Oral Transmission of Trypanosoma cruzi, Brazilian Amazon.
On December 29, 2017, a 51-year-old woman with acute febrile syndrome visited a tertiary care center for infectious diseases (Fundagao 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 Labrea, a municipality 850 km south of Manaus, where she visited often (Table). A common exposure factor among them was ingestion of acai berry juice, produced by local dealers in the outskirts of Labrea 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[degrees]C in the family refrigerator in Labrea, 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 [approximately equal to]10 mL of blood was collected into heparin-containing tubes. Next, 100 [micro]L 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[degrees]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 [micro]L 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 acai 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 [micro]L into 1 mL liver infusion tryptose medium containing 20% inactivated fetal calf serum and 40 mg/ mL gentamycin sulfate and incubated it at 27[degrees]C. We made triplicate cultures and used inverted optical microscopy to search daily for flagellate forms.
We placed 200 [micro]L of the agai culture in 1.5-mL microtubes with 500 [micro]L of phosphate-buffered saline at pH 7.2, incubated the sample in a water bath for 15 minutes at 98[degrees]C, and centrifuged it at 3,500 rpm for 3 minutes. We removed 200 [micro]L 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 (COII7) and the glucose-phosphate isomerase (GPI8) 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 acai 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 agai juice (Figure 1, panel C). T. cruzi from human samples and agai juice showed an identical 150-bp band of miniexon 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 agai 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 agai juice were the same.
All patients who simultaneously exhibited febrile syndrome had consumed agai 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 acai juice is a source of oral contamination with T. cruzi. Circumstantial association between outbreaks and contaminated acai 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 acai pulp extraction. Another hypothesis is that contamination occurred during collection and manipulation of acai 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 acai juice. On the basis of our demonstration of this route of contamination, legislation should be revised to possibly require pasteurization of acai juice (14).
We thank Nelson Fe, Flavio Fe, 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.
Dr. Santana is a scientist in the Fundagao de Medicina Tropical Dr. Heitor Vieira Dourado. His research interests include entomology and epidemiology of neglected infectious diseases, especially Chagas disease and malaria.
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Address for correspondence: Marcus V.G. Lacerda, Fundacao de Medicina Tropical Dr Heitor Vieira Dourado, Av Pedro Teixeira 25, Manaus 69040-000, AM, Brazil; email: email@example.com
Author affiliations: Fundagao de Medicina Tropical Dr Heitor Vieira Dourado, Manaus, Brazil (R.A.G. Santana, M.G.V.B. Guerra, D.R. Sousa, K. Couceiro, J.V. Ortiz, M. Oliveira, L.S. Ferreira, G.A.V. Silva, G.C. Melo, G.M. Vergel, W.M. Monteiro, M.V.G. Lacerda, J.A.O. Guerra); Universidade do Estado do Amazonas, Manaus (R.A.G. Santana, M.G.V.B. Guerra, D.R. Sousa, K. Couceiro, J.V. Ortiz, M. Oliveira, K.R. Souza, I. C. Tavares, R.F. Morais, G.C. Melo, W.M. Monteiro, J. M.B.B. Ferreira, J.A.O. Guerra); Fundagao de Vigilancia em Saude do Amazonas, Manaus (G.M. Vergel, B.C. Albuquerque, A.R.L. Arcanjo); Instituto Leonidas & Maria Deane, Fiocruz, Manaus (M.V.G. Lacerda); Instituto de Higiene e Medicina Tropical, Universidade Nova de Lisboa, Lisbon, Portugal (H. Silveira)
Caption: Figure 1. Agaf berry juice sample from Brazilian Amazon. A) A 50 mL-tube after centrifugation shows 3 layers: 1, pulp, 2, intermediate fat (box); and 3: supernatant. B) Top view of layer 2 (arrow). C) Fresh preparation of layer 2 showing Trypanosoma cruzi flagellated form (arrow).
Caption: Figure 2. Comparison of Trypanosoma cruziapal juice samples and Chagas disease patient blood samples, Brazilian Amazon. A) Alignment of GPI sequences from apal juice samples and patient blood samples. B-C) Phylogenetic position of T cruzi responsible for the 2017 Chagas disease outbreak in the Brazilian Amazon, based on the cytocrome oxidase subunit II gene sequences (bestfit model: Hasegawa-Kishino-Yano) and on the GPI gene sequences (best-fit model: Kimura 2-parameter). The following standard strains obtained from GenBank (discrete typing units [strain name, access no. for COII-GPY]) were used: TcI (SilvioX10 cl4, EU302222.1-Silvio10cl1-AY540730.1), TcII (Esmeraldo cl3, AF359035.1-AY540728.1), TcIII (M6241 cl6, AF359032.1- AY484478.1), TcIV (CANIII cl1-AF359030.1), TcV (Mn cl2, DQ343718.1-AY484480.1), and TcVI (CL Brener, DQ343645.1-XM_815802.1). B, blood; C, culture; GPI, glucose-phosphate isomerase; P0, patient number; X, xenodiagnosis; (i) repetition number. Scale bars indicate number of mutations per site.
Table. Basic demographics and diagnostic methods used to confirm acute Chagas disease in 10 patients, Brazilian Amazon * Patient age, Patient y/sex Date of diagnosis Blood smear 1 51/F 2017 Dec 29 + 2 19/F 2017 Dec 29 + 3 22/M 2017 Dec 29 + 4 35/F 2018 Jan 5 + 5 1/F 2018 Jan 5 + 6 21/F 2018 Dec 1 + 7 65/F 2018 Dec 1 + 8 16/F 2018 Dec 1 - 9 11/M 2018 Dec 1 + 10 51/F 2018 Dec 1 + Patient Xenodiagnosis Culture 1 + + 2 + + 3 + + 4 + + 5 NP + 6 + - 7 + + 8 + NP 9 NP NP 10 NP NP *NP, not performed; +, positive for Trypanosoma cruzi; -, negative for T. cruzi.
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|Author:||Santana, Rosa Amelia G.; Guerra, Maria Gragas V.B.; Sousa, Debora R.; Couceiro, Katia; Ortiz, Jessic|
|Publication:||Emerging Infectious Diseases|
|Date:||Jan 1, 2019|
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