Volume 19, Number 10—October 2013
Chagas Disease and Breast-feeding
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Chagas disease (infection by the protozoan Trypanosoma cruzi) is a major parasitic disease of the Americas and one of the main neglected tropical diseases. Although various routes of transmission are recognized, the risk for transmission of the infection through breast-feeding has not clearly been established. We reviewed the literature on transmission of T. cruzi through breast-feeding to provide breast-feeding mothers with Chagas disease with medical guidance. Although data from animal studies and human studies are scarce, we do not recommend that mothers with Chagas disease discontinue breast-feeding, unless they are experiencing the acute phase of the disease, reactivated disease resulting from immunosuppression, or bleeding nipples. In these cases, thermal treatment of milk before feeding the infant may be considered.
Chagas disease (infection by the protozoan Trypanosoma cruzi) is a major parasitic disease in the Americas and one of the main neglected tropical diseases. T. cruzi is transmitted to humans primarily through the infected feces of triatomine bugs that contain metacyclic trypomastigotes (vectorial transmission). Other modes of transmission include transmission through infected blood and organs, vertical transmission, oral transmission (through consumption of contaminated food or drink), and transmission through laboratory accidents. The estimated number of infections in North, South, and Central America fell from ≈20 million in 1981 to ≈8–10 million in 2005; the reduction is mainly attributed to vector control campaigns and screening of blood donations in disease-endemic areas (1). However, the increase in mobile populations has led to the emergence of Chagas disease in non–disease-endemic areas where vectors are noncompetent and where the infection may be transmitted by other routes. A considerable proportion of migrants from Latin America are women, which turns the focus to preventing possible transmission from infected mother to child. The risk for congenital transmission from an infected mother may range from 0.13% to 17%, and the likelihood of congenital infection appears to correlate with maternal parasite density (2,3). Screening is recommended during pregnancy to detect mothers who may transmit T. cruzi to the fetus, even though no specific means of preventing congenital infection during pregnancy are available (4). The possibility of transmission through breast-feeding may be particularly relevant because, if breast-feeding is a route for transmission after delivery, such transmission may be preventable. Although some early publications identify breast-feeding as a possible route for T. cruzi infection, such data are scarce, and few animal studies exist (5–8).
Apart from other benefits, exclusive breast-feeding is the ideal way to provide nutrition during the first 6 months of life (9), and interruption of breast-feeding in resource-poor settings does not seem feasible unless the risks clearly outweigh possible benefits. If transmission occurs, treatment of acute infections is more successful in infants and children, and the treatment is also better tolerated (i.e., causes fewer side effects) in infants and children (10,11). The risk for transmission of infection through breast-feeding and whether any means are available to minimize this risk should be determined. The objective of this study was, therefore, to review the literature on transmission of T. cruzi through breast-feeding to adequately inform breast-feeding mothers with Chagas disease.
We searched the literature in PubMed (www.ncbi.nlm.nih.gov/pubmed), EMBASE (www.elsevier.com/online-tools/embase), and Google Scholar (http://scholar.google.com/) for all published articles until January 2013, using the terms “breast-feeding” and “Chagas,” “breastfeeding” and “Trypanosoma cruzi,” “milk” and “Chagas,” and “milk” and “Trypanosoma cruzi.” No language, age, or sex restrictions were used. Both animal and human studies were considered. Direct access to some of the older publications was not possible, and information about results and conclusions was obtained from other articles.
