivorous Gambusia affinis fish were continuously reared and widely introduced (5,6). After 1980, chronic political instability resulted in the progressive breakdown of malaria control activities (2).

Although existing malaria control efforts have focused mainly on the Kabul area, little is known about the situation in the irrigated rice-growing high-risk areas of northeastern Afghanistan (7). During 1996–2001, from 202,767 to 395,581 malaria cases were reported annually, sharply increasing in 2002 and 2003 with 590,176 and 591,441 cases confirmed, respectively (7), and 3 million cases estimated annually (8). Takhar and Kundoz Provinces were most affected (7). In late 2003, P. falciparum incidence ranged from 0.002% in Wardak to 31% in Takhar Province. The other malaria cases were attributable to P. vivax (7). Our aim was to analyze the current status, risk factors, and epidemiology of malaria in Kundoz Province, a previously underreported risk area.

The Study

Figure

Thumbnail of Plasmodium vivax (Pv) and P. falciparum (Pf) malaria cases reported in Kundoz Province, northern Afghanistan, January 2001–December 2005.

Figure. Plasmodium vivax (Pv) and P. falciparum (Pf) malaria cases reported in Kundoz Province, northern Afghanistan, January 2001–December 2005.

Newly contracted (excluding all follow-up patients with P. vivax relapses) malaria cases were confirmed by light microscopy, using standard Giemsa staining according to the World Health Organization (WHO) national malaria treatment and diagnosis guidelines (79), and were detected passively in febrile patients seeking treatment in the Provincial Malaria Center, Kundoz City, from January 2001 through December 2005. Annual cases of P. vivax and P. falciparum malaria reported from Kundoz Province from January 2001 through December 2005 are depicted in the Figure. A marked increase in case numbers of both vivax and falciparum malaria occurred from 2001 through 2002, showing an 8.9-fold increase for P. falciparum. After 2002, the height of the epidemic, malaria case numbers steadily declined, with P. vivax cases falling to 10,946 and P. falciparum cases falling to only 27 during 2005. With an estimated population of 3,058,100, the annual incidence rates for P. falciparum malaria in Kundoz Province were from 0.0088 (in 2005) to 4.39 (in 2002) per 1,000 person-years; for P. vivax, the rates were from 3.57 (in 2005) to 13.37 (in 2002) per 1,000 person-years.

From January 2004 through December 2005, adult anopheline mosquitoes were collected outdoors by using New Standard Miniature Light Traps (No. 1012, John W. Hook Co., Gainesville, FL, USA) without an additional CO2 generator and indoors by using an aspirator in the rice-growing areas of Kundoz City, Kanam, Khanabad, Angor Bag, Alchira, Malaghi, and Jan Guzar. Light Traps were set in housing areas within a 5-km radius of rice fields, which are located in or close to towns, villages, and housing areas. Anopheline larval monitoring was carried out using the WHO-recommended Frisbee disk method (10) once a month from May through October in rice fields associated with mosquito trapping sites. Results represent mean values obtained after 10 replicates.

Indoor trapping showed the following: of 299 anopheline mosquitoes trapped in 2004, 82.6% were A. pulcherrimus, 16.7% were A. superpictus, and 0.7% were A. culicifacies; of 403 anophelines trapped in 2005, 81.1% were A. pulcherrimus and 18.9% were A. superpictus (11). All specimens were female and blood-fed.

Outdoor entomologic surveys showed the following: of 439 anophelines collected in 2004, 60.1% were A. pulcherrimus, 30.0% were A. hyrcanus, and 9.9% were A. superpictus; of 456 anophelines collected in 2005, 47.4% were A. hyrcanus, 42.1% were A. pulcherrimus, and 10.5% were A. superpictus. Among all mosquitoes trapped, 80.8% were female, and 22.9% of these were blood-fed. The mean trap rate was 4.8 ± 3.9 anophelines per trap night (range 0–17 per trap night).

Anopheline adult outdoor abundance peaked in late August, with the following percentage monthly means: May (1.2%), June (9.5%), July (18.6%), August (35.2%), September (26.8%), and October (8.7%). Anopheline larval monitoring yielded 54.7% A. hyrcanus (0–68 larvae per dip; mean 12.3), and 45.3% A. pulcherrimus (0–49 larvae per dip; mean 9.8). No A. superpictus or A. culicifacies larvae could be detected in rice field samples. Anopheline larval abundance peaked in late July and early August with the following monthly means: May (0%), June (17.9%), July (32.3%), August (36.2%), September (12.8%), and October (0.8%).

The P. falciparum and P. vivax polymorphs VK 210 and VK 247 circumsporozoite protein (CSP) positivity rates in anopheline pools (5 females per species) trapped indoors and outdoors from 2004 through 2005 were detected by using the VecTest Malaria Panel Assay dipstick ELISA (Medical Analysis Systems, Inc., Camarillo, CA, USA) and are listed in the Table. The available data indicate that A. superpictus is the principal P. falciparum vector. Three A. pulcherrimus pools positive for P. falciparum CSP indicate that this species may be partly involved in P. falciparum malaria transmission. Plasmodium CSP positivity values were higher in indoor-trapped A. superpictus (2004: χ2 = 4.9; df = 1; p = 0.025). Of P. vivax CSP-positive pools, 90.6% were VK 247-reactive, and 9.4% were reactive against both VK 247 and VK 210, indicating a similar P. vivax genospecies distribution pattern as reported previously from eastern Afghanistan (12).

