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Preliminary observations of the urbanization and domiciliation of the American cutaneous leishmaniasis in Rio Branco, Acre, Western Amazon

ABSTRACT

Background:

The American cutaneous leishmaniasis (ACL) is expanding in peri-urban environments.

Methods:

An entomological survey was conducted in the area of the occurrence of an autochthonous urban case of ACL. Sandflies and a parasitological slide of the human case were submitted for molecular diagnosis.

Results:

Nyssomyia whitmani and Ny. antunesi were the most frequently collected species. Ny. whitmani and Bichromomyia flaviscutellata were positive for Leishmania guyanensis and L. lainsoni, respectively. The human case tested positive for L. lainsoni.

Conclusions:

Sandflies and Leishmania parasites present in urban forest may occur frequently in nearby domiciliary environments; thus, these areas must be monitored.

Keywords:
Health Surveillance; Leishmania; Psychodidae; Urban population

In the state of Acre, American cutaneous leishmaniasis (ACL) is one of the most relevant diseases for public health, with cases reported in all municipalities, most of which are concentrated in the Vale do Acre region. Predominantly, the cases are of populations that live in rural and forest areas; when they live in urban areas, transmission occurs due to activities related to the forest11. Melchior LAK, Brilhante AF, Chiaravalloti-Neto F. Spatial and temporal distribution of American cutaneous leishmaniasis in Acre state, Brazil. Infect Dis Poverty. 2017;6(1):99..

Epidemiological studies in the region, involving entomological, human, and domestic animal surveys, detected the circulation of several Leishmania species in different hosts, and a high diversity of vector species, mainly in the rural and wild environments, was found22. Teles CB, Medeiros JF, Santos AP, Freitas LA, Katsuragawa TH, Cantanhede LM, et al. Molecular characterization of American Cutaneous Leishmaniasis in the triborder area of Assis Brasil, Acre State, Brazil. Rev Inst Med Trop Sao Paulo. 2015;57(4):343-7.,33. Brilhante AF, Lima L, Zampieri RA, Nunes VLB, Dorval MEC, Malavazi PFNDS, et al. Leishmania (Viannia) braziliensis type 2 as probable etiological agent of canine cutaneous leishmaniasis in Brazilian Amazon. PLoS One. 2019;30;14(4):e0216291.,44. Brilhante AF, Lima L, de Ávila MM, Medeiros-Sousa AR, de Souza JF, Dos Santos NP, et al. Remarkable diversity, new records and Leishmania detection in the sand fly fauna of an area of high endemicity for cutaneous leishmaniasis in Acre state, Brazilian Amazonian Forest. Acta Trop. 2021;223:106103.. Although, the presence of sandfly vectors in forest fragments in urban areas has been observed55. Araujo-Pereira T, Fuzari AA, Filho JDA, Pita-Pereira D, Britto C, Brazil RP. Sand fly fauna (Diptera: Psychodidae: Phlebotominae) in an area of leishmaniasis transmission in the municipality of Rio Branco, state of Acre, Brazil. Parasit Vectors. 2014;7(1):1-5.; the circulation of Leishmania spp. between vectors and human cases is linked to forest or rural areas.

Changes in the environment and landscape may alter the dynamics of vectors and hosts and, consequently, the transmission of etiological agents. As ACL presents a high diversity of causative parasites and vector species, distinct epidemiological profiles may be identified in different regions of Brazil66. da Costa SM, Cordeiro JLP, Rangel EF. Environmental suitability for Lutzomyia (Nyssomyia) whitmani (Diptera: Psychodidae: Phlebotominae) and the occurrence of American cutaneous leishmaniasis in Brazil. Parasit Vectors . 2018;11(1):1-10.,77. Caldart ET, Sevá ADP, Pinto-Ferreira F, Pereira Pachoal AT, de Oliveira JS, Cortela IB, et al. American cutaneous leishmaniasis associated with degradation of native forest, regardless of economic, social and infrastructure vulnerability. Zoonoses Public Health. 2021;68(4):327-43..

In response to the demand from the Entomological Surveillance Service of the municipality of Rio Branco to clarify aspects of the transmission of an ACL autochthonous urban case in the Conjunto Universitário neighborhood, an entomological survey was carried out, aiming to identify the sandfly fauna and to investigate the presence of Leishmania DNA in female sandflies and in the human case. During three nights between August 27 and September 1, 2021, five Center for Disease Control and Prevention (CDC) automatic light traps were installed from 5:00 pm to 7:00 am in three environments: inside the house, in the kitchen, and in the hallway near the bedrooms (n=2); in the backyard, without the presence of domestic animals and vegetation, with the floor being completely cemented and clean (n=1), and in an urban forest fragment (approximately 100 m from the house) composed mainly of primary forest (n=2). Collection with a Shannon trap was undertaken in the backyard for one night, from 17:00 to 22:00 h, by two individuals.

