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Volume 27, Number 12—December 2021
Research Letter

Coxiella burnetii in 3 Species of Turtles in the Upper Midwest, United States

William E. SanderComments to Author , Richard King, William Graser, Joshua M. Kapfer, Aubrey I. Engel, Laura Adamovicz, and Matthew C. Allender
Author affiliations: University of Illinois Urbana‒Champaign, Urbana, Illinois, USA (W. E. Sander, A.I. Engel, L. Adamovicz, M.C. Allender); Northern Illinois University, DeKalb, Illinois, USA (R. King); Kane County Forest Preserve, Geneva, Illinois, USA (W. Graser); University of Wisconsin‒Whitewater, Whitewater, Wisconsin, USA (J.M. Kapfer)

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Abstract

Coxiella burnetii, the causative bacterium of the zoonotic disease Q fever, has been documented in many different species. We describe documented turtles that were PCR positive for C. burnetii from multiple locations in Illinois and Wisconsin, USA. Assessing the conservation implications, reservoir potential, and zoonotic risk requires further research.

Two studies have identified Coxiella burnetii in poikilotherms (vertebrates that cannot regulate body temperature physiologically); both studies originated in India. Two tortoises had antibodies to C. burnetii by capillary agglutination testing of their serum samples in Uttar Pradesh (1). Additional reptiles, including snakes and skinks, had serum samples positive for C. burnetii in a separate study in Karnataka (2). Although both studies are useful in clarifying how this bacterium might interface with reptiles, there is no other evidence to support the role played by this large class of vertebrates (3). Furthermore, serologic assays applied to species that they were not designed for are difficult to interpret (Appendix).

Serologic testing, typically using indirect immunofluorescence assay, is the primary method used to diagnose C. burnetii infection, which causes Q fever in humans and coxiellosis in domestic ruminants (4). Additional serologic testing includes complement fixation and ELISA (5). Serologic assay benefits include commercial availability and insights into acute, treated, and chronic patients, depending on titers (6). Several PCR-based assays have been developed for detection of C. burnetii in samples from nontraditional mammals, birds, and arthropods (7). PCR provides a simple and reliable method for detection of the bacterium even retrospectively from tissues (6). Therefore, we tested turtles from multiple locations in Illinois and Wisconsin, USA, for C. burnetii.

This study was approved by the institutional animal care and use committees of the University of Illinois (20258), Northern Illinois University (LA16–0016), and University of Wisconsin‒Whitewater (K145011020Q). The Wildlife Epidemiology Laboratory, based at the University of Illinois College of Veterinary Medicine, continually conducts long-term, prospective health assessments of several turtle species across Illinois and neighboring states in natural habitats. Reptiles can be an excellent proxy for the health of environments, and many turtle species have small home ranges with diverse diets reflecting local conditions (8).

As part of these annual surveys, turtle species collected have various morphometric data, blood samples, or oral and cloacal swab specimens obtained before being released. Several diagnostic tests are performed with these samples, such as PCR screening for several pathogens, including C. burnetii. Other pathogenic organisms include Ambystoma tigrinum virus, Bohle iridovirus, Terrapene herpesvirus 1, Terrapene herpesvirus 2, epizootic hematopoietic necrosis virus, Emydomyces testavorans, frog virus 3, Emydid herpesvirus 1, Emydoidea herpesvirus 1 (in Blanding’s turtles), Mycoplasma agassizii, M. testudineum, Salmonella spp., and Testudinid herpesvirus 2 (9).

We extracted DNA from frozen, combined oral/cloacal swab specimens from each turtle by using the DNA Blood Mini Kit (QIAGEN, https://www.qiagen.com). We assessed spectrophotometrically DNA concentration and purity by using NanoDrop 1000 (Thermo Fisher Scientific Inc., https://www.thermofisher.com). We performed quantitative PCR by using a QuantStudio3 Real Time PCR System (Applied Biosystems, https://www.thermofisher.com) and a TaqMan primer‒probe assay targeting the C. burnetti icd gene as described (10).

We assayed all samples, standards, and nontemplate controls in triplicate and quantified positive samples by using a 7-point standard curve (101–107 target copies). Samples were considered positive if all 3 replicates had a lower cycle threshold value than the lowest detected standard dilution. We used a highly sensitive and specific quantitative PCR for C. burnetti.

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Location (gray areas) of turtles PCR positive for Coxiella burnetii, by county, Wisconsin (top) and Illinois (bottom), USA.

Figure. Location (gray areas) of turtles PCR positive for Coxiella burnetii, by county, Wisconsin (top) and Illinois (bottom), USA.

During 2019, samples from 5/605 turtles encountered across 8 counties showed positive results for quantitative PCRs, indicating presence of C. burnetii (Figure). We collected positive samples from 3 Blanding’s turtles (Emydoidea blandingii), 1 painted turtle (Chrysemys picta), and 1 ornate box turtle (Terrapene ornata). These positive turtles were found in Kane and Lee Counties in Illinois and Sauk County in Wisconsin. We did not perform serologic analysis for these animals. One Blanding’s turtle had a microchip and transmitter, was sampled again during 2020, and showed a negative PCR result. All of these turtles were found within a 1-hour drive to the Illinois‒Wisconsin state border within protected preserves. However, the 3 locations in which the 5 turtles varied in proximity to farms, livestock, industry, residential areas, and major highways; we found no geographic associations. All other screening tests showed negative results for pathogenic organisms for these 5 animals.

C. burnetii is a ubiquitous bacterium that has been found in many different species, often without pathogenicity (4). A variety of species of turtles are sampled annually in Illinois and surrounding areas through the Wildlife Epidemiology Laboratory. Over time, the testing for various organisms has expanded, especially as additional tests are validated. Screening for the bacterium that causes Q fever has been conducted for many species but infrequently in poikilotherms. These results show that the bacteria can be detected in these species and should be further researched to understand additional sources of this reportable disease, including potential management or regulatory decisions.

Continued investigation and screening in poikilotherms for zoonotic pathogens should be prioritized to understand the potential risk from additional hosts. The pet trade is a potential avenue of risk for exposure between humans and turtles. As these pathogens of concern are better characterized, the implications of different and varied hosts will drive the need for continued One Health research and dialogue between environmental, animal, and human health professionals.

Dr. Sander is an assistant professor of preventive medicine and public health and director of the DVM/MPH joint degree program in the Department of Veterinary Clinical Medicine, University of Illinois College of Veterinary Medicine, Urbana, IL. His primary research interest is One Health approaches, including the interface of infectious disease and toxicities between humans and animals both domestically and internationally.

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Acknowledgments

We thank the students and employees of the Wildlife Epidemiology Laboratory at the University of Illinois College of Veterinary Medicine for providing assistance; and Joseph Mozuch, Jarod Lorenz, Jacquelyn Kincanon, and Kari Rebman for providing assistance with the Wisconsin fieldwork.

This study was supported by the State of Illinois (Wildlife grants (T-104-R-2 and T-111-R-1). Support for the Wisconsin fieldwork was provided by a donation to The Nature Conservancy by the family of Orie and Elinor Loucks.

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References

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Cite This Article

DOI: 10.3201/eid2712.211278

Original Publication Date: November 04, 2021

Table of Contents – Volume 27, Number 12—December 2021

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William E. Sander, Department of Veterinary Clinical Medicine, University of Illinois at Urbana‒Champaign, 1008 W Hazelwood Dr, Urbana, IL 61801-3028, USA

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Page created: September 09, 2021
Page updated: November 21, 2021
Page reviewed: November 21, 2021
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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