Sero-epidemiological evaluation of changes in Plasmodium falciparum and Plasmodium vivax transmission patterns over the rainy season in Cambodia
In Cambodia, malaria transmission is low and most cases occur in forested areas. Sero-epidemiological techniques can be used to identify both areas of ongoing transmission and high-risk groups to be targeted by control interventions. This study utilizes repeated cross-sectional data to assess the ri...
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Published in | Malaria journal Vol. 11; no. 1; p. 86 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
BioMed Central Ltd
25.03.2012
BioMed Central BMC |
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Abstract | In Cambodia, malaria transmission is low and most cases occur in forested areas. Sero-epidemiological techniques can be used to identify both areas of ongoing transmission and high-risk groups to be targeted by control interventions. This study utilizes repeated cross-sectional data to assess the risk of being malaria sero-positive at two consecutive time points during the rainy season and investigates who is most likely to sero-convert over the transmission season.
In 2005, two cross-sectional surveys, one in the middle and the other at the end of the malaria transmission season, were carried out in two ecologically distinct regions in Cambodia. Parasitological and serological data were collected in four districts. Antibodies to Plasmodium falciparum Glutamate Rich Protein (GLURP) and Plasmodium vivax Merozoite Surface Protein-1(19) (MSP-1(19)) were detected using Enzyme Linked Immunosorbent Assay (ELISA). The force of infection was estimated using a simple catalytic model fitted using maximum likelihood methods. Risks for sero-converting during the rainy season were analysed using the Classification and Regression Tree (CART) method.
A total of 804 individuals participating in both surveys were analysed. The overall parasite prevalence was low (4.6% and 2.0% for P. falciparum and 7.9% and 6.0% for P. vivax in August and November respectively). P. falciparum force of infection was higher in the eastern region and increased between August and November, whilst P. vivax force of infection was higher in the western region and remained similar in both surveys. In the western region, malaria transmission changed very little across the season (for both species). CART analysis for P. falciparum in the east highlighted age, ethnicity, village of residence and forest work as important predictors for malaria exposure during the rainy season. Adults were more likely to increase their antibody responses to P. falciparum during the transmission season than children, whilst members of the Charay ethnic group demonstrated the largest increases.
In areas of low transmission intensity, such as in Cambodia, the analysis of longitudinal serological data enables a sensitive evaluation of transmission dynamics. Consecutive serological surveys allow an insight into spatio-temporal patterns of malaria transmission. The use of CART enabled multiple interactions to be accounted for simultaneously and permitted risk factors for exposure to be clearly identified. |
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AbstractList | In Cambodia, malaria transmission is low and most cases occur in forested areas. Sero-epidemiological techniques can be used to identify both areas of ongoing transmission and high-risk groups to be targeted by control interventions. This study utilizes repeated cross-sectional data to assess the risk of being malaria sero-positive at two consecutive time points during the rainy season and investigates who is most likely to sero-convert over the transmission season.
In 2005, two cross-sectional surveys, one in the middle and the other at the end of the malaria transmission season, were carried out in two ecologically distinct regions in Cambodia. Parasitological and serological data were collected in four districts. Antibodies to Plasmodium falciparum Glutamate Rich Protein (GLURP) and Plasmodium vivax Merozoite Surface Protein-1(19) (MSP-1(19)) were detected using Enzyme Linked Immunosorbent Assay (ELISA). The force of infection was estimated using a simple catalytic model fitted using maximum likelihood methods. Risks for sero-converting during the rainy season were analysed using the Classification and Regression Tree (CART) method.
A total of 804 individuals participating in both surveys were analysed. The overall parasite prevalence was low (4.6% and 2.0% for P. falciparum and 7.9% and 6.0% for P. vivax in August and November respectively). P. falciparum force of infection was higher in the eastern region and increased between August and November, whilst P. vivax force of infection was higher in the western region and remained similar in both surveys. In the western region, malaria transmission changed very little across the season (for both species). CART analysis for P. falciparum in the east highlighted age, ethnicity, village of residence and forest work as important predictors for malaria exposure during the rainy season. Adults were more likely to increase their antibody responses to P. falciparum during the transmission season than children, whilst members of the Charay ethnic group demonstrated the largest increases.
