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Trypanosoma cruzi genotyping supports a common source of infection in a school-related oral outbreak of acute Chagas disease in Venezuela

Published online by Cambridge University Press:  02 April 2013

Z. DÍAZ-BELLO ,
M. C. THOMAS ,
M. C. LÓPEZ ,
R. ZAVALA-JASPE ,
O. NOYA ,
B. ALARCÓN DE NOYA  and
T. ABATE
Z. DÍAZ-BELLO
Affiliation:
Sección de Inmunología, Instituto de Medicina Tropical, Facultad de Medicina, Universidad Central de Venezuela, Caracas, Venezuela
M. C. THOMAS
Affiliation:
Instituto de Parasitología y Biomedicina López Neyra – CSIC – Parque Tecnológico de Ciencias de la Salud, Granada, España
M. C. LÓPEZ
Affiliation:
Instituto de Parasitología y Biomedicina López Neyra – CSIC – Parque Tecnológico de Ciencias de la Salud, Granada, España
R. ZAVALA-JASPE
Affiliation:
Sección de Inmunología, Instituto de Medicina Tropical, Facultad de Medicina, Universidad Central de Venezuela, Caracas, Venezuela
O. NOYA
Affiliation:
Sección de Biohelmintiasis, Instituto de Medicina Tropical, Facultad de Medicina, Universidad Central de Venezuela, Caracas, Venezuela Cátedra de Parasitología, Escuela de Medicina Luis Razetti, Universidad Central de Venezuela, Caracas, Venezuela
B. ALARCÓN DE NOYA
Affiliation:
Sección de Inmunología, Instituto de Medicina Tropical, Facultad de Medicina, Universidad Central de Venezuela, Caracas, Venezuela Cátedra de Parasitología, Escuela de Medicina Luis Razetti, Universidad Central de Venezuela, Caracas, Venezuela
T. ABATE*
Affiliation:
Sección de Biología Molecular, Instituto de Medicina Tropical, Facultad de Medicina, Universidad Central de Venezuela, Caracas, Venezuela
*
*Author for correspondence: Dr T. Abate, Instituto de Medicina Tropical ‘Dr. Félix Pifano’, Universidad Central de Venezuela, Apartado Postal 47.706, Los Chaguaramos, Caracas 1041-A, Venezuela. (Email: [email protected])
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Summary

Trypanosoma cruzi I, a discrete typing unit (DTU) found in human infections in Venezuela and other countries of the northern region of South America and in Central America, has been recently classified into five intra-DTU genotypes (Ia, Ib, Ic, Id, Ie) based on sequence polymorphisms found in the spliced leader intergenic region. In this paper we report the genotype identification of T. cruzi human isolates from one outbreak of acute orally acquired Chagas disease that occurred in a non-endemic region of Venezuela and from T. cruzi triatomine and rat isolates captured at a guava juice preparation site which was identified as the presumptive source of infection. The genotyping of all these isolates as TcId supports the view of a common source of infection in this oral Chagas disease outbreak through the ingestion of guava juice. Implications for clinical manifestations and dynamics of transmission cycles are discussed.

Keywords

Acute Chagas disease outbreakDTU genotypesoral transmissionTrypanosoma cruzi
Type
Original Papers
Information
Epidemiology & Infection , Volume 142 , Issue 1 , January 2014 , pp. 156 - 162
Copyright
Copyright © Cambridge University Press 2013 

INTRODUCTION

Chagas disease (CD) is a parasitic illness with an estimated prevalence of eight million infected people in Latin America, although the information currently available does not reflect the true extent of the problem [1]. Trypanosoma cruzi, its aetiological agent, is mainly transmitted to humans by different Reduviidae insect vectors or by blood transfusion. Congenital transmission from chronically infected women occurs in 2–8% of pregnancies depending on the endemic area [Reference Carlier and Torrico2, 3]. New epidemiological modes of infection have been detected such as oral transmission and domestic adaptation of wild triatomines. The oral route of transmission is well documented and constitutes a mode of infection that leads to microepidemics and outbreaks of a more severe clinical form of acute CD [Reference Coura4–Reference Shikanai-Yasuda and Carvalho8]. The latter via transmission is currently acquiring relevance due to its association with a high mortality rate. The severity of CD also depends on the genetic diversity of T. cruzi and the competence of the host immune system.

