BioMed Research International
Volume 2016 (2016), Article ID 6456031, 8 pages
http://dx.doi.org/10.1155/2016/6456031

Research Article

Epidemiology of American Tegumentary Leishmaniasis and Trypanosoma cruzi Infection in the Northwestern Argentina

Carlos L. Hoyos,¹ Silvana P. Cajal,¹ Marisa Juarez,¹ Jorge D. Marco,1,2 Anahí M. Alberti D’Amato,² Melina Cayo,³ Irma Torrejón,³ Rubén O. Cimino,1,4 Patricio Diosque,² Alejandro J. Krolewiecki,1,2 Julio R. Nasser,1,4 and José F. Gil1,5

¹Instituto de Investigaciones en Enfermedades Tropicales, Sede Regional Orán, Universidad Nacional de Salta, 4530 Salta, Argentina
²Instituto de Patología Experimental (IPE-CONICET), Facultad de Ciencias de la Salud, Universidad Nacional de Salta, 4400 Salta, Argentina
³Instituto de Biología de la Altura (InBiAl), Universidad Nacional de Jujuy, Jujuy, Argentina
⁴Cátedra de Química Biológica, Facultad de Ciencias Naturales, Universidad Nacional de Salta, 4400 Salta, Argentina
⁵Instituto de Investigaciones en Energía no Convencional (INENCO-CONICET), Universidad Nacional de Salta, 4400 Salta, Argentina

Received 23 July 2016; Accepted 7 September 2016

Academic Editor: Jose Vasconcelos

Copyright © 2016 Carlos L. Hoyos et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Background. Endemic areas of tegumentary leishmaniasis (TL) in Salta, Argentina, present some overlap zones with the geographical distribution of Chagas disease, with mixed infection cases being often detected. Objectives. The purpose of this study was to determine the magnitude of Leishmania sp. infection and potential associated risk factors, the serologic prevalence of T. cruzi, and the presence of T. cruzi-Leishmania sp. mixed infection in a region of the northwest of Argentina. Methods. Cross-sectional studies were conducted to detect TL prevalence and T. cruzi seroprevalence. A case-control study was conducted to examine leishmaniasis risk factors. Results. Prevalence of TL was 0.17%, seroprevalence of T. cruzi infection was 9.73%, and mixed infection proportion—within the leishmaniasic patients group—was 16.67%. The risk factors associated with TL transmission were sex, age, exposure to bites at work, staying outdoors more than 10 hours/day, bathing in the river, and living with people who had lesions or were infected during the study. Discussion. The endemic pattern of TL seems to involve exposure of patients to vectors in wild as well as peridomestic environment. Cases of T. cruzi infection are apparently due to migration. Therefore, a careful epidemiological surveillance is necessary due to the contraindication of antimonial administration to chagasic patients.

1. Introduction

Tegumentary leishmaniasis (TL) is caused by protozoan parasites belonging to the genus Leishmania. Clinical manifestations of this disease include single, multiple, disseminated cutaneous, and mucocutaneous forms [1]. The species Leishmania (Viannia) braziliensis, L. (V.) guyanensis, L. (L.) amazonensis, and L. (V.) panamensis have been reported from northern Argentina [2–4], although the vast majority is caused by L. (V.) braziliensis. In this region, Leishmania spp. are transmitted by the bite of the female sandfly belonging to the genus Lutzomyia (Diptera, Psychodidae, and Phlebotominae). Migonemyia migonei (França 1920), Evandromyia cortelezzii (Brèthes 1923), Evandromyia sallesi (Galvão & Coutinho 1940), Psathyromyia shannoni (Dyar 1929), Psathyromyia punctigeniculata (Floch & Abonnenc, 1944), and Nyssomyia neivai (Pinto 1926) have been reported in northern Argentina [5, 6]; and particularly Ny. neivai, Mg. migonei, and cortelezzii complex have been proposed as potential vectors [7, 8].

The described scenarios of TL transmission in Argentina include four cycles’ patterns: (a) wild cycle with transmission in primary or residual vegetation, (b) with eventual peridomestic transmission due to wild or secondary vegetation changes, (c) with peridomestic transmission in contiguous domiciles with the residual vegetation, and (d) peridomestic cycle in rural, ruralized periurban, or urban-rural interface environment [9]. However, the potential existence of urban transmission has been reported, which represents an important change in the transmission pattern paradigm of this disease at the regional scale [10]. Oran and San Martin departments (Salta province) are the areas with the greatest risk of transmission in the country, which reported the highest number of cases to the overall TL incidence in Argentina [10, 11].