As early as 1913, Nattan-Larrier reported finding T. cruzi in the milk of laboratory animals (12). Disko and Krampitz found T. cruzi trypomastigotes in the milk of experimentally infected mice, which was not attributable to contamination of milk with blood. However, they did not subsequently demonstrate infection of suckling mice (13). In 1972, Miles examined the milk of mice in the acute phase of the disease and detected T. cruzi trypomastigotes and antibodies against T. cruzi, but concluded that, experimentally, even in the acute phase of the disease, transmission through breast-feeding was rare (14). In another study, Campos et al. found that nursing mice born to lactating females in the acute phase of the infection were not infected (15). Another study on vertical transmission of T. cruzi among chronically infected laboratory rats did not demonstrate transmission through breast-feeding, and histopathologic examination of the mammary glands of the infected rats did not reveal the parasites (16). More recently, Martins et al. inoculated 15 female mice with Y strain T. cruzi trypomastigote forms a few hours after they gave birth, and breast-feeding of offspring was continued. Despite confirmed infection in female mice, no infection through breast-feeding was documented in the 142 offspring examined (examination of fresh blood by microscopy) (17). Other authors have not been able to confirm experimental transmission through breast-feeding during the acute phase of the disease (18–21), and researchers have hypothesized that maternal antibodies transferred with the milk may play a protective role (14,22).
Studies that examined pasteurization and microwave treatment of human milk to prevent transmission of Chagas disease have demonstrated transmission when human milk contaminated with Y strain trypomastigotes was orally administered to mice. However, such transmission occurred under experimental conditions, not natural breast-feeding, and the milk was artificially contaminated. In 1 experiment, batches of laboratory mice were orally or intraperitoneally inoculated with human milk that was contaminated with T. cruzi trypomastigotes and pasteurized, contaminated with T. cruzi and not pasteurized, or not contaminated with T. cruzi. Only mice that were given contaminated nonpasteurized milk (orally or intraperitoneally) were infected (detected by examination of peripheral blood) (23). In a similar study, mice that received either infected or noninfected microwave-treated milk (63°C, domestic microwave oven 2,450 MHz, 700 W), orally or intraperitoneally, were not infected (negative parasitologic and serologic results), whereas mice that received contaminated milk that had not been microwaved acquired the infection (24).
Studies involving metacyclic trypomastigotes from triatomine feces have found that contaminated milk seems to be an adequate medium (when compared with other types of food and water) for oral transmission of T. cruzi to mice, and this fact has been attributed to its moisture and nutrient content (25). In certain animal experiments, infection through the oral route (not breast-feeding) has been established by using blood trypomastigotes, and the success of this mode of transmission appeared dependent on the size of the inoculum used (26,27). Transmission of T cruzi by breast-feeding is possible in animal models, but oral infections may be difficult to establish unless metacyclic forms of the parasite are involved.
Two reports from 1936 and 1983 describe finding trypomastigotes in the milk of mothers in the acute phase of Chagas disease. Mazza et al. (5) reported transmission through lactation; in the other study, the newborn was not breast-fed (28). However, another publication later indicated that in the study by Mazza et al., the collected milk was contaminated by blood (29). Medina-Lopes reported 2 cases of acute Chagas disease in infants that had been acquired through breast-feeding from mothers in the chronic phase. In 1 of these cases, no parasites were found in the milk, and the source of the infection was postulated to be infected blood because the mother had bleeding nipples. In the other case, congenital, vector-borne, and transfusion-associated transmission were excluded, and transmission was suspected to have occurred through breast-feeding (6,7).
In 1988, Bittencourt et al. were unable to demonstrate transmission of infection through breast-feeding. Samples of milk/colostrum from 78 mothers in the chronic phase of the disease were studied (5 mothers had parasitemia at the time of milk collection). Results of the following were negative: the parasitologic study of all sample-inoculated mice and the serologic tests of serum samples from 97 breast-fed children born free of infection (22).
In 1990, Shikanai-Yasuda et al. published a series of reports of cases of acute Chagas disease, and breast-feeding was considered a possible route of transmission for 2 patients (30). Amato Neto et al. (31) could not document the presence of T. cruzi in the colostrum and breast milk of 40 women with Chagas disease through direct observation, culture, and inoculation. The possibility of using a larger study population and/or more efficient diagnostic techniques was highlighted (31).
Other studies that examined maternal transmission of T. cruzi included breast-feeding as a possible contributing factor, but once again, this mode of transmission could not be demonstrated. In 2004, Rassi et al. found 2 cases of maternal transmission of infection in 2 patients who had also been breast-fed, but this mechanism could not be established, and the infections may have resulted from vertical transmission (32).
