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1.
Virus Res ; 314: 198766, 2022 06.
Article in English | MEDLINE | ID: mdl-35364118

ABSTRACT

Rat hepatitis E virus (HEV-C1) in the Orthohepevirus C species has been reported to cause zoonotic infection and hepatitis in humans. HEV-C1 strains have been detected from wild rats in many countries in Europe, Asia, and North America. However, in Japan, no HEV-C1 strains have been identified. In the present study, 5 (1.2%) of 428 wild rats (Rattus norvegicus or R. rattus) were positive for anti-HEV-C1 IgG. Although all 428 rat sera were negative for HEV-C1 RNA, it was detectable in 20 (19.8%) of 101 rat fecal samples collected on a swine farm, where HEV (genotype 3b, HEV-3b) was prevalent and wild rats were present. In addition, HEV-C1 RNA was detectable in the intestinal contents and liver tissues of 7 (18.9%) of 37 additional rats captured on the same farm. The HEV-C1 strain (ratEJM1703495L) obtained in this study shared only 75.8-84.7% identity with reported HEV-C1 strains over the entire genome but propagated efficiently in cultured cells. HEV-3b strains were detected in the rats' intestinal contents, with 97.3-99.5% identity to those in pigs on the same farm, but were undetectable in rat liver tissues, suggesting that wild rats do not support the replication of HEV-3b of swine origin.


Subject(s)
Hepatitis E virus , Hepatitis E , Swine Diseases , Animals , Hepatitis E/veterinary , Hepatitis E virus/genetics , Japan , Phylogeny , RNA , RNA, Viral/genetics , Rats , Swine
2.
Parasit Vectors ; 12(1): 389, 2019 Aug 05.
Article in English | MEDLINE | ID: mdl-31383002

ABSTRACT

BACKGROUND: Two transmission patterns of Sarcoptes scabiei in host mammal communities have been reported based on microsatellite-level genetic studies in the last two decades. While one involves restrictions among different host taxa, the other is associated with predator-prey interactions between different host taxa. In contrast to these observations, the present study reports a possible irregular case of transmission of S. scabiei between herbivorous Japanese serow and omnivorous Caniformia mammals in Japan, though under very weak predator-prey relationships. METHODS: DNA from 93 Sarcoptes mites isolated from omnivorous Caniformia (such as the domestic dog, raccoon dog, raccoon and Japanese marten), omnivorous Cetartiodactyla (wild boar) and herbivorous Cetartiodactyla (Japanese serow) in Japan were analyzed by amplifying nine microsatellite markers. Principal components analyses (PCA), Bayesian clustering analyses using STRUCTURE software, and phylogenetic analyses by constructing a NeighborNet network were applied to determine the genetic relationships among mites associated with host populations. RESULTS: In all the analyses, the genetic differentiation of Sarcoptes mites from wild boars and Japanese serows was observed. Conversely, considerably close genetic relationships were detected between Caniformia-derived and Japanese serow-derived mites. Because the predator-prey interactions between the omnivorous Caniformia and herbivorous Japanese serow are quite limited and epidemiological history shows at least a 10-year lag between the emergence of sarcoptic mange in Japanese serow and that in Caniformia, the transmission of S. scabiei from Caniformia to Japanese serow is highly suspected. CONCLUSIONS: The close genetic relationships among mites beyond Host-taxon relationships and without obvious predator-prey interactions in Caniformia and Japanese serow deviate from previously reported S. scabiei transmission patterns. This type of cryptic relationship of S. scabiei populations may exist in local mammalian communities worldwide and become a risk factor for the conservation of the remnant and fragmented populations of wild mammals.


Subject(s)
Caniformia/parasitology , Sarcoptes scabiei/genetics , Scabies/veterinary , Sus scrofa/parasitology , Animals , Herbivory , Japan , Phylogeny , Ruminants/parasitology , Scabies/transmission , Skin/parasitology
3.
Ticks Tick Borne Dis ; 10(2): 344-351, 2019 02.
Article in English | MEDLINE | ID: mdl-30501980