In several areas of Latin America (including northern Argentina) the geographical distribution of TL overlaps with transmission areas of American trypanosomiasis (Chagas disease). The World Health Organization estimates that 8 to 10 million people are infected worldwide, mostly in Latin America where the disease is endemic [12]; this is caused by Trypanosoma cruzi and it is transmitted by several species of triatomine insects, Triatoma infestans being the most important in Argentina. In the last century, the progressive urbanization and the intensive migration of infected individuals increased the risk of transmission by blood transfusion and congenital route in nonendemic regions [13]. In restricted areas located in the east and northeast of Salta province, corresponding to the Gran Chaco ecoregion, vectorial transmission of T. cruzi still occurs but not in the rain forest ecoregion (Yunga ecoregion).

Mixed infections due to Leishmania sp. and T cruzi have been reported in patients showing clinical symptoms of TL, ranging between 12% and 70% [2, 14–16]. Prevalence of Leishmania sp. and T. cruzi mixed infection is unknown for northern Salta. Cross-reactivity between T. cruzi and Leishmania sp. infections has been reported when some serological tests were evaluated [2, 16, 17], possibly due to the close phylogenetic relationship between these parasites. The occurrence of Leishmania sp. and T. cruzi mixed infections also has therapeutic implications. Antimonial drugs used to treat leishmaniasis have potential cardiac toxicity [18–20], which is an important concern in patients infected by T. cruzi because about 30% of people infected by this parasite develop chronic cardiomyopathy [21].

In the present study, we examined the prevalence of single infections by Leishmania sp. and T. cruzi as well as the proportion of mixed infections due to both parasites in people living in the northern of Argentina. Demographic, behavioral, and environmental variables have also been studied as potential risk factors associated with transmission of cutaneous leishmaniasis. The epidemiologic pattern here observed can occur in several countries in Latin America and this research can provide information to optimize global and local prevention measures of public health.

2. Materials and Methods

2.1. Area and Population Studied

Hipólito Yrigoyen (Orán Department, Salta, Argentina) is located at 23°14′S, 64°16′W, 323 m.a.s.l. in large-scale farming and forest exploitation area, with subtropical climate. It is within the perimeter of the Pedemontana rain forest. This urban place has a population of 10 363 inhabitants (Primary Health Care Record, 2009). The study population included people who lived in Hipólito Yrigoyen between 2001 and 2011.

2.2. Study Design

This research included two cross-sectional studies, a tegumentary leishmaniasis case-control study, and the report of mixed infection for Leishmania sp. and T. cruzi.

A cross-sectional study was conducted in 2009 to determine the prevalence of Leishmania sp. (LP) taking into account the active cases of TL (ACTL) and total population of Hipólito Yrigoyen (HYTP: population censed by the PHC):

The seroprevalence of T. cruzi infection (TCSP) corresponding to 2009 was also calculated through a cross-sectional study. The sample size was 113 people. It was calculated considering an expected prevalence 5% with 4% of accuracy and confidence level of 95% using the Epidat software v3.1 (Epidat Xunta de Galicia, Santiago de Compostela, Spain and Pan-American Health Organization, Washington, DC). Seventy-nine quasi-randomly selected households were studied (Figure 1(b)). Of all household members, only those who wanted to participate voluntarily were selected (one person or more per household). The seroprevalence (TCSP) was calculated as the number of seropositive people for T. cruzi infection (TCP) over the sample size (SS):

(a)

(b)

Figure 1: (a) HY within Argentina. (b) The black dots indicate households’ distribution, where the sampling was conducted in the HY locality.

Also, the mixed infection proportion within group of patients with TL in 2009 was calculated (Figure 2).

Figure 2: Flow chart showing the groups of patients and noninfected people included in prevalence (LP) and case-control study of leishmaniasis and T. cruzi seroprevalence (TCSP) infection. Mixed infections detected (T. cruzi-Leishmania) from 13 patients with active leishmaniasis ulcer in 2009 are also shown. Diagnostic of T. cruzi infection applied to the 100 people to detect both seropositive people to calculate T. cruzi seroprevalence and select the negative control people for the case-control study. People positive for ELISA-leishmaniasis or leishmanin skin test (LST) may have been exposed to the Leishmania parasite. The cross-reaction of both ELISA and leishmanin skin test with chagasic infection does not distinguish whether the person was exposed to Leishmania parasite or is infected with T. cruzi. Due to this, the people positive for Chagas lab tests were not included as controls in the case-control study.