The females were dissected for investigation of flagellated parasites in their guts, with subsequent molecular analysis. Undissected females and males were identified following the Galati taxonomic key88. Galati EAB. Morfologia e terminologia de Phlebotominae (Diptera: Psychodidae). Classificação e identificação de táxons das Américas. Vol I. Apostila da Disciplina Bioecologia e Identificação de Phlebotominae do Programa de Pós-Graduação em Saúde Pública. Faculdade de Saúde Pública da Universidade de São Paulo, São Paulo, 132p, 2021. Available from: https://www.fsp.usp.br/egalati/
https://www.fsp.usp.br/egalati/...
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The patient's clinical information is not reported here because it was not possible to access the data. According to information from the Entomological Surveillance of Rio Branco and the Central Laboratory of Public Health of Rio Branco (Laboratório Central de Saúde Pública de Rio Branco, LACEN-AC), the patient was a male, 21 years old, student, who had not visited forest areas in recent years. The patient presented with three lesions suggestive of cutaneous leishmaniasis on one of his legs, from which the amastigote forms were detected in the parasitological examination.

This project is part of the umbrella project “LeishAcre: Ecoepidemiological studies on leishmaniasis in Acre” and has been approved by the Ethics Committee in Research with Human Beings of the Federal University of Acre (CEP-UFAC) under the opinion number CAAE 26901619.4.0000.5010.

The Giemsa slide with a sample of the ulcer from the patient with a positive diagnosis and 41 dissected sandfly females were sent to the Institute of Biosciences of the University of São Paulo for molecular tests, which were performed using the high melting resolution (HRM) technique99. Zampieri RA, Laranjeira-Silva MF, Muxel SM, Stocco de Lima AC, Shaw JJ, Floeter-Winter LM. High Resolution Melting Analysis Targeting hsp70 as a Fast and Efficient Method for the Discrimination of Leishmania Species. PLoS Negl Trop Dis. 2016;29;10(2):e0004485.. HRM approaches can detect differences in the melting profiles of PCR products as a result of variations in nucleotide composition, such as single nucleotide polymorphisms (SNPs) or other mutation types. The hsp70 coding sequence is a polymorphic gene able to discriminate Leishmania species and, compared to most others, it is among the targets with the highest species-level discriminatory power1010. Van der Auwera G, Dujardin JC. Species typing in dermal leishmaniasis. Clin Microbiol Rev. 2015;28(2):265-94.. Briefly, DNA samples were subjected to real-time PCR, in which three distinct hsp70 gene regions (amplicons 1, 2, and 3) were amplified independently. HRM analyses were performed at the end of each real-time PCR reaction. HRM profiles and specific melting temperatures (Tm) were determined and compared to the Tm obtained from DNA samples of reference strains of Leishmania spp.

During the entomological survey with CDC traps, 129 (58 females and 71 males) sandflies belonging to 14 species were collected (Table 1), and no insects were collected using Shannon traps. Of the 41 females submitted for molecular analysis, one of Bichromomyia flaviscutellata was positive, with a profile of L. lainsoni and three females of Ny. whitmani were positive, with a profile compatible with that of L. guyanensis (Figure 1). The positive specimens were collected in the forest fragment, and none of the 41 dissected females contained flagellated forms under bright field light microscopy. Regarding the slide of the human case, the HRM profile was compatible with that of L. lainsoni (Figure 1).

TABLE 1:
Sandflies in a residential area of Rio Branco municipality, Acre, Brazilian Western Amazon in 2021.

FIGURE 1:
Melting temperatures obtained from HRM profiles. Average Tm values based on dissociation curves of hsp70-amplicons 1, 2, and 3 from the field samples (black dots) and Leishmania reference strains (red dots). Each species and sample were tested in duplicate. Reference strains: I: L. (L.) infantum (MCER/BR/1981/M6445); A: L. (L.) amazonensis (MHOM/BR/1973/M2269); M: L. (L.) mexicana (MNYC/BZ/62/M379); L: L. (V.) lainsoni (MHOM/BR/81/M6426); B: L. (V.) braziliensis (MHOM/BR/1975/M2903); G: L. (V.) guyanensis (MHOM/BR/1975/M4147); N: L. (V.) naiffi (MDAS/BR/1979/M5533); S: L. (V.) shawi (MCEB/BR/84/M8408). Field samples: phlebo 14: Bi. flaviscutellata; phlebo 15, 19, and 21: Ny. whitmani. Each species and samples were tested in duplicate and the data obtained were plotted using the GraphPad Prism v. 8.0.0 software.

