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Natural infection of Lutzomyia longipalpis (Lutz & Neiva, 1912) by Leishmania infantum in a municipality with a high incidence of visceral leishmaniasis in the Brazilian Midwest

ABSTRACT

Background:

Here, Leishmania presence in sand flies from Três Lagoas, Mato Grosso do Sul, Brazil, after visceral leishmaniasis (VL) was investigated.

Methods:

In April 2022, two light traps were deployed within and around the residence for two days post-VL case report.

Results:

A total of 120 Lutzomyia longipalpis were collected. Suprapyloric flagellates were found in a female sand fly with eggs and residual blood during midgut dissection. Sequencing of ITS1 and cytb fragments confirmed Leishmania infantum DNA and identified Homo sapiens as the blood source, respectively.

Conclusions:

This study emphasizes the importance of monitoring sand flies in VL endemic areas.

Keywords:
Lutzomyia longipalpis; Natural infection; Leishmania infantum; Brazil

Visceral leishmaniasis (VL) is a severe disease caused by the protozoan parasite Leishmania infantum that affects both humans and other mammals on a global scale11. Bruschi F, Gradoni L. The leishmaniases: Old neglected tropical diseases. vol. 1. 1 ed. Berlim, Germany: Springer International Publishing; 2018.. In Brazil, VL is a significant public health challenge that notably affects the northeastern and southeastern regions of the country22. Ministério da Saúde (MS). Banco de dados do Sistema Único de Saúde-DATASUS. Banco de Dados Do Sistema Único de Saúde-DATASUS. 2022.. The disease is transmitted through the bites of infected female sand flies, with domestic dogs serving as the parasite's primary reservoir, posing complex obstacles to disease control11. Bruschi F, Gradoni L. The leishmaniases: Old neglected tropical diseases. vol. 1. 1 ed. Berlim, Germany: Springer International Publishing; 2018..

Mato Grosso do Sul state (MS) is an endemic area for VL. Nonetheless, until the early 1990s, the disease was confined to the geographical region of Corumbá and Ladário municipalities located along the border with Bolivia33. de Oliveira ALL, Paniago AMM, Sanches MA, Dorval MEC, Oshiro ET, Leal CRB, et al. Asymptomatic infection in family contacts of patients with human visceral leishmaniasis in Três Lagoas, Mato Grosso do Sul State, Brazil. Cad Saude Publica. 2008;24(12):2827-33.. Since 2000, the municipality of Três Lagoas has witnessed recurrent urban VL outbreaks, registering nearly 30 autochthonous cases within the preceding three years, leading to elevated fatality rates33. de Oliveira ALL, Paniago AMM, Sanches MA, Dorval MEC, Oshiro ET, Leal CRB, et al. Asymptomatic infection in family contacts of patients with human visceral leishmaniasis in Três Lagoas, Mato Grosso do Sul State, Brazil. Cad Saude Publica. 2008;24(12):2827-33.,44. Carvalho GB de A, Caldeira JVC, de Oliveira MD, Oda JY, Machado AM, Machado AR da SR. Epidemiological characterization and spatial distribution of visceral leishmaniasis cases in Três Lagoas - MS, Brazil in the period of 2007-2021. Res Soc Dev. 2021;10(16):1-13.. The recent upsurge in VL outbreaks and heightened mortality rates within the municipality have spurred apprehensions among Brazilian authorities, with a cumulative tally of 27 human cases documented in the preceding three-year period22. Ministério da Saúde (MS). Banco de dados do Sistema Único de Saúde-DATASUS. Banco de Dados Do Sistema Único de Saúde-DATASUS. 2022.,44. Carvalho GB de A, Caldeira JVC, de Oliveira MD, Oda JY, Machado AM, Machado AR da SR. Epidemiological characterization and spatial distribution of visceral leishmaniasis cases in Três Lagoas - MS, Brazil in the period of 2007-2021. Res Soc Dev. 2021;10(16):1-13.. Moreover, it is noteworthy that the distribution of VL occurrences spans both urban neighborhoods and rural zones of Três Lagoas, where the year-round presence of sand fly vectors has been well-documented44. Carvalho GB de A, Caldeira JVC, de Oliveira MD, Oda JY, Machado AM, Machado AR da SR. Epidemiological characterization and spatial distribution of visceral leishmaniasis cases in Três Lagoas - MS, Brazil in the period of 2007-2021. Res Soc Dev. 2021;10(16):1-13..

