Figures
Citation: Valdez-Tah A, Ibarra-Cerdeña CN (2021) Call to action: A literature review of Chagas disease risk in California 1916–2018. PLoS Negl Trop Dis 15(2): e0009035. https://doi.org/10.1371/journal.pntd.0009035
Editor: Helton da Costa Santiago, Universidade Federal de Minas Gerais, BRAZIL
Published: February 25, 2021
Copyright: © 2021 Valdez-Tah, Ibarra-Cerdeña. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: AVT thanks to the programs of Comexus-Fulbright Visiting Scholar and UC Mexus-Conacyt, both in 2016-17 and a second-year granted by UC Mexus-Conacyt from 2017-18, for a postdoctoral stay at the Department of Anthropology-UC Irvine. CNIC acknowledges financial support from the Secretaría de Educación Pública-Cinvestav (Project: FIDSC2018/160). The funders had no role in study design, data collection, and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Human Chagas disease (CD), caused by the Trypanosoma cruzi infection, is considered nonendemic in the United States of America [https://www.cdc.gov/parasites/chagas/gen_info/detailed.html#intro; consulted March 29, 2020], assuming that this chronic affection’s epidemiology is different from that of Latin American countries. The attention is mostly focused on blood bank screening, organ donation, and vertical (mother to child) transmission [1]. This approach can overlook the potential for autochthonous transmission of T. cruzi, particularly in the light of a recent acknowledgment about the role that vectorial transmission may have on the CD in the USA. A low awareness among physicians about CD risk besides its migratory origin can contribute to an existing underreporting rate, thus masking the accurate estimation of CD burden in the USA [2].
Cases of autochthonous infection in the USA are not accurately tracked since it is only mandatory to report it in seven states, i.e., Arizona, Arkansas, Louisiana, Mississippi, Tennessee, Texas, and Massachusetts [3]. However, as it occurs in Latin America, where the index of suspicion is much higher, acute T. cruzi infections in immunocompetent individuals can pass undiagnosed and undetected among residents [4]. In the USA, 238,091 cases are estimated as of 2012 [5]. This analysis highlighted the role of Latin immigrants in the CD burden, with California being the state with the highest estimated number of cases.
Although imported CD cases are undoubtedly a matter of concern, there are also environmental conditions leading to autochthonous infections [6]. New encounters between humans and triatomine bugs are often associated with the destruction of or invasion into vertebrate hosts’ habitats, compromised housing structures, or both. Disruption of host burrows provokes the bugs to seek new refugees, and their attraction to artificial light often leads them to nearby human dwellings [7]. Multiple publications have highlighted the southern USA as an area where autochthonous infection occurs, mainly because of the high proportion of impoverished residents living in substandard housing infested by triatomines [7–10].
It is essential to improve our knowledge of T. cruzi infection risk components because there are parasite reservoirs among wildlife species and vectors living in contact with humans [11]. This is especially found in less-studied regions such as California, where the epidemiological, parasitological, and entomological patterns of T. cruzi transmission might resemble those of other endemic areas. Surveillance of infection prevalence among local populations of Triatominae is critical for accurate assessment of the public health risk. We attempt to contribute to this with an extensive historical literature review of records of autochthonous T. cruzi and human-related data for CD in California. This method of review provides a contemporary account of this topic’s breadth of knowledge. There has been no recent review of this theme at the state level to the best of our knowledge, as has already been conducted in some other states, such as Texas [12].
We summarized a historical account of triatomines reports, infection with T. cruzi in triatomines, mammals and humans (CD), and human-triatomine interaction for California counties. We found 62 articles published between 1916 and 2018 encompassing 35 countries (Table 1), mostly from the greater Los Angeles area, metropolitan San Diego, Sierra Nevada’s foothills, and the Morongo Basin (Fig 1A and 1B).