In Brazil, ACL is expanding to peri-urban and urban environments, where human cases have been reported, and some vectors have been collected from households66. da Costa SM, Cordeiro JLP, Rangel EF. Environmental suitability for Lutzomyia (Nyssomyia) whitmani (Diptera: Psychodidae: Phlebotominae) and the occurrence of American cutaneous leishmaniasis in Brazil. Parasit Vectors . 2018;11(1):1-10.. This scenario has also been reported in Argentina, a neighboring country1111. Moya SL, Szelag EA, Manteca-Acosta M, Quintana MG, Salomón OD. Update of the Phlebotominae Fauna with New Records for Argentina and Observations on Leishmaniasis Transmission Scenarios at a Regional Scale. Neotrop Entomol. 2022;51(2):311-23., where the adaptation of some sandfly species to urban and domestic environments has been observed owing to environmental changes and alterations. In this case, some species that were previously wild take on a peri-urban or urban profile under the pressure of these changes1212. Sánchez Uzcátegui YDV, Vasconcelos Dos Santos T, Silveira FT, Ramos PKS, Dos Santos EJM, Póvoa MM. Phlebotomines (Diptera: Psychodidae) from a Urban Park of Belém, Pará State, Northern Brazil and Potential Implications in the Transmission of American Cutaneous Leishmaniasis. J Med Entomol. 2020;9;57(1):281-8..

In this study, the predominant species were Ny. whitmani and Ny. antunesi, the latter collected indoors, and the other species collected in the forest fragment near the residences. Since the first studies with sandflies in Rio Branco, species of epidemiological importance have been collected in urban environments and forest fragments, evidencing the urbanization process of some species such as Ny. antunesi and Ny. whitmani55. Araujo-Pereira T, Fuzari AA, Filho JDA, Pita-Pereira D, Britto C, Brazil RP. Sand fly fauna (Diptera: Psychodidae: Phlebotominae) in an area of leishmaniasis transmission in the municipality of Rio Branco, state of Acre, Brazil. Parasit Vectors. 2014;7(1):1-5., which was found to be infected by parasites of the genus Leishmania in this study. These observations have also been reported in other cities in the Amazon region such as Belém1212. Sánchez Uzcátegui YDV, Vasconcelos Dos Santos T, Silveira FT, Ramos PKS, Dos Santos EJM, Póvoa MM. Phlebotomines (Diptera: Psychodidae) from a Urban Park of Belém, Pará State, Northern Brazil and Potential Implications in the Transmission of American Cutaneous Leishmaniasis. J Med Entomol. 2020;9;57(1):281-8., Porto Velho1313. Silva ANR, Júnior AMP, de Paulo PFM, da Silva MS, Castro TS, Costa GDS, Freitas MTS, Rodrigues MMS, Medeiros JF. Detection of Leishmania species (Kinetoplastida, Trypanosomatidae) in phlebotomine sand flies (Diptera, Psychodidae) from Porto Velho, Northern Brazil. Acta Trop . 2021;213:105757., and Sinop1414. Thies SF, Bronzoni RVM, Michalsky ÉM, Santos ESD, Silva DJFD, Dias ES, Damazo AS. Aspects on the ecology of phlebotomine sand flies and natural infection by Leishmania hertigi in the Southeastern Amazon Basin of Brazil. Acta Trop . 2018;177:37-43..

For the detection of Leishmania DNA, most positive specimens were Ny. whitmani, emphasizing its high rate of infection. This species is recognized as a vector of ACL agents and is implicated in the transmission of three species of Leishmania: L. braziliensis, L. guyanensis, and L. shawi. In the last two species, Ny. whitmani acts as a maintenance vector for enzootic cycles66. da Costa SM, Cordeiro JLP, Rangel EF. Environmental suitability for Lutzomyia (Nyssomyia) whitmani (Diptera: Psychodidae: Phlebotominae) and the occurrence of American cutaneous leishmaniasis in Brazil. Parasit Vectors . 2018;11(1):1-10.. This species is one of the vectors with the widest geographical distribution in Brazil and is considered a complex of cryptic species, which may have different behavior profiles in different Brazilian ecosystems, as well as a species that has been adapting and tolerating environmental changes66. da Costa SM, Cordeiro JLP, Rangel EF. Environmental suitability for Lutzomyia (Nyssomyia) whitmani (Diptera: Psychodidae: Phlebotominae) and the occurrence of American cutaneous leishmaniasis in Brazil. Parasit Vectors . 2018;11(1):1-10..