The data on transmission of T. cruzi through breast-feeding in humans are scarce; reports are not recent and the findings have several limitations. Additional data on methods used to diagnose infection and exclude other forms of transmission in these studies are summarized in the Table.
In mice, oral transmission of T. cruzi infection through human milk contaminated with trypomastigotes is possible, although natural transmission through breast-feeding has not been clearly demonstrated in recent studies. Infection in laboratory mice acquired after oral or intraperitoneal administration of human milk contaminated with T. cruzi trypomastigotes may be prevented by thermal treatment (pasteurization or microwave treatment at 63°C) of milk, which can inactivate the trypomastigotes. Such treatment of milk may therefore be an option for lactating mothers who have the acute form of the infection or bleeding nipples.
In humans, the oral route is an efficient mode of transmission for T. cruzi, as has been demonstrated in recent outbreaks of infection acquired through contaminated food and fruit juices (33–35). Ingestion of food or drink contaminated with vector feces (containing metacyclic trypomastigotes) or crushed insects is the most likely mode of oral infection (36). The concentration of the ingested inoculum may result in the different clinical manifestations and variations in attack rates reported in outbreaks (34).
Milk appears to be an adequate medium for transmission of T. cruzi because of its moisture and nutrient content and, in the case of human milk, body temperature would also be favorable (the parasite can be destroyed in dry vector feces and by high temperatures) (23,24,36). Despite this, except for some dated cases, in humans, transmission through breast-feeding has not been reported.
A further consideration to account for the relative lack of infections transmitted through breast-feeding is that, if they occur at all, blood-form trypomastigotes would be expected to occur in human milk and not metacyclic trypomastigotes, which are found in the vector. Blood, metacyclic, and culture trypomastigotes are similar in form and structure, but the different forms may have different surface glycoproteins, which are used for cell invasion (17,37). Metacyclic trypomastigotes may have specialized surface molecules (such as gp82, a member of the gp85/ trans-sialidase superfamily, or pepsin-susceptible gp90 isoforms, which make parasites highly invasive against target cells after contact with gastric juice) with functions for mucosal invasion that are not present in blood-form trypomastigotes. The latter, in turn, express other molecules that facilitate dissemination within the host (38–40). Even though trypomastigote forms of the Y strain of T. cruzi, which expresses glycoprotein 82 in metacyclic forms and should have high infectivity, were used in some experiments, transmission through breast-feeding could not be demonstrated. Blood-form trypomastigotes may therefore not be as efficient as metacyclic trypomastigotes in establishing mucosal invasion of the gastrointestinal tract (partly because of their decreased capacity to migrate through the gastric mucin layer), even though oral infections with blood trypomastigotes have been demonstrated experimentally with the possibility of infection depending on amount of inoculum. Peptic digestion may also destroy some of the infective forms, mainly blood trypomastigotes (40).
On the basis of the data examined, oral infection through breast-feeding does not appear to be an efficient mode of transmission for T. cruzi. In humans, milk contamination by T. cruzi has been described only in isolated cases. In the acute phase, patent parasitemia occurs, but T. cruzi has been demonstrated in breast milk only in 1 case (transmission did not occur because the newborn was not breast-fed) (27). In the chronic phase, parasitemia is usually low grade and tends to fluctuate. A couple of cases of acute infection in breast-feeding infants of mothers in the chronic phase have been reported, but transmission may have resulted from the ingestion of blood from bleeding nipples (6,7). In older studies, it is not always clear how accurately vertical and other modes of transmission had been excluded with the diagnostic tools available at the time, and in other cases, breast-feeding is contemplated only as a possible route of infection. Many of the studies reported were performed some years ago, and current novel techniques, such as PCR, may aid in detecting low parasite loads. On the other hand, new techniques may even yield equivocal results (e.g., because of the presence of infected blood but not true contamination of milk by T. cruzi) if contamination with infected blood were below the level of detection found with other methods. In humans, transmission of T. cruzi through maternal milk (not contaminated with infected blood) may not be considered clearly proven.