In Venezuela, a significant outbreak of acute CD occurred in December 2007 affecting 103 persons at a school in an urban neighbourhood of Caracas where vector transmission had not been reported previously [Reference Alarcón de Noya9]. The infection was associated with Panstrongylus geniculatus, a sylvatic triatomine vector that is in a progressive process of domiciliation [Reference Reyes-Lugo10–Reference Carrasco12] and which had been considered as an inefficient T. cruzi transmission vector. The outbreak was suspected of being linked to the ingestion of contaminated guava juice prepared under unsupervised hygienic conditions by a supplier in a distant slum on the western mountain slopes of the city, where triatomines were present. A significant positive correlation was found between ingestion of guava juice and risk of infection [Reference Alarcón de Noya9].

T. cruzi shows a genetic diversity that has been associated with the observed variability of clinical manifestations, geographical distribution and preferential parasite–vector interactions. To characterize the population structure, T. cruzi has been subdivided into six discrete typing units (DTUs), namely TcI, TcII, TcIII, TcIV, TcV and TcVI [Reference Zingales13]. T. cruzi I (TcI) isolates are predominant in Venezuela and other countries of the northern region of South America and in Central America [Reference Añez14–Reference Carrasco17]. TcI has been mainly associated with low parasitaemia level in peripheral blood and very mild clinical symptoms. However, many symptomatic cases of severe acute CD patients infected with TcI in endemic regions of Venezuela and Colombia have also been described [Reference Añez14, Reference Triana18, Reference Salazar, Schijman and Triana19]. Five intra-DTU TcI genotypes (Ia, Ib, Ic, Id, Ie) have been described based on sequence polymorphisms found in the mini-exon gene's intergenic region [Reference Herrera20–Reference Cura22]. So far, strains associated with documented cases of oral transmission have been characterized as TcII [Reference Steindel23] and TcI [Reference Marcili24, Reference Andrade25]. In this context we decided to determine the intra-DTU TcI genotypes of T. cruzi isolates from the orally transmitted outbreak described above which also allowed us to understand the current circulating infecting strains. Preliminary results revealed a marked genetic homogeneity, with all of the isolates belonging to the TcI lineage.

METHODS

T. cruzi isolates

The parasite isolates were obtained by haemoculture from peripheral blood of three patients orally infected in an urban outbreak at a school in Caracas, Venezuela, in December 2007 (including the index case); from the faeces of one infected P. geniculatus triatomine, and from the blood of a rat captured at the guava juice preparation site which was identified as the source of infection [Reference Alarcón de Noya9]. In addition, a cultured human stock from B. Alarcón de Noya's laboratory, isolate PM [Reference Maekelt26], as well as Munanta (DTU TcI), Ikiakarora (DTU TcIII) and Guateque (DTU TcVI) strains from M. C. López's laboratory [Reference Thomas27] were included (Table 1).

Table 1. Description of Trypanosoma cruzi isolates

DTU, Discrete typing unit.

DNA extraction and PCR amplifications

Total DNA extraction from samples was performed by resuspension of parasite pellets in lysis solution (150 mm NaCl, 0·1 m EDTA, 0·1 mg Proteinase K, 0·4% SDS) and incubated for 2 h at 50°C, followed by phenol-chloroform extractions and RNAse treatment. DNA pellets were resuspended in distilled water and stored at −20°C. Amplification of spliced leader intergenic region (SL-IR) was performed in a multiplex reaction with primers TC (CCCCCCTCCCAGGCCACACTG), TC1 (GTGTCCGCCACCTCCTTCGGGCC) and TC2 (CCTGCAGGCACACGTGTGTGTG) [Reference Souto28, Reference Fernandes29]. PCR was performed in a final volume of 25 μl containing 100 ng template DNA, 100 pmol of each primer, 2·5 mm of each dNTP, 2·5 U Taq polymerase, 2·5 μl of 10× Taq polymerase buffer, and 1·5 mm MgCl2. Amplification was performed in a MJR PTC-100 thermocycler (MJ Research, USA) as follows: one step of 1 min denaturation at 94°C, 27 cycles at 94 °C for 30 s, 55°C for 30 s, 72°C for 30 s and a final extension step at 72°C for 5 min. Ribosomal subunit amplification with primers D71 (AAGGTGCGTCGACAGTGTGG) and D72 (TTTTCAGAATGGCCAACAGT) were also performed [Reference Souto28] in a final volume of 25 μl containing 100 ng template DNA, 100 pmol of each primer, 2·5 mm of each dNTP, 2·5 U Taq polymerase, 2·5 μl of 10× Taq polymerase buffer and 1·5 mm MgCl2. The PCR products were analysed by 1·5% agarose gel electrophoresis for SL-IR amplification and by 12% acrylamide gel electrophoresis for 24Sα amplification. In both cases the DNA was detected by ethidium bromide staining and visualized under ultraviolet light. PCR products of 350 bp and 300 bp for SL-IR amplification were expected for TcI and for TcII, TcV and TcVI, respectively, while no bands were expected for TcIII and TcIV [Reference Zingales30]. A product of 110 bp for 24Sα rDNA amplification was expected for TcI, TcIII and TcV, and products of 120 bp and 125 bp, for TcIV and for TcII and TcVI, respectively.

