- Open Access
Population-level estimates of the proportion of Plasmodium vivax blood-stage infections attributable to relapses among febrile patients attending Adama Malaria Diagnostic Centre, East Shoa Zone, Oromia, Ethiopia
© The Author(s) 2017
- Received: 7 April 2017
- Accepted: 18 July 2017
- Published: 27 July 2017
Malaria is ranked as the leading communicable disease in Ethiopia, where Plasmodium falciparum and Plasmodium vivax are co-endemic. The incidence of P. vivax is usually considered to be less seasonal than P. falciparum. Clinical cases of symptomatic P. falciparum exhibit notable seasonal variation, driven by rainfall-dependent variation in the abundance of Anopheles mosquitoes. A similar peak of clinical cases of P. vivax is usually observed during the rainy season. However, the ability of P. vivax to relapse causing new blood-stage infections weeks to months after an infectious mosquito bite can lead to substantial differences in seasonal patterns of clinical cases. These cannot be detected with currently available diagnostic tools and are not cleared upon treatment with routinely administered anti-malarial drugs.
A health- facility based cross-sectional study was conducted in Adama malaria diagnostic centre from May 2015 to April 2016. Finger-prick blood samples were collected for thin and thick blood film preparation from participants seeking treatment for suspected cases of febrile malaria. Informed consent was obtained from each study participant or their guardians. Seasonal patterns in malaria cases were analysed using statistical models, identifying the peaks in cases, and the seasonally varying proportion of P. vivax cases attributable to relapses.
The proportion of patients with malaria detectable by light microscopy was 36.1% (1141/3161) of which P. vivax, P. falciparum, and mixed infections accounted for 71.4, 25.8 and 2.8%, respectively. Of the febrile patients diagnosed, 2134 (67.5%) were males and 1919 (60.7%) were urban residents. The model identified a primary peak in P. falciparum and P. vivax cases from August to October, as well as a secondary peak of P. vivax cases from February to April attributable to cases arising from relapses. During the secondary peak of P. vivax cases approximately 77% (95% CrI 68, 84%) of cases are estimated to be attributable to relapses. During the primary peak from August to October, approximately 40% (95% CrI 29, 57%) of cases are estimated to be attributable to relapses.
It is not possible to diagnose whether a P. vivax case has been caused by blood-stage infection from a mosquito bite or a relapse. However, differences in seasonal patterns of P. falciparum and P. vivax cases can be used to estimate the population-level proportion of P. vivax cases attributable to relapses. These observations have important implications for the epidemiological assessment of vivax malaria, and initiating therapy that is effective against both blood stages and relapses.
- P. vivax
Plasmodium vivax is the most widely distributed species of malaria in the world, causing an estimated 8.5 (6.6–10.8) million clinical cases per year . Across the globe, there are about 3 billion people at risk of P. vivax infection . Despite this large burden of disease, P. vivax is often overlooked compared to Plasmodium falciparum, which is responsible for the majority of malaria-associated deaths, predominantly in young children and pregnant women in sub-Saharan Africa. Ethiopia together with India, Indonesia, and Pakistan accounts for more than 80% of the global P. vivax burden .
About 75% of the landmass of Ethiopia is either malarious or potentially malarious and an estimated total of 68% of the Ethiopian population live at altitudes below 2000 m and are considered to be at risk of malaria. In Ethiopia, P. falciparum and P. vivax account for about 60 and 40% of all malaria cases, respectively . Malaria transmission is generally seasonal and unstable with substantial spatial and inter- and intra-annual variation. The seasonality is attributed to variation in the vector population (due to variation in the suitability of climatic conditions for vector breeding) across different months of the year. In general, two main seasons for the transmission of malaria are known in Ethiopia: the major transmission season from September to December following the main rainy season from June to August and the minor transmission season from April to May following the shorter rainy season in March, although the transmission seasons generally vary from region to region depending on climatic conditions such as temperature, rainfall, and humidity . In some parts of the country where temperature and rainfall conditions are nearly always favorable the transmission of malaria occurs throughout the year. In Ethiopia, most malaria control interventions are initiated during wet seasons. The co-existence of both P. falciparum and P. vivax in Ethiopia creates challenges for prevention, control and elimination of the disease. Anopheles arabiensis is the main malaria vector although Anopheles pharoensis, Anopheles funestus and Anopheles nili also transmit malaria .