As previously postulated in laboratory studies, in humans, a combination of several factors likely account for the low efficiency of breast-feeding as a possible mode of transmission of T. cruzi infection. These include the low number of trypomastigotes ingested by the lactating infant, the biologic forms and strains of T. cruzi involved, the passage of protective maternal antibodies, and the destruction of some parasites by gastric juice.
A limitation of this review was that some of the articles dated back several decades and were not readily available. Some information about these studies was obtained from other articles.
Published studies on the transmission of T. cruzi through breast-feeding are scarce. After reviewing the various studies, and given the demonstrated benefits of breast-feeding (especially in lower income disease-endemic countries where a safe and inexpensive alternative may not be available), we conclude that discontinuing or interrupting breast-feeding by mothers with chronic Chagas disease is not recommended. If the mother has fissures or bleeding nipples, temporary discontinuation of breast-feeding may be recommended, although thermal treatment (pasteurization or microwaving) of expressed milk before feeding the infant may be a safe alternative. When mothers are in the acute phase of the disease (an infrequent situation that will occur almost exclusively in disease-endemic countries) or have reactivated disease (resulting from immunosupression, in which circulating parasitemia level may be high), breast-feeding may pose a risk for the infant. The benefits of using thermally treated expressed milk should be considered on an individual basis. To avoid any possibility of transmission, human milk banks should exclude mothers with Chagas disease as donors. As other modes of transmission of Chagas disease come under control (vector-borne transmission and transmission through infected blood/organs), further studies are needed on the possibility of transmission through breast-feeding, as this could occur even in countries where the disease is nonendemic.
Dr Norman is a consultant in tropical medicine and parasitology at the Ramón y Cajal Hospital in Madrid, Spain. Her research interests are neglected tropical diseases and emerging pathogens.
Dr López-Vélez directs the Tropical Medicine and Parasitology Unit of the Ramón y Cajal Hospital and is associate professor of medicine at Alcalá University in Madrid, Spain. His research interests include Chagas disease and other aspects of immigrant medicine.
We thank the staff at the Tropical Medicine Unit, Ramón y Cajal Hospital, for technical assistance.
This work was supported by the Spanish Ministry of Science and Innovation and the Instituto de Salud Carlos III within the Network of Tropical Diseases Research RICET RD06/0021/0020.
- Organización Panamericana de la salud. Estimación cuantitativa de la enfermedad de Chagas en las Américas. OPS/HDM/CD/425–06. Montevideo (Uruguay); 2006.
- Oliveira I, Torrico F, Muñoz J, Gascon J. Congenital transmission of Chagas disease: a clinical approach. Expert Rev Anti Infect Ther. 2010;8:945–56.
- Brutus L, Castillo H, Bernal C, Salas NA, Schneider D, Santalla JA, Detectable Trypanosoma cruzi parasitemia during pregnancy and delivery as a risk factor for congenital Chagas disease. Am J Trop Med Hyg. 2010;83:1044–7.
- Carlier Y, Torrico F, Sosa-Estani S, Russomando G, Luquetti A, Freilij H, Congenital Chagas disease: recommendations for diagnosis, treatment and control of newborns, siblings and pregnant women. PLoS Negl Trop Dis. 2011;5:e1250.
- Mazza S, Montaña A, Benitez C, Janzi EC. Transmisión de Schizotrypanum cruzi al niño por leche de la madre con enfermedad de Chagas. Mis Est Patol Reg Arg (M.E.P.R.A) 1936; 28: 41–6. In: Medina-Lopes MD, Macedo V. Trypanossoma cruzi no colostro humano. Rev Soc Bras Med Trop. 1983;16:170.
- Medina-Lopes MD. Transmissao materno-infantil da doença de Chagas. Brasilia, 1983 (Dissertaçao de Mestrado-Nucleo de Medicina Tropical e Nutriçao da Universidade de Brasilia). In: Bittencourt AL. Possible risk factors for vertical transmission of Chagas’ disease. Rev Inst Med Trop Sao Paulo. 1992;34:403–8 .
