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Presence of Lutzomyia longipalpis and Nyssomyia whitmani in Entre Rios, Argentina

ABSTRACT

The objective of this study was to evaluate the presence of Lutzomyia longipalpis in the Argentine city of Concordia, in the province of Entre Rios, without record of this species despite previous samplings, but with canine cases of visceral leishmaniasis and Lu. longipalpis reports both, from Northern Argentine localities and from the city of Salto, Uruguay, located just across the river and the international border. This study confirms the presence of Lu. longipalpis and Nyssomyia whitmani, related to the risk of visceral and tegumentary leishmaniasis, respectively, in Concordia-Entre Rios. The presence of Lu. longipalpis confirms the ongoing dispersal along the Uruguay river basin. The presence of these species in the study area alerts about the risk of transmission of Leishmania spp.

KEYWORDS:
Lutzomyia longipalpis; Nyssomyia whitmani; Dispersal; Argentina

INTRODUCTION

Leishmaniasis, a worldwide health issue with special relevance in public health, is considered a vectorial emergent or re-emergent disease. Processes such as urbanization and landscape modification favor vector colonization of an environment modified by humans especially in the Americas11. Lainson R, Rangel EF. Lutzomyia longipalpis and the ecoepidemiology of American visceral leishmaniasis, with particular reference to Brazil: a review. Mem Inst Oswaldo Cruz. 2005;100:811-27.,22. Shaw J. The leishmaniases: survival and expansion in a changing world. A mini-review. Mem Inst Oswaldo Cruz. 2007;102:541-7..

The urban cycle of visceral leishmaniasis (VL) includes the incriminated agents Leishmania infantum and Lutzomyia longipalpis as parasite and vector, respectively11. Lainson R, Rangel EF. Lutzomyia longipalpis and the ecoepidemiology of American visceral leishmaniasis, with particular reference to Brazil: a review. Mem Inst Oswaldo Cruz. 2005;100:811-27.,33. Chagas E. Primeira verificação em individuo vivo, da leishmaniose visceral no Brasil. Bras Med. 1936;50:221-2.,44. Deane LM, Deane MP. Leishmaniose visceral urbana (no cão e no homem) em Sobral, Ceará. Hospital. 1955;47:75-87.. Since its urban showing up in 2004 at the North border with Paraguay, Lu. longipalpis dispersed in Argentina from the Northeastern region to the South reaching Chajari (Entre Rios) 600 km far away in approximately seven years, and establishing the Latin-American Southernmost registry at the moment in Salto (Republica Oriental del Uruguay)55. Satragno D, Faral-Tello P, Canneva B, Verger L, Lozano A, Vitale E, et al. Autochthonous outbreak and expansion of canine visceral leishmaniasis, Uruguay. Emerg Infect Dis. 2017;23:536-8.,66. Salomón OD, Feliciangeli MD, Quintana MG, Afonso MM, Rangel EF. Lutzomyia longipalpis urbanisation and control. Mem Inst Oswaldo Cruz. 2015;110:831-46..

For tegumentary leishmaniasis (TL), more phlebotominae species are incriminated as vectors, being in Argentina L. braziliensis the principal parasite associated to outbreaks77. Salomón OD, Acardi SA, Liotta DJ, Fernández MS, Lestani E, López D, et al. Epidemiological aspects of cutaneous leishmaniasis in the Iguazu falls area of Argentina. Acta Trop. 2009;109:5-11., with Nyssomyia neivai as its principal vector except for the outbreak in Puerto Iguazu (Misiones) where Ny. whitmani was incriminated77. Salomón OD, Acardi SA, Liotta DJ, Fernández MS, Lestani E, López D, et al. Epidemiological aspects of cutaneous leishmaniasis in the Iguazu falls area of Argentina. Acta Trop. 2009;109:5-11.. Well documented human cases date from the first outbreak in 1984, however there are known cases since 191677. Salomón OD, Acardi SA, Liotta DJ, Fernández MS, Lestani E, López D, et al. Epidemiological aspects of cutaneous leishmaniasis in the Iguazu falls area of Argentina. Acta Trop. 2009;109:5-11..

In the case of these last two species, their occurrence in Northeastern Argentina is more sporadic. According to current references, Ny. neivai was found in cities by the river Parana, whereas Ny. whitmani was not captured in the provinces of Corrientes nor in Entre Rios77. Salomón OD, Acardi SA, Liotta DJ, Fernández MS, Lestani E, López D, et al. Epidemiological aspects of cutaneous leishmaniasis in the Iguazu falls area of Argentina. Acta Trop. 2009;109:5-11.1010. Salomón OD, Fernández MS, Santini MS, Saavedra S, Montiel N, Ramos M, et al. Distribución de Lutzomyia longipalpis en la Mesopotamia Argentina. Medicina (B Aires). 2011;71:22-6..