An unmatched case-control study was conducted to identify risk factors associated with TL cases. The TL cases included in the case-control study were patients living in Hipólito Yrigoyen and diagnosed between 2001 and 2009. The control population was selected within the cross-sectional sample used to calculate the T. cruzi seroprevalence infection (Figure 2). A survey was conducted in both cases and on the control people through a structured epidemiological questionnaire. After each person was interviewed, 6 mL of venous blood was drawn by clinical laboratory technicians and allowed to clot at room temperature. The sera were obtained by centrifugation at 3500 rotations per min for 5 min, then aliquoted into 1.5 mL tubes, and stored at −20°C until tested.

The variables registered were age, sex, occupation (exposure to vector bites at work), recreational habits (staying outdoors for more than 10 h and bathing in the river), personal preventive measures, household data (i.e., location, construction material, proximity to sites of possible development of sandflies, distance from crop fields and primary vegetation, knowledge about and application of preventive measures), living with people who were infected or had lesions, and aspects indicating knowledge about TL [22–24]. The data from the questionnaire were managed using the application EpiData Entry version 3.1 [25]; the resulting database was exported to the R statistical software for respective analysis.

The people included in each study group mentioned above were defined according to the diagnostic criteria described below.

2.3. Diagnostic Procedures

The patients were evaluated in the field by the personnel at Instituto de Investigaciones en Enfermedades Tropicales (IIET) at Universidad Nacional de Salta, the San Vicente de Paul Hospital in Orán, and Eva Peron Hospital in Hipólito Yrigoyen.

The sera and blood samples collected in the field were transported to the IIET for processing. The parasitological diagnostic of Leishmania was made in the IIET and the patients were derived from Hipólito Yrigoyen Hospital. Both diagnostic procedures such as serological, parasitological, and molecular techniques were performed following the protocols established in previous studies. The commercial kits were applied according to manufacturer’s instructions.

2.4. Diagnostic Criteria

Diagnostic criteria included the following.

2.4.1. Leishmaniasis Cases

Included were individuals who had lesions clinically compatible with TL and visualization of amastigotes of Leishmania sp. in Giemsa-stained smears and/or positive reaction of serum samples by enzyme-linked immunosorbent assay (ELISAg) homogenate protein of L (V.) guyanensis [15] and/or positive reaction to leishmanin skin test [4, 5].

2.4.2. T. cruzi Infection

The subjects were considered infected with T. cruzi when serum samples by ELISA and Indirect hemagglutination (IHA) tests (Wiener Lab, Argentina) were reactive. The samples with discordant results between ELISA and IHA were examined by recombinant ELISA 3.0 (Wiener Lab, Argentina) and Immunofluorescence test [26] or Polymerase Chain Reaction (PCR) [27]. The recombinant ELISA 3.0 was reported as specific test for T. cruzi infection detection without cross-reaction with Leishmania [17, 28].

2.4.3. Mixed Infections

Included were patients with TL and positive results for at least two tests for T. cruzi infection, mentioned above.

2.4.4. Controls in Case-Control Study

Included were individuals living in Hipólito Yrigoyen who were not grouped as leishmaniasis cases and/or T. cruzi infected.

2.5. Data Analysis

The prevalence of Leishmania sp., seroprevalence of T. cruzi infections, and mixed infection proportion with 95% Confidence Intervals (CI) were calculated using the EPIDAT software version 3.1.

In the case-control study, the independent continuous and discreet variables were, respectively, categorized or dichotomized. Univariate and multivariate logistic regression (LR) analysis were carried out. The Odds Ratios (OR) and 95% CI were calculated to assess the link between the TL cases and potential risk factors. The variables with OR > 1 and in univariate logistic regression analysis were tested in a multivariate analysis to establish a model involving the least number of variables that best explains the dependent variable (TL cases).

The final model was obtained using the stepwise technique, a procedure that combines forward method (it starts from a model only with the constant or independent variable, followed by progressive introduction of variables in the equation, provided they are significant) and backward method (all the variables are initially considered in the model, and those lacking significance are then progressively eliminated) [29]. The Akaike Information Criterion (AIC) was used as selection criterion. AIC calculation is based on minimization of the loss of information function, penalizing for the number of variables introduced that seeks the model that best adjusts to the data with the minimum number of possible variables, thus producing simpler models [30, 31]. The model that has been chosen minimizes the AIC. Data were considered statistically significant if . All statistical analysis for case-control study was performed using R software version 2.15.2 [32].