The amplification products for SL-IR were directly sequenced using the dideoxy chain termination method, and also purified from agarose gels using the Qualex kit (Qiagen, Germany) and cloned in p-GEM T vector (Promega, USA), using the blue/white selection with IPTG/X-gal for the identification of transformants. DNA from each one of the three clones was isolated with the SV Minipreps DNA Purification System (Promega) and the two chains sequenced using the dideoxy chain termination method.

DNA sequence and molecular phylogenetic analysis

Multiple sequence alignments were performed using ClustalW2 [Reference Goujon31] and edited in BioEdit v. 7.0.9 (Ibis Biosciences, USA).

RESULTS

In order to characterize the infecting strain that caused the orally acquired CD acute infection, parasites were isolated from three patients from the Caracas outbreak and also from a triatomine and a rat captured at the guava juice preparation site (identified as the source of infection), grown and genotyped. Thus, genomic DNA (gDNA) from the different isolates was purified and PCR performed. As PCR controls, gDNA purified from known T. cruzi strains such as Munanta (DTU TcI), Ikiakarora (DTU TcIII) and Guateque (DTU TcVI) were employed as DNA template. As observed in Figure 1 a, amplification of SL-IR in a multiplex reaction using the TC, TC1 and TC2 primers generated a 350 bp product when the T. cruzi gDNAs isolated from the three patients from Caracas (lanes 1–3), and those isolated from the triatomine (lane 5), the rat (lane 6) and control DTU TcI (lane C2) were employed. A single amplification band of 300 bp was generated when DTU TcVI gDNA (lane C3) was employed as DNA template and none when DTU TcIII gDNA (lane C1) was used. These data indicated that all the analysed parasite strains belonged to DTU TcI. This typing was corroborated by the PCR performed with specific primers for 24S amplification which produced amplified bands with the expected size for DTU TcI strains (Fig. 1 b).

Fig. 1. Gel electrophoresis of PCR products from T. cruzi isolates. (a) 1·5% Agarose gel electrophoresis of SL-IR amplicons. (b) 12% Acrylamide gel electrophoresis of 24Sα amplicons. Lane M, 100 bp DNA ladder (hyperladder IV, Bioline, UK); lanes 1–3, isolates 1593, 1595 and 1598 from patients infected in the Caracas outbreak; lane 4, laboratory strain PM; lane 5, isolate AC1 from an infected Panstrongylus geniculatus triatomine captured at the guava juice preparation site; lane 6, isolate RATA 6 from an infected rat captured at the guava juice preparation site; lanes C1, C2, C3, T. cruzi control strains Ikiakora (DTU TcIII), Munanta (DTU TcI) and Guateque (DTU TcVI).

The SL-IR amplified products were directly sequenced but also cloned into pGEM-T Easy Vector (Promega), in order to reveal the possible existence of mixed TcI SL-IR genotypes. The DNA from different clones was purified and subsequently sequenced. Sequence alignment of the different PCR products (whose electropherograms exhibited no nucleotide ambiguity) and clones corresponding to the isolated parasites in all the patients from Caracas were seen to be identical, indicating that they were all infected by a T. cruzi population belonging to a single TcI genotype. The sequences of the different PCR products and clones corresponding to the amplicons generated with the DNA of the parasites isolated from the triatomine and the rat were also identical to those obtained from the parasites isolated from the patients.