ABSTRACT

Ehrlichiosis is a tick-borne bacterial disease caused by pathogens of the Ehrlichia genus. Although human ehrlichiosis has not been reported in Japan, Ehrlichia spp., which are closely related to Ehrlichia chaffeensis, were detected in several species of ixodid ticks. In this study, the presence of Ehrlichia spp. in ticks in Japan was studied by using isolation and molecular detection methods. In total, 1237 ticks were collected from vegetation in western, central, and eastern parts of Japan. The ticks were tested for detection of ehrlichial DNA with a nested polymerase chain reaction and/or isolation by inoculation of mice with the homogenate. Ehrlichial DNA was detected in 29 of these ticks. The ehrlichial DNAs, groEL and 16S rRNA genes, detected in Ixodes turdus showed a high similarity to those of E. chaffeensis with 94.7% and 99.2% identity, respectively. Ehrlichia sp. HF and Candidatus Neoehrlichia mikurensis were also detected in I. ovatus. Furthermore, Ehrlichia sp. HF was isolated from laboratory mice that were intraperitoneal inoculated with I. ovatus tick homogenate. Some ehrlichial agents detected in Ixodes ticks might be a previously unknown Ehrlichia species. In this study, Candidatus N. mikurensis was detected in I. ovatus ticks. Because I. ovatus is distributed widely and cases of its tick bite in humans are ubiquitously reported in Japan, there is a potential for ehrlichiosis to be endemic to Japan, necessitating intensive surveillance of this infectious disease.


Subject(s)
Ehrlichia/isolation & purification , Ehrlichiosis/epidemiology , Ticks/microbiology , Animals , Chaperonin 60/genetics , DNA, Bacterial/genetics , DNA, Ribosomal/genetics , Ehrlichia/genetics , Ehrlichia chaffeensis/genetics , Female , Ixodes/microbiology , Japan/epidemiology , Male , Mice , Phylogeny , Polymerase Chain Reaction , RNA, Ribosomal, 16S/genetics
4.
Int J Syst Evol Microbiol ; 65(Pt 2): 734-737, 2015 Feb.
Article in English | MEDLINE | ID: mdl-25406232

ABSTRACT

Mycoplasma haemomuris is causative of infectious anaemia or splenomegaly in rodents. We examined the nucleotide sequences of the non-ribosomal genes, rnpB and dnaK, in strains of the species M. haemomuris detected in small field mice and black rats. rnpB nucleotide sequences in strains of the species M. haemomuris isolated from small field mice and black rats had only 89 % sequence similarity, suggesting their separation into two distinct subgroups. dnaK had a nucleotide sequence similarity of 84 % between the subgroups. These results support the classification of M. haemomuris into two genetically distinct subgroups. Here we propose the establishment of these subgroups as 'Candidatus Mycoplasma haemomuris subsp. musculi', detected in small field mice (Apodemus argenteus), and 'Candidatus Mycoplasma haemomuris subsp. ratti', detected in black rats (Rattus rattus).


Subject(s)
Murinae/microbiology , Mycoplasma/classification , Phylogeny , Rats/microbiology , Animals , DNA, Bacterial/genetics , Genes, Bacterial , Molecular Sequence Data , Sequence Analysis, DNA
5.
Jpn J Infect Dis ; 67(2): 111-4, 2014.
Article in English | MEDLINE | ID: mdl-24647253

ABSTRACT

A total of 138 animals from 7 species (Apodemus agrarius, Bandicota indica, Crocidura suaveolens, Mus caroli, Mus formosanus, Rattus losea, and Suncus murinus) captured in Taichung, located in central Taiwan, and Kinmen Island, an island off the shore of China, were examined for the presence of Anaplasma phagocytophilum. The presence of the bacteria, which causes human granulocytic anaplasmosis, was examined by nested PCR targeting the16S rDNA. Twelve animals (8.7%) from M. caroli and R. losea, and 25 (18.1%) from A. agrarius, B. indica, M. caroli, and R. losea were infected with A. phagocytophilum and Anaplasma bovis, respectively. Phylogenetic analysis revealed that partial 16S rDNA sequences in the 12 aforementioned animals showed higher similarity to the sequences related to A. phagocytophilum detected in wild rodents (Rattus and Niviventer) from southeast China. The sequences of the other 25 animals belonged to the A. bovis clade. We demonstrated that small wild mammals were infected with A. phagocytophilum and A. bovis in Taichung and Kinmen Island, Taiwan.


Subject(s)
Anaplasma phagocytophilum/isolation & purification , Animals, Wild/microbiology , Ehrlichiosis/veterinary , Anaplasma phagocytophilum/classification , Anaplasma phagocytophilum/genetics , Animals , Cluster Analysis , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , Ehrlichiosis/epidemiology , Ehrlichiosis/microbiology , Mammals , Molecular Sequence Data , Phylogeny , Polymerase Chain Reaction , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA , Sequence Homology, Nucleic Acid , Taiwan/epidemiology
