Complete Genome Sequence of Campylobacter fetus subsp. testudinum Strain Pet-3, Isolated from a Lizard (Hydrosaurus pustulatus).

The whole-genome sequence for Campylobacter fetus subsp. testudinum, a pathogen isolated from humans and turtles, has been reported recently. We present another completed genome sequence of the C. fetus subsp. testudinum strain pet-3, which was isolated from a lizard in Taiwan, for further genomic comparison study.

Occurrence and molecular characterization of reptilian Campylobacter fetus strains isolated in Taiwan.

The number of people who raise reptiles as pets has increased, but information about zoonotic Campylobacter carried by reptiles is limited. A survey of zoonotic Campylobacter species isolated from reptiles was undertaken to understand the possibility of this zoonotic bacterial pathogen causing human infection. A total of 179 fresh reptile fecal samples were collected from human-raised, pet shop and wild reptiles to survey the Campylobacter species. Basic biochemical reactions and 16S rRNA gene sequencing were used to identify the Campylobacter species. In the 179 fecal samples, 6.7% (12/179) were Campylobacter positive; all positive samples were identified as Campylobacter fetus. For the different reptile species, the prevalence of C. fetus in turtles was 9.7% (10/103), 1.7% (1/56) in lizards and 5.0% (1/20) in snakes. Based on published C. fetus subspecies-specific sequences, 9 of the C. fetus bacterial isolates were identified as C. fetus subsp. fetus by multiplex PCR. In addition, multilocus sequence typing (MLST) was used to analyze the Campylobacter epidemiology and population genetics. Most of the C. fetus strains isolated from the reptiles were genetically distinct from classical mammalian C. fetus. Only the new type of ST-43, isolated from Chelonoidis carbonaria (turtle), was closely related to mammalian strains. Strain Campy-pet-3 possesses a urease activity in this study is the first to be described in C. fetus and this strain is the only one of lizard origin. This study provides the first information of Campylobacter species distribution in reptilian feces and supports the possibility of zoonotic Campylobacter infectious diseases caused by reptiles.

Fragment of tegument protein pp65 of human cytomegalovirus induces autoantibodies in BALB/c mice.

INTRODUCTION: Human cytomegalovirus (HCMV) infection has been implicated in the development of autoimmunity, including systemic lupus erythematosus (SLE). Previously we reported that HCMV phosphoprotein 65 (pp65) could induce early onset of autoantibody and glomerulonephritis on lupus-prone NZB/W mice. This study further examined whether the B cell epitope(s) in pp65 is able to drive the development of autoantibody. METHODS: Sera from SLE patients or HCMVpp65-immunized mice were analyzed for anti-nuclear antibody by immunoblotting, enzyme-linked immunosorbent assay (ELISA), immunofluorescent stain and Crithidia luciliae stain. The deposition of immunoglobulin to the kidney was also examined by immunofluorescent stain. The interactions between pp65 sub-fragment to cellular proteins were revealed by yeast two-hybrid analyses. RESULTS: Our results showed that most SLE patients possessed antibodies to the C-terminal half of the HCMVpp65 antigen. Of these positive sera, 73% were also positive to the pp65336-439 sub-fragment. The immunization of pp65336-439 induced formation of multiple anti-nuclear antibodies, including anti-chromatin, anti-centriole, anti-mitotic spindle type I/II (MSA I/II) and a significant elevation of anti-double-stranded DNA (anti-dsDNA) antibodies on BALB/c mice. Yeast two-hybrid analyses revealed the binding of pp65336-439 sub-fragment to cellular proteins. Immunoglobulin deposition on glomeruli was also detected on pp65336-439-immunized mice. CONCLUSIONS: Our data suggested that HCMVpp65336-439 sub-fragment may induce cross-reactive antibodies to several nuclear antigens, which could contribute to the development of autoimmunity in genetic-suspected individuals.