2.6. Ethical Approval

All the people included in the study agreed to participate by signing an informed consent form (ICF). The project and ICF were approved by the Ethics Committee of the School of Health Sciences at the National University of Salta and the “Fundación Huesped.”

3. Results

In 2009, only 18 cases of TL were diagnosed in Hipólito Yrigoyen, which represented a TL prevalence of 0.17% (CI 0.09–0.26). The age range of study patients was 7–69 years with an average of (SD).

Of the 113 samples analyzed to detect T. cruzi infection, 67 (59%) corresponded to females and 46 (41%) to males. Their age ranged between 7 and 74, with an average of (SD) years. There was no statistically significant difference in prevalence between males and females (). The seroprevalence for this infection was 9.73% (CI 3.83–15.64) in 2009. The frequencies of cases according to age and sex are summarized in Table 1.

Table 1: Number of individuals included in the study, percentage (%) of individuals infected with T. cruzi according to sex and age group. Indication of the overall prevalence in Hipólito Yrigoyen for 2009. : infected individuals according to sex and age; : total sample in seroprevalence of T. cruzi study.

Sex
Female
(%)
Male
(%)

Total infected
5/67 ()
6/46 ()

Age

Infected (%)

10–35
62
4 (6.45)

36–55
28
3 (10.7)

>55
23
4 (10.4)

Total
113
11 (9.73)

Positive results were obtained for T. cruzi infection in three patients with TL in 2009 (Table 2), which represents a mixed infection proportion of 16.67% CI (3.58–41.42) within the group of 18 patients with TL.

Table 2: Results of samples with mixed infection. SMEAR: visualization of amastigotes of Leishmania sp. in Giemsa-stained smears; ELISAg: ELISA based on homogenate protein of L (V.) guyanensis; LST: reaction to leishmanin skin test; ELISA Rec: recombinant ELISA Kit; IHA: indirect hemagglutination; TIF: test of Immunofluorescence; PCR: Polymerase Chain Reaction. nd: no data (samples were not evaluated with TIF).

Leishmania infection tests
T. cruzi infection tests

Smear
ELISAg
LST
ELISA Rec.
IHA
TIF
PCR

Patient code
HI 54
+
+
+
+
+
+
−

HI 55
+
+
+
−
+
nd
+

HI 58
+
+
+
+
+
nd
+

The samples for the case-control study included 33 cases of TL (18 actives cases in 2009 and 15 cases registered in the 2001–2008 period) and 88 controls (Figure 2). The control group consisted of individuals without positive diagnosis for leishmaniasis and Chagas diseases according to criteria above described.

The variables that showed significant association () with the presence of TL (case) in univariate LR analysis were sex, age, exposure to vector bites at work, staying outdoors for more than 10 h (so), bathing in the river, and living with people who were infected or had lesions during the study period (Table 3). These variables were included in a multivariate logistic regression analysis and final model obtained using the stepwise method. This model includes only 3 predictive variables (sex, age, and so) that explained the occurrence of TL cases (Table 3). The AIC value was 122.2

 The selected model:

Table 3: Crude OR and adjusted OR for the factors associated with the presence of tegumentary leishmaniasis. OR, Odds Ratio; CI, Confidence Interval. Significant association at ; highly significant association at ; highly significant association at .

Logistic regression
OR (CI 95%)
univariate analysis
OR (CI 95%)
multivariate analysis

Sex

    Female
1
1

    Male
5.47 (2.21–13.54)
6.05 (2.2–16.64)

Age (years)

     >16
1
1

     7–15
4.37 (1.39–13.8)
7.73 (2.05–29.16)

Exposure to vector bites at work

    Unexposed
1

    Exposed
2.68 (1.14–6.3)

Permanence > 10 hours outdoors (SO)

    No
1
1

    Yes
4.67 (1.23–17.78)
4.16 (0.97–17.77)

Bathing in the river

    No
1

    Yes
3.89 (1.59–9.54)

Living with infected people

    No
1

    Yes
3.17 (1.23–8.15)

4. Discussion

In the north of Salta province, TL levels are hyperendemic in some sites and periods [33, 34]. This situation is worsened by the presence of cases of Chagas disease, which may further generate cases of mixed infections, causing a synergistic problem for the health care system. In the locality Hipólito Yrigoyen, TL prevalence values of 0.17, 0.79, and 0.18% were previously reported [33, 34]. The prevalence calculated in the present study (0.17%; CI 0.08–0.26) is similar, which indicates a level of active transmission that persists over time. However, high incidence foci are likely to occur in short exposure periods in this area [5].