Conclusions

Our results show that malaria quickly reemerged in rice-growing Kundoz Province of northeastern Afghanistan. This may be due to various factors: 1) introduction of P. falciparum and P. vivax malaria by returning refugees (13); 2) environmental changes caused by intensified rice growing in close proximity to towns, villages, and housing areas and therefore within flight range of endemic anopheline vectors (3,5); 3) increased abundance and breeding of the local principal vectors of P. vivax malaria stemming from intensified rice growing and irrigation systems that serve as preferred breeding sites for A. pulcherrimus and A. hyrcanus (3,5); and 4) absence of widespread biological and chemical vector control measures, including effective larviciding in flooded rice fields (8).

Habitat and breeding site preferences of malaria vectors may play a major role in the differing epidemiologies of local P. falciparum malaria and rice-field–dependent, exophilic and endophilic P. vivax malaria. Possible reasons for the decline in annual malaria cases after 2002, especially in endophilic P. falciparum malaria not dependent on rice fields, may include the introduction of insecticide-treated bednets, increased indoor spraying, and improved treatment and health education (7,8), as well as inhibiting climatic conditions (e.g., the extraordinarily cold 2005 spring/summer season). Current P. vivax malaria incidence rates indicate that future control efforts should emphasize large-scale management of potential mosquito breeding sites in rice-growing areas, including biological or chemical larviciding or both. The effectiveness of personal protection from exophilic P. vivax malaria vectors such as A. hyrcanus may be enhanced by simultaneous use of skin repellents and insecticide-treated clothing (14,15).

Dr Faulde is assistant professor of medical entomology and parasitology on the medical faculty, University of Bonn, Germany, and director and senior adviser in medical entomology/zoology of the Bundeswehr Medical Service. His research interests include modes of transmission, epidemiology of, and field-based “Near-Real-Time” surveillance systems for arthropod- and rodentborne diseases.

Acknowledgment

We thank the Afghan Ministry of Public Health, WHO, and HealthNet International for logistical support; Doud Akbari and Sabine Barz for technical assistance; and Richard G. Robbins, US Armed Forces Pest Management Board, for critically reviewing the manuscript.

References

  1. Abdur Rab M, Freeman TW, Rahim S, Durrani N, Simon-Taha A, Rowland M. High altitude epidemic malaria in Bamian Province, central Afghanistan. East Mediterr Health J. 2003;9:2329.PubMed
  2. Kolaczinski J, Graham K, Fahim A, Brooker S, Rowland M. Malaria control in Afghanistan: progress and challenges. Lancet. 2005;365:150612. DOIPubMed
  3. Artem`ev MM, Anufrieva VN, Zharov AA, Flerova OA. Problem of malaria and the malaria control measures in northern Afghanistan. 3. Anopheles mosquitoes in the rice-growing areas. Med Parazitol (Mosk). 1977;46:40613.PubMed
  4. Ministry of Public Health. Islamic Republic of Afghanistan. National Malaria Strategic Plan 2006–2010. [cited 2007 Apr 18]. Available from http://www.who.int/malaria/docs/complex_emergencies_db/AfghanistanStrategicPlanRBM.pdf
  5. Onori E, Nushin MK, Cullen JE, Yakubi GH, Mohammed K, Christal FA. An epidemiological assessment of the residual effect on DDT on Anopheles hyrcanus sensu lato and A. pulcherrimus (Theobald) in the north eastern region of Afghanistan. Trans R Soc Trop Med Hyg. 1975;69:23642. DOIPubMed
  6. Polevoj NI. Experiment on Gambusia transportation from Tazik SSR into north-east Afghanistan and its application in the antimalaria campaign. WHO/MAL.73.795; 1973.
  7. World Health Organization. Roll back malaria monitoring and evaluation. Afghanistan. [cited 2007 Feb 1]. Available from http://www.rbm.who.int/wmr2005/profiles/afghanistan.pdf
  8. World Health Organization. WHO Afghanistan activities. [cited 2007 Feb 1]. Available from http://www.who.int/disasters/repo/13773.pdf
  9. World Health Organization. Basic laboratory methods in medical parasitology. Geneva: the Organization; 1991.
  10. Service MW. Mosquito ecology—field sampling methods. 2nd ed. London: Elsevier Applied Science; 1993.
  11. Glick JI. Illustrated key to the female Anopheles of southwestern Asia and Eqypt (Diptera: Culicidae). Mosq Syst. 1992;24:12553.
  12. Rowland M, Mohammed N, Rehman H, Hewitt S, Mendis C, Ahmad M, Anopheline vectors and malaria transmission in eastern Afghanistan. Trans R Soc Trop Med Hyg. 2002;96:6206. DOIPubMed
  13. Rowland M, Rab MA, Freeman T, Durrani N, Rehman N. Afghan refugees and the temporal and spatial distribution of malaria in Pakistan. Soc Sci Med. 2002;55:206172. DOIPubMed
  14. World Health Organization. Vectors of diseases: hazards and risks for travelers—Part I. Wkly Epidemiol Rec. 2001;25:18994.
  15. Faulde M, Uedelhoven W. A new clothing impregnation method for personal protection against ticks and biting insects. Int J Med Microbiol. 2006;292(Suppl 1):2259. DOI

Figure

Table

Suggested citation for this article: Faulde MK, Hoffmann R, Fazilat KM, Hoerauf A. Malaria re-emergence in northern Afghanistan. Emerg Infect Dis [serial on the Internet]. 2007 Sep [date cited]. Available from http://wwwnc.cdc.gov/eid/article/13/9/06-1325

DOI: 10.3201/eid1309.061325

Table of Contents – Volume 13, Number 9—September 2007

Comments to the Authors

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

Michael K. Faulde, Central Institute of the Bundeswehr Armed Forces Medical Service, Department of Medical Entomology/Zoology, PO Box 7340, D-56065, Koblenz, 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