In areas of low transmission intensity, such as in Cambodia, the analysis of longitudinal serological data enables a sensitive evaluation of transmission dynamics. Consecutive serological surveys allow an insight into spatio-temporal patterns of malaria transmission. The use of CART enabled multiple interactions to be accounted for simultaneously and permitted risk factors for exposure to be clearly identified. Doc number: 86 Abstract Background: In Cambodia, malaria transmission is low and most cases occur in forested areas. Sero-epidemiological techniques can be used to identify both areas of ongoing transmission and high-risk groups to be targeted by control interventions. This study utilizes repeated cross-sectional data to assess the risk of being malaria sero-positive at two consecutive time points during the rainy season and investigates who is most likely to sero-convert over the transmission season. Methods: In 2005, two cross-sectional surveys, one in the middle and the other at the end of the malaria transmission season, were carried out in two ecologically distinct regions in Cambodia. Parasitological and serological data were collected in four districts. Antibodies to Plasmodium falciparum Glutamate Rich Protein (GLURP) and Plasmodium vivax Merozoite Surface Protein-119 (MSP-119 ) were detected using Enzyme Linked Immunosorbent Assay (ELISA). The force of infection was estimated using a simple catalytic model fitted using maximum likelihood methods. Risks for sero-converting during the rainy season were analysed using the Classification and Regression Tree (CART) method. Results: A total of 804 individuals participating in both surveys were analysed. The overall parasite prevalence was low (4.6% and 2.0% for P. falciparum and 7.9% and 6.0% for P. vivax in August and November respectively). P. falciparum force of infection was higher in the eastern region and increased between August and November, whilst P. vivax force of infection was higher in the western region and remained similar in both surveys. In the western region, malaria transmission changed very little across the season (for both species). CART analysis for P. falciparum in the east highlighted age, ethnicity, village of residence and forest work as important predictors for malaria exposure during the rainy season. Adults were more likely to increase their antibody responses to P. falciparum during the transmission season than children, whilst members of the Charay ethnic group demonstrated the largest increases. Discussion: In areas of low transmission intensity, such as in Cambodia, the analysis of longitudinal serological data enables a sensitive evaluation of transmission dynamics. Consecutive serological surveys allow an insight into spatio-temporal patterns of malaria transmission. The use of CART enabled multiple interactions to be accounted for simultaneously and permitted risk factors for exposure to be clearly identified. Abstract Background In Cambodia, malaria transmission is low and most cases occur in forested areas. Sero-epidemiological techniques can be used to identify both areas of ongoing transmission and high-risk groups to be targeted by control interventions. This study utilizes repeated cross-sectional data to assess the risk of being malaria sero-positive at two consecutive time points during the rainy season and investigates who is most likely to sero-convert over the transmission season. Methods In 2005, two cross-sectional surveys, one in the middle and the other at the end of the malaria transmission season, were carried out in two ecologically distinct regions in Cambodia. Parasitological and serological data were collected in four districts. Antibodies to Plasmodium falciparum Glutamate Rich Protein (GLURP) and Plasmodium vivax Merozoite Surface Protein-119 (MSP-119) were detected using Enzyme Linked Immunosorbent Assay (ELISA). The force of infection was estimated using a simple catalytic model fitted using maximum likelihood methods. Risks for sero-converting during the rainy season were analysed using the Classification and Regression Tree (CART) method. Results A