Following the intra-DTU TcI classification first proposed by Herrera et al. [Reference Herrera20] and expanded by Cura et al. [Reference Cura22], when the first 60 bp of the SL-IR were aligned with reference sequences, it was observed that all the isolates from the Caracas outbreak presented a gap of 8 nt at position 20–27, as well as other single nucleotide polymorphisms (SNPs), considered as hallmarks of the DTU TcId (Fig. 2). These observations indicated that the triatomine and rat were also infected by a T. cruzi population belonging to the same TcI genotype.

Fig. 2. Multiple alignment of 60-nt region within the SL-IR of the T. cruzi I sequences analysed. Partial reference sequences reported in [Reference Herrera20, Reference Cura22] are shown in bold: CGC (AM259467), JLC (AM259468), X380C (AM259472), JD1C (AM259478) and PALV2-2 Cl5 (GQ398812.1). Gaps (∼), conserved sites (.).

On the other hand, a SL-IR sequence divergence was observed in clones corresponding to the laboratory PM strain which was isolated from a patient with vector-acquired CD [Reference Maekelt26]. These sequences did not have the characteristic 8-nt gap of DTU TcId. Instead they bore the SNP characteristic of the SL-IR sequences from parasites belonging to DTUs TcIa and TcIb (Fig. 2) which was taken as an indication that the laboratory strain was a mixed population of TcIa and TcIb genotypes.

DISCUSSION

In this study we have demonstrated that three patients (including the index case) from an important outbreak of acute CD occurring at a school in an urban neighbourhood of Caracas, and a triatomine and a rat captured at the guava juice preparation site identified as the source of the parasite contamination, were all infected by a T. cruzi population belonging to the same TcI genotype. These observations strongly suggest that a single strain was implicated in this outbreak and reinforce the fact that the guava juice preparation site was the source of the infection, identifying the oral route of transmission as a common mechanism of infection [Reference Alarcón de Noya9]. On the other hand, our results indicate that the T. cruzi isolate PM, obtained from a patient with vector-acquired CD [Reference Maekelt26], was a mixed population of TcIa and TcIb genotypes. Recently, natural mixed populations of TcIa and TcId have been reported in faecal samples of Triatoma infestans from Paraguay [Reference Cura22] and in heart, blood and skin chagoma samples from an Argentinean patient [Reference Burgos32].

According to current molecular evidence, TcI is one of the parental DTUs in the hybridization events that, separated by periods of clonal evolution, explain the genetic diversity of the extant T. cruzi populations. In Venezuela and Colombia, TcI isolates have been associated not only with low parasitaemia and very mild clinical symptoms, but also with severe acute symptomatic cases and death [Reference Añez14, Reference Salazar, Schijman and Triana19, Reference Herrera20]. TcI has a notable intra-DTU diversity, recently classified into five genotypes (Ia, Ib, Ic, Id, Ie) [Reference Herrera20–Reference Cura22], although it could not be definitely associated with the diversity of TcI biological characteristics observed, i.e. transmission cycles, host preferences, clinical manifestations or geographical distribution [Reference O'Connor and Bosseno33, Reference Mejía-Jaramillo34]. In Colombia, an association was found for TcId with sylvatic populations of Rhodnius prolixus and wild reservoirs [Reference Falla and Herrera21]. We here report its association with sylvatic populations of P. geniculatus. The close contact with infected sylvatic species might explain oral outbreaks in areas without a history of vector transmission. In fact, Caracas is a densely populated urban area currently considered non-endemic for CD, since active vector transmission had not been reported previously. However, a local sylvatic triatomine vector, P. geniculatus, is present in the surrounding mountain area where the nocturnal incursion of sylvatic infected triatomine bugs has allowed the opportunity of easy contamination of unprotected food and beverages with T. cruzi [Reference Alarcón de Noya9].