(A) County-level distribution of the literature reviewed of autochthonous Trypanosoma cruzi transmission and Chagas disease in California 1916–2017; (B) Published reports of county-level abundance distribution of Triatomine species; (C) Published reports of county-level incidence of natural infection of T. cruzi among triatomines and mammals; and (D) Published reports of the distribution of human exposure (manifested as bites) to triatomines, reported at the county level. Counties in white are more likely regions with no reports. Geographic boundaries were obtained from the 2016 TIGER/Line shapefiles prepared by the United States Census Bureau. TIGER/Line Shapefiles (machine-readable data files): Current County and Equivalent National Shapefile. 2016.
Between 1916 and 1930, T. cruzi was reported for the first time in the USA in San Diego County. The Los Angeles and San Diego counties account for up to 1,000 and 2,500 records, respectively. The T. cruzi infection prevalence was estimated for 34 of 56 localities in 13 counties (Fig 1C), ranging from 9% to 100% among triatomines and 0.62% to 100% among six wild mammals and dogs (Tables 2 and 3). The most abundant triatomine species in California is Triatoma protracta (98% of the 4,951 records), followed by Triatoma rubida and Paratriatoma hirsuta.
The first report of domestic incidence was recorded in the 1940s. In 38.8% of the publications reporting collection site for triatomines (19/49), at least one was collected inside human habitation. Domestic triatomine incidence was associated with dispersion from the vicinity of residences in semirural, canyon, or mountain-foothill areas (involved removal of mammal hosts and triatomine nest); during the monsoon, houselights are attractive to triatomines, especially while mating and/or seeking blood-meals.
Twenty-two publications reported 164 triatomine bites and ensuing anaphylactic reactions among residents of 11 California counties (Fig 1D), 80% of them taking place inside dwellings. Tuolumne and Los Angeles counties reported the largest number of cases. At least four patients with Romaña signs have been reported since 1964.
In publications around the 1950s, the bulk of domestic triatomines reports and human exposure came from residents’ testimonies, from Kern, Riverside, Fresno, and San Diego counties, and from descriptions of clinical cases (S1 Text). Although in California, CD is not mandatory to report. In 2008 and 2010, the Californian Vector-Borne Department Section recorded reports of vector inside homes and bites. A different perspective of this interaction are the 24 distinct common names in English, Spanish, and a Native American language for the insect found across the literature. This might suggest it’s a more common interaction than previously thought. This has been indicated by ethno-entomology studies and reports among indigenous peoples within the CD endemic areas (Table 4) [38].
Research on human-triatomine interaction in California involved two surveys conducted 50 years apart. The State Department of Health conducted a study in 1962 in Mariposa and Tuolumne counties that recorded more than 101 bite cases. In 2012, Los Angeles’ residents reported bites resembling the swelling (called Chagoma) produced by triatomines, and rural residents in Santa Barbara were found with immunoglobulin G (IgG) against the T. protracta saliva. Along with this, human blood-meals have been found in free-roaming triatomines [47].
In 1982, the first autochthonous human case of CD was reported for California in Tuolumne county: a 50-year-old woman from Lake Don Pedro [48]. Thereafter a broad serological survey, the only type in the states’ history, was conducted among three groups of residents, revealing antibodies in 2.5% to 0.7% of the population. The second case was reported in Simi Valley in 2016 and discovered through a routine screening test in blood-donation, a 19-year-old white male, locally born and raised, with no acknowledged bite but who had presumably been exposed during outdoor activities [49].
This review of the autochthonous transmission of T. cruzi in California is the first one in more than 50 years. A temporal analysis of the publications shows an early scientific effort to compare some endemic areas; 80% of the articles were published before the early 1980s (Table 1). Amid the current debate about autochthonous transmission in the Southern USA, evidence of an ongoing domestic cycle and T. cruzi human infection has been found [7,9]. Our review shows evidence that the current assessment of public health risk among California residents is mostly based on outdated and is nonpublicly acknowledged.
