Epidemiology of Disappearing Plasmodium vivax Malaria: A Case Study in Rural Amazonia

Carregando...
Imagem de Miniatura
Citações na Scopus
78
Tipo de produção
article
Data de publicação
2014
Título da Revista
ISSN da Revista
Título do Volume
Editora
PUBLIC LIBRARY SCIENCE
Autores
BARBOSA, Susana
GOZZE, Amanda B.
LIMA, Nathalia F.
BATISTA, Camilla L.
BASTOS, Melissa da Silva
NICOLETE, Vanessa C.
FONTOURA, Pablo S.
GONCALVES, Raquel M.
VIANA, Susana Ariane S.
MENEZES, Maria Jose
Citação
PLOS NEGLECTED TROPICAL DISEASES, v.8, n.8, article ID e3109, 13p, 2014
Projetos de Pesquisa
Unidades Organizacionais
Fascículo
Resumo
Background: New frontier settlements across the Amazon Basin pose a major challenge for malaria elimination in Brazil. Here we describe the epidemiology of malaria during the early phases of occupation of farming settlements in Remansinho area, Brazilian Amazonia. We examine the relative contribution of low-density and asymptomatic parasitemias to the overall Plasmodium vivax burden over a period of declining transmission and discuss potential hurdles for malaria elimination in Remansinho and similar settings. Methods: Eight community-wide cross-sectional surveys, involving 584 subjects, were carried out in Remansinho over 3 years and complemented by active and passive surveillance of febrile illnesses between the surveys. We used quantitative PCR to detect low-density asexual parasitemias and gametocytemias missed by conventional microscopy. Mixed-effects multiple logistic regression models were used to characterize independent risk factors for P. vivax infection and disease. Principal Findings/Conclusions: P. vivax prevalence decreased from 23.8% (March-April 2010) to 3.0% (April-May 2013), with no P. falciparum infections diagnosed after March-April 2011. Although migrants from malaria-free areas were at increased risk of malaria, their odds of having P. vivax infection and disease decreased by 2-3% with each year of residence in Amazonia. Several findings indicate that low-density and asymptomatic P. vivax parasitemias may complicate residual malaria elimination in Remansinho: (a) the proportion of subpatent infections (i. e. missed by microscopy) increased from 43.8% to 73.1% as P. vivax transmission declined; (b) most (56.6%) P. vivax infections were asymptomatic and 32.8% of them were both subpatent and asymptomatic; (c) asymptomatic parasite carriers accounted for 54.4% of the total P. vivax biomass in the host population; (d) over 90% subpatent and asymptomatic P. vivax had PCR-detectable gametocytemias; and (e) few (17.0%) asymptomatic and subpatent P. vivax infections that were left untreated progressed to clinical disease over 6 weeks of follow-up and became detectable by routine malaria surveillance.