The interruption of P. vivax transmission is not easy because of its unique biological features, most notably, the ability for relapses to cause new blood-stage infections weeks to months after the initial infectious mosquito bite . In contrast to P. falciparum, which has only sporozoite induced infections, P. vivax blood-stage parasitaemia can arise from either mosquito-borne sporozoites or liver-stage hypnozoites. Hypnozoites arise from P. vivax sporozoites that invade liver-stage hepatocytes and lie dormant for weeks to years before activating to cause relapses . Assigning the exact source of any given blood stage infection (parasitaemia) observed in endemic settings is usually impossible, but the force of infection attributable to sporozoites versus hypnozoites may still be inferred at a population level [8–10].
Relapse may well be the predominant origin of most P. vivax clinical attacks throughout the endemic areas. Failure to systematically attack the hypnozoite reservoir of P. vivax not only results in repeated clinical attacks and serious illness, but also creates further opportunities for transmission to others . The time to first relapse after primary infection has been observed to be approximately 3 months in Ethiopia . When the transmission season ceases as a consequence of decline and/or absence of the mosquito population, most vivax malaria cases in the dry season are likely due to hypnozoite reactivation. Although hypnozoites do not contribute to clinical disease until activated, these dormant stages of the parasite ultimately play a vital role in sustaining transmission as they are refractory to blood-stage antimalarial drugs and interventions to reduce transmission. Furthermore, hypnozoites also ensure the ability of P. vivax to survive in climatic conditions that cannot sustain P. falciparum transmission [13, 14].
Representing an important reservoir for new infections, P. vivax hypnozoites are less susceptible to conventional malaria control interventions such as insecticides, bed nets, diagnostic methods, and almost all chemoprophylactic or chemotherapeutic interventions . Only one class of drugs, 8-aminoquinolines, has been proven to successfully prevent relapses, with primaquine being the only drug from this class currently licensed for use. In most endemic countries chloroquine (CQ) and primaquine (PQ) have been used as the first-line therapies for P. vivax infections except where P. vivax is resistant to CQ . There are currently insufficient measures in place to ensure the safe delivery of PQ within the context of glucose-6-phosphate dehydrogenase deficiency (G6PDd) risk . As PQ may cause a life threatening haemolytic anemia in patients with G6PD deficiency, it is not recommended to patients whose G6PD deficiency status is not known.
Estimates of the force of blood-stage infections arising from primary infections and relapses are important for designing intervention strategies although their relative contributions in endemic settings are not well established. The seasonality of P. vivax primary infections can be estimated from the seasonality of P. falciparum infections since they are transmitted by the same vectors. A statistical model has been developed to estimate the incidence and seasonality of P. vivax primary infection and relapse , given longitudinal data with genotyped samples. The seasonal pattern of P. falciparum infections provides approximate estimates of the seasonal pattern of P. vivax primary infections. In co-endemic settings, P. falciparum is often the first species to show a decline in incidence during successful control campaigns with P. vivax generally being slower to respond to the same interventions. As a result significant reductions in P. vivax case burden may only become evident a few years after decreases of P. falciparum, due to the hidden reservoir of silent P. vivax hypnozoites . It is uncertain how relapses contribute to the burden of P. vivax malaria in areas of seasonal transmission settings. Effective control strategies for P vivax will be aided by improving our understanding of the proportion of clinical cases of P. vivax caused by relapses. The objective of this study was to estimate the proportion of clinical cases of P. vivax attributable to relapses in Adama malaria diagnostic centre, East Shoa Zone, Oromia, Ethiopia.