Regarding the low number of human CD cases in California, our literature review shed light on a set of circumstances that have difficulted the report of official autochthonous cases. First, human-triatomine interaction was assessed in terms of risk of anaphylaxis—common in the Southwest—but not for T. cruzi transmission. Only one bite case was followed up by a screen test. A triatomine bite is nonreactive among 85% to 95% of the cases, reducing the chances of seeking medical care and suspicion of T. cruzi infection [50]. Secondly, there is no routine screening program at the primary care level in California, and mandatory blood-donor screening is not adequate for capturing T. cruzi infection among both Latino immigrants and residents [1]. Current efforts in this sense target Latino immigrants. Therefore, as potential autochthonous cases, individuals might not meet risk criteria about the country of birth, ethnicity, and a history of travel to an endemic country. The lack of specifically assessed locally acquired infection and large-scale serological surveys might have failed to detect autochthonous cases. Lastly, physicians might be unaware of the local risk and fail to encourage patients to get tested [2]. Health providers have underestimated CD cases because they believe it to be “a South American problem,” leading to misdiagnosis [51]. In patients’ cases, they may decline to seek healthcare if feeling healthy during the CD indeterminate phase (nonsymptomatic), when having limited access to healthcare, i.e., among the low-income and homeless individuals, or when choosing to avoid a perceived stigma [52]. In the USA, mainstream stereotypes are that CD is a “tropical exotic” disease prevalent among so-called “illegal aliens” and it is associated with poverty.
Compared to what occurs in Latin America, a generally higher housing standard in the USA has been a main contributor for the low incidence of reports of domestic triatomines and human CD [47]. However, both the historical domestic incidence and recent data documented here suggest that residences might harbor vector colonies [53]. While triatomine oviposition, nymphal development, and T. cruzi infection may occur outdoors, we believe that T. cruzi transmission in California might have some similarities with Texas, and Mexican endemic triatomines are not domestic but disperse from surrounding areas. Human-triatomine interaction also occurs outdoors due to the free-roaming vector that feeds on human hosts given the opportunity [7,10]. In California, outdoor activities within forests and natural parks are widely popular, for instance, during 2018, a total of 269,055 hunting licenses were granted, and campsite attendance reached 7,265,525 overnight stays.
Socioenvironmental changes of the last five decades in California have not been followed by research on their effects on human-triatomine interaction and T. cruzi transmission. Loss of habitat and human settlements (and increasing numbers of pets) have led to an increasing encroachment upon the natural habitat of triatomines and their mammal hosts. This might raise the chances of triatomine domestic incidence due to their flexibility in habitat and host requirements, including dogs and other mammals (rodents, opossums, raccoons, etc.). Examples of Triatoma sanguisuga in Louisiana came after the disruption of hurricane Katrina; there was a change of infestations in human dwellings [53].
County-level maps of reports only partially reflect the T. cruzi distribution in California. This is due to the scarcity/absence of records in some areas and early discovery of the association triatomine-woodrat that might be biased to the field research. An ecological niche modeling approach of the geographic distribution of vector species indicates favorable host habitat in many unsurveyed regions of California [54].
Our review in California highlights that a critical and accurate assessment of the public health risk for T. cruzi and CD needs research/intervention on the:
- Spatial modeling of pattern occurrences of triatomine and T. cruzi infection for further robust analysis on habitat suitability and risk due to socioenvironmental changes;
- Dynamics and mechanisms of transmission: spatial variation of triatomine activity, infection levels and their reliance on humans-blood, dynamics of dispersal flights and free-roaming triatomines feeding habits;
- Identification of sylvatic, synanthropic, and domestic (especially dogs) animal blood-sources and determination of infection variability;
- Identification of the T. cruzi circulating strains and an analysis of the parasite’s genetic variation;
- Large-scale systematic programs of active surveillance, rigorous population-based data collection, and comprehensive assessment to determine infection prevalence and morbidity to identify factors that might inform policy and program-driven actions, especially among the vulnerable (impoverished residents living in substandard housing);
- Improvement of local knowledge local about epidemiology and ecology and the criteria for public health promotion to raise awareness among residents, physicians, and clinicians;
- Active screening of heart failure patients, hunters/campers, and pregnant women; and
- Continuing medical education programs on diagnosis and treatment among physicians.