A multilocus microsatellite typing of T. cruzi DTU I [Reference Llewellyn16] showed a sylvatic TcI genotype predominance in the Venezuelan adult intradomiciliary triatomine sampled, including Triatoma maculata, P. geniculatus, and R. prolixus. The TcI sylvatic genotype was different from the domestic one observed in TcI strains from infected humans sampled across the country. In Colombia, TcId has also been mainly associated with sylvatic triatomines and reservoir populations suggesting, in both countries, a possible and progressive introduction of a sylvatic sub-DTU I in the domestic environment, independent of the transmission route of the parasite or the species of the triatomine vector.

In a broader study TcId was also found in a variety of peridomestic, domestic and sylvatic triatomines, as well as in wild reservoirs and in human samples from South America [Reference Cura22]. These data are also consistent with the epidemiological changes that are taking place with regard to CD transmission since P. geniculatus had been considered as an inefficient T. cruzi transmission vector.

A preferential cardiac tropism for TcId has been suggested [Reference Burgos32]. This tropism was consistent with the clinical manifestations of patients from the Caracas outbreak, where in 61 (59%) of the 103 confirmed cases, one or more abnormalities were observed on ECG recordings, 75% were symptomatic, 20·3% required hospitalization and a child aged 5 years died of acute chagasic myocarditis [Reference Alarcón de Noya9].

This report shows that T. cruzi isolates from sylvatic vectors and reservoirs, as well as isolates from humans infected in an orally acquired CD outbreak in a non-endemic region of Venezuela belong to a same T. cruzi I genotype, TcId. The similarity in the parasite isolates from three patients of the urban oral outbreak and the triatomine and the rat captured at the guava juice preparation site, allows us to suggest that the source of infection was common for these persons and the vector.

Although further analysis with more isolates is needed, this work contributes to the knowledge and possible association between the oral route of transmission, the severity of the disease and the genotypes of T. cruzi isolates, providing evidence that DTU TcId can successfully infect humans by the oral route.

ACKNOWLEDGEMENTS

This work received financial support from Sección de Inmunología, Instituto de Medicina Tropical, Universidad Central de Venezuela; Fondo Nacional de Ciencia y Tecnología (travelling expenses of Z.D. for a research cooperation with Spain, grant no. G-2005000387), (T.A., grant no. 2006000216); Plan Nacional I+D+i, MINECO, Spain (M.C.T. and M.C.L., grant nos. BFU2010-1670 and SAF2012-35777); FEDER (M.C.T. and M.C.L). M. C. Thomas, M. C. López, O. Noya and B. Alarcón de Noya are members of the NHEPACHA network (Latin American Network for Chagas disease) and PAICET network (Tri-Continental Altantic Platform for Research and Control of Tropical Diseases).

DECLARATION OF INTEREST

None.