total of 804 individuals participating in both surveys were analysed. The overall parasite prevalence was low (4.6% and 2.0% for P. falciparum and 7.9% and 6.0% for P. vivax in August and November respectively). P. falciparum force of infection was higher in the eastern region and increased between August and November, whilst P. vivax force of infection was higher in the western region and remained similar in both surveys. In the western region, malaria transmission changed very little across the season (for both species). CART analysis for P. falciparum in the east highlighted age, ethnicity, village of residence and forest work as important predictors for malaria exposure during the rainy season. Adults were more likely to increase their antibody responses to P. falciparum during the transmission season than children, whilst members of the Charay ethnic group demonstrated the largest increases. Discussion In areas of low transmission intensity, such as in Cambodia, the analysis of longitudinal serological data enables a sensitive evaluation of transmission dynamics. Consecutive serological surveys allow an insight into spatio-temporal patterns of malaria transmission. The use of CART enabled multiple interactions to be accounted for simultaneously and permitted risk factors for exposure to be clearly identified. BACKGROUNDIn Cambodia, malaria transmission is low and most cases occur in forested areas. Sero-epidemiological techniques can be used to identify both areas of ongoing transmission and high-risk groups to be targeted by control interventions. This study utilizes repeated cross-sectional data to assess the risk of being malaria sero-positive at two consecutive time points during the rainy season and investigates who is most likely to sero-convert over the transmission season. METHODSIn 2005, two cross-sectional surveys, one in the middle and the other at the end of the malaria transmission season, were carried out in two ecologically distinct regions in Cambodia. Parasitological and serological data were collected in four districts. Antibodies to Plasmodium falciparum Glutamate Rich Protein (GLURP) and Plasmodium vivax Merozoite Surface Protein-1(19) (MSP-1(19)) were detected using Enzyme Linked Immunosorbent Assay (ELISA). The force of infection was estimated using a simple catalytic model fitted using maximum likelihood methods. Risks for sero-converting during the rainy season were analysed using the Classification and Regression Tree (CART) method. RESULTSA total of 804 individuals participating in both surveys were analysed. The overall parasite prevalence was low (4.6% and 2.0% for P. falciparum and 7.9% and 6.0% for P. vivax in August and November respectively). P. falciparum force of infection was higher in the eastern region and increased between August and November, whilst P. vivax force of infection was higher in the western region and remained similar in both surveys. In the western region, malaria transmission changed very little across the season (for both species). CART analysis for P. falciparum in the east highlighted age, ethnicity, village of residence and forest work as important predictors for malaria exposure during the rainy season. Adults were more likely to increase their antibody responses to P. falciparum during the transmission season than children, whilst members of the Charay ethnic group demonstrated the largest increases. DISCUSSIONIn areas of low transmission intensity, such as in Cambodia, the analysis of longitudinal serological data enables a sensitive evaluation of transmission dynamics. Consecutive serological surveys allow an insight into spatio-temporal patterns of malaria transmission. The use of CART enabled multiple interactions to be accounted for simultaneously and permitted risk factors for exposure to be clearly identified. In Cambodia, malaria transmission is low and most cases occur in forested areas. Sero-epidemiological techniques can be used to identify both areas of ongoing transmission and high-risk groups to be targeted by control interventions. This study utilizes repeated cross-sectional data to assess the