Supporting information
S1 Text. Domestic and peri-domestic reports of human bites and human exposure to vectors.
https://doi.org/10.1371/journal.pntd.0009035.s001
(DOCX)
Acknowledgments
AV-T thanks Dr. Leo Chavez, who hosted her during her postdoctoral stay at UC Irvine. We would like to thank the Vector Control of the California Department of Public Health for the Triatoma database submitted for testing during February 2008 and July 2012. Thanks to Natalia Heredia and Erick de la Barrera for the English edition.
References
- 1. Bern C, Messenger LA, Whitman JD, Maguire JH. Chagas Disease in the United States: a Public Health Approach. Clin Microbiol Rev. 2019;27;33(1):e 00023–19. pmid:31776135
- 2. Stimpert KK, Montgomery SP. Physician awareness of Chagas disease, USA. Emerg Infect Dis. 2010;16(5): 871–872. pmid:20409389
- 3. Bennett C, Straily A, Haselow D, Weinstein S, Taffner R, Yaglom H, et al. Chagas Disease Surveillance Activities—Seven States, 2017. MMWR Morb Mortal Wkly Rep. 2018;67: 738–741. pmid:29975678
- 4. Castro Y, Marcus R. Epidemiology of Chagas disease in the USA: high-risk patient populations for screening. Curr Trop Med Rep. 2019;6: 8–12.
- 5. Manne-Goehler J, Chukwuemeka AU, Montgomery SP, Wirtz VJ. Estimating the burden of Chagas Disease in the United States. PLoS Negl Trop Dis. 2016;10: e0005033. pmid:27820837
- 6. Shender L, Lewis M, Rejmanek D, Mazet J. Molecular diversity of Trypanosoma cruzi detected in the vector Triatoma protracta from California, USA. PloS Negl Trop Dis. 2016a;10: e0004291. pmid:26797311
- 7. Lynn MK, Bossak BH, Sandifer PA, Watson A, Nolan MS. Contemporary autochthonous human Chagas disease in the USA. Acta Trop. 2020;205: 105361. pmid:32006523
- 8. Garcia MN, Aguilar D, Gorchakov R, Rossmann SN, Montgomery SP, Rivera H, et al. Case report: evidence of autochthonous Chagas disease in southeastern Texas. Am J Trop Med Hyg. 2015;92: 325–330. pmid:25371187
- 9. Curtis-Robles R, Zecca IB, Roman-Cruz V, Carbajal ES, Auckland LD, Flores I, et al. Trypanosoma cruzi (Agent of Chagas Disease) in Sympatric Human and Dog Populations in "Colonias" of the Lower Rio Grande Valley of Texas. Am J Trop Med Hyg. 2017 96(4): 805–814. pmid:28167589
- 10. Beard CB, Pye G, Steurer FJ, Rodriguez R, Campman R, Peterson AT, et al. Chagas disease in a domestic transmission cycle, southern Texas, USA. Emerg Infect Dis. 2003;9: 103–105. pmid:12533289
- 11. Georgieva AY, Gordon ERL, Weirauch C. Sylvatic host associations of Triatominae and implication for Chagas disease reservoirs: a review and new host records based on archival specimens. PeerJ. 2017. 5: e3826, pmid:28948106
- 12. Garcia MN, Woc-Colburn L, Aguilar D, Hotez PJ, Murray KO. Historical Perspectives on the Epidemiology of Human Chagas Disease in Texas and Recommendations for Enhanced Understanding of Clinical Chagas Disease in the Southern United States. PLoS Negl Trop Dis. 2015;9: e0003981. pmid:26540273
- 13. Wood SF, Wood FD. Nocturnal aggregation and invasion of homes in southern California by insect vectors of Chagas’ disease. J Econ Entomol. 1964b;57: 775–776.
- 14. Wood SF. The distribution of California insect vectors harboring Trypanosoma cruzi Chagas. Bull S Calif Acad Sci. 1950b;49(3): 98–100.