The presence of Leishmania DNA in Bi. flavistutellata, collected from a forest fragment, is reported here for the first time in Acre. In previous studies, this species has been reported in urban and peri-urban areas of Rio Branco55. Araujo-Pereira T, Fuzari AA, Filho JDA, Pita-Pereira D, Britto C, Brazil RP. Sand fly fauna (Diptera: Psychodidae: Phlebotominae) in an area of leishmaniasis transmission in the municipality of Rio Branco, state of Acre, Brazil. Parasit Vectors. 2014;7(1):1-5. and in forest areas in other locations of the state44. Brilhante AF, Lima L, de Ávila MM, Medeiros-Sousa AR, de Souza JF, Dos Santos NP, et al. Remarkable diversity, new records and Leishmania detection in the sand fly fauna of an area of high endemicity for cutaneous leishmaniasis in Acre state, Brazilian Amazonian Forest. Acta Trop. 2021;223:106103.. In Rondônia, a neighboring state Bi. flaviscutellata was found in greater density in preserved forests and with females engorged with human blood1515. Pereira Júnior AM, Souza ABN, Castro TS, da Silva MS, de Paulo PFM, Ferreira GEM, de Medeiros JF. Diversity, natural infection and blood meal sources of phlebotomine sandflies (Diptera, Psychodidae) in the western Brazilian Amazon. Mem Inst Oswaldo Cruz. 2019;114:e190170., which demonstrates that this species is still dependent on the forest environment.

The human ACL in Acre has generally been attributed to rural and/or forestry cases, whether of individuals who live in these areas or those who occasionally visit these areas for leisure, ecotourism, or exploratory activities such as forest extraction and hunting11. Melchior LAK, Brilhante AF, Chiaravalloti-Neto F. Spatial and temporal distribution of American cutaneous leishmaniasis in Acre state, Brazil. Infect Dis Poverty. 2017;6(1):99.. It is also important to highlight that in the Acre state, six species of Leishmania cause dermotropic forms in humans, with the exception of L. lindenbergi22. Teles CB, Medeiros JF, Santos AP, Freitas LA, Katsuragawa TH, Cantanhede LM, et al. Molecular characterization of American Cutaneous Leishmaniasis in the triborder area of Assis Brasil, Acre State, Brazil. Rev Inst Med Trop Sao Paulo. 2015;57(4):343-7.. Thus, in this study, we reported the occurrence of the first autochthonous urban case of ACL in Acre, which was attributed to L. lainsoni, with the presence of incriminated sandflies species in the domestic environment and the circulation of vectors and Leishmania in the surroundings.

Thus, it is concluded that in Rio Branco City, some sandfly species frequent the domiciliary environment (indoor and peridomicile) in urban areas close to forest fragments; among them, Leishmania spp. vectors are suspected and recognized. Additionally, detection in forest fragments of sandfly females was positive for Leishmania spp. DNA indicates the need for periodic monitoring to verify the possibility of determining urban transmission foci. This preliminary observation serves as a warning for health surveillance in Rio Branco for decision making regarding preventive and control measures for this disease. Furthermore, the expansion of surveillance in other urban and peri-urban areas of the city is suggested.

ACKNOWLEDGMENTS

To the residents for allowing the entomological survey to be carried out. To the Conselho Nacional de Desenvolvimento Científico e Tecnológico - CNPq for the scholarship granted to EAS and ACGC. To the Programa de Apoio a Pós-Graduação (PROAP-CAPES) for the financial support.