In this sense, the objective of this study was to evaluate the presence of Lu. longipalpis in the Argentine city of Concordia (Entre Rios), having no registered captures in previous studies.

MATERIAL AND METHODS

Area of study

The sampling was developed in the city of Concordia, Entre Rios - Argentina (31°18′S 58°00′W), placed within the Pampean phytogeographic region (Pampean Uruguayan phytogeographic district), on the border with the Eastern Republic of Uruguay through the Uruguay river and connected by an international bridge (Figure 1A). The city has a population of 149,450 inhabitants and a density of 63.8 inhab/km2 (INDEC, Census 2010). Climate is temperate with an annual maximum mean temperature of 24.8 °C (31.8 °C in January and February) and an annual minimum mean temperature of 13.1 °C (19.3 °C in January and February) (Sistema Meteorologico Nacional).

Figure 1
A) Location of the study area (black point) in South America, bordering the Eastern Republic of Uruguay; B) Study area showing the four landscapes sampled and the distribution of the sites (points). Stars highlight the sites with phlebotomine occurrence. The sampling period was from January 30th to February 2nd,2017

The fieldwork took place between January 30th and February 2nd, 2017, during the austral summer. With the purpose of sampling all the study area, the city was divided into four landscape strata: urban, semiurban, periurban and coastal, using the images provided by GoogleEarth© and GoogleStreet Maps©. Each landscape was divided into 400 x 400 m quadrants (Figure 1B) that were then random selected, so that the number of sampled quadrants per landscape was proportional to the total surface (Quadrants/surface total (km22. Shaw J. The leishmaniases: survival and expansion in a changing world. A mini-review. Mem Inst Oswaldo Cruz. 2007;102:541-7.): urban 30/5.57; semiurban 104/20.44; periurban 30/6.33; Coastal 14/3.33).

The landscape urban is the central area with paved streets and low density of vegetation, the surface measures 2, 5.57 km.

Sand flies were captured with REDILA-BL minilight traps1010. Salomón OD, Fernández MS, Santini MS, Saavedra S, Montiel N, Ramos M, et al. Distribución de Lutzomyia longipalpis en la Mesopotamia Argentina. Medicina (B Aires). 2011;71:22-6.. Each trap was active from approximately 5:00 p.m. to 8:30 a.m. of the next day. Traps were placed 1.5 m above the ground during three consecutive nights in each landscape: 5 traps in urban, 18 traps in semiurban, 5 traps in periurban and 2 traps in coastal landscape.

Each trap was placed in a domestic unit of the sampling quadrant, selected by the criterion descripted by Feliciangeli et al.1111. Feliciangeli M, Delgado O, Suarez B, Bravo A. Leishmania and sand flies: proximity to woodland as a risk factor for infection in a rural focus of visceral leishmaniasis in west central Venezuela. Trop Med Int Health. 2006;11:1785-91. choosing sites with the higher probability of urban phlebotomine occurrence due to habitat conditions. The geographic coordinates of all the sampled sites were recorded with a Global Positioning System (Garmin Trex10®). In all the domestic units, an informed consent was signed by the adult who authorized the entry.

During the sampling days, the weather was windy with intermittent rain.

All phlebotominae sandflies were dried and preserved prior to processing. The specimens were cleared with lacto-phenol and identified according to Galati1212. Galati EA. Classificação de Phlebotominae. In: Rangel EF, Lainson R, organizadores. Flebotomíneos do Brasil. Rio do Janeiro: Fiocruz; 2003. p.23-51. under a microscope (Zeiss, 400x).

RESULTS

The sampling effort was of 30 trap/night. Of the total studied sites, we found phlebotomine specimens in 10%. These sites with phlebotomine were distributed and located at three out of the four sampled landscapes (urban, semiurban and periurban), being the coastal the only one without phlebotomines (Figure 1B).

We captured a total of 8 phlebotomines, belonging to two species: Lu. longipalpis and Ny. whitmani. There were two male Lu. Longipalpis, one in the semiurban landscape and the other in the periurban landscape, but we found six female Ny. whitmani in the urban landscape.

During the sampling nights, mean maximum temperatures ranged from 30.4 °C to 33.8 °C, and mean minimum ranged between 20.9 °C and 22.6 °C.