The study was conducted in Adama malaria diagnostic centre, East Shoa Zone, Oromia, Ethiopia from 15 May 2015 through 15 April 2016. The health centre is dedicated to malaria diagnosis as it does not perform any other types of diagnosis. Adama town (8°33′N 39°17′E) is located 100 km from Addis Ababa, Ethiopia. People from the Adama town and the surrounding rural areas preferentially use this laboratory for malaria diagnosis over hospitals and other surrounding health centres. The population of Adama within reach of the health centre is approximately 324,000. As individuals can obtain malaria diagnosis and treatment at other facilities, this can be considered as an upper limit on the population denominator. The laboratory technicians at this centre are WHO certified microscopists. In the study area, malaria transmission is seasonal like many endemic regions of Ethiopia and both P. falciparum and P. vivax co-exist. Although malaria transmission varies from year to year depending on rainfall patterns, the major transmission season in the study area usually runs from August through December with a minor transmission season from May through June.
Self-reporting febrile patients seeking malaria diagnosis were included in this study. Demographic characteristics of individuals presenting at Adama malaria diagnostic centre were systematically registered on the logbook (routine procedures). Blood samples were obtained through finger prick method for thick and thin smears. The slides were stained with a 10% Giemsa solution to be examined under 100× microscopes for the presence of malaria parasites. The slides were independently read by two skilled microscopists. Ethiopia adopted species-specific malaria treatment policy making species identification very crucial for proper prescription of the right anti-malarial drugs. Those febrile individuals who were negative for malaria were advised to undertake further diagnosis for their febrile illness at hospitals or elsewhere. Patients with confirmed cases of P. vivax received an unsupervised 3-day treatment of chloroquine (total 25 mg/kg) without primaquine, while cases of confirmed P. falciparum and mixed infections (P. falciparum and P. vivax) received artemether–lumefantrine.
Ethical clearance for this study was obtained from Aklilu Lemma Institute of Pathobiology Institutional Review Board. Informed consents were obtained from participating individuals.
Demographic characteristics of the study participants
Number positive (%)
Age groups (in years)
Data on recorded cases of clinical malaria
People presenting at health centre
Clinical malaria case
P. vivax a
P. falciparum a
P. vivax and P. falciparum
Estimated parameters of the statistical model. Parameters are presented as median and 95% credible intervals of the estimated posterior distribution
Mean proportion/number of P. falciparum cases per month
9.4% (8.4, 10.4%)
27 (21, 33)
Ratio of cases in dry season to wet season
0.69 (0.55, 0.84)
0.56 (0.28, 0.79)
Seasonal shape parameter
2.3 (1.5, 4.3)
3.0 (1.7, 7.0)
Offset for seasonal peak (0 = May 2015)
4.9 (4.4, 5.4)
5.1 (4.6, 5,5)
Primary P. vivax cases relative to P. falciparum cases
1.17 (0.77, 1.49)
1.91 (1.19, 2.65)
Relapses P. vivax cases relative to P. falciparum cases
1.72 (1.35, 2.12)
0.71 (0.13, 1.39)
Lag of relapse cases compared to primary cases
5.9 (5.2, 6.5)
4.8 (0.8, 10.8)
Standard deviation of case numbers
10.3 (7.4, 16.3)
Figure 3b shows the estimated proportion of clinical cases of P. vivax attributable to relapses. Although the line of best fit does suggest substantial seasonal variation in the cases attributable to relapses, the credible intervals are very wide, spanning most of the range from 0 to 100%. This suggests that the model and data interpreted in this manner does not have sufficient statistical power to identify the seasonal variation in relapses.
In this study, the proportion of individuals with malaria was 36.1% (1141/3161) as diagnosed by light microscopy. The highest incidence of malaria was during the peak malaria transmission season for the study site from August to October. Malaria cases were highest among age group 6–15 years (49.5%), followed by the <5 age group (40.0%) (Table 1). It is apparent that most malaria mortality and morbidity in endemic settings occurs in children under 5 years of age. Malaria cases were highest among rural (46.4%, 576/1242) residents compared to urban residents (29.4%, 565/1919). Inhabitants of urban areas may have lower exposure to mosquito bites than rural inhabitants and hence have lower malaria incidences. Males had a slightly higher proportion of confirmed malaria cases (38.5%) than females (32.0%). The presence of sex-specific occupational variation in the study area (mainly outdoor activities in males and indoor activities in females) may account for variable exposure to mosquito bites and hence lower incidence of malaria cases in the latter.