- 15. Wood S. Trypanosoma cruzi: new foci of enzootic Chagas’ disease in California. Exp Parasitol. 1975f;38: 153–160. pmid:809291
- 16. Stevens L, Dorn PL, Hobson J, de la Rua NM, Lucero DE, Klotz JH, et al. Vector blood meals and Chagas disease transmission potential, United States. Emerg Infect Dis. 2012;18:646–649. pmid:22469536
- 17. Hwang WS, Guanyang Z, Maslov D, Weirauch C. Short report: infection rates of Triatoma protracta (Uhler) with Trypanosoma cruzi in Southern California and molecular identification of trypanosomes. Am J Trop Med Hyg. 2010;83: 1020–1022. pmid:21036830
- 18. Klotz SA, Dorn PL, Klotz JH, Pinnas JL, Weirauch C, Kurtz JR, et al. Feeding behavior of triatomines from the southwestern United States: An update on potential risk for transmission of Chagas disease. Acta Trop. 2009;111: 114–118. pmid:19524078
- 19. Mehringer PJ, Wood SF. A resampling of wood rat houses and human habitations in Griffith Park, Los Angeles, for Triatoma protracta and Trypansoma cruzi. Bull S Calif Acad Sci. 1958;52: 46–56.
- 20. Ryckman RE. Triatoma protracta infected with Trypanosoma cruzi at Riverside, California (Hemiptera: Reduviidae). Pan-Pac Entomol. 1952a;28(1): 58.
- 21.
Vector-Borne Sector, California Department of Public Health; 2018. Database: Triatoma submitted for testing. Available from requesting VBS California Department of Public Health.
- 22. Sjogren RD, Ryckman RE. Epizootiology of Trypanosoma cruzi in southwestern North America. Part VIII: Nocturnal flights of Triatoma protracta (Uhler) as indicated by collections at black light traps (Hemiptera: Reduviidae: Triatominae). J Med Entomol. 1966;3: 81–92. pmid:5941571
- 23. Wood SF. Conenose bug annoyance in Griffith Park in 1958. Bull So Calif Acad Sci. 1960b;59: 50–52.
- 24. Augustson GF, Wood SF. Notes on Californian mammals ecto-Parasites from the Sierra Nevada Hills of Madera County. Bull So Calif Acad Sci. 1953;52: 46–56.
- 25. Wood SF. Conenose bug annoyance and Trypanosoma cruzi Chagas in Griffith Park, Los Angeles. Bull So Calif Acad Sci. 1953;52(3): 105–109.
- 26. Wood S. An Additional California Locality for Trypanosoma cruzi Chagas in the Western Cone-Nosed Bug, Triatoma protracta (Uhler). J Parasitol. 1944a;30(3): 199.
- 27. Wood SF. Observations on vectors of Chagas’ disease in the United States. I. California. Bull So Calif Acad Sci. 1942c;41: 61–69.
- 28. Wood SF, Wood FD. Ecological relationships of Triatoma p. protracta (Uhler) in Griffith Park, Los Angeles, California. Pac Insects. 1967;9: 537–550.
- 29. Wood SF. Bug annoyance in the Sierra Nevada foothills of California. Bull So Calif Acad Sci. 1951a;50: 106–112.
- 30. Wood SF, Anderson RC. Conenose bugs triatoma) visit unoccupied boy’s camp in Los Angeles. J Med Entolmol. 1965;1: 347–348. pmid:14280486
- 31. Ryan CP, Hughes E, Howard EB. American Trypanosomiasis (Chagas’ Disease) in a striped skunk. J Wildl Dis. 1985;21: 175–176. pmid:3923215
- 32. Wood SD, Hughes H. A mammal host of Trypanosoma cruzi Chagas in Griffin Park, Los Angeles, California. Bull So Calif Acad Sci. 1953;52: 103–104.
- 33. Wood FD. Natural and experimental infection of Triatoma protracta Uhler and mammals in California with American human trypanosomiasis. Am Jour Trop Med. 1934a;14: 497–517.
- 34. Wood FD, Wood SF. Occurrence of haematozoa in some California birds and mammals. J Parasitol. 1937;23: 197–201.
- 35. Wood SF. Mammal blood parasite records from southwestern United States and Mexico. J Parasitol. 1952a;38: 85–86.
