Volume 25, Number 1—January 2019
Oral Transmission of Trypanosoma cruzi, Brazilian Amazon
In the Brazilian Amazon, the suspected source of infection in an outbreak of acute Chagas disease involving 10 patients was Euterpe oleracea (açaí berry) juice. Patient blood and juice samples contained Trypanosoma cruzi TcIV, indicating oral transmission of the Chagas disease agent.
In Latin America, Chagas disease is prevalent in 21 countries and is one of the most worrisome public health problems on the subcontinent. The social and economic effects among poor and neglected populations are high (1). Increasing reports of outbreaks of acute Chagas disease have come to the attention of public health authorities, who regard the disease as emerging in the Amazon (2). For most reported outbreaks, epidemiologic investigation points to nonvectored transmission, implicating juices from local fruits (3). A major suspected source of infection is Euterpe oleracea, the açaí berry, consumed widely as a drink made from a blended pulp (4).
On December 29, 2017, a 51-year-old woman with acute febrile syndrome visited a tertiary care center for infectious diseases (Fundação de Medicina Tropical Dr Heitor Vieira Dourado; FMT-HVD) in Manaus, the capital of Amazonas state, Brazil, where malaria is endemic. A routine thick blood smear was negative for Plasmodium spp. but positive for Trypanosoma cruzi trypomastigotes. The patient mentioned 3 sick relatives in Manaus and 6 more in Lábrea, a municipality 850 km south of Manaus, where she visited often (Table). A common exposure factor among them was ingestion of açaí berry juice, produced by local dealers in the outskirts of Lábrea and sent to Manaus for consumption. Thick blood smears from the other 9 patients, all with acute febrile syndrome, were positive for T. cruzi. Of these 10 patients, 8 were clinically assessed at FMT-HVD and submitted samples for direct xenodiagnosis and peripheral blood for T. cruzi culture and PCR. A sample of the same juice drunk by all the patients, maintained at −20°C in the family refrigerator in Lábrea, was collected by local health authorities and sent to the reference laboratory in Manaus. All patients with a diagnosis of acute Chagas disease were prescribed benznidazole for 60 days (5).
Blood samples were obtained by venipuncture from 8 of the 10 patients, and ≈10 mL of blood was collected into heparin-containing tubes. Next, 100 μL whole blood was distributed into 3 mL liver infusion tryptose medium containing 20% inactivated fetal calf serum and 40 mg/mL gentamycin sulfate and then incubated at 27°C. Inverted optical microscopy was used daily to search for flagellate forms. Xenodiagnosis was conducted by using 20 stage 3 nymphs of Rhodnius robustus and R. prolixus bugs. We centrifuged 5 μL blood at 4,000 rpm for 10 min and collected the buffy coat for DNA extraction by using the PureLink Kit (Invitrogen, https://www.thermofisher.com).
On December 11, a sample of the açaí juice was transported on ice to FMT-HVD, where it was immediately thawed and centrifuged in 50-mL tubes at 3,000 rpm for 5 minutes. After centrifugation, 3 layers were observed: pulp, an intermediate layer containing fat, and supernatant (Figure 1, panels A and B). From each phase, we suspended 300 μL into 1 mL liver infusion tryptose medium containing 20% inactivated fetal calf serum and 40 mg/mL gentamycin sulfate and incubated it at 27°C. We made triplicate cultures and used inverted optical microscopy to search daily for flagellate forms.
We placed 200 μL of the açaí culture in 1.5-mL microtubes with 500 μL of phosphate-buffered saline at pH 7.2, incubated the sample in a water bath for 15 minutes at 98°C, and centrifuged it at 3,500 rpm for 3 minutes. We removed 200 μL of supernatant for genotyping.
The nontranscribed spacer of the mini-exon gene was amplified according to the multiplex protocol described elsewhere (6). The 150-bp product is characteristic of T. cruzi zymodeme Z3 of discrete typing units (DTUs) TcIII or TcIV; 100 bp is characteristic of T. rangeli, 200 bp of T. cruzi TcI, and 250 bp of T. cruzi TcII. Mini-exon gene analysis cannot distinguish between TcIII and TcIV.
