Downloaded from:

Similar documents
Cutaneous Leishmaniasis : Global overview

Description of Warileya lumbrerasi n. sp. (Diptera: Psychodidae) from Peru

Recommendations for Coping with Leishmaniasis: A Review of Control Strategies. Centro de Convenções de Reboças Red Room 17: 00h

World Health Organization Department of Communicable Disease Surveillance and Response

Neglected Diseases (NDs) Landscape in Brazil and South America

CONTROLE DAS LEISHMANIOSES O QUE FALTA FAZER? Centro de Convenções de Reboças Red Room 17: 00h

Evidence for Leishmania (Viannia) Parasites in the Skin and Blood of Patients Before and After Treatment

Leishmaniasis in the WhO european region

Development of Mathematical models predicting the density of vectors: Case of sandflies vectors of leishmaniasis

Control of leishmaniasis

Control of leishmaniasis

Lutzomyia migonei is a permissive vector competent for Leishmania infantum

Etiologic Agent of an Epidemic of Cutaneous Leishmaniasis in Tolima, Colombia

Susceptibility of Spiny Rats (Proechimys semispinosus) to Leishmania (Viannia) panamensis and Leishmania (Leishmania) chagasi

SUMMARY. Cutaneous leishmaniasis with only skin involvement: single to multiple skin ulcers, satellite lesions and nodular lymphangitis.

The epidemiology and control of leishmaniasis in Andean countries. Epidemiologia e controle da leishmaniose nos países andinos

Citation for the original published paper (version of record): N.B. When citing this work, cite the original published paper.

Summary of Cases & Epidemiology Aspects of Leishmaniasis in Thailand

Survey of Wild Mammal Hosts of Cutaneous Leishmaniasis Parasites in Panamá and Costa Rica

Biomédica ISSN: Instituto Nacional de Salud Colombia

Leishmaniasis. CDR R.L. Gutierrez Oct 2014

CUTANEOUS LEISHMANIASIS

AEDES AEGYFTI AS A FACTOR IN THE INTERNATIONAL SPREAD OF YELLOW FEVER. Statement presented by the Delegations of Brazil, Cuba and Panama

0 BSERVATIONS ON THE PARASITE LEIiSHMANIA MEXICANA AMAZONENSIS AND ITS NATURAL INFECTION OF THE SAND FLY LUTZOMYIA OLMECA NOCIW

Animal Models of Leishmaniasis Relevant to Vaccine Development. David Sacks Laboratory of Parasitic Diseases NIAID, NIH

The Most Common Parasitic Infections In Yemen. Medical Parasitology

Epidemiological Study of Cutaneous Leishmaniasis in Tuz

Seasonality of Lutzomyia fairtigi (Diptera: Psychodidae: Phlebotominae), a species endemic to Eastern Colombia

Multilevel modelling of the incidence of visceral leishmaniasis in Teresina, Brazil

Visceral leishmaniasis: an endemic disease with global impact

1. YELLOW FEVER BACKGROUND 2. YELLOW FEVER IN SOUTH AMERICA

Vector Hazard Report: Malaria, Leishmaniasis and Dengue Risk in Honduras

Elimination of VL in the Indian subcontinent is it achievable?

Leishmaniasis, Kala Azar(The Black Fever)

Clinical Picture of Cutaneous Leishmaniases Due to Leishmania (Leishmania) mexicana in the Yucatan Peninsula, Mexico

Studying the Dynamics of Visceral Leishmaniasis Epidemic in India - A System Dynamic Approach for Policy Development

Proven and putative vectors of American cutaneous leishmaniasis in Brazil: aspects of their biology and vectorial competence

The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters.

Leishmania (Viannia) naiffi: rare enough to be neglected?

Analytical evaluation of Malaria Research Papers in MEDLINE & SCI during the period of &

Leishmaniasis. MAJ Kris Paolino September 2014

Experimental hut to study the indoor behaviour and effects of insecticide-treated bednets on phlebotomine sand flies (Diptera: Psychodidae)

Anopheles darlingi and Anopheles marajoara (Diptera: Culicidae) susceptibility to pyrethroids in an endemic area of the Brazilian Amazon

Prevalence of Cutaneous Leishmaniasis among HIV and Non-HIV Patients attending some Selected Hospitals in Jos Plateau State

Downloaded from:

Series Editors Samuel J. Black, University of Massachusetts, Amherst, MA, US.A. J. Richard Seed, University of North Carolina, Chapel Hill, NC, US.A.