The incidence of P. vivax appears to decrease more slowly than that of P. falciparum in areas where both species coexist . As the incidence of malaria is reduced, the proportion of all cases due to P. vivax increases and predominates in the area. During the peak transmission season, both falciparum and vivax malaria cases appear at health facilities. As the transmission season ceases following the unfavourable weather conditions for vector breeding, P. falciparum cases decline while vivax malaria cases continue appearing at health facilities because of latent liver-stage infections. Thus, the appearance of P. falciparum cases after a pause of transmission signals the beginning of the next malaria transmission season. The continuation of P. vivax cases even after the primary transmission season underscores the need for effective intervention strategies against liver-stage parasites in Ethiopia. However, with currently available technology, it is not possible to diagnose latent liver stages. Another point worth noting is the complaints of treatment fatigue by individuals receiving treatment for P. vivax. As Ethiopia’s national treatment guideline does not allow PQ for the radical cure, the inevitable recurrence of P. vivax after CQ therapy has made people less interested to seek health facilities. Plasmodium vivax cases appearing at health facilities during the non-transmission season likely arise from reactivation of dormant liver-stages. These individuals had P. vivax primary infections sometime ago during the previous transmission seasons and did not receive PQ for radical cure for their illness. The infections that arise from the reactivation of dormant liver-stage in the dry season may not be transmitted from infected individuals to uninfected ones as the vectors responsible for active transmission are non-existent due to the unsuitability of the weather conditions in the dry season. Indeed, in the transmission season P. vivax cases are presumed to be both from new mosquito infections and relapse unlike the vivax malaria episodes in the dry season that emanate from the latter. As a consequence, clearance of acute vivax malaria requires two distinct classes of drugs: blood schizonticide(s) (to terminate the acute attack), and hypnozoitocide(s) (to prevent subsequent acute attacks) [15, 16]. Prevention of infections arising from relapse is challenging as it is less susceptible to the conventional malaria control interventions such as insecticides, bed nets, diagnostic methods and almost all chemotherapeutic interventions . The distinct biological characteristics of P. vivax present challenges for its control and elimination. Insecticide-treated mosquito nets (ITNs) and indoor residual spraying (IRS), for instance, are not always as effective against P. vivax as they are against P. falciparum. The reservoir of P. vivax infection in the human liver stage (hypnozoites), can result in cases occurring without the bite of infectious vectors.
Several historical studies have shown that P. falciparum and P. vivax substantially contribute to malaria morbidity in Ethiopia, in relative proportions of approximately 60 and 40% [20–22], respectively, although their relative proportions vary both temporally and spatially. The predominance of P. vivax cases in the study site is consistent with a globally reported epidemiological trend in P. vivax and P. falciparum co-endemic regions where the proportion of P. vivax cases increases as total malaria cases are reduced via malaria control interventions. However, to definitively show this for the study site in Adama would require additional data from before the roll out of insecticide treated nets.
The statistical model applied here utilizes routinely collected data on monthly cases of P. falciparum and P. vivax to estimate the proportion of P. vivax cases attributable to relapses. Notably, the results of this study are consistent with the findings from an analysis of data from cohorts of Papua New Guinean children that indicate that approximately 81% (95% CI 42, 94%) of clinical cases of P. vivax are attributable to relapses  and that the proportion of P. vivax infections attributable to relapses is highest in the dry season . However, it should be noted that there are some challenges in interpreting the data due to the seasonality in non-malaria cases reporting to the health centre (Fig. 1b). The seasonal variation in non-malaria cases could be due to (1) seasonally varying incidence of other infectious diseases; (2) sub-microscopic symptomatic cases of malaria; or (3) individuals systematically over-accessing resources at the health centre during the malaria transmission season. Given these uncertainties, it is unclear whether the true seasonal pattern of cases of clinical malaria in the population as a whole is better represented by the proportion of cases of confirmed P. vivax and P. falciparum, or by total case numbers.
When the statistical model is applied to the data on proportion of cases with P. vivax there is a clear secondary peak of P. vivax cases in February to March (Fig. 2a). However when the statistical model is applied to total P. vivax cases, there is much less evidence for a secondary peak of P. vivax cases from February to March (Fig. 3a). In both cases, the proportion of P. vivax cases attributable to relapses is predicted to be highest during February to March, although there is not enough signal for a significant pattern when data are analysed using total cases.