The role of Lutzomyia longipalpis as the main vector of Le. infantum is widely acknowledged in Brazil, with this species exhibiting a broad distribution across geographic regions, coinciding with instances of autochthonous VL55. Andrade-Filho JD, Scholte RGC, Amaral ALG, Shimabukuro PHF, Carvalho OS, Caldeira RL. Occurrence and Probability Maps of Lutzomyia longipalpis and Lutzomyia cruzi (Diptera: Psychodidae: Phlebotominae) in Brazil. J Med Entomol. 2017;54(5):1430-4.. Furthermore, the capacity of Lu. longipalpis to sustain late-stage infections involving diverse Leishmania species has been recognized, and prior documentation has affirmed the natural infection of this species with Le. infantum66. Rêgo FD, Soares RPP. Lutzomyia longipalpis: an update on this sand fly vector. An Acad Bras Cienc. 2021;93(3):1-29.. However, the prevailing strategies for VL control have proven ineffective, culminating in Três Lagoas becoming the second-most afflicted municipality regarding reported cases22. Ministério da Saúde (MS). Banco de dados do Sistema Único de Saúde-DATASUS. Banco de Dados Do Sistema Único de Saúde-DATASUS. 2022.. Consequently, there is a recommendation for heightened entomological surveillance activities within locales reporting human cases to detect local transmission and instigate pertinent control measures. Thus, the focal aim of this study was to delineate the outcomes of entomological surveillance triggered by a report of human VL within the confines of the Três Lagoas Municipality.

A suspected case of autochthonous human VL was reported during local communicable disease surveillance in April 2022. The afflicted individual was a resident of the Jardim Novo Aeroporto neighborhood. Despite Três Lagoas municipality (20°45'35'' S, 51°41'42'' W), situated within the state of MS, Brazil (Figure 1), being an established endemic region for VL, efforts to substantiate the autochthonous nature of this particular case were undertaken. This approach was aligned with the guidelines provided by the National Program for the Prevention and Control of Visceral Leishmaniasis. The sand fly collection was conducted using light traps for two nights in April 2022 in the intradomicile and peridomicile areas, where dogs and a chicken coop were observed. All insects were separated and transported live in rearing boxes to the field laboratory for midgut dissection and taxonomic identification.

FIGURE 1:
Location of the collection site within Três Lagoas, Mato Grosso do Sul, Brazil.

Sand flies were promptly processed at the Entomology Laboratory of the Zoonosis Control Center of the municipality. Female specimens were dissected using sterile needles to expose the midgut, and the presence of flagellate forms was evaluated using optical microscopy (at 400x and 1000x magnification). Furthermore, the sand flies were identified based on morphological characteristics77. Galati EAB. Phlebotominae (Diptera, Psychodidae): classification, morphology and terminology of adults and identification of American Taxa. In: Rangel E, Shaw J, editors. Brazilian Sand Flies Biol. Taxon. Med. Importance Control, vol. 1. 1 ed. Springer International Publishing; 2018. p. 9-212.. For positive samples, the midguts were triturated and preserved in 1.5mL tubes containing 1x phosphate-buffered saline (pH 7.2) at -20°C until DNA extraction. Whole DNA was extracted using 5% Chelex solution. Moreover, the presence of Leishmania was monitored through PCR using the 13A/13B primers88. Reale S, Maxia L, Vitale F, Glorioso NS, Caracappa S, Vesco G. Detection of Leishmania infantum in dogs by PCR with lymph node aspirates and blood. J Clin Microbiol. 1999;37(9):2931-5. and ITS1-PCR99. Schönian G, Nasereddin A, Dinse N, Schweynoch C, Schallig H, Presber W, et al. PCR diagnosis and characterization of Leishmania in local and imported clinical samples. Diagn Microbiol Infect Dis. 2003;47(1):349-58., while species identification was achieved via Sanger sequencing. PCR was performed using the reference strains of Le. infantum (MHOM/BR/1974/PP75) and Le. braziliensis (MHOM/BR/1975/M2903) were used as the positive and negative controls, respectively.

DNA extracted from the female displaying blood in the midgut underwent PCR targeting the cytb gene to identify the source of the blood1010. Steuber S, Abdel-Rady A, Clausen PH. PCR-RFLP analysis: A promising technique for host species identification of blood meals from tsetse flies (Diptera: Glossinidae). Parasitol Res. 2005;97(3):247-54.. Within the PCR, DNA extracted from Gallus gallus served as the positive control, whereas DNA from male sand flies was used as the negative control. Following a positive PCR result, the product was purified, subjected to Sanger sequencing, and subsequently analyzed by comparison with sequences cataloged in GenBank database1111. Carvalho GM de L, Rêgo FD, Tanure A, Silva ACP, Dias TA, Paz GF, et al. Bloodmeal Identification in Field-Collected Sand Flies From Casa Branca, Brazil, Using the Cytochrome b PCR Method. J Med Entomol . 2017;54(4):1049-54..

