Literature DB >> 20113586

Using museum collections to detect pathogens.

C Miguel Pinto, B Dnate Baxter, J Delton Hanson, Francisca M Mendez-Harclerode, John R Suchecki, Mario J Grijalva, Charles F Fulhorst, Robert D Bradley.   

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Year:  2010        PMID: 20113586      PMCID: PMC2958016          DOI: 10.3201/eid1602.090998

Source DB:  PubMed          Journal:  Emerg Infect Dis        ISSN: 1080-6040            Impact factor:   6.883


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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 (). 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 (). 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 (). 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) () under previously standardized conditions and positive controls (). 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 (); however, no definitive DNA-based confirmation had been performed (,). 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 (). 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 (), 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 (), 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.
  6 in total

1.  Trypanosoma cruzi (Chagas) (Protozoa: Kinetoplastida) in invertebrate, reservoir, and human hosts of the lower Rio Grande valley of Texas.

Authors:  J E Burkholder; T C Allison; V P Kelly
Journal:  J Parasitol       Date:  1980-04       Impact factor: 1.276

2.  Detection of Trypanosoma cruzi by DNA amplification using the polymerase chain reaction.

Authors:  D R Moser; L V Kirchhoff; J E Donelson
Journal:  J Clin Microbiol       Date:  1989-07       Impact factor: 5.948

Review 3.  Chagas disease in Texas: recognizing the significance and implications of evidence in the literature.

Authors:  Elaine Jennifer Hanford; F Benjamin Zhan; Yongmei Lu; Alberto Giordano
Journal:  Soc Sci Med       Date:  2007-04-16       Impact factor: 4.634

4.  A MOLECULAR EXAMINATION OF RELATEDNESS, MULTIPLE PATERNITY, AND COHABITATION OF THE SOUTHERN PLAINS WOODRAT (NEOTOMA MICROPUS).

Authors:  B Dnate' Baxter; Francisca M Mendez-Harclerode; Charles F Fulhorst; Robert D Bradley
Journal:  J Mammal       Date:  2009-08-01       Impact factor: 2.416

5.  Comparison of polymerase chain reaction methods for reliable and easy detection of congenital Trypanosoma cruzi infection.

Authors:  Myrna Virreira; Faustino Torrico; Carine Truyens; Cristina Alonso-Vega; Marco Solano; Yves Carlier; Michal Svoboda
Journal:  Am J Trop Med Hyg       Date:  2003-05       Impact factor: 2.345

6.  Molecular typing of Trypanosoma cruzi isolates, United States.

Authors:  Dawn M Roellig; Emily L Brown; Christian Barnabé; Michel Tibayrenc; Frank J Steurer; Michael J Yabsley
Journal:  Emerg Infect Dis       Date:  2008-07       Impact factor: 6.883

  6 in total
  12 in total

Review 1.  Chagas Disease in the United States: a Public Health Approach.

Authors:  Caryn Bern; Louisa A Messenger; Jeffrey D Whitman; James H Maguire
Journal:  Clin Microbiol Rev       Date:  2019-11-27       Impact factor: 26.132

2.  Natural history collections-based research: progress, promise, and best practices.

Authors:  Bryan S McLean; Kayce C Bell; Jonathan L Dunnum; Bethany Abrahamson; Jocelyn P Colella; Eleanor R Deardorff; Jessica A Weber; Amanda K Jones; Fernando Salazar-Miralles; Joseph A Cook
Journal:  J Mammal       Date:  2015-11-24       Impact factor: 2.416

3.  Parasites and vector-borne pathogens of southern plains woodrats (Neotoma micropus) from southern Texas.

Authors:  Roxanne A Charles; Sonia Kjos; Angela E Ellis; J P Dubey; Barbara C Shock; Michael J Yabsley
Journal:  Parasitol Res       Date:  2011-11-23       Impact factor: 2.289

Review 4.  Trypanosoma cruzi and Chagas' Disease in the United States.

Authors:  Caryn Bern; Sonia Kjos; Michael J Yabsley; Susan P Montgomery
Journal:  Clin Microbiol Rev       Date:  2011-10       Impact factor: 26.132

5.  Southern plains woodrats (Neotoma micropus) from southern Texas are important reservoirs of two genotypes of Trypanosoma cruzi and host of a putative novel Trypanosoma species.

Authors:  Roxanne A Charles; Sonia Kjos; Angela E Ellis; John C Barnes; Michael J Yabsley
Journal:  Vector Borne Zoonotic Dis       Date:  2012-11-05       Impact factor: 2.133

6.  Bats, Trypanosomes, and Triatomines in Ecuador: New Insights into the Diversity, Transmission, and Origins of Trypanosoma cruzi and Chagas Disease.

Authors:  C Miguel Pinto; Sofía Ocaña-Mayorga; Elicio E Tapia; Simón E Lobos; Alejandra P Zurita; Fernanda Aguirre-Villacís; Amber MacDonald; Anita G Villacís; Luciana Lima; Marta M G Teixeira; Mario J Grijalva; Susan L Perkins
Journal:  PLoS One       Date:  2015-10-14       Impact factor: 3.240

7.  High local diversity of Trypanosoma in a common bat species, and implications for the biogeography and taxonomy of the T. cruzi clade.

Authors:  Veronika M Cottontail; Elisabeth K V Kalko; Iain Cottontail; Nele Wellinghausen; Marco Tschapka; Susan L Perkins; C Miguel Pinto
Journal:  PLoS One       Date:  2014-09-30       Impact factor: 3.240

8.  Worldwide Engagement for Digitizing Biocollections (WeDigBio): The Biocollections Community's Citizen-Science Space on the Calendar.

Authors:  Elizabeth R Ellwood; Paul Kimberly; Robert Guralnick; Paul Flemons; Kevin Love; Shari Ellis; Julie M Allen; Jason H Best; Richard Carter; Simon Chagnoux; Robert Costello; Michael W Denslow; Betty A Dunckel; Meghan M Ferriter; Edward E Gilbert; Christine Goforth; Quentin Groom; Erica R Krimmel; Raphael LaFrance; Joann Lacey Martinec; Andrew N Miller; Jamie Minnaert-Grote; Thomas Nash; Peter Oboyski; Deborah L Paul; Katelin D Pearson; N Dean Pentcheff; Mari A Roberts; Carrie E Seltzer; Pamela S Soltis; Rhiannon Stephens; Patrick W Sweeney; Matt von Konrat; Adam Wall; Regina Wetzer; Charles Zimmerman; Austin R Mast
Journal:  Bioscience       Date:  2018-01-17       Impact factor: 8.589

9.  Habitat Management to Reduce Human Exposure to Trypanosoma cruzi and Western Conenose Bugs (Triatoma protracta).

Authors:  Lisa Shender; Michael Niemela; Patricia Conrad; Tracey Goldstein; Jonna Mazet
Journal:  Ecohealth       Date:  2016-08-11       Impact factor: 3.184

10.  Toward an Ecological Framework for Assessing Reservoirs of Vector-Borne Pathogens: Wildlife Reservoirs of Trypanosoma cruzi across the Southern United States.

Authors:  Carolyn L Hodo; Sarah A Hamer
Journal:  ILAR J       Date:  2017-12-15
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