- Medina-Lopes M das D. Transmissao do. Trypanosoma cruzi em um caso durante o aleitamento, em área nao endémica. Rev Soc Bras Med Trop. 1988;21:151–3.
- Carlier Y, Truyens C. Maternal-fetal transmission of Trypanosoma cruzi. In: Telleria J, Tibayrenc M, editors. American trypanosomiasis: Chagas disease—one hundred years of research. New York: Elsevier Inc.;2010.pp. 539–82.
- United Nations Children’s Fund (UNICEF). Infant and young children feeding [cited 2013 Aug 9]. 2012 May 25. www.unicef.org/nutrition/index_breastfeeding.html
- Schijman AG, Altcheh J, Burgos JM, Biancardi M, Bisio M, Levin MJ, Aetiological treatment of congenital Chagas' disease diagnosed and monitored by the polymerase chain reaction. J Antimicrob Chemother. 2003;52:441–9.
- Altcheh J, Moscatelli G, Moroni S, Garcia-Bournissen F, Freilij H. Adverse events after the use of benznidazole in infants and children with Chagas disease. Pediatrics. 2011;127:e212–8.
- Nattan-Larrier L. Sur le passage des trypanosomes dans le lait. Rev Pathol Comp. 1913;13:282–5.
- Disko R, Krampitz HE. Das Auftreten von Trypanosoma cruzi in der Milch infizierter Mause. Z Tropenmed Parasitol. 1971;22:56–66 .
- Miles MA. Trypanosoma cruzi–milk transmission of infection and immunity from mother to young. Parasitology. 1972;65:1–9.
- Campos R, Pinto PLS, Moreira AA, Amato Neto V, Duarte MI, de SantÁna EJ, Experimental study on the transmission of Chagas´ disease by milk [in Portuguese]. Rev Hosp Clin Fac Med Sao Paulo. 1988;43:146–7 .
- Moreno EA, Quintero AC, Alarcón ME, Lugo de Yarbuh A, Moreno SC, Araujo S, Investigaciones sobre la transmisión vertical de Trypanosoma cruzi en ratas Wistar crónicamente infectadas [cited 2012 Oct 3]. Boletín de Malariología y Salud Ambiental. 2006;46. http://www.scielo.org.ve/scielo.php?script=sci_arttext&pid=S1690-46482006000200007&lng=es
- Martins LP, Castanho RE, Nogueira AB, Silva OT, Gusmao AS. Incidence of Trypanosoma cruzi transmission through breastfeeding during acute experimental Chagas disease. Braz J Infect Dis. 2011;15:116–8 .
- Fine J. Is trypanosomiasis in the lactating rat transmitted to the suckling young? Ann Trop Med Parasitol. 1933;27:180–1.
- Werner H. Uber die Frage der placentaren Trypanosomen Infektionen und Ubertragung von Trypanosomen und Antikorpern durch die Milch auf das Neugeborene. Zeitschriff Tropenmed Parasitol. 1954;5:422–42.
- Pinto PLS, Campos R, Santana EJ, Moreira AAB, Amato-Neto V, Duarte MYS, Estudo experimental sobre a transmissão da doença de Chagas por meio do leite. Rev Inst Med Trop Sao Paulo. 1989;31(Suppl.7):S15.
- Moreno EA, Rivera IM, Moreno SC, Alarcón ME, Lugo-Yarbuh A. Transmisión vertical de Trypanosoma cruzi en ratas Wistar durante la fase aguda de la infección. Invest Clin. 2003;44:241–54 .
- Bittencourt AL, Sadigursky M, Da Silva AA, Menezes CA, Marianetti MM, Guerra SC, Evaluation of Chagas disease transmission through breast-feeding. Mem Inst Oswaldo Cruz. 1988;83:37–9.
- Ferreira CS, Martinho PC, Amato Neto V, Cruz RR. Pasteurization of human milk to prevent transmission of Chagas disease. Rev Inst Med Trop Sao Paulo. 2001;43:161–2 and.