In the state of MS, Lu. Longipalpis has been documented in at least 44 municipalities, including Três Lagoas, where it has emerged as the predominant species within both intra and peridomiciliary environments1212. Oliveira GMG de, Figueiró Filho EA, Andrade GM de C, Araújo LA de, Oliveira MLG de, Cunha RV da. Survey of phlebotomine sand flies (Diptera: Psychodidae: Phlebotominae) in Três Lagoas Municipality, Mato Grosso do Sul State, Brazil, an area of intense transmission of American visceral leishmaniasis. Rev Pan-Amazônica Saúde. 2010;1(3):83-94.,1313. Neitzke-Abreu HC, Costa GB, da Silva MN, Palacio E, da Silva Cardoso A, de Almeida PS, et al. Geographic distribution of human leishmaniasis and phlebotomine sand flies in the State of Mato Grosso do Sul, Brazil. Parasit Vectors. 2022;15(1):1-7.. In this study, 120 sand flies were collected, all belonging to Lu. longipalpis. Specifically, three specimens were collected in the intradomicile (two males and one female), whereas the remaining 117 specimens were collected in the peridomicile (84 males and 33 females). All female specimens were dissected immediately to expose their midguts. Notably, during the dissection of a female from the peridomiciliary area, seemingly toward the conclusion of the gonotrophic cycle (as evidenced by the presence of mature eggs and remnants indicative of blood digestion), suprapyloric promastigote forms were detected (Supplementary File 1). Furthermore, 13A/13B (Figure 2) and ITS1 PCRs confirmed the presence of Leishmania, and DNA sequencing of the ITS1 amplicon (300-350bp) allows the identification of these flagellates as Le. infantum (GenBank accession number OQ675107).

FIGURE 2:
Representative agarose gel of molecular identification of Leishmania in Lutzomyia longipalpis from Três Lagoas, Mato Grosso do Sul, Brazil. Lanes: MM, molecular weight marker (100 bp); 1, sand fly sample; 2, Leishmania braziliensis (MHOM/BR/1975/M2903) strain used as positive control; 3, non-template control.

Considering that the female sand fly displaying Leishmania infection demonstrated residual blood remnants indicative of recent feeding, a cytb-PCR analysis was performed to ascertain the source of this blood meal. DNA sequencing indicated the presence of human (Homo sapiens) DNA in the blood sample, with an identity match exceeding 99%. Notably, no other female specimens displayed discernible indications of recent blood ingestion.

The described results support the determination of autochthony in VL cases and the implementation of the following control activities (i.e., residual insecticide application in residences and dog surveys). Notably, ecological parameters related to vector-host interactions are key to understanding vector capacity1414. Galvis-Ovallos F, Da Silva MD, Bispo GBDS, De Oliveira AG, Neto JRG, Malafronte RDS, et al. Canine visceral leishmaniasis in the metropolitan area of São Paulo: Pintomyia fischeri as potential vector of Leishmania infantum. Parasite. 2017;24(2).. The condition of the female at the end of the gonotrophic cycle suggested that it was close to oviposition and was searching for a new blood meal. Furthermore, the presence of human blood in the intestine suggests that this female may have attempted to feed on humans of significant epidemiological importance, considering the state of infection with flagellates.

The circulation of an infected female highlights the need for constant monitoring of this zoonosis in the study area, particularly to intensify measures to control canine reservoirs and vectors. Effective prevention and control of VL require a thorough understanding of the epidemiology and ecology of the disease, including the role of vector insects in its transmission. Thus, the results presented in this report reinforce the importance of entomological surveillance activities as support for prevention and control programs for zoonosis, providing evidence for identifying risk areas to support public health decision-making.

ACKNOWLEDGEMENTS

We thank the DNA sequencing facility as part of the Fiocruz Network of Technological Platforms at Instituto René Rachou - Fiocruz Minas for assistance and DNA sequencing services.