- 36. Wood SF. Blood parasites of mammals of the California Sierra Nevada foothills, with special reference to Trypanosoma cruzi and Hepatozoon leptosoma sp. n. Bull So Calif Acad Sci. 1962;61: 161–176.
- 37. Navin TR, Roberto RR, Juranek DD, Limpakarnjanarat K, Mortenson EW, Clover JR, et al. Human and sylvatic Trypanosoma cruzi infection in California. AJPH. 1985;75: 366–369. pmid:3919598
- 38. Costa-Neto EM. The use of insects in folk medicine in the State of Bahia, Northeastern Brazil, with notes in insects reports elsewhere in Brazilian folk medicine. Hum Ecol. 2002;30: 245–263.
- 39. Kofoid CA, McCulloh I. On Trypanosoma triatomae, a new flagellate from a hemipteran bug from the nests of the wood rat Neotoma fuscipes. Univ California Publ Zool. 1916;16: 113–126.
- 40.
Kofoid y Donat 1933b. South American Trypanosomiasis of the human type—occurrence in mammals in the United States. California and Western Medicine. 1933b;38: 245–249.
- 41. Wood SD, Wood FD. New locations for Chagas’ trypanosome in California. Bull So Calif Acad Sci. 1964a;63: 104–111.
- 42. Wood SF. Conenose bug (Triatoma) annoyance and Trypanosoma cruzi in southwestern nationaI monuments. Bull So Calif Acad Sci. 1953b;52: 57–60.
- 43. Walsh JD, Jones JP. Public health significance of the cone-nosed bug, Triatoma protracta (Uhler), in the Sierra Nevada foothills of California. Calif Vector Views. 1962;9: 33–38.
- 44. Swezey R. Kissing bug bite in Los Angeles. Arch Intern. 1963;112: 977–980. pmid:14065009
- 45. Scott K. Ken Scott catches the "kissing bug". PCO News. 1963;23: 17.
- 46. Dolhun EP, Antes AW. Case report: a case of cardboard boxes likely facilitating the biting of a patient by Trypanosoma cruzi-infected triatomine bugs. Am J Trop Med Hyg. 2016;95: 1115–1157. pmid:27601526
- 47. Klotz SA, Schmidt JO, Dorn PL, Ivanyi C, Sullivan KR, Stevens L. Free-roaming kissing bugs, vectors of Chagas disease, feed often on humans in the Southwest. Am J Med. 2014b;127: 421–426. pmid:24398362
- 48. Schiffler R, Mansur G, Navin T, Limpakarnjanarat K. Indigenous Chagas’ disease (American trypanosomiasis) in California. JAMA. 1984;251: 2983–2984. pmid:6425516
- 49. Hernandez S, Flores CA, Viana GM, Sanchez DR, Traina MI, Meymandi SK. Autochthonous transmission of Trypanosoma cruzi in Southern California. Open Forum Infect. 2016;20: pmid:28018928
- 50. Wood SF. Reaction of man to the feeding of Triatoma protracta (Hemiptera: Reduviidae). National Pest Control Operator News. 1975a;35: 19–21.
- 51. Friedman S, Parks E, Yasmin S. Hidden threat: the kissing bug and Chagas disease. NBC 5 Dallas-Fort Worth. 2016 [Cited 2018 Jan 27]. Available from: http://www.nbcdfw.com/investigations/Hidden-Threat-The-Kissing-Bug-and-Chagas-Disease 345192802.html.
- 52. Ingber A, Garcia MN, Leon J, Murray KO. Chagas disease Knowledge and Risk Behaviors of the homeless population in Houston, TX. J Racial Ethn Health Disparities. 2018;5: 229–234. pmid:28567616
- 53. Dorn P, Perniciaro L, Yabsley M, Roellig D, Balsamo G, Diaz J. Autochthonous transmission of Trypanosoma cruzi, Louisiana. Emerg Infect Dis. 2007;13: 605–607. pmid:17553277
- 54. Ibarra-Cerdeña CN, Sanchez-Cordero V, Townsend P Ramsey JM. Ecology of North American triatominae. Acta Trop. 2009;110: 178–186. pmid:19084490