All samples were also subjected to mitochondrial and nuclear DNA typing by analyzing polymorphisms in the cytochrome oxidase subunit II (COII) (7) and the glucose-phosphate isomerase (GPI) (8) genes, respectively. The amplified PCR products were purified by using the Wizard SV Gel and PCR Clean-up System kit (Promega, https://www.promega.com.br) and sequenced. Sequencing was performed with an ABI 3130 DNA sequencer (Applied Biosystems, https://www.thermofisher.com). We followed the BigDye Terminator v3.1 Cycle Sequencing Kit protocol (Applied Biosystems) by using 10–40 ng of purified PCR product in the sequencing reaction and the same primers used for COII and GPI gene amplification by PCR. We used sequences from standard strains: TcI (Silvio X10 cl1), TcII (Esmeraldo cl3), TcIII (M6241 cl6), TcIV (CANIII cl1), TcV (Mn cl2), and TcVI (CL Brener). Maximum-likelihood phylogenetic trees were inferred by using W-IQ-TREE (9).
During the outbreak, 8 patients who had drunk the açaí juice were clinically assessed at FMT-HVD. Parasite culture was successful for 6 and xenodiagnoses for 7. A total of 5 T. cruzi strains were isolated by blood culture and xenodiagnosis. All 8 patients were T. cruzi positive by PCR. Blood culture, xenodiagnoses, and PCR were not performed for 2 patients because they did not attend follow-up at FMT-HVD; their diagnoses were based only on thick blood smears.
After 24 h of incubation, we observed flagellated motile forms in the intermediate layer of fat of centrifuged açaí juice (Figure 1, panel C). T. cruzi from human samples and açaí juice showed an identical 150-bp band of mini-exon compatible with T. cruzi zymodeme Z3 (6), consistent with COII and GPI sequencing results. Parasites differed in position 507 (G/C) of the GPI sequence (Figure 2, panel A). COII sequences were compatible with T. cruzi III mitochondrial ancestral lineage (7). This set of samples and the reference strains TcIII, TcIV, TcV, and TcVI formed a single cluster that shared a characteristic mitochondrial genome distinct from both TcI and TcII (Figure 2, panel B). GPI sequence analysis showed that the human blood and açaí juice T. cruzi samples could be consistently classified as TcIV DTU (8) (Figure 2, panel C). Alignments of sequences from COII and GPI T. cruzi genes showed that the parasites in the açaí juice were the same.
All patients who simultaneously exhibited febrile syndrome had consumed açaí juice from the same source in the previous weeks. They were all infected with the same T. cruzi DTU as that in the juice, strongly suggestive that in the Brazilian Amazon, contaminated açaí juice is a source of oral contamination with T. cruzi. Circumstantial association between outbreaks and contaminated açaí juice has been suggested by previous studies from South America (10–12), but our evidence of an acute Chagas disease outbreak in which oral transmission could be implicated is robust because patients and a sample of the juice consumed were analyzed in a paired manner.
The most probable hypothesis for contamination of the juice is based on the attraction of contaminated triatomines by the light used during nighttime açaí pulp extraction. Another hypothesis is that contamination occurred during collection and manipulation of açaí berries without use of proper hygiene before mashing (1). Triatomine infestation of Amazonian palm trees also supports the potential for oral T. cruzi contamination of humans (13).
Experimental contamination of food with T. cruzi shows that parasite survival varies with the type of food and presence or absence of refrigeration (14,15). In this study, we hypothesized that the long survival of the parasite is associated with freezing the sample in the presence of cryoprotectants probably present in the fatty content of the açaí juice. On the basis of our demonstration of this route of contamination, legislation should be revised to possibly require pasteurization of açaí juice (14).
Dr. Santana is a scientist in the Fundação de Medicina Tropical Dr. Heitor Vieira Dourado. His research interests include entomology and epidemiology of neglected infectious diseases, especially Chagas disease and malaria.
We thank Nelson Fé, Flávio Fé, and Yolanda Noguthi for technical support in the laboratory.
This study was supported by the National Council for Scientific and Technological Development and by the Amazonas Research Foundation.
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Table of Contents – Volume 25, Number 1—January 2019
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Marcus V.G. Lacerda, Fundação de Medicina Tropical Dr Heitor Vieira Dourado, Av Pedro Teixeira 25, Manaus 69040-000, AM, Brazil