risk of being malaria sero-positive at two consecutive time points during the rainy season and investigates who is most likely to sero-convert over the transmission season. In 2005, two cross-sectional surveys, one in the middle and the other at the end of the malaria transmission season, were carried out in two ecologically distinct regions in Cambodia. Parasitological and serological data were collected in four districts. Antibodies to Plasmodium falciparum Glutamate Rich Protein (GLURP) and Plasmodium vivax Merozoite Surface Protein-1.sub.19 (MSP-1.sub.19 ) were detected using Enzyme Linked Immunosorbent Assay (ELISA). The force of infection was estimated using a simple catalytic model fitted using maximum likelihood methods. Risks for sero-converting during the rainy season were analysed using the Classification and Regression Tree (CART) method. A total of 804 individuals participating in both surveys were analysed. The overall parasite prevalence was low (4.6% and 2.0% for P. falciparum and 7.9% and 6.0% for P. vivax in August and November respectively). P. falciparum force of infection was higher in the eastern region and increased between August and November, whilst P. vivax force of infection was higher in the western region and remained similar in both surveys. In the western region, malaria transmission changed very little across the season (for both species). CART analysis for P. falciparum in the east highlighted age, ethnicity, village of residence and forest work as important predictors for malaria exposure during the rainy season. Adults were more likely to increase their antibody responses to P. falciparum during the transmission season than children, whilst members of the Charay ethnic group demonstrated the largest increases. In areas of low transmission intensity, such as in Cambodia, the analysis of longitudinal serological data enables a sensitive evaluation of transmission dynamics. Consecutive serological surveys allow an insight into spatio-temporal patterns of malaria transmission. The use of CART enabled multiple interactions to be accounted for simultaneously and permitted risk factors for exposure to be clearly identified. BACKGROUND: In Cambodia, malaria transmission is low and most cases occur in forested areas. Sero-epidemiological techniques can be used to identify both areas of ongoing transmission and high-risk groups to be targeted by control interventions. This study utilizes repeated cross-sectional data to assess the risk of being malaria sero-positive at two consecutive time points during the rainy season and investigates who is most likely to sero-convert over the transmission season. METHODS: In 2005, two cross-sectional surveys, one in the middle and the other at the end of the malaria transmission season, were carried out in two ecologically distinct regions in Cambodia. Parasitological and serological data were collected in four districts. Antibodies to Plasmodium falciparum Glutamate Rich Protein (GLURP) and Plasmodium vivax Merozoite Surface Protein-119 (MSP-119) were detected using Enzyme Linked Immunosorbent Assay (ELISA). The force of infection was estimated using a simple catalytic model fitted using maximum likelihood methods. Risks for sero-converting during the rainy season were analysed using the Classification and Regression Tree (CART) method. RESULTS: A total of 804 individuals participating in both surveys were analysed. The overall parasite prevalence was low (4.6% and 2.0% for P. falciparum and 7.9% and 6.0% for P. vivax in August and November respectively). P. falciparum force of infection was higher in the eastern region and increased between August and November, whilst P. vivax force of infection was higher in the western region and remained similar in both surveys. In the western region, malaria transmission changed very little across the season (for both species). CART analysis for P. falciparum in the east highlighted age, ethnicity, village of residence and forest work as important predictors for malaria exposure during the rainy season. Adults were more likely to increase their antibody responses to