DISCUSSION

This study reports the presence of Lu. longipalpis and Ny. whitmani in Concordia-Entre Rios, Southern to the Southernmost previous record in Argentina, despite the historical sampling in the area. The presence of Ny. whitmany is interesting as its distribution up to now seemed discontinuous along the residual gallery forest of the Parana and Uruguay rivers, while the report of Lu. longipalpis support the hypothesis of an ongoing dispersal, expanding to territories without previous records22. Shaw J. The leishmaniases: survival and expansion in a changing world. A mini-review. Mem Inst Oswaldo Cruz. 2007;102:541-7.. Some major constructions among others had taken place in the study area, the binational dam of Salto Grande, the main pipeline of Entre Rios and the national motorway N° 14 that had changed the physiognomy of the landscape. According to different authors, these changes triggered climate changes, demographic and transit of goods and services profiles at the local level, contributing to vector dispersal especially when there is ecological continuity and least cost steps1313. Fischer D, Moeller P, Thomas SM, Naucke TJ, Beierkuhnlein C. Combining climatic projections and dispersal ability: a method for estimating the responses of sandfly vector species to climate change. PLoS Negl Trop Dis. 2011;5:e1407.1515. Correa Antonialli SA, Torres TG, Paranhos Filho AC, Tolezano JE. Spatial analysis of American Visceral Leishmaniasis in Mato Grosso do Sul State, Central Brazil. J Infect. 2007;54:509-14..

The presence of Lu. longipalpis and Ny. whitmani in the study area alerts about the transmission risk of Leishmania spp. in latitudes which are not considered receptive or vulnerable.

To present, Lu. longipalpis Southernmost distribution in Argentina was 30°46'00"S 57°59'00"W, Chajari - Entre Rios1010. Salomón OD, Fernández MS, Santini MS, Saavedra S, Montiel N, Ramos M, et al. Distribución de Lutzomyia longipalpis en la Mesopotamia Argentina. Medicina (B Aires). 2011;71:22-6., but American Southernmost location where individuals of this species were found was 31°23'18"S 57°57'38"W Salto -R.O. del Uruguay1616. Salomón OD, Basmajdian Y, Fernández MS, Santini MS. Lutzomyia longipalpis in Uruguay: the first report and the potential of visceral leishmaniasis transmission. Mem Inst Oswaldo Cruz. 2011;106:381-2.. The results of this study update this distribution to 31°23'32"S 58°01'01"W Concordia-Entre Rios, supporting the risk of Lu. longipalpis dispersal already shown in other studies under certain conditions of temperature and humidity and exceptional ones66. Salomón OD, Feliciangeli MD, Quintana MG, Afonso MM, Rangel EF. Lutzomyia longipalpis urbanisation and control. Mem Inst Oswaldo Cruz. 2015;110:831-46..

The number of individuals obtained from both species is very low, but the climate conditions according to the records during the study were not optimal for the activity of phlebotomines1717. Santini MS, Fernández MS, Cavia R, Salomón OD. Co-occurrence and seasonal and environmental distributions of the sandflies Lutzomyia longipalpis and Nyssomyia whitmani in the city of Puerto Iguazu, northeastern Argentina. Med Vet Entomol. 2018;32:197-205.. Even though the scenario is adverse and there is eventual recent colonization, Lu. longipalpis was found in the anthropogenic environments1818. Santini MS, Utges ME, Berrozpe P, Manteca Acosta M, Casas N, Heuer P, et al. Lutzomyia longipalpis presence and abundance distribution at different micro-spatial scales in an urban scenario. PLoS Negl Trop Dis. 2015;9:e0003951.. In this sense, while the odds of permanent colonization by Lu. longipalpis in the current climate and landscape context are low, the presence of Lu. longipalpis, the outbreak of canine cases that took place in Salto-Uruguay55. Satragno D, Faral-Tello P, Canneva B, Verger L, Lozano A, Vitale E, et al. Autochthonous outbreak and expansion of canine visceral leishmaniasis, Uruguay. Emerg Infect Dis. 2017;23:536-8. and the occurrence of canine cases of LV in Concordia (National Health Surveillance System - Argentina) warn about the risk of autochthonous transmission of L. infantum in the region.

