The rice rat Euryoryzomys russatus, a competent amplifying host of Rickettsia parkeri strain Atlantic rainforest for the tick Amblyomma ovale

• Published in: Ticks and tick-borne diseases 2018-07, Vol.9 (5), p.1133-1136
• Main Authors: Krawczak, Felipe S., Labruna, Marcelo B.
• Format: Article
• Language: English
• Subjects: Animals; Antibodies, Bacterial - blood; Brazil - epidemiology; Cofeeding; Disease Transmission, Infectious; DNA, Bacterial - genetics; Horizontal transmission; Ixodidae; Ixodidae - microbiology; Larva - microbiology; Nymph - microbiology; Rats - parasitology; Rickettsia - genetics; Rickettsia - immunology; Rickettsia - isolation & purification; Rickettsia Infections - blood; Rickettsia Infections - epidemiology; Rickettsia Infections - immunology; Rickettsia Infections - transmission; Rickettsiae; Sigmodontinae - microbiology; Sigmodontinae - parasitology; Spotted fever; Tick Infestations - epidemiology; Tick Infestations - parasitology
• ISSN: 1877-959X; 1877-9603
• DOI: 10.1016/j.ttbdis.2018.04.013

Rickettsia parkeri strain Atlantic rainforest (SAR) is the etiological agent of a spotted fever group rickettsiosis in Brazil, where it is transmitted to humans by the tick Amblyomma ovale. A previous study demonstrated that R. parkeri SAR was successfully maintained in A. ovale ticks by transstadial and transovarial passages; however, because this agent induced lower reproduction rates in A. ovale, the participation of a vertebrate amplifier host, yet to be determined, was speculated. Since the rice rat Euryoryzomys russatus was demonstrated to be the most important host for immature stages of A. ovale in a focus of R. parkeri SAR transmission, the present study evaluated the competence of rice rats to act as amplifying host of R. parkeri SAR for A. ovale ticks. Rice rats were infested with R. parkeri SAR-infected A. ovale nymphs, and four days later with uninfected A. ovale larvae. Rickettsial transmission to rats was confirmed by seroconversion to R. parkeri antigens. Detached engorged larvae were allowed to molt to nymphs, in which rickettsial DNA was detected in up to 60% (mean: 20%) of the specimens. When part of these nymphs was allowed to feed on susceptible rice rats, rickettsial transmission was confirmed by seroconversion, indicating that there was successful horizontal transmission of R. parkeri SAR from infected nymphs to uninfected larvae in the previous acquisition infestations. Because we used naïve, susceptible rats, we infer that this horizontal transmission occurred via a systemic infection (rickettsemia) in the rat. Our results, coupled with previous epidemiological studies, suggest that under natural conditions rice rats could be acting as amplifying hosts of R. parkeri SAR to A. ovale ticks.