P. falciparum during the transmission season than children, whilst members of the Charay ethnic group demonstrated the largest increases. DISCUSSION: In areas of low transmission intensity, such as in Cambodia, the analysis of longitudinal serological data enables a sensitive evaluation of transmission dynamics. Consecutive serological surveys allow an insight into spatio-temporal patterns of malaria transmission. The use of CART enabled multiple interactions to be accounted for simultaneously and permitted risk factors for exposure to be clearly identified. Background In Cambodia, malaria transmission is low and most cases occur in forested areas. Sero-epidemiological techniques can be used to identify both areas of ongoing transmission and high-risk groups to be targeted by control interventions. This study utilizes repeated cross-sectional data to assess the risk of being malaria sero-positive at two consecutive time points during the rainy season and investigates who is most likely to sero-convert over the transmission season. Methods In 2005, two cross-sectional surveys, one in the middle and the other at the end of the malaria transmission season, were carried out in two ecologically distinct regions in Cambodia. Parasitological and serological data were collected in four districts. Antibodies to Plasmodium falciparum Glutamate Rich Protein (GLURP) and Plasmodium vivax Merozoite Surface Protein-1.sub.19 (MSP-1.sub.19 ) were detected using Enzyme Linked Immunosorbent Assay (ELISA). The force of infection was estimated using a simple catalytic model fitted using maximum likelihood methods. Risks for sero-converting during the rainy season were analysed using the Classification and Regression Tree (CART) method. Results A total of 804 individuals participating in both surveys were analysed. The overall parasite prevalence was low (4.6% and 2.0% for P. falciparum and 7.9% and 6.0% for P. vivax in August and November respectively). P. falciparum force of infection was higher in the eastern region and increased between August and November, whilst P. vivax force of infection was higher in the western region and remained similar in both surveys. In the western region, malaria transmission changed very little across the season (for both species). CART analysis for P. falciparum in the east highlighted age, ethnicity, village of residence and forest work as important predictors for malaria exposure during the rainy season. Adults were more likely to increase their antibody responses to P. falciparum during the transmission season than children, whilst members of the Charay ethnic group demonstrated the largest increases. Discussion In areas of low transmission intensity, such as in Cambodia, the analysis of longitudinal serological data enables a sensitive evaluation of transmission dynamics. Consecutive serological surveys allow an insight into spatio-temporal patterns of malaria transmission. The use of CART enabled multiple interactions to be accounted for simultaneously and permitted risk factors for exposure to be clearly identified. |
ArticleNumber | 86 |
Audience | Academic |
Author | Sokny, Mao Sochanta, Tho Somony, Heng Theisen, Michael Erhart, Annette Soares, Irene S Cook, Jackie Lemmens, Kristel Claes, Filip Coosemans, Marc D'Alessandro, Umberto Speybroeck, Nico |
AuthorAffiliation | 4 Centre for Medical Parasitology at Department of International Health, Immunology and Microbiology, University of Copenhagen, Copenhagen, Denmark 5 Departamento de Análises Clínicas e Toxicológicas, Faculdade de Ciências Farmacêuticas, Universidade de São Paulo, São Paulo State, Brazil 1 Institute of Tropical Medicine, Nationalestraat 155, Antwerp 2000, Belgium 2 Ecole de santé publique, Université Catholique de Louvain, Clos Chapelle-aux-Champs, Brussels 1200, Belgium 3 National Center for Malaria Control, Parasitology and Entomology, Phnom Penh, Cambodia 6 Disease Control and Elimination, Medical Research Council Unit, Fajara, The Gambia |