References

REFERENCES

1. World Health Organization. Report of the scientific working group on Chagas disease. 2007 (http://whqlibdoc.who.int/hq/2007/TDR_SWG_09_spa.pdf). Accessed June 2012.Google Scholar
2. Carlier, Y, Torrico, F. Congenital infection with Trypanosoma cruzi from mechanism of transmisión to strategies for diagnosis and control. Revista da Sociedade Brasileria de Medicina Tropical 2003; 36: 767–771.CrossRefGoogle Scholar
3. World Health Organization. Control of Chagas disease. Second report of the WHO Expert Committee. World Health Organization, Technical Report Series 2002; 905: 59–90.Google Scholar
4. Coura, JR, et al. Emerging Chagas' disease in Amazonian Brazil. Trends in Parasitology 2002; 18: 171–176.CrossRefGoogle ScholarPubMed
5. Nóbrega, AA, et al. Oral transmission of Chagas disease by consumption of açaí palm fruit, Brazil. Emerging Infectious Diseases 2009; 15: 653–655.CrossRefGoogle ScholarPubMed
6. Ríos, JF, et al. Probable outbreak of oral transmission of Chagas disease in Turbo, Antioquia. Biomedica 2011; 31: 185–195.CrossRefGoogle ScholarPubMed
7. Santalla, Vargas J, et al. First reported outbreak of Chagas disease in the Bolivian Amazonia: report of 14 acute cases by oral transmission of Trypanosoma cruzi in Guayaramerín, Beni-Bolivia. Biofarbo 2011; 19: 52–58.Google Scholar
8. Shikanai-Yasuda, MA, Carvalho, NB. Oral transmission of Chagas disease. Clinical Infectious Diseases 2012; 54: 845–852.CrossRefGoogle ScholarPubMed
9. Alarcón de Noya, B, et al. Large urban outbreak of orally acquired acute Chagas disease at a school in Caracas, Venezuela. Journal of Infectious Diseases 2010; 201: 1308–1315.CrossRefGoogle Scholar
10. Reyes-Lugo, M. Panstrongylus geniculatus Latreille 1811 (Hemiptera: Reduviidae: Triatominae), vector of Chagas disease in the home environment of North-Central Venezuela. Revista Biomédica 2009; 20: 180–205.Google Scholar
11. Feliciangeli, MD, et al. Mixed domestic infestation by Rhodnius prolixus Stal, 1859 and Panstrongylus geniculatus Latreille, 1811, vector incrimination, and seroprevalence for Trypanosoma cruzi among inhabitants in El Guamito, Lara State, Venezuela. American Journal of Tropical Medicine and Hygiene 2004; 71: 501–505.CrossRefGoogle ScholarPubMed
12. Carrasco, HJ, et al. Risk of Trypanosoma cruzi I (Kinetoplastida: Trypanosomatidae) transmission by Panstrongylus geniculatus (Hemiptera: Reduviidae) in Caracas (Metropolitan District) and neighboring States, Venezuela. International Journal for Parasitology 2005; 35: 1379–1384.CrossRefGoogle ScholarPubMed
13. Zingales, B, et al. A new consensus for Trypanosoma cruzi intraspecific nomenclature: second revision meeting recommends TcI to TcVI. Memorias do Instituto Oswaldo Cruz 2009; 104: 1051–1054.CrossRefGoogle ScholarPubMed
14. Añez, N, et al. Predominance of lineage I among Trypanosoma cruzi isolates from Venezuelan patients with different clinical profiles of acute Chagas Disease. Tropical Medicine and International Health 2004; 9: 1319–1326.CrossRefGoogle ScholarPubMed
15. Samudio, F, et al. Predominance of Trypanosoma cruzi I among Panamanian sylvatic isolates. Acta Tropica 2007; 101: 178–181.CrossRefGoogle ScholarPubMed
16. Llewellyn, MS, et al. Genome-scale multilocus microsatellite typing of Trypanosoma cruzi discrete typing unit I reveals phylogeographic structure and specific genotypes linked to human infection. PLoS Pathogens 2009; 5: e1000410.CrossRefGoogle ScholarPubMed
17. Carrasco, HJ, et al. Geographical distribution of Trypanosoma cruzi genotypes in Venezuela. PLoS Neglected Tropical Diseases 2012; 6: e1707.CrossRefGoogle ScholarPubMed
18. Triana, O, et al. Trypanosoma cruzi: variability of stocks from Colombia determined by molecular karyotype and minicircle Southern blot analysis. Experimental Parasitology 2006; 113: 62–66.CrossRefGoogle ScholarPubMed
19. Salazar, A, Schijman, AG, Triana, O. High variability of Colombian Trypanosoma cruzi lineage I stocks as revealed by low-stringency single primer-PCR minicircle signatures. Acta Tropica 2006; 100: 110–118.CrossRefGoogle ScholarPubMed
20. Herrera, C, et al. Identifying four Trypanosoma cruzi I isolate haplotypes from different geographic regions in Colombia. Infection, Genetics and Evolution 2007; 7: 535–539.CrossRefGoogle ScholarPubMed
