Cultivation at 37°C enhances Borrelia burgdorferi sensu stricto infectivity for hamsters

Marygorret Obonyo, Ulrike G. Munderloh, Thien N. Sam, Timothy J. Kurtti

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9 Scopus citations


Borrelia burgdorferi sensu stricto (s.s.), the causative agent of Lyme disease in North America is transmitted to the mammalian host by ticks belonging to the genus, Ixodes. Antibodies to several spirochetal proteins, most notably outer surface protein C (OspC), have been observed in early infection in both humans and laboratory animals. Thus, the expression of these proteins have been postulated to play a role in tick transmission and spirochetal infectivity for the mammalian host. B. burgdorferi strain JMNT was induced to produce increased levels of OspC by cultivation in BSK medium at 37°C. To diminish expression of OspC, spirochetes were cultivated at 31°C. Spirochetes shifted down from 37°C to 31°C or up from 31°C to 37°C for 1 week contained equivalent amounts of OspC. To evaluate spirochetal infectivity, hamsters were inoculated subcutaneously with 1×104 or 1×106 spirochetes grown at the above-mentioned temperatures. Hamsters inoculated with spirochetes expressing high amounts of OspC all became infected, irrespective of the inoculum size. None of the hamsters inoculated with 1×104 spirochetes grown at 31°C or in cultures shifted down from 37°C to 31°C were infected. All infected hamsters, confirmed by isolation of spirochetes in ear and/or bladder cultures, had an antibody response to OspC. In contrast, all non-infected hamsters lacked antibodies to OspC. We conclude that cultivation of spirochetes at 37°C enhances their infectivity for hamsters. This study also suggests there is a correlation between enhancement of OspC expression and spirochetal infectivity for hamsters.

Original languageEnglish (US)
Pages (from-to)33-39
Number of pages7
JournalMedical Microbiology and Immunology
Issue number1
StatePublished - 2002

Bibliographical note

Funding Information:
Acknowledgements This work is part of the Ph.D. dissertation of Marygorret Obonyo. We thank Dr. Tom Schwan (Rocky Mountain Laboratories, National Institute of Health) for providing us with mAb H5332, H4610, and H9724 against OspA, OspB and flagellin, respectively. We thank Dr. Bettina Wilske (Pettenkofer Institute, Germany) for providing the mAb L22 6C4 against OspC. This work was supported by Public Health Service grant no AR37909 to T.J.K.


  • Borrelia burgdorferi
  • Lyme disease
  • Outer surface protein C


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