AuthorAffiliation_xml | – name: 3 National Center for Malaria Control, Parasitology and Entomology, Phnom Penh, Cambodia – name: 2 Ecole de santé publique, Université Catholique de Louvain, Clos Chapelle-aux-Champs, Brussels 1200, Belgium – name: 5 Departamento de Análises Clínicas e Toxicológicas, Faculdade de Ciências Farmacêuticas, Universidade de São Paulo, São Paulo State, Brazil – name: 6 Disease Control and Elimination, Medical Research Council Unit, Fajara, The Gambia – name: 4 Centre for Medical Parasitology at Department of International Health, Immunology and Microbiology, University of Copenhagen, Copenhagen, Denmark – name: 1 Institute of Tropical Medicine, Nationalestraat 155, Antwerp 2000, Belgium |
Author_xml | – sequence: 1 givenname: Jackie surname: Cook fullname: Cook, Jackie email: jcook@itg.be organization: Institute of Tropical Medicine, Nationalestraat 155, Antwerp 2000, Belgium. jcook@itg.be – sequence: 2 givenname: Nico surname: Speybroeck fullname: Speybroeck, Nico – sequence: 3 givenname: Tho surname: Sochanta fullname: Sochanta, Tho – sequence: 4 givenname: Heng surname: Somony fullname: Somony, Heng – sequence: 5 givenname: Mao surname: Sokny fullname: Sokny, Mao – sequence: 6 givenname: Filip surname: Claes fullname: Claes, Filip – sequence: 7 givenname: Kristel surname: Lemmens fullname: Lemmens, Kristel – sequence: 8 givenname: Michael surname: Theisen fullname: Theisen, Michael – sequence: 9 givenname: Irene S surname: Soares fullname: Soares, Irene S – sequence: 10 givenname: Umberto surname: D'Alessandro fullname: D'Alessandro, Umberto – sequence: 11 givenname: Marc surname: Coosemans fullname: Coosemans, Marc – sequence: 12 givenname: Annette surname: Erhart fullname: Erhart, Annette |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/22443375$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.4269/ajtmh.2000.62.746 10.3201/eid1603.090732 10.1046/j.1365-3156.2003.01179.x 10.1016/S0065-308X(09)69005-9 10.1007/3-540-29967-X_3 10.1016/j.actatropica.2009.05.016 10.1016/S0035-9203(96)90406-X 10.1016/j.vaccine.2008.02.020 10.1186/1475-2875-9-373 10.1016/j.actatropica.2007.01.007 10.1086/644781 10.1186/1475-2875-8-142 10.1186/1475-2875-4-58 10.1016/j.pt.2004.05.004 10.1128/CDLI.2.1.30-34.1995 10.1186/1475-2875-10-195 10.1093/intimm/8.6.905 10.1073/pnas.0408725102 10.4269/ajtmh.2001.64.97 10.1016/j.pt.2007.08.023 10.1186/1475-2875-6-37 10.1128/IAI.71.8.4320-4325.2003 10.1016/S0169-4758(97)01061-2 10.1086/652456 10.4269/ajtmh.1999.60.357 10.1371/journal.ppat.1000912 10.1016/S0140-6736(73)92361-1 10.1186/1475-2875-7-195 10.1016/S1473-3099(09)70177-X 10.1371/journal.pone.0008022 10.1186/1475-2875-9-108 10.1186/1475-2875-7-28 10.1371/journal.pone.0029025 10.1371/journal.pone.0025137 10.1186/1475-2875-6-82 |
ContentType | Journal Article |
Copyright | COPYRIGHT 2012 BioMed Central Ltd. 2012 Cook et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Copyright ©2012 Cook et al; licensee BioMed Central Ltd. 2012 Cook et al; licensee BioMed Central Ltd. |
Copyright_xml | – notice: COPYRIGHT 2012 BioMed Central Ltd. – notice: 2012 Cook et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. – notice: Copyright ©2012 Cook et al; licensee BioMed Central Ltd. 2012 Cook et al; licensee BioMed Central Ltd. |
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References | 7719909 - Clin Diagn Lab Immunol. 1995 Jan;2(1):30-4 18234102 - Malar J. 2008;7:28 20502681 - PLoS Pathog. 2010 May;6(5):e1000912 16265903 - Curr Top Microbiol Immunol. 2005;297:71-102 15040560 - Trop Med Int Health. 2004 Feb;9(2):230-7 21980386 - PLoS One. 2011;6(9):e25137 15193565 - Trends Parasitol. 2004 Jul;20(7):333-9 17389041 - Malar J. 2007;6:37 21767376 - Malar J. 2011;10:195 19481997 - Acta Trop. 2009 Oct;112(1):1-7 19622411 - Adv Parasitol. 2009;69:299-352 19695492 - Lancet Infect Dis. 2009 Sep;9(9):555-66 17988945 - Trends Parasitol. 2007 Dec;23(12):575-82 15275075 - Parasitol Today. 1997 Jun;13(6):227-31 9015495 - Trans R Soc Trop Med Hyg. 1996 Nov-Dec;90(6):614-20 19848588 - J Infect Dis. 2009 Nov 15;200(10):1509-17 18342997 - Vaccine. 2008 Apr 7;26(16):1963-71 16336671 - Malar J. 2005;4:58 15792998 - Proc Natl Acad Sci U S A. 2005 Apr 5;102(14):5108-13 18471797 - Acta Trop. 2008 Jun;106(3):207-12 8671680 - Int Immunol. 