B Bastrenta/ +, N Mita*, R Buitrago*, F Vargas*, M Flores*, M Machane*, N Yacsik*, M Torrez*, F Le Pont**, F Brenière***

Infestation of peridomestic Attalea phalerata palms by Rhodnius stali, a vector of Trypanosoma cruzi in the Alto Beni, Bolivia

Lutzomyia longipalpis and the eco-epidemiology of American visceral leishmaniasis, with particular reference to Brazil - A Review

Duane J. Gubler, ScD Professor and Founding Director, Signature Research Program in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore

We are IntechOpen, the world s leading publisher of Open Access books Built by scientists, for scientists. International authors and editors

BOVA Network - Building Out Vector-borne diseases in sub-saharan Africa. First BOVA Open Network Meeting IEDE-UCL, London, 28 th March 2018

Navigating vaccine introduction: a guide for decision-makers JAPANESE ENCEPHALITIS (JE) Module 1. Does my country need JE vaccine?

Departamento de Parasitologia, Instituto de Ciências Biológicas 3

Ana Maria Marassá [1], Eunice Aparecida Bianchi Galati [2], Denise Pimentel Bergamaschi [3] and Cleide Aschenbrenner Consales [4] INTRODUCTION METHODS

Proceedings of the World Small Animal Veterinary Association Sydney, Australia 2007

HSJ HEALTH SCIENCE JOURNAL VOLUME 2, ISSUE 4 (2008)

Impact of Olyset long lasting nets to control transmission of anthroponotic cutaneous leishmaniasis in central Iran

Global distribution maps of the leishmaniases

Schedule NIMBioS Investigative Workshop: Malaria-Leishmania Co-infection May 26-28, 2015

Serological tests fail to discriminate dogs with visceral leishmaniasis that transmit Leishmania infantum to the vector Lutzomyia longipalpis

Fact sheet. Yellow fever

The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters.

Frequently Asked Questions on Visceral Leishmaniasis (Kala-azar)

Molecular diagnosis of cutaneous leishmaniasis in an endemic area of Acre State in the Amazonian Region of Brazil

Surveillance for Visceral Leishmaniasis in Iraq

Introduction Leishmaniasis is a group of zoonotic infections caused by protozoan parasites of the genus Leishmania; an estimated persons are

Blood Smears Only 6 October Sample Preparation and Quality Control 15B-K

Laurenti, Marcia D.; Chaves, Luis F

Correspondence should be addressed to Edelberto Santos Dias;

INTRODUCTION MATERIALS AND METHODS

Downloaded from:

Malaria Control in an Agro-industrial Settlement of Rondônia (Western Amazon Region, Brazil)

Correlation of Aedes aegypti infestation indices in the urban area of Merida, Mexico

Atlas of insecticide resistance in malaria vectors of the WHO African region

Prevention of arboviral diseases. Willem Takken & Sander Koenraadt Laboratory of Entomology Wageningen University and Research

Irma Fatima Agrela/ +, Maria Dora Feliciangeli

Running head: VECTOR-BORNE DISEASES: MALARIA IN SUB-SAHARAN AFRICA 1

Resource Allocation for Malaria Prevention. Bahar Yetis Kara

Subclinical Form of the American Visceral Leishmaniasis

Visceral leishmaniasis in Brazil: rationale and concerns related to reservoir control

Repellent Soap. The Jojoo Mosquito. Africa s innovative solution to Malaria prevention. Sapphire Trading Company Ltd

Citation PLoS Neglected Tropical Diseases, 8. the original author and source are

Lesion aspirate culture for the diagnosis and isolation of Leishmania spp. from patients with cutaneous leishmaniasis

Treatment of Cutaneous Leishmaniasis with Allopurinol and Stibogluconate

Natural infection of Didelphis aurita (Mammalia: Marsupialia) with Leishmania infantum in Brazil

Leishmania amazonensis DNA in wild females of Lutzomyia cruzi (Diptera: Psychodidae) in the state of Mato Grosso do Sul, Brazil