Another finding of this work is the presence of Ny. whitmani in the study area. So far, the studies carried out in other cities of the Mesopotamia Argentina do not report the presence of this species, but identified specimens of Ny. neivai and other phlebotomine species88. Berrozpe P, Lamattina D, Santini MS, Araujo AV, Utgés ME, Salomón OD. Environmental suitability for Lutzomyia longipalpis in a subtropical city with a recently established visceral leishmaniasis transmission cycle, Argentina. Mem Inst Oswaldo Cruz. 2017;112:674-80.1010. Salomón OD, Fernández MS, Santini MS, Saavedra S, Montiel N, Ramos M, et al. Distribución de Lutzomyia longipalpis en la Mesopotamia Argentina. Medicina (B Aires). 2011;71:22-6.,1414. Kent AD, Dos Santos TV, Gangadin A, Samjhawan A, Mans DR, Schallig HD. Studies on the sand fly fauna (Diptera: Psychodidae) in high-transmission areas of cutaneous leishmaniasis in the Republic of Suriname. Parasit Vectors. 2013;6:318.. Ny. whitmani is a species that is mainly found in rural areas and in zones with primary or secondary vegetation1919. de Souza CF, Quaresma PF, Andrade Filho JD, Bevilacqua PD. Phlebotomine fauna in the urban area of Timóteo, State of Minas Gerais, Brazil. Acta Trop. 2014;134:72-9.,2020. Rangel EF, Lainson R. Proven and putative vectors of American cutaneous leishmaniasis in Brazil: aspects of their biology and vectorial competence. Mem Inst Oswaldo Cruz. 2009;104:937-54.. However, in this study the specimens captured were from the urban landscape1818. Santini MS, Utges ME, Berrozpe P, Manteca Acosta M, Casas N, Heuer P, et al. Lutzomyia longipalpis presence and abundance distribution at different micro-spatial scales in an urban scenario. PLoS Negl Trop Dis. 2015;9:e0003951., perhaps due to a probable trend towards urban occupation that this species shows2020. Rangel EF, Lainson R. Proven and putative vectors of American cutaneous leishmaniasis in Brazil: aspects of their biology and vectorial competence. Mem Inst Oswaldo Cruz. 2009;104:937-54.. Although its presence is incipient, these results could be related to regions of intense agriculture leading to a possible anthroponization of the vector2121. Zeilhofer P, Kummer OP, Santos ES, Ribeiro AL, Missawa NA. Spatial modelling of Lutzomyia (Nyssomyia) whitmani s.l. (Antunes & Coutinho, 1939) (Diptera: Psychodidae: Phlebotominae) habitat suitability in the state of Mato Grosso, Brazil. Mem Inst Oswaldo Cruz. 2008;103:653-60..

Finally, considering the foregoing, active surveillance is recommended for Lu. longipalpis and Ny. whitmani with periodic monitoring in the areas adjacent to known records. Likewise, there is a need to develop instruments for decision makers, starting from validated models that allow timely identification in space environments with risk of incipient vector colonization, estimating the likelihood of transmission risk for leishmaniasis in regular and exceptional conditions, considering climate or environmental change scenarios in order to reduce the risk of occurrence of human and canine cases of LV and/or LT.

  • FUNDING
    This study was developed with research funding provided in 2014 by the National Ministry of Health and the National Ministry of Science, Technology and Productive Innovation (PICTO-2014- 3549) which title is: Vigilancia y control integrado para Dengue y Leishmaniasis para la generación espacios saludables. Trabajo multi-sectorial e inter-ministerial.

ACKNOWLEDGMENTS

To all the neighbors who opened their homes to us to carry out this study. Also to the entire team work, to Epidemiologia de Entre Rios and the municipality of Concordia, especially to: Jerónimo Garcilazo Amatti, Carlos Uranga, Vanesa Alejandra Defeis, Silvana Gabriela Bressan, Gastón Morilla, Maria Helena Hernández, Juan Cruz Iglesias, Marcelo Mazzula a Fernando Carmona.