Seasonal patterns in clinical cases of P. vivax may not accurately reflect seasonal patterns in the incidence of P. vivax blood-stage infections. The incidence of P. vivax relapses is believed to be highest immediately after the initial infectious mosquito bite , but possibly with a delay of a few weeks [17, 24]. However, the model fit to the data suggests a delay of 5–6 months between exposure during the peak malaria transmission season and the incidence of clinical cases of P. vivax attributable to relapses. This could be due to the relapse phenotype of Ethiopian P. vivax parasites [25, 26], or may be a consequence of induced immune responses. An adaptive antibody response targeting the primary blood-stage P. vivax infection may provide protection against high density parasitaemia and clinical episodes arising from relapses, particularly if the relapse and primary infection are clonal . Indeed, it is plausible that a relapse may only cause a clinical case of P. vivax if: (1) it occurs after a sufficient duration such that short-term adaptive responses generated by the primary infection have waned [28, 29]; and (2) the relapsing parasite is not a full sibling of the parasites that caused the primary infection .
It is apparent that the treatment of P. vivax patients with primaquine radical cure may reduce relapse associated morbidity. However, many malaria endemic countries have not mandated routine glucose-6-phosphate dehydrogenase (G6PD) testing before initiating PQ for radical cure of patients infected by P. vivax malaria. This has led to the absence of PQ prescription or inconsiderate prescription and administration of PQ to P. vivax patients without being concerned about patients’ G6PD status and associated complications . Indeed, the single greatest obstacle to PQ prescription is the rational fear of complications associated with this drug in G6PD deficient patients. Towards this end, a study conducted in the Gambella region of Ethiopia showed the presence of G6PD deficiency in Nilotic ethnic group  that represents less than 1% of the total population. Further assessments of G6PD deficiency nationwide will help abate relapse-associated morbidity by providing PQ for radical cure.
Data on the incidence of P. falciparum and P. vivax cases are often routinely collected at various levels of the public health system. By comparing the seasonal patterns in P. falciparum and P. vivax cases, this method suggests that after the primary malaria transmission in Adama, Ethiopia up to 77% (95% CrI 68, 84%) of P. vivax cases are attributable to relapses. This provides an indication of the burden of P. vivax malaria that can be prevented if more individuals are treated with primaquine during the wet season, either following a primary case of P. vivax in the wet season or by mass treatment of asymptotic individuals in the wider population. This is the first study in Ethiopia to address population-level estimates of the proportion of P. vivax clinical cases attributable to relapses among febrile patients. As relapses present a challenge to control and elimination programmes, the hypnozoite needs to be the focus of specific intervention programmes for the realization of malaria elimination. These observations have important implications for the epidemiological assessment of vivax malaria, and initiating therapy that is effective against both blood stages and relapses.
This study estimated the proportion of clinical cases of P. vivax attributable to relapses, which has important implications for the epidemiological assessment of vivax malaria and initiating therapy that is effective against both blood stages and relapses. The study provides an indication of the burden of P. vivax malaria that can be prevented if more individuals are treated with primaquine during the wet season, either following a primary case of P. vivax or by mass treatment of asymptomatic individuals in the wider population. The model suggest that 70% of P. vivax infections are suggested to have arisen from relapse during February to April, while 40% of P. vivax cases resulted from relapse during August to October 2015. The model also shows the occurrence of the relapse phenotype of Ethiopian P. vivax parasites with a delay of 5–6 months between exposure during the peak malaria transmission season and the incidence of clinical cases of P. vivax attributable to relapses. Undoubtedly, the successful control and elimination of P. vivax malaria calls for specific and additional interventions, particularly against the liver stage of the parasite.
LG conceived and designed the study, MTW analysed the data, LG and MTW wrote the paper. Both authors read and approved the final manuscript.
We are grateful to all the study participants, as well as their parents or legal guardians who made themselves available for these studies. We also thank laboratory staff at the Adama malaria diagnostic centre, Tewabech Lemma and Tsehay Orlando for their assistance with patient recruitment and microscopic slide readings.