Leishmaniaand Leishmaniasis

The feature of papers and citation analysis of eleven journals in tropical medicine indexed by Science Citation Index Expanded

Leishmaniasis: A forgotten disease among neglected people

Policy and technical topics: Selected neglected tropical diseases targeted for elimination: kala-azar, leprosy, yaws, filariasis and schistosomiasis

Some Ecological Aspects of Phlebotomine Sand Flies in an Endemic Focus of Cutaneous Leishmaniasis in Iran

SUDAN BASIC COUNTRY DATA

Mixed infection of Leishmania infantum and Leishmania braziliensis in rodents from endemic urban area of the New World

WHO Malaria Surveillance Reference Manual. Dr Abdisalan M Noor, Team Leader, Surveillance, Monitoring and Evaluation Webinar, 29 May 2018

Suggested Exercises and Projects 395

Trypanosomiasis. Introduction. Epidemiology. Global Epidemiology. Trypanosomiasis Risk in UK Travellers

The Mediterranean Fruit Fly in Central America

Leishmania panamensis transmission in the domestic environment: the results of a prospective epidemiological survey in Santander, Colombia

Transcription:

Campbell-Lendrum, D; Dujardin, JP; Martinez, E; Feliciangeli, MD; Perez, JE; de Silans, L; Desjeux, P (2001) Domestic and peridomestic transmission of American cutaneous leishmaniasis: Changing epidemiological patterns present new control opportunities. Memorias do Instituto Oswaldo Cruz, 96 (2). pp. 159-62. ISSN 0074-0276 Downloaded from: http://researchonline.lshtm.ac.uk/17165/ DOI: Usage Guidelines Please refer to usage guidelines at http://researchonline.lshtm.ac.uk/policies.html or alternatively contact researchonline@lshtm.ac.uk. Available under license: Creative Commons Attribution Non-commercial http://creativecommons.org/licenses/by-nc/3.0/

Mem Inst Oswaldo Cruz, Rio de Janeiro, Vol. 96(2): 159-162, February 2001 Domestic and Peridomestic Transmission of American Cutaneous Leishmaniasis: Changing Epidemiological Patterns Present New Control Opportunities Diarmid Campbell-Lendrum/ +, Jean-Pierre Dujardin*, Eddy Martinez**, M Dora Feliciangeli***, J Enrique Perez****, Laura Ney Marcelino Passerat de Silans*****, Philippe Desjeux****** London School of Hygiene and Tropical Medicine, Keppel St., London WC1E 7HT, UK *UMR IRD-CNRS 9926, Montpellier, France/Instituto Nacional de Laboratorios de Salud, La Paz, Bolivia **Institut de Recherche pour le Développement, La Paz, Bolivia ***Universidad de Carabobo, Maracay, Venezuela ****Instituto de Medicina Tropical Alexander von Humboldt, Universidad Peruana Cayetano Heredia, Lima, Peru *****FNS/SEOPE/Núcleo de Entomologia, João Pessoa, PB, Brazil ******World Health Organization, Geneva, Switzerland Predictions that deforestation would reduce American cutaneous leishmaniasis incidence have proved incorrect. Presentations at a recent international workshop, instead, demonstrated frequent domestication of transmission throughout Latin America. While posing new threats, this process also increases the effectiveness of vector control in and around houses. New approaches for sand fly control and effective targeting of resources are reviewed. Key words: American cutaneous leishmaniasis - deforestation - domestication - transmission - control 159 This paper is a summary of the EUROLEISH workshop on Phlebotomine sandfly control in the New World with special reference to peridomestic transmission, 26 August 1999, Montpellier, France, funded by the European Community. + Corresponding author. Fax: +44-20-7323.5687. E-mail: D.Campbell-Lendrum@lshtm.ac.uk Received 22 February 2000 Accepted 11 October 2000 In undisturbed Neotropical forests, the Leishmania species which cause American cutaneous leishmaniasis (ACL) and mucocutaneous leishmaniasis (MCL), are transmitted amongst sylvatic mammals by the bite of phlebotomine sand flies. The close association between forest, wild mammal reservoirs and sand flies has previously led to predictions that deforestation would lead to local eradication of some of the most important Leishmania species, including Leishmania braziliensis in the State of São Paulo, Brazil (Sampaio 1951), and Leishmania panamensis in Panama (Herrer & Christensen 1976). Presentations at a recent EUROLEISH workshop (August 26, Montpellier, France) demonstrated that such optimistic predictions were far from accurate. Researchers from throughout South America described how the unprecedented deforestation of recent decades has instead been accompanied by an increase in ACL and MCL cases, and documented various examples of sand fly and Leishmania species responding to human encroachment by invading the domestic environment. The increasing importance of domestic transmission is leading to reconsideration of the view that cutaneous leishmaniasis and mucocutaneous leishmaniasis in the New World can, for the most part, be considered occupational diseases since they are directly related to professional activities in enzootic areas, especially in forests (WHO 1990). E Martinez (La Paz, Bolivia) described the recent definition of the role of Lutzomyia nuneztovari anglesi as a domestic vector of L. amazonensis in the new sub-andean focus of Cajuta, Bolivia (Martinez et al. 1998). Lu. n. anglesi was incriminated on the basis of repeated isolation and culture of the same parasite species from sand flies as from human patients, high sand fly densities inside houses, high anthropophily, and similar geographical distributions of sand flies and human cases (Martinez et al. 1999). L. amazonensis had not previously been isolated from Lu. n. anglesi, which acts as a domestic vector for L. braziliensis elsewhere in Bolivia (Torrez et al. 1999). This site is at a relatively high altitude (1450-2100 m a.s.l.) suggesting possible expansion of the distribution of L. amazonensis from previously reported foci in the lowlands of Bolivia, where it had been considered a sylvatic parasite. Infections were detected in dogs, adding to the accumulating indirect evi-