- Santos Ferreira C, Amato Neto V, Gakiya E, Bezerra RC, Alarcón RS. Microwave treatment of human milk to prevent transmission of Chagas disease. Rev Inst Med Trop Sao Paulo. 2003;45:41–2.
- Calvo-Méndez ML, Nogueda-Torres B, Alejandre-Aguilar R, Cortés-Jiménez M. Experimental Trypanosoma cruzi infection via contaminated water and food. Rev Latinoam Microbiol. 1994;36:67–9 .
- Araujo RGM, Nery ACS, Bueno LM, Turolo da Silva O, Silva de Gusmão A. Infecçao experimental do Trypanosoma cruzi utilizando a via oral. Rev Soc Bras Med Trop. 1998;31(Suppl III):50–1.
- Lima CMP, Camandaroba ELP, Andrade SG. Influencia da cepa do Trypanosoma cruzi na infecçao experimental de camundongos pela via digestiva. Rev Soc Bras Med Trop. 2000;33(Suppl II):110–1.
- Medina-Lopes MD, Macedo V. Trypanossoma cruzi no colostro humano. Rev Soc Bras Med Trop. 1983;16:170.
- Jörg ME. Transmission of Trypansoma cruzi via human milk [in Spanish]. Rev Soc Bras Med Trop. 1992;25:83 .
- Shikanai-Yasuda MA, Lopes MH, Tolezano JE, Umezawa E, Amato Neto V, Barreto AC, Acute Chagas´ disease: transmission routes, clinical aspects and response to specific therapy in diagnosed cases in an urban centre [in Portuguese]. Rev Inst Med Trop Sao Paulo. 1990;32:16–27.
- Amato Neto V, Matsubara L, Campos R, Moreira AA, Pinto PL, Faccioli R, Trypanosoma cruzi in the milk of women with chronic Chagas disease [in Portuguese]. Rev Hosp Clin Fac Med Sao Paulo. 1992;47:10–1 .
- Rassi A, Amato Neto V, Rassi GG, Amato VS, Rassi Júnior A, Luquetti AO, A retrospective search for maternal transmission of Chagas infection from patients in the chronic phase [in Portuguese]. Rev Soc Bras Med Trop. 2004;37:485–9.
- Nóbrega AA, Garcia MH, Tatto E, Obara MT, Costa E, Sobel J, Oral transmission of Chagas disease by consumption of Açaí palm fruit, Brazil. Emerg Infect Dis. 2009;15:653–5.
- Alarcón de Noya B, Díaz-Bello Z, Colmenares C, Ruiz-Guevara R, Mauriello L, Zavala-Jaspe R, Large urban outbreak of orally acquired acute Chagas disease at a school in Caracas, Venezuela. J Infect Dis. 2010;201:1308–15.
- Shikanai-Yasuda MA, Barbosa Carvalho N. Oral transmission of Chagas disease. Clin Infect Dis. 2012;54:845–52.
- Miles MA. Orally acquired Chagas disease: lessons from an urban school outbreak. J Infect Dis. 2010;201:1282–4.
- Yoshida N. Molecular basis of mammalian cell invasion by Trypanosoma cruzi. An Acad Bras Cienc. 2006;78:87–111.
- Yoshida N. Molecular mechanisms of Trypanosoma cruzi infection by oral route. Mem Inst Oswaldo Cruz. 2009;104(Suppl 1):101–7.
- Hoft DF. Differential mucosal infectivity of different life stages of Trypanosoma cruzi. Am J Trop Med Hyg. 1996;55:360–4 .
- Cortez C, Yoshida N, Bahia D, Sobreira TJP. Structural basis of the interaction of a Trypanosoma cruzi surface molecule implicated in oral infection with host cells and gastric mucin. PLoS ONE. 2012;7:e4215.
Suggested citation for this article: Norman FF, López-Vélez R. Chagas disease and breast-feeding. Emerg Infect Dis [Internet]. 2013 Oct [date cited]. http://dx.doi.org/10.3201/eid1910.130203
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