REFERENCES

  • 1
    Lainson R, Rangel EF. Lutzomyia longipalpis and the ecoepidemiology of American visceral leishmaniasis, with particular reference to Brazil: a review. Mem Inst Oswaldo Cruz. 2005;100:811-27.
  • 2
    Shaw J. The leishmaniases: survival and expansion in a changing world. A mini-review. Mem Inst Oswaldo Cruz. 2007;102:541-7.
  • 3
    Chagas E. Primeira verificação em individuo vivo, da leishmaniose visceral no Brasil. Bras Med. 1936;50:221-2.
  • 4
    Deane LM, Deane MP. Leishmaniose visceral urbana (no cão e no homem) em Sobral, Ceará. Hospital. 1955;47:75-87.
  • 5
    Satragno D, Faral-Tello P, Canneva B, Verger L, Lozano A, Vitale E, et al. Autochthonous outbreak and expansion of canine visceral leishmaniasis, Uruguay. Emerg Infect Dis. 2017;23:536-8.
  • 6
    Salomón OD, Feliciangeli MD, Quintana MG, Afonso MM, Rangel EF. Lutzomyia longipalpis urbanisation and control. Mem Inst Oswaldo Cruz. 2015;110:831-46.
  • 7
    Salomón OD, Acardi SA, Liotta DJ, Fernández MS, Lestani E, López D, et al. Epidemiological aspects of cutaneous leishmaniasis in the Iguazu falls area of Argentina. Acta Trop. 2009;109:5-11.
  • 8
    Berrozpe P, Lamattina D, Santini MS, Araujo AV, Utgés ME, Salomón OD. Environmental suitability for Lutzomyia longipalpis in a subtropical city with a recently established visceral leishmaniasis transmission cycle, Argentina. Mem Inst Oswaldo Cruz. 2017;112:674-80.
  • 9
    Salomón OD, Ramos LK, Quintana MG, Acardi SA, Santini MS, Schneider A. Distribucion de vectores de leishmaniasis visceral en la provincia de Corrientes, 2008. Medicina (B Aires). 2009;69:625-30.
  • 10
    Salomón OD, Fernández MS, Santini MS, Saavedra S, Montiel N, Ramos M, et al. Distribución de Lutzomyia longipalpis en la Mesopotamia Argentina. Medicina (B Aires). 2011;71:22-6.
  • 11
    Feliciangeli M, Delgado O, Suarez B, Bravo A. Leishmania and sand flies: proximity to woodland as a risk factor for infection in a rural focus of visceral leishmaniasis in west central Venezuela. Trop Med Int Health. 2006;11:1785-91.
  • 12
    Galati EA. Classificação de Phlebotominae. In: Rangel EF, Lainson R, organizadores. Flebotomíneos do Brasil. Rio do Janeiro: Fiocruz; 2003. p.23-51.
  • 13
    Fischer D, Moeller P, Thomas SM, Naucke TJ, Beierkuhnlein C. Combining climatic projections and dispersal ability: a method for estimating the responses of sandfly vector species to climate change. PLoS Negl Trop Dis. 2011;5:e1407.
  • 14
    Kent AD, Dos Santos TV, Gangadin A, Samjhawan A, Mans DR, Schallig HD. Studies on the sand fly fauna (Diptera: Psychodidae) in high-transmission areas of cutaneous leishmaniasis in the Republic of Suriname. Parasit Vectors. 2013;6:318.
  • 15
    Correa Antonialli SA, Torres TG, Paranhos Filho AC, Tolezano JE. Spatial analysis of American Visceral Leishmaniasis in Mato Grosso do Sul State, Central Brazil. J Infect. 2007;54:509-14.
  • 16
    Salomón OD, Basmajdian Y, Fernández MS, Santini MS. Lutzomyia longipalpis in Uruguay: the first report and the potential of visceral leishmaniasis transmission. Mem Inst Oswaldo Cruz. 2011;106:381-2.
  • 17
    Santini MS, Fernández MS, Cavia R, Salomón OD. Co-occurrence and seasonal and environmental distributions of the sandflies Lutzomyia longipalpis and Nyssomyia whitmani in the city of Puerto Iguazu, northeastern Argentina. Med Vet Entomol. 2018;32:197-205.
  • 18
    Santini MS, Utges ME, Berrozpe P, Manteca Acosta M, Casas N, Heuer P, et al. Lutzomyia longipalpis presence and abundance distribution at different micro-spatial scales in an urban scenario. PLoS Negl Trop Dis. 2015;9:e0003951.
  • 19
    de Souza CF, Quaresma PF, Andrade Filho JD, Bevilacqua PD. Phlebotomine fauna in the urban area of Timóteo, State of Minas Gerais, Brazil. Acta Trop. 2014;134:72-9.
  • 20
    Rangel EF, Lainson R. Proven and putative vectors of American cutaneous leishmaniasis in Brazil: aspects of their biology and vectorial competence. Mem Inst Oswaldo Cruz. 2009;104:937-54.
  • 21
    Zeilhofer P, Kummer OP, Santos ES, Ribeiro AL, Missawa NA. Spatial modelling of Lutzomyia (Nyssomyia) whitmani s.l. (Antunes & Coutinho, 1939) (Diptera: Psychodidae: Phlebotominae) habitat suitability in the state of Mato Grosso, Brazil. Mem Inst Oswaldo Cruz. 2008;103:653-60.

Publication Dates

  • Publication in this collection
    22 Oct 2018
  • Date of issue
    2018

History

  • Received
    18 Apr 2018
  • Accepted
    17 July 2018
Instituto de Medicina Tropical de São Paulo Av. Dr. Enéas de Carvalho Aguiar, 470, 05403-000 - São Paulo - SP - Brazil, Tel. +55 11 3061-7005 - São Paulo - SP - Brazil
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