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- World Health Organization. Control and elimination of Plasmodium vivax malaria: a technical brief. Geneva: World Health Organization; 2015.Google Scholar
- Arnott A, Barry AE, Reeder JC. Understanding the population genetics of Plasmodium vivax is essential for malaria control and elimination. Malar J. 2012;11:14.View ArticlePubMedPubMed CentralGoogle Scholar
- World Health Organization. World malaria report. Geneva: World Health Organization; 2013.Google Scholar
- Deressa W, Ali A, Enqusellassie F. Self-treatment of malaria in rural communities, Butajira, southern Ethiopia. Bull World Health Organ. 2003;81:261–8.PubMedPubMed CentralGoogle Scholar
- Highland Malaria Project (HIML). New systems for predicting malaria epidemics in the East African Highlands. Intercountry Workshop Proceeding 2002. Nairobi; 2002. http://www.lshtm.ac.uk/dcvbu/himal/Documents/kisumu.pdf.
- Abose T, Ye-Ebiyo Y, Olana D, Alamirew D, Beyene Y, Regassa L, et al. Reorientation and definition of the role of malaria vector control in Ethiopia; the epidemiology and control of malaria with special emphasis to the distribution, behavior and susceptibility to insecticides of anopheline vectors and chloroquine resistance in Ziway, Central Ethiopia and other areas. Addis Ababa; 1998.Google Scholar
- Mueller I, Galinski MR, Baird JK, Carlton JM, Kochar DK, Alonso PL, et al. Key gaps in the knowledge of Plasmodium vivax, a neglected human malaria parasite. Lancet Infect Dis. 2009;9:555–66.View ArticlePubMedGoogle Scholar
- Imwong M, Snounou G, Pukrittayakamee S, Tanomsing N, Kim JR, Nandy A, et al. Relapses of Plasmodium vivax infection usually result from activation of heterologous hypnozoites. J Infect Dis. 2007;195:927–33.View ArticlePubMedGoogle Scholar
- Koepfli C, Schoepflin S, Bretscher M, Lin E, Kiniboro B, Zimmerman PA, et al. How much remains undetected? Probability of molecular detection of human plasmodia in the field. PLoS ONE. 2011;6:e19010.View ArticlePubMedPubMed CentralGoogle Scholar
- Robinson LJ, Wampfler R, Betuela I, Karl S, White MT, Li Wai Suen CS, et al. Strategies for understanding and reducing the Plasmodium vivax and Plasmodium ovale hypnozoite reservoir in Papua New Guinean Children: a randomised placebo-controlled trial and mathematical model. Plos Med. 2015;12:e1001891.View ArticlePubMedPubMed CentralGoogle Scholar
- Baird JK. Malaria caused by Plasmodium vivax: recurrent, difficult to treat, disabling, and threatening to life- averting the infectious bite preempts these hazards. Pathog Glob Health. 2013;107:475–9.View ArticleGoogle Scholar
- Schwartz E, Sidi Y. New Aspects of Malaria Imported from Ethiopia. Clin Infect Dis. 1998;26:1089–91.View ArticlePubMedGoogle Scholar
- Hulden L, Hulden L. Activation of the hypnozoite: a part of Plasmodium vivax life cycle and survival. Malar J. 2011;10:90.View ArticlePubMedPubMed CentralGoogle Scholar
- White MT, Shirreff G, Karl S, Ghani AC, Mueller I. Variation in relapse frequency and the transmission potential of Plasmodium vivax malaria. Proc Biol Sci. 2016;283:20160048.View ArticlePubMedPubMed CentralGoogle Scholar
- Price RN, Auburn S, Marfurt J, Cheng Q. Phenotypic and genotypic characterisation of drug-resistant Plasmodium vivax. Trends Parasitol. 2012;28:522–9.View ArticlePubMedPubMed CentralGoogle Scholar
- Howes RE, Dewi M, Piel FB, Monteiro WM, Battle KE, Messina JP, et al. Spatial distribution of G6PD deficiency variants across malaria-endemic regions. Malar J. 2013;12:418.View ArticlePubMedPubMed CentralGoogle Scholar