21. Falla, A, Herrera, C, et al. Haplotype identification within Trypanosoma cruzi I in Colombian isolates from several reservoirs, vectors and humans. Acta Tropica 2009; 110: 15–21.CrossRefGoogle ScholarPubMed
22. Cura, CI, et al. Trypanosoma cruzi I genotypes in different geographical regions and transmission cycles based on a microsatellite motif of the intergenic spacer of spliced-leader genes. International Journal for Parasitology 2010; 40: 1599–1607.CrossRefGoogle ScholarPubMed
23. Steindel, M, et al. Characterization of Trypanosoma cruzi isolated from humans, vectors, and animal reservoirs following an outbreak of acute human Chagas disease in Santa Catarina State, Brazil. Diagnostic Microbiology and Infectious Disease 2008; 60: 25–32.CrossRefGoogle ScholarPubMed
24. Marcili, A, et al. Trypanosoma cruzi in Brazilian Amazonia: Lineages TCI and TCIIa in wild primates, Rhodnius spp. and in humans with Chagas disease associated with oral transmission. International Journal for Parasitology 2009; 39: 615–623.CrossRefGoogle ScholarPubMed
25. Andrade, SG, et al. Biological, biochemical and molecular features of Trypanosoma cruzi strains isolated from patients infected through oral transmission during a 2005 outbreak in the state of Santa Catarina, Brazil: its correspondence with the new T. cruzi Taxonomy Consensus (2009). Memorias do Instituto Oswaldo Cruz 2011; 106: 948–956.CrossRefGoogle Scholar
26. Maekelt, GA. The complement fixation test for Chagas disease. Zeitschrift Tropenmedizin und Parasitologie 1960; 11: 155–166.Google Scholar
27. Thomas, MC, et al. Plasticity of the histone H2A genes in a Brazilian and six Colombian strains of Trypanosoma cruzi . Acta Tropica 2000; 25: 203–210.CrossRefGoogle Scholar
28. Souto, RP, et al. DNA markers define two major phylogenetic lineages of Trypanosoma cruzi . Molecular and Biochemical Parasitology 1996; 83: 141–152.CrossRefGoogle ScholarPubMed
29. Fernandes, O, et al. Brazilian isolates of Trypanosoma cruzi from humans and triatomines classified into two lineages using mini-exon and ribosomal RNA sequences. American Journal of Tropical Medicine and Hygiene 1998; 58: 807–811.CrossRefGoogle ScholarPubMed
30. Zingales, B, et al. The revised Trypanosoma cruzi subspecific nomenclature: Rationale, epidemiological relevance and research applications. Infection, Genetics and Evolution 2012; 12: 240–253.CrossRefGoogle ScholarPubMed
31. Goujon, M, et al. A new bioinformatics analysis tools framework at EMBL-EBI (2010). Nucleic Acids Research 2010; 38 (Suppl.): W695–699.CrossRefGoogle Scholar
32. Burgos, JM, et al. Molecular identification of Trypanosoma cruzi discrete typing units in end-stage chronic Chagas heart disease and reactivation after heart transplantation. Clinical Infectious Diseases 2010; 51: 485–495.CrossRefGoogle ScholarPubMed
33. O'Connor, O, Bosseno, MF, et al. Genetic clustering of Trypanosoma cruzi I lineage evidenced by intergenic miniexon gene sequencing. Infection, Genetics and Evolution 2007; 7: 587–593.CrossRefGoogle ScholarPubMed
34. Mejía-Jaramillo, AM, et al. Geographical clustering of Trypanosoma cruzi I groups from Colombia revealed by low-stringency single specific primer-PCR of the intergenic regions of spliced-leader gene. Parasitology Research 2009; 104: 399–410.CrossRefGoogle Scholar
Figure 0

Table 1. Description of Trypanosoma cruzi isolates

Figure 1

Fig. 1. Gel electrophoresis of PCR products from T. cruzi isolates. (a) 1·5% Agarose gel electrophoresis of SL-IR amplicons. (b) 12% Acrylamide gel electrophoresis of 24Sα amplicons. Lane M, 100 bp DNA ladder (hyperladder IV, Bioline, UK); lanes 1–3, isolates 1593, 1595 and 1598 from patients infected in the Caracas outbreak; lane 4, laboratory strain PM; lane 5, isolate AC1 from an infected Panstrongylus geniculatus triatomine captured at the guava juice preparation site; lane 6, isolate RATA 6 from an infected rat captured at the guava juice preparation site; lanes C1, C2, C3, T. cruzi control strains Ikiakora (DTU TcIII), Munanta (DTU TcI) and Guateque (DTU TcVI).

Figure 2

Fig. 2. Multiple alignment of 60-nt region within the SL-IR of the T. cruzi I sequences analysed. Partial reference sequences reported in [20, 22] are shown in bold: CGC (AM259467), JLC (AM259468), X380C (AM259472), JD1C (AM259478) and PALV2-2 Cl5 (GQ398812.1). Gaps (∼), conserved sites (.).