REFERENCES

  • 1
    Melchior LAK, Brilhante AF, Chiaravalloti-Neto F. Spatial and temporal distribution of American cutaneous leishmaniasis in Acre state, Brazil. Infect Dis Poverty. 2017;6(1):99.
  • 2
    Teles CB, Medeiros JF, Santos AP, Freitas LA, Katsuragawa TH, Cantanhede LM, et al. Molecular characterization of American Cutaneous Leishmaniasis in the triborder area of Assis Brasil, Acre State, Brazil. Rev Inst Med Trop Sao Paulo. 2015;57(4):343-7.
  • 3
    Brilhante AF, Lima L, Zampieri RA, Nunes VLB, Dorval MEC, Malavazi PFNDS, et al. Leishmania (Viannia) braziliensis type 2 as probable etiological agent of canine cutaneous leishmaniasis in Brazilian Amazon. PLoS One. 2019;30;14(4):e0216291.
  • 4
    Brilhante AF, Lima L, de Ávila MM, Medeiros-Sousa AR, de Souza JF, Dos Santos NP, et al. Remarkable diversity, new records and Leishmania detection in the sand fly fauna of an area of high endemicity for cutaneous leishmaniasis in Acre state, Brazilian Amazonian Forest. Acta Trop. 2021;223:106103.
  • 5
    Araujo-Pereira T, Fuzari AA, Filho JDA, Pita-Pereira D, Britto C, Brazil RP. Sand fly fauna (Diptera: Psychodidae: Phlebotominae) in an area of leishmaniasis transmission in the municipality of Rio Branco, state of Acre, Brazil. Parasit Vectors. 2014;7(1):1-5.
  • 6
    da Costa SM, Cordeiro JLP, Rangel EF. Environmental suitability for Lutzomyia (Nyssomyia) whitmani (Diptera: Psychodidae: Phlebotominae) and the occurrence of American cutaneous leishmaniasis in Brazil. Parasit Vectors . 2018;11(1):1-10.
  • 7
    Caldart ET, Sevá ADP, Pinto-Ferreira F, Pereira Pachoal AT, de Oliveira JS, Cortela IB, et al. American cutaneous leishmaniasis associated with degradation of native forest, regardless of economic, social and infrastructure vulnerability. Zoonoses Public Health. 2021;68(4):327-43.
  • 8
    Galati EAB. Morfologia e terminologia de Phlebotominae (Diptera: Psychodidae). Classificação e identificação de táxons das Américas. Vol I. Apostila da Disciplina Bioecologia e Identificação de Phlebotominae do Programa de Pós-Graduação em Saúde Pública. Faculdade de Saúde Pública da Universidade de São Paulo, São Paulo, 132p, 2021. Available from: https://www.fsp.usp.br/egalati/
    » https://www.fsp.usp.br/egalati/
  • 9
    Zampieri RA, Laranjeira-Silva MF, Muxel SM, Stocco de Lima AC, Shaw JJ, Floeter-Winter LM. High Resolution Melting Analysis Targeting hsp70 as a Fast and Efficient Method for the Discrimination of Leishmania Species. PLoS Negl Trop Dis. 2016;29;10(2):e0004485.
  • 10
    Van der Auwera G, Dujardin JC. Species typing in dermal leishmaniasis. Clin Microbiol Rev. 2015;28(2):265-94.
  • 11
    Moya SL, Szelag EA, Manteca-Acosta M, Quintana MG, Salomón OD. Update of the Phlebotominae Fauna with New Records for Argentina and Observations on Leishmaniasis Transmission Scenarios at a Regional Scale. Neotrop Entomol. 2022;51(2):311-23.
  • 12
    Sánchez Uzcátegui YDV, Vasconcelos Dos Santos T, Silveira FT, Ramos PKS, Dos Santos EJM, Póvoa MM. Phlebotomines (Diptera: Psychodidae) from a Urban Park of Belém, Pará State, Northern Brazil and Potential Implications in the Transmission of American Cutaneous Leishmaniasis. J Med Entomol. 2020;9;57(1):281-8.
  • 13
    Silva ANR, Júnior AMP, de Paulo PFM, da Silva MS, Castro TS, Costa GDS, Freitas MTS, Rodrigues MMS, Medeiros JF. Detection of Leishmania species (Kinetoplastida, Trypanosomatidae) in phlebotomine sand flies (Diptera, Psychodidae) from Porto Velho, Northern Brazil. Acta Trop . 2021;213:105757.
  • 14
    Thies SF, Bronzoni RVM, Michalsky ÉM, Santos ESD, Silva DJFD, Dias ES, Damazo AS. Aspects on the ecology of phlebotomine sand flies and natural infection by Leishmania hertigi in the Southeastern Amazon Basin of Brazil. Acta Trop . 2018;177:37-43.
  • 15
    Pereira Júnior AM, Souza ABN, Castro TS, da Silva MS, de Paulo PFM, Ferreira GEM, de Medeiros JF. Diversity, natural infection and blood meal sources of phlebotomine sandflies (Diptera, Psychodidae) in the western Brazilian Amazon. Mem Inst Oswaldo Cruz. 2019;114:e190170.

Publication Dates

  • Publication in this collection
    16 Dec 2022
  • Date of issue
    2022

History

  • Received
    14 July 2022
  • Accepted
    18 Oct 2022
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