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Nilgai antelope display no signs of infection upon experimental challenge with a virulent Babesia bovis strain

  • Tammi L. Johnson,
  • Kelly A. Persinger,
  • Naomi S. Taus,
  • Sara K. Davis,
  • Karen C. Poh,
  • Lowell S. Kappmeyer,
  • Jacob M. Laughery,
  • Janaína Capelli-Peixoto,
  • Kimberly H. Lohmeyer,
  • Massaro W. Ueti,
  • Pia U. Olafson

摘要

Background

Bovine babesiosis is caused by infection with the protozoal parasite Babesia bovis, which is transmitted by Rhipicephalus (Boophilus) spp. It can cause mortality rates up to 90% in immunologically naive Bos taurus cattle. In south Texas, R. (B.) microplus is known to infest nilgai antelope (Boselaphus tragocamelus); however, their susceptibility to infection with Bbovis and their role in the transmission of the parasite remain unknown. In this study, we challenged nilgai antelope with Bbovis and evaluated their susceptibility to infection.

Methods

Nilgai were needle inoculated with ≈108 Bbovis-parasitized erythrocytes (merozoites) or a homogenate of Bbovis-infected larval ticks (sporozoite) delivered intravenously. Bos taurus beef calves were inoculated in parallel, as this strain of Bbovis is lethal to cattle. Temperature and hematocrit were monitored daily over the course of each study, and whole blood was collected for molecular [polymerase chain reaction (PCR)] and serological [indirect enzyme-linked immunosorbent assay (ELISA)] diagnostic evaluation. Histological sections of nilgai cerebral tissue were examined for evidence of infection. Recipient bovine calves were sub-inoculated with blood from nilgai challenged with either stage of the parasite, and they were monitored for clinical signs of infection and evaluated by a PCR diagnostic assay. Red blood cells (RBCs) from prechallenged nilgai and Btaurus beef cattle were cultured with an in vitro Bbovis merozoite culture to examine colonization of the RBCs by the parasite.

Results

Nilgai did not display clinical signs of infection upon inoculation with either the merozoite or sporozoite stage of Bbovis. All nilgai were PCR-negative for the parasite, and they did not develop antibodies to Bbovis. No evidence of infection was detected in histological sections of nilgai tissues, and in vitro culture analysis indicated that the nilgai RBCs were not colonized by Bbovis merozoites. Cattle subinoculated with blood from challenged nilgai did not display clinical signs of infection, and they were PCR-negative up to 45 days after transfer.

Conclusions

Nilgai do not appear to be susceptible to infection with a strain of Bbovis that is lethal to cattle. Tick control on these alternative hosts remains a critical priority, especially given their potential to disseminate ticks over long distances.

Graphical Abstract