REFERENCES

  • 1
    Bruschi F, Gradoni L. The leishmaniases: Old neglected tropical diseases. vol. 1. 1 ed. Berlim, Germany: Springer International Publishing; 2018.
  • 2
    Ministério da Saúde (MS). Banco de dados do Sistema Único de Saúde-DATASUS. Banco de Dados Do Sistema Único de Saúde-DATASUS. 2022.
  • 3
    de Oliveira ALL, Paniago AMM, Sanches MA, Dorval MEC, Oshiro ET, Leal CRB, et al. Asymptomatic infection in family contacts of patients with human visceral leishmaniasis in Três Lagoas, Mato Grosso do Sul State, Brazil. Cad Saude Publica. 2008;24(12):2827-33.
  • 4
    Carvalho GB de A, Caldeira JVC, de Oliveira MD, Oda JY, Machado AM, Machado AR da SR. Epidemiological characterization and spatial distribution of visceral leishmaniasis cases in Três Lagoas - MS, Brazil in the period of 2007-2021. Res Soc Dev. 2021;10(16):1-13.
  • 5
    Andrade-Filho JD, Scholte RGC, Amaral ALG, Shimabukuro PHF, Carvalho OS, Caldeira RL. Occurrence and Probability Maps of Lutzomyia longipalpis and Lutzomyia cruzi (Diptera: Psychodidae: Phlebotominae) in Brazil. J Med Entomol. 2017;54(5):1430-4.
  • 6
    Rêgo FD, Soares RPP. Lutzomyia longipalpis: an update on this sand fly vector. An Acad Bras Cienc. 2021;93(3):1-29.
  • 7
    Galati EAB. Phlebotominae (Diptera, Psychodidae): classification, morphology and terminology of adults and identification of American Taxa. In: Rangel E, Shaw J, editors. Brazilian Sand Flies Biol. Taxon. Med. Importance Control, vol. 1. 1 ed. Springer International Publishing; 2018. p. 9-212.
  • 8
    Reale S, Maxia L, Vitale F, Glorioso NS, Caracappa S, Vesco G. Detection of Leishmania infantum in dogs by PCR with lymph node aspirates and blood. J Clin Microbiol. 1999;37(9):2931-5.
  • 9
    Schönian G, Nasereddin A, Dinse N, Schweynoch C, Schallig H, Presber W, et al. PCR diagnosis and characterization of Leishmania in local and imported clinical samples. Diagn Microbiol Infect Dis. 2003;47(1):349-58.
  • 10
    Steuber S, Abdel-Rady A, Clausen PH. PCR-RFLP analysis: A promising technique for host species identification of blood meals from tsetse flies (Diptera: Glossinidae). Parasitol Res. 2005;97(3):247-54.
  • 11
    Carvalho GM de L, Rêgo FD, Tanure A, Silva ACP, Dias TA, Paz GF, et al. Bloodmeal Identification in Field-Collected Sand Flies From Casa Branca, Brazil, Using the Cytochrome b PCR Method. J Med Entomol . 2017;54(4):1049-54.
  • 12
    Oliveira GMG de, Figueiró Filho EA, Andrade GM de C, Araújo LA de, Oliveira MLG de, Cunha RV da. Survey of phlebotomine sand flies (Diptera: Psychodidae: Phlebotominae) in Três Lagoas Municipality, Mato Grosso do Sul State, Brazil, an area of intense transmission of American visceral leishmaniasis. Rev Pan-Amazônica Saúde. 2010;1(3):83-94.
  • 13
    Neitzke-Abreu HC, Costa GB, da Silva MN, Palacio E, da Silva Cardoso A, de Almeida PS, et al. Geographic distribution of human leishmaniasis and phlebotomine sand flies in the State of Mato Grosso do Sul, Brazil. Parasit Vectors. 2022;15(1):1-7.
  • 14
    Galvis-Ovallos F, Da Silva MD, Bispo GBDS, De Oliveira AG, Neto JRG, Malafronte RDS, et al. Canine visceral leishmaniasis in the metropolitan area of São Paulo: Pintomyia fischeri as potential vector of Leishmania infantum. Parasite. 2017;24(2).
  • Financial Support: This research was funded by the Fundação de Amparo à Pesquisa do Estado de Minas Gerais - FAPEMIG (grant number PPM-00792-18 to JDAF) and Conselho Nacional de Desenvolvimento Científico e Tecnológico - CNPq (grant number 166380/2020-2 to FDR and 302701/2016-8 to JDAF).

Publication Dates

  • Publication in this collection
    22 Sept 2023
  • Date of issue
    2023

History

  • Received
    05 June 2023
  • Accepted
    25 Aug 2023
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