Palavras-chave
Referências
  1. Aguas R, 2008, PLOS ONE, V3, pe1767
  2. Alexander N, 2005, AM J TROP MED HYG, V73, P140
  3. Barreto ML, 2011, LANCET, V377, P1877, DOI 10.1016/S0140-6736(11)60202-X
  4. Bereczky S, 2007, MICROBES INFECT, V9, P103, DOI 10.1016/j.micinf.2006.10.014
  5. Beurskens M, 2009, AM J TROP MED HYG, V81, P366
  6. Branch O, 2005, MALARIA J, V4, DOI 10.1186/1475-2875-4-27
  7. MARCELO L, 1994, AM J TROP MED HYG, V51, P16
  8. Camargo LMA, 1996, AM J TROP MED HYG, V55, P32
  9. Castro MC, 2006, P NATL ACAD SCI USA, V103, P2452, DOI 10.1073/PNAS.0510576103
  10. Confalonieri UEC, 2014, ACTA TROP, V129, P33, DOI 10.1016/j.actatropica.2013.09.013
  11. da Silva NS, 2010, T ROY SOC TROP MED H, V104, P343, DOI 10.1016/j.trstmh.2009.12.010
  12. da Silva-Nunes M, 2008, AM J TROP MED HYG, V79, P624
  13. da Silva-Nunes M, 2012, ACTA TROP, V121, P281, DOI 10.1016/j.actatropica.2011.10.001
  14. da Silva-Nunes M, 2007, MEM I OSWALDO CRUZ, V102, P341
  15. Douglas NM, 2013, J INFECT DIS, V208, P801, DOI 10.1093/infdis/jit261
  16. Felger I, 2012, PLOS ONE, V7, DOI 10.1371/journal.pone.0045542
  17. Hahn MB, 2014, PLOS ONE, V9, DOI 10.1371/journal.pone.0085725
  18. KLEIN TA, 1990, J AM MOSQUITO CONTR, V6, P700
  19. Ladeia-Andrade S, 2009, AM J TROP MED HYG, V80, P452
  20. Lindblade KA, 2013, EXPERT REV ANTI-INFE, V11, P623, DOI [10.1586/eri.13.45, 10.1586/ERI.13.45]
  21. LOURENCODEOLIVEIRA R, 1989, MEM I OSWALDO CRUZ, V84, P501
  22. Magris M, 2007, TROP MED INT HEALTH, V12, P392, DOI 10.1111/j.1365-3156.2006.01801.x
  23. Males S, 2008, CLIN INFECT DIS, V46, P516, DOI 10.1086/526529
  24. MARQUES AC, 1987, PARASITOL TODAY, V3, P166
  25. McKenzie FE, 2006, J PARASITOL, V92, P1281, DOI 10.1645/GE-911R.1
  26. Njama-Meya D, 2004, TROP MED INT HEALTH, V9, P862, DOI 10.1111/j.1365-3156.2004.01277.x
  27. Norris DE, 2004, ECOHEALTH, V1, P19, DOI 10.1007/s10393-004-0008-7
  28. Oliveira-Ferreira J, 2010, MALARIA J, V9, DOI 10.1186/1475-2875-9-115
  29. Parker BS, 2013, MALARIA J, V12, DOI 10.1186/1475-2875-12-178
  30. PERIGNON JL, 1994, MEM I OSWALDO CRUZ, V89, P51
  31. Portugal S, 2011, NAT MED, V17, P732, DOI 10.1038/nm.2368
  32. Prata A, 1988, Rev Soc Bras Med Trop, V21, P51
  33. Roshanravan B, 2003, AM J TROP MED HYG, V69, P45
  34. Sattabongkot J, 2004, TRENDS PARASITOL, V20, P192, DOI 10.1016/j.pt.2004.02.001
  35. SAWYER D, 1993, SOC SCI MED, V37, P1131, DOI 10.1016/0277-9536(93)90252-Y
  36. Scopel KKG, 2004, ACTA TROP, V90, P61, DOI 10.1016/j.actratropica.2003.11.002
  37. Shanks GD, 2012, ADV PARASIT, V80, P301, DOI 10.1016/B978-0-12-397900-1.00006-2
  38. Sinka ME, 2010, PARASITE VECTOR, V3, DOI 10.1186/1756-3305-3-72
  39. Stresman G, 2012, MALARIA J, V11, DOI 10.1186/1475-2875-11-353
  40. Sturrock HJW, 2013, PLOS MED, V10, DOI 10.1371/journal.pmed.1001467
  41. TADEI WP, 1988, REV I MED TROP, V30, P221
  42. Vittor AY, 2009, AM J TROP MED HYG, V81, P5
  43. Vittor AY, 2006, AM J TROP MED HYG, V74, P3
  44. Wampfler R, 2013, PLOS ONE, V8, DOI 10.1371/journal.pone.0076316
  45. WHO, 2013, WORLD MALARIA REPORT 2013, P1
  46. World Health Organization, 2012, DIS SURV MAL EL OP M
  47. Zimmerman R H, 1997, Rev Panam Salud Publica, V2, P18, DOI 10.1590/S1020-49891997000700004