- Ross A, Koepfli C, Schoepflin S, Timinao L, Siba P, Smith T, et al. The incidence and differential seasonal patterns of Plasmodium vivax primary infections and relapses in a cohort of children in Papua New Guinea. PLoS Negl Trop Dis. 2016;10:e0004582.View ArticlePubMedPubMed CentralGoogle Scholar
- Howes RE, Battle KE, Mendis KN, Smith DL, Cibulskis RE, Baird JK, et al. Global Epidemiology of Plasmodium vivax. Am J Trop Med Hyg. 2016;95:15–34.View ArticlePubMedPubMed CentralGoogle Scholar
- Griffin JT. The interaction between seasonality and pulsed interventions against malaria in their effects on the reproduction number. PLoS Comput Biol. 2015;11:e1004057.View ArticlePubMedPubMed CentralGoogle Scholar
- Nigatu W, Abebe M, Dejene A. Plasmodium vivax and P. falciparum epidemiology in Gambella, south-west Ethiopia. Trop Med Parasitol. 1992;43:181–5.PubMedGoogle Scholar
- Olana D, Chibsa S, Teshome D, Mekasha A, Graves PM, Reithinger R. Malaria, Oromia regional state, Ethiopia, 2001–2006. Emerg Infect Dis. 2011;17:1336–7.View ArticlePubMedPubMed CentralGoogle Scholar
- Ramos JM, Reyes F, Tesfamariam A. Change in epidemiology of malaria infections in a rural area in Ethiopia. J Travel Med. 2005;12:155–6.View ArticleGoogle Scholar
- White NJ. Determinants of relapse periodicity in Plasmodium vivax malaria. Malar J. 2011;10(297):23.Google Scholar
- Roy M, Bouma MJ, Ionides EL, Dhiman RC, Pascual M. The potential elimination of Plasmodium vivax malaria by relapse treatment: insights from a transmission model and surveillance data from NW India. PLoS Neg Trop Dis. 2013;7:e1979.View ArticleGoogle Scholar
- Battle KE, Karhunen MS, Bhatt S, Gething PW, Howes RE, Golding N, et al. Geographical variation in Plasmodium vivax relapse. Malar J. 2014;13:144.View ArticlePubMedPubMed CentralGoogle Scholar
- Lover AA, Coker RJ. quantifying effect of geographic location on epidemiology of Plasmodium vivax Malaria. Emerg Infect Dis. 2013;19:1058–65.View ArticlePubMedPubMed CentralGoogle Scholar
- Collins WE, Jeffery GM, Roberts JM. A retrospective examination of reinfection of humans with Plasmodium vivax. Am J Trop Med Hyg. 2004;70:642–4.PubMedGoogle Scholar
- Cole-Tobian JL, Michon P, Biasor M, Richards JS, Beeson JG, Mueller I, et al. Strain-specific Duffy binding protein antibodies correlate with protection against infection with homologous compared to heterologous Plasmodium vivax strains in Papua New Guinean children. Infect Immun. 2009;77:4009–17.View ArticlePubMedPubMed CentralGoogle Scholar
- Longley RJ, Reyes-Sandoval A, Montoya-Díaz E, Dunachie S, Kumpitak C, Nguitragool W, et al. Acquisition and longevity of antibodies to Plasmodium vivax preerythrocytic antigens in Western Thailand. Clin Vaccine Immunol. 2016;23:117–24.View ArticlePubMed CentralGoogle Scholar
- Bright AT, Manary MJ, Tewhey R, Arango EM, Wang T, Schork NJ, et al. A high resolution case study of a patient with recurrent Plasmodium vivax infections shows that relapses were caused by meiotic siblings. PLoS Negl Trop Dis. 2014;8:e2882.View ArticlePubMedPubMed CentralGoogle Scholar
- Rishikesh K, Saravu K. Primaquine treatment and relapse in Plasmodium vivax malaria. Pathog Glob Health. 2016;110:1–8.View ArticlePubMedPubMed CentralGoogle Scholar
- Tsegaye A, Golassa L, Mamo H, Erko B. Glucose-6-phosphate dehydrogenase deficiency among malaria suspects attending Gambella hospital, southwest Ethiopia. Malar J. 2014;13:438.View ArticlePubMedPubMed CentralGoogle Scholar