160 Changing Patterns of ACL Transmission Diarmid Campbell-Lendrum et al. dence that dogs act as alternative reservoirs for a range of cutaneous leishmaniasis parasites (Reithinger & Davies 1999). E Perez (Lima, Peru) gave an account of L. peruviana transmission by Lu. verrucarum and Lu. peruensis in the Andean highlands of Peru. In this region, transmission is overwhelmingly domestic, possibly involving domestic dogs as reservoir hosts, with indoor (rather than peridomestic) sand fly abundance providing the best predictor of transmission rate in humans. Further evidence for indoor transmission was provided by a case-control study, which identified significant house-related risk factors, and by the absence of any relationship between risk and either age or gender. However, evidence from the case-control study and from a village-based cohort study both demonstrated that risk increased with nocturnal visits to crops (e.g. for irrigation). MD Feliciangeli (Maracay, Venezuela) described how an analysis of over 41,250 cases of cutaneous leishmaniasis reported in Venezuela reveals an increase from approximately 600 cases/ year in 1955 to 2000/yr in 1998, and a spread from sylvatic to peridomestic/domestic (Feliciangeli 1997) and even peri-urban foci (MD Feliciangeli, unpublished data). This trend has also been accompanied by a recent increase in transmission of visceral leishmaniasis [caused by L. infantum/ chagasi and transmitted by Lu. longipalpis (Feliciangeli et al. 1999)] and an emergence in periurban areas, associated with an increase in poverty and malnutrition (Aguilar et al. 1998). Full descriptions of reported cases are now organized in a Geographical Information System (GIS) format, allowing the rapid mapping of changes in the geographic, ecological and epidemiological pattern of transmission. These examples constitute convincing evidence that the increasing domestication of cutaneous leishmaniasis transmission, already well characterized in deforested areas of Brazil (e.g. Tolezano 1994, Gomes 1994, Brandão-Filho et al. 1999), is widespread in Latin American. OPPORTUNITIES FOR CONTROL The consequent shift in the burden of disease towards children and women poses a new threat, but also presents new opportunities for control. Until recently, the interruption of ACL transmission has generally been considered unfeasible, due to its perceived sylvatic nature (Desjeux 1996). In domestic and peri-domestic transmission foci, however, interventions that decrease sand fly abundances and biting rates in and around houses may reduce disease incidence; some promising results were reported. J-P Dujardin (La Paz, Bolivia) described early results of fieldwork in the Yungas region (Bolivia), where Lu. n. anglesi is a highly endophagic vector for L. braziliensis. Pyrethroid (deltamethrin) impregnated ribbons were placed around the doors and windows of bedrooms in three villages. The intervention resulted in a marked decrease in sand fly densities inside protected houses compared to unprotected controls, and most importantly, ACL incidence was also significantly lower in protected houses (one case/400 inhabitants) during the trial compared to the same period of the previous year (10/400: Fisher s exact test, P = 0.011), or to the control houses (5/245: Fisher s exact test, P = 0.032). E Martinez reported that the same intervention also greatly reduced the abundance of Lu. n. anglesi inside houses in the L. amazonensis focus, from an average of 40.8 females/cdc trap/ night in unprotected control houses to 1.08 in protected houses. E Perez described how indoor spraying of the insecticide lambdacyhalothrin (ICON) reduced transmission of L. peruviana in recent trials in Peru, consistent with results of DDT trials in the 40 s. Insecticide-treated bednets have also previously been demonstrated to protect users against the bites of the ACL vector Lu. youngi in Colombia (Alexander et al. 1995), and may therefore reduce domestic ACL transmission. Taken together, these results raise hopes for insecticide-based interventions in many foci. LIMITATIONS AND FUTURE RESEARCH NEEDS Such interventions may not always be effective, however. MD Feliciangeli described how the use of deltamethin impregnated curtains had failed to reduce domestic abundance of Lu. ovallesi and Lu. gomezi in Venezuela, due to the practical difficulties of blocking all entrances to irregularly constructed house. This suggests that they will consequently reduce neither human-sand fly contact nor disease transmission. A presentation by L Passerat de Silans (João Pessoa, Brazil) further illustrated the difficulties of controlling even exclusively domestic and peridomestic transmission cycles. In Northeast Brazil, pyrethroid insecticides (deltamethrin and cypermethrin) are applied inside and outside houses to control visceral leishmaniasis. Repeated entomological surveys showed that these measures significantly reduced sand fly densities inside all houses for approximately two months, but that densities subsequently returned to pre-control levels. Bioassays suggested that this was due to gradual loss of residual insecticide activity on the adobe house walls, which are typical of the region. Outdoor densities of Lu. longipalpis remained un-

