Affiliation:
1. Department of Entomology, University of Minnesota, St. Paul, Minnesota 55108
2. Max von Pettenkofer-Institut für Hygiene und Medizinische Mikrobiologie, Ludwig-Maximilians-Universität München, Munich, Germany
Abstract
ABSTRACT
We describe the isolation and characterization of
Rickettsia monacensis
sp. nov. (type strain, IrR/Munich
T
) from an
Ixodes ricinus
tick collected in a city park, the English Garden in Munich, Germany. Rickettsiae were propagated in vitro with
Ixodes scapularis
cell line ISE6. BLAST analysis of the 16S rRNA, the citrate synthase, and the partial 190-kDa rickettsial outer membrane protein A (rOmpA) gene sequences demonstrated that the isolate was a spotted fever group (SFG) rickettsia closely related to several yet-to-be-cultivated rickettsiae associated with
I. ricinus
. Phylogenetic analysis of partial
rompA
sequences demonstrated that the isolate was genotypically different from other validated species of SFG rickettsiae.
R. monacensis
also replicated in cell lines derived from the ticks
I. ricinus
(IRE11) and
Dermacentor andersoni
(DAE100) and in the mammalian cell lines L-929 and Vero, causing cell lysis. Transmission electron microscopy of infected ISE6 and Vero cells showed rickettsiae within the cytoplasm, pseudopodia, nuclei, and vacuoles. Hamsters inoculated with
R. monacensis
had immunoglobulin G antibody titers as high as 1:16,384, as determined by indirect immunofluorescence assay. Western blot analyses demonstrated that the hamster sera cross-reacted with peptides from other phylogenetically distinct rickettsiae, including rOmpA.
R. monacensis
induced actin tails in both tick and mammalian cells similar to those reported for
R. rickettsii. R. monacensis
joins a growing list of SFG rickettsiae that colonize ticks but whose infectivity and pathogenicity for vertebrates are unknown.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
200 articles.
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