Effects of treatment and drug resistance on the transmission dynamics of malaria in endemic areas

被引:44
作者
Chiyaka, Christinah [1 ]
Garira, Winston [1 ]
Dube, Shadreck [2 ]
机构
[1] Natl Univ Sci & Technol, Dept Appl Math, Bulawayo, Zimbabwe
[2] Natl Univ Sci & Technol, Dept Appl Biol Biochem, Bulawayo, Zimbabwe
关键词
Malaria; Treatment; Resistance; Endemic; Delay; Reproductive number; PLASMODIUM-FALCIPARUM; ANTIMALARIAL RESISTANCE; ANOPHELES MOSQUITOS; CHLOROQUINE USE; SPREAD; MODELS; INFECTION; PARASITES; PYRIMETHAMINE; EVOLUTION;
D O I
10.1016/j.tpb.2008.10.002
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
We present a mathematical model for malaria treatment and spread of drug resistance in an endemic population. The model considers treated humans that remain infectious for some time and partially immune humans who are also infectious to mosquitoes although their infectiousness is always less than their non immune counterparts. The model is formulated by considering delays in the latent periods in both mosquito and human populations and in the period within which partial immunity is lost. Qualitative analysis of the model including positivity and boundedness of solutions is performed. Analysis of the reproductive numbers shows that if the treated humans become immediately uninfectious to mosquitoes then treatment will always reduce the number of sensitive infections. If however treated humans are infectious then for treatment to effectively reduce the number of sensitive infections, the ratio of the infectious period of the treated humans to the infectious period of the untreated humans multiplied by the ratio of the transmission rate from a treated human to the transmission rate of an untreated human should be less than one. Our results show that the spread of drug resistance with treatment as a control strategy depends on the ratio of the infectious periods of treated and untreated humans and on the transmission rates from infectious humans with resistant and sensitive infections. Numerical analysis is performed to assess the effects of treatment on the spread of resistance and infection. The study provides insight into the possible intervention strategies to be employed in malaria endemic populations with resistant parasites by identifying important parameters. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:14 / 29
页数:16
相关论文
共 54 条
[31]   Reemergence of chloroquine-sensitive Plasmodium falciparum malaria after cessation of chloroquine use in Malawi [J].
Kublin, JG ;
Cortese, JF ;
Njuniu, EM ;
Mukadam, RAG ;
Wirima, JJ ;
Kazembe, PN ;
Djimdé, AA ;
Kouriba, B ;
Taylor, TE ;
Plowe, CV .
JOURNAL OF INFECTIOUS DISEASES, 2003, 187 (12) :1870-1875
[32]   GLOBAL STABILITY FOR THE SEIR MODEL IN EPIDEMIOLOGY [J].
LI, MY ;
MULDOWNEY, JS .
MATHEMATICAL BIOSCIENCES, 1995, 125 (02) :155-164
[33]  
LIU DQ, 1995, B WORLD HEALTH ORGAN, V73, P483
[34]   Molecular characterisation of drug-resistant Plasmodium falciparum from Thailand [J].
Dinora Lopes ;
Kanchana Rungsihirunrat ;
Fátima Nogueira ;
Aree Seugorn ;
José Pedro Gil ;
Virgilio E do Rosário ;
Pedro Cravo .
Malaria Journal, 1 (1)
[35]   RELATIONSHIP BETWEEN BODY SIZE OF ADULT ANOPHELES-GAMBIAE SL AND INFECTION WITH THE MALARIA PARASITE PLASMODIUM-FALCIPARUM [J].
LYIMO, EO ;
KOELLA, JC .
PARASITOLOGY, 1992, 104 :233-237
[36]  
Mcdonald G., 1957, The epidemiology and control of malaria
[37]   Association of house spraying with suppressed levels of drug resistance in Zimbabwe [J].
Mharakurwa, S ;
Mutambu, SL ;
Mudyiradima, R ;
Chimbadzwa, T ;
Chandiwana, SK ;
Day, KP .
MALARIA JOURNAL, 2004, 3 (1)
[38]   Recovery of chloroquine sensitivity and low prevalence of the Plasmodium falciparum chloroquine resistance transporter gene mutation K76T following the discontinuance of chloroquine use in Malawi [J].
Mita, T ;
Kaneko, A ;
Lum, JK ;
Bwijo, B ;
Takechi, N ;
Zungu, IL ;
Tsukahara, T ;
Tanabe, K ;
Kobayakawa, T ;
Björkman, A .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 2003, 68 (04) :413-415
[39]   Towards an understanding of the mechanism of pyrimethamine-sulfadoxine resistance in Plasmodium falciparum:: Genotyping of dihydrofolate reductase and dihydropteroate synthase of Kenyan parasites [J].
Nzila, AM ;
Mberu, EK ;
Sulo, J ;
Dayo, H ;
Winstanley, PA ;
Sibley, CH ;
Watkins, WM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (04) :991-996
[40]   Potential impact of intermittent preventive treatment (IPT) on spread of drug-resistant malaria [J].
O'Meara, Wendy Prudhomme ;
Smith, David L. ;
McKenzie, F. Ellis .
PLOS MEDICINE, 2006, 3 (05) :633-642