Mem Inst Oswaldo Cruz, Rio de Janeiro, Vol. 96(2), February 2001 161 affected throughout the trial period (Passerat de Silans et al. 1998). These results illustrate the urgent requirement for a series of large scale intervention trials against the domestic transmission of ACL, in order to quantify the potential reduction in the burden of disease in a range of ecological settings. Even allowing for the development of appropriate control tools, the limited availability of health resources in most endemic countries will necessitate prioritization of interventions to where they will have greatest effect. For example, in São Paulo, Brazil, the current control policy for cutaneous leishmaniasis (transmitted domestically by Lu. intermedia) is to carry out house spraying only in localities with at least two notified cases (Gomes & Neves 1998). Logistic constraints, however, mean that in most endemic areas case notification systems fail to achieve full geographic coverage and usually lack information on the particular parasite and vector species responsible. D Campbell-Lendrum (London, UK), described how GIS techniques may be used to extract maximum information from available data on intensity of leishmaniasis transmission and vector and parasite species. Ecological (e.g. temperature, vegetation) determinants of these distributions may be analyzed, and the observed relationships used to generate predictions for unsurveyed areas. These would improve estimates of the distribution of populations at risk, and of vector and parasite species, providing better evidence for allocation of control resources and the selection of appropriate interventions. The final presentation and overall summary was made by P Desjeux (Geneva, Switzerland), representing the World Health Organization. Dr Desjeux thanked the workshop participants for raising awareness of the challenges posed by the changing epidemiological situation of the New World leishmaniases. He stressed that research should continue on the characterization of complex zoonotic transmission cycles (both sylvatic and domestic), which continue to make control more challenging than for anthroponotic leishmaniasis diseases in other regions. The results of the few intervention trials presented in this workshop and elsewhere, however, offer sufficient encouragement to believe that cost-effective campaigns against domestic transmission of the New World leishmaniases are an achievable goal. International co-operation will be essential to achieving this aim; vectors and parasites cross national boundaries, and this workshop confirmed that experience from one country is often of great relevance to others within the region. The sharing of research findings, the central aim of the EUROLEISH workshops, is an essential first step on this path. ACKNOWLEDGEMENTS To Katrin Kuhn for summarizing the workshop proceedings, and Clive Davies for comments on the manuscript. REFERENCES Aguilar CM, Fernandez E, Fernandez R, Cannova DC, Ferrer E, Cabrera Z, Souza WJ, Coutinho