Volume 16, Number 2—February 2010
Using Museum Collections to Detect Pathogens
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|EID||Pinto CM, Baxter BD, Hanson JD, Méndez-Harclerode FM, Suchecki JR, Grijalva MJ, et al. Using Museum Collections to Detect Pathogens. Emerg Infect Dis. 2010;16(2):356-357. https://dx.doi.org/10.3201/eid1602.090998|
|AMA||Pinto CM, Baxter BD, Hanson JD, et al. Using Museum Collections to Detect Pathogens. Emerging Infectious Diseases. 2010;16(2):356-357. doi:10.3201/eid1602.090998.|
|APA||Pinto, C. M., Baxter, B. D., Hanson, J. D., Méndez-Harclerode, F. M., Suchecki, J. R., Grijalva, M. J....Bradley, R. D. (2010). Using Museum Collections to Detect Pathogens. Emerging Infectious Diseases, 16(2), 356-357. https://dx.doi.org/10.3201/eid1602.090998.|
To the Editor: Natural history museum collections have evolved in recent years to meet the challenges of current and future interdisciplinary scientific studies. Many natural history museums have built tissue collections and made digital information (e.g., photographs, publications, geographic coordinates) freely available on the Internet. These collections provide endless opportunities to conduct studies, including temporal and spatial surveys of emerging and reemerging pathogens (1). We report an example of a museum collection being useful in detecting Trypanosoma cruzi, the etiologic agent of Chagas disease, in the southern plains woodrat (Neotoma micropus) in southern Texas. This finding is of interest in the epidemiology of Chagas disease because the climatic characteristics and demographics of the region are similar to areas in Latin America where Chagas disease is an important zoonotic agent that infects ≈20 million persons (2).
Tissue samples from N. micropus woodrats archived in the Natural Science Research Laboratory at the Museum of Texas Tech University were evaluated for T. cruzi DNA by PCR methods. All samples were originally collected during March 2001–June 2003 from the Chaparral Wildlife Management Area in southern Texas (28º18′N, 99º24′W), 86 km west of the Mexico–US border; some samples had been used previously in other research projects (3). Individual rodents were captured with live traps (n = 13) or by excavating middens in which all the nest occupants were collected by hand (n = 146). Animals were later euthanized and tissue samples (heart, kidney, liver, lung, muscle, spleen) were obtained. Tissues were immediately frozen in liquid nitrogen and permanently stored in ultralow-temperature freezers. We extracted 1 DNA sample from each animal’s liver for use in this survey. DNA amplification was performed by using primers specific to T. cruzi (TCZ1 and TCZ2) (4) under previously standardized conditions and positive controls (5). T. cruzi DNA was detected in 42 (26.4%) of 159 woodrat samples tested. Males were infected significantly more often (31/82) than females (11/73); sex was not determined for 4 individuals (Score test for a binomial proportion, z = –4.0, p<0.01). Adults had a nonsignificant higher prevalence (24/92) than all other individuals in the remaining age categories combined (14/54) (age was not determined for 13 individuals) (Score test for a binomial proportion, z = –0.02, p = 0.98). Middens that harbored infected individuals (n = 28, mean = 1.8) were not significantly (t = 0.79, df = 84, p = 0.43) more populated than middens that harbored uninfected individuals (n = 58, mean = 1.6).
Woodrats had been shown by using microscopy to be infected by T. cruzi and T. cruzi–like organisms (6); however, no definitive DNA-based confirmation had been performed (6,7). The results of this research confirm the infection of N. micropus woodrats with T. cruzi and show a higher prevalence than that reported in previous studies that used other diagnostic methods. These results also point to woodrats as a potentially important reservoir of T. cruzi in North America. We hypothesize that the high prevalence is a consequence of the nest-building habits of these rodents. These nests are complexes of dry branches, grasses, and leaves, with a mean diameter of 84 cm, and offer easy access and permanent refuge to triatomine bugs. Woodrats have been found in association with at least 5 triatomine species: Triatoma gerstaeckeri, T. lecticularia, T. neotomae, T. protracta, and T. sanguisuga (8). Another factor for consideration is woodrats’ multigenerational midden use, which may enable the permanent occurrence of triatomine colonies and therefore maintain long-term circulation of T. cruzi. Whereas recent characterizations of North American strains have included isolates from other mammalian reservoir hosts (9), the genotyping of parasites from N. micropus woodrats and other woodrats is still to be done.
Despite successful results from tracking pathogens by using material deposited in natural history museum collections (10), this practice is not common. We suggest that natural history museum collections be used more frequently, especially for surveying and genotyping T. cruzi in mammals, because of the importance of such information in clarifying the epidemiology and the evolutionary history of this pathogen.
Nisha Garg, Jian-Jun Wen, and Carlos Machado graciously supplied positive controls. Robert Baker, Heath Garner, and Kathy MacDonald provided access to DNA samples. Special thanks to Lisa Longhofer, Brian Amman, Darin Carroll, Michelle Haynie, Nevin Durish, Mary Lou Milazzo, and Ciro Milazzo for collecting specimens. Thanks to David Synatske and Donald Ruthven for access to the study area.
Specimens were collected by using funds provided by a National Institutes of Health grant (AI-41435, “Ecology of emerging arenaviruses in the southwestern United States”) to C.F.F. and R.D.B.; funding for laboratory work was provided by Texas Tech University Association of Biologists to C.M.P.
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- Baxter BD, Méndez-Harclerode F, Fulhorst CF, Bradley RD. Genetics of social behavior: a molecular examination of relatedness, multiple maternity, and cohabitation of the southern plains woodrat (Neotoma micropus). J Mammal. 2009;90:819–31.
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Please use the form below to submit correspondence to the authors or contact them at the following address:
C. Miguel Pinto, Department of Mammalogy and Sackler Institute for Comparative Genomics, American Museum of Natural History, New York, NY 10024, USA
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