1996 Jun;8(6):905-15 772232 - J Trop Med Hyg. 1975 Sep;78(9):194-200 20415536 - J Infect Dis. 2010 Jun 1;201(11):1764-74 20202412 - Emerg Infect Dis. 2010 Mar;16(3):392-9 10772546 - Southeast Asian J Trop Med Public Health. 1998 Dec;29(4):685-91 11304067 - Am J Trop Med Hyg. 2000 Jun;62(6):746-51 20409349 - Malar J. 2010;9:108 19323029 - Southeast Asian J Trop Med Public Health. 2009 Jan;40(1):18-29 18826573 - Malar J. 2008;7:195 12874308 - Infect Immun. 2003 Aug;71(8):4320-5 19558695 - Malar J. 2009;8:142 2094587 - Bull World Health Organ. 1990;68 Suppl:191-6 17598897 - Malar J. 2007;6:82 4125305 - Lancet. 1973 Sep 8;2(7828):547-51 19946627 - PLoS One. 2009;4(11):e8022 10466961 - Am J Trop Med Hyg. 1999 Mar;60(3):357-63 22174947 - PLoS One. 2011;6(12):e29025 11425182 - Am J Trop Med Hyg. 2001 Jan-Feb;64(1-2 Suppl):97-106 21182774 - Malar J. 2010;9:373 LC Okell (2084_CR1) 2009; 200 GE Weiss (2084_CR36) 2010; 6 J Cook (2084_CR4) 2011; 6 W Van Bortel (2084_CR31) 2010; 9 K Mendis (2084_CR27) 2001; 64 LJ Bruce-Chwatt (2084_CR8) 1975; 78 M Theisen (2084_CR23) 1995; 2 A Erhart (2084_CR32) 2005; 4 L Turner (2084_CR37) 2011; 6 LJ Bruce-Chwatt (2084_CR7) 1973; 2 T Bousema (2084_CR5) 2010; 201 I Mueller (2084_CR19) 2009; 9 N Steenkeste (2084_CR28) 2010; 9 S Incardona (2084_CR15) 2007; 6 P Corran (2084_CR3) 2007; 23 L Durnez (2084_CR21) 2011; 10 K Maitland (2084_CR17) 1996; 90 G Chowell (2084_CR29) 2009; 8 R Perraut (2084_CR10) 2000; 62 N Protopopoff (2084_CR25) 2009; 4 GW Agak (2084_CR11) 2008; 26 HD Trung (2084_CR16) 2004; 9 C Drakeley (2084_CR26) 2009; 69 RR Taylor (2084_CR34) 1996; 8 G Snounou (2084_CR20) 2004; 20 AH Achtman (2084_CR33) 2005; 297 G Del Giudice (2084_CR9) 1990; 68 L Dysoley (2084_CR14) 2008; 106 T Abe (2084_CR30) 2009; 40 ND Thang (2084_CR22) 2008; 7 AA Mehrizi (2084_CR39) 2009; 112 PH Corran (2084_CR2) 2008; 7 T Bousema (2084_CR6) 2010; 16 K Maitland (2084_CR18) 1997; 13 M Ak (2084_CR38) 1998; 29 SM Kinyanjui (2084_CR12) 2007; 6 CC John (2084_CR35) 2003; 71 IS Soares (2084_CR24) 1999; 60 CJ Drakeley (2084_CR13) 2005; 102 |
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Snippet | In Cambodia, malaria transmission is low and most cases occur in forested areas. Sero-epidemiological techniques can be used to identify both areas of ongoing... Background In Cambodia, malaria transmission is low and most cases occur in forested areas. Sero-epidemiological techniques can be used to identify both areas... Doc number: 86 Abstract Background: In Cambodia, malaria transmission is low and most cases occur in forested areas. Sero-epidemiological techniques can be... BACKGROUNDIn Cambodia, malaria transmission is low and most cases occur in forested areas. Sero-epidemiological techniques can be used to identify both areas... BACKGROUND: In Cambodia, malaria transmission is low and most cases occur in forested areas. Sero-epidemiological techniques can be used to identify both areas... Abstract Background In Cambodia, malaria transmission is low and most cases occur in forested areas. Sero-epidemiological techniques can be used to identify... |
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SubjectTerms | Adolescent Adult Aged Aged, 80 and over Animals Antibodies, Protozoan - blood Cambodia Cambodia - epidemiology Child Child, Preschool Classification and regression tree Cross-Sectional Studies Demographic aspects Disease transmission Distribution Elimination Enzyme-Linked Immunosorbent Assay Female Field study Humans Infant Infant, Newborn Malaria Malaria, Falciparum - epidemiology Malaria, Falciparum - transmission Malaria, Vivax - epidemiology Malaria, Vivax - transmission Male Middle Aged Plasmodium falciparum Plasmodium falciparum - immunology Plasmodium vivax Plasmodium vivax - immunology Principal components analysis Risk Factors Seasons Seroepidemiologic Studies Serology Towns Young Adult |
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Title | Sero-epidemiological evaluation of changes in Plasmodium falciparum and Plasmodium vivax transmission patterns over the rainy season in Cambodia |
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