In the case-control study, the associated variables would be reflecting the existence of a complex pattern of transmission. Male sex and staying outdoors for more than 10 hours would be indicators of a sylvatic mode of transmission, facilitated by labour, subsistence, or recreational activities (in rural environments and/or deforestation areas, or hunting and fishing activities), as it is indicated in regions where TL is endemic [9, 24, 33]. The significantly higher proportion of infected children compared to that of adults found in this analysis (OR = 7.73; CI: 2.05–29.16) suggests the existence of other patterns of transmission in Hipólito Yrigoyen. The incidence of TL in children has been cited as an indicator of peridomiciliary transmission, especially in localities adjacent to primary and/or secondary vegetation [4, 22–24, 33].

In addition, a high density of sandflies has been detected in the vegetation near to the irrigation channels located in the outskirts of the city (Figure 1) [35], showing a species diversity similar to that found in a nearby place where there was a high rate of infection [5, 36]. Many families go to these sites for recreational purposes in times of high temperature and risk leishmaniasis transmission (7 pm to 10 pm approximately) with the consequent risk of being bitten by infected sandflies and contracting leishmaniasis, as reported in a study of spatial distribution of TL cases [37].

The presence of active TL cases among elderly people that remain mostly in their houses and of sandflies in the center of the town [35] offers another plausible epidemiologic situation of disease transmission (but with low probability) in urban environments because lower abundance of sandflies was recorded here [35]. Indeed, in Hipólito Yrigoyen, house courtyards have vegetation patches that can be colonized by sandflies from the periphery, according to the characteristics of metapopulation dynamics [10].

On the other hand, in the study area, the possibility of vector-borne transmission of T. cruzi has been discarded, because no insects or indicators of their presence have been found in the annual activities of entomological surveillance of triatomines carried out by Primary Health Care System in recent and historical monitoring. Thus, cases of T. cruzi infection in Hipólito Yrigoyen would be associated with migratory processes (movement principally of rural populations from Argentina and Bolivia of the Gran Chaco ecoregion where Chagas disease is endemic) [13]. The T. cruzi seroprevalence found in this work is low compared with the prevalence value observed in rural populations of endemic areas (25%) [38], and it is high compared with other regions without endemic transmission [39]. In turn, infected children may have acquired infection by congenital transmission, as reported in previous studies of this type of transmission in the province of Salta [40].

The proportion of T. cruzi-Leishmania sp. mixed infection within the group of patients with TL reported in the north of Salta reaches 30 and 40% [2, 14, 15] and does not show differences from the percentage obtained in this study. Knowing the level of this condition in the population allows us to explore the factors involved in the origin and persistence of mixed infections. In addition, because antimonials are cardiotoxic, a careful diagnosis and implementation of alternative treatments are needed to avoid further complications.

The complex situation in Hipólito Yrigoyen in reference to TL is aggravated by the coexistence of T. cruzi infection. The transmission pattern involves mainly natural areas, but the possibility of a peridomiciliary transmission in the outskirts of the city cannot be ruled out. This situation demands the involvement of different stakeholders to control the magnitude of disease incidence, implementing prevention strategies and taking into account biogeographical and sociocultural characteristics, as well as human-induced environmental changes and situations that pose a risk.

The present work provides epidemiological information of potential determinants of TL occurrence in Hipólito Yrigoyen, its magnitude, and situation of T. cruzi infection in the same area. This information is useful for the local health system because it may contribute to a better planning of the surveillance systems and to the design of prevention strategies in the area. These epidemiological patterns of mixed infections can occur in other countries were T. cruzi transmission does not exist or was interrupted and tegumentary leishmaniasis is endemic.

Competing Interests

The authors declare that they have no competing interests.

Acknowledgments

The authors wish to thank Carlos Villalpando, Elizabeth Corro, Yolanda Abán, Nadia Gonzalez, and Norma Acosta, for their support during fieldwork and the Med. Nicanor Sosa of the Municipality of Hipólito Yrigoyen for logistic support during permanence in the study area. This study was supported by the Consejo de Investigación de la Universidad Nacional de Salta (CIUNSa), the PICT 2013-3213, PICT 2014-1579, and Fundación Mundo Sano.

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