SG 1998. Urban visceral leishmaniasis in Venezuela. Mem Inst Oswaldo Cruz 93: 15-16. Alexander B, Usma MC, Cadena H, Quesada BL, Solarte Y, Roa W, Travi BL 1995. Evaluation of deltamethrin-impregnated bednets and curtains against phlebotomine sandflies in Valle del Cauca, Colombia. Med Vet Entomol 9: 279-283. Brandão-Filho SP, Campbell-Lendrum D, Brito MEF, Shaw JJ, Davies CR 1999. Epidemiological surveys confirm increasing burden of cutaneous leishmaniasis in north-east Brazil. Trans R Soc Trop Med Hyg 93: 488-494. Desjeux P 1996. Leishmaniasis. Public health aspects and control. Clin Dermatol 14: 417-424. Feliciangeli MD 1997. Hourly activity of Lutzomyia ovallesi and L. gomezi (Diptera: Psychodidae), vectors of cutaneous leishmaniasis in northcentral Venezuela. J Med Entomol 34:110-115. Feliciangeli MD, Rodriguez N, De Guglielmo Z, Rodriguez A 1999. The re-emergence of American visceral leishmaniasis in an old focus in Venezuela. II. Vectors and parasites. Parasite 6: 113-120. Gomes AC 1994. Sand fly vectorial ecology in the State of São Paulo. Mem Inst Oswaldo Cruz 89: 457-460. Gomes AC, Neves VL 1998. Strategy and perspectives for the control of cutaneous leishmaniasis in the State of São Paulo. Rev Soc Bras Med Trop 31: 553-558. Herrer A, Christenson HA 1976. Natural cutaneous leishmaniasis among dogs in Panama. Am J Trop Med Hyg 25: 59-63. Martinez E, Le Pont F, Torrez M, Telleria J, Vargas F, Munoz M, De Doncker S, Dujardin JC, Dujardin JP 1998. A new focus of cutaneous leishmaniasis due to Leishmania amazonensis in a sub-andean region of Bolivia. Acta Trop 15: 97-106. Martinez E, Le Pont F, Torrez M, Telleria J, Vargas F, Dujardin JC, Dujardin JP 1999. Lutzomyia nuneztovari anglesi (Le pont & Desjeux, 1984) as a vector of Leishmania amazonensis in a sub-andean leishmaniasis focus of Bolivia. Am J Trop Med Hyg 61: 846-849. Passerat de Silans LNM, Dedet JP, Arias JR 1998. Field monitoring of cypermethrin residual effect on the mortality rates of the phlebotomine sand fly Lutzomyia longipalpis in the State of Paraíba, Brazil. Mem Inst Oswaldo Cruz 93: 339-344. Reithinger R, Davies CR 1999. Is the domestic dog (Canis familiaris) a reservoir host of American cutaneous leishmaniasis? A critical review of the current evidence. Am J Trop Med Hyg 61: 530-541. Sampaio LF 1951. Medicina rural o aparecimento, a

162 Changing Patterns of ACL Transmission Diarmid Campbell-Lendrum et al. expansão e o fim da leishmaniose no estado de São Paulo. Rev Bras Med 8: 717-721. Tolezano JE 1994. Ecoepidemiological aspects of American cutaneous leishmaniasis in the State of São Paulo, Brazil. Mem Inst Oswaldo Cruz 89: 427-434. Torrez M, Lopez M, Le Pont F, Martinez E, Munoz M, Hervas D, Yaksic N, Arevalo J, Sossa D, Dedet JP, Dujardin JPM 1999. Lutzomyia nuneztovari anglesi (Diptera: Psychodidae) as a probable vector of Leishmania braziliensis in the Yungas, Bolivia. Acta Trop 71: 311-316. WHO 1990. Control of the leishmaniases: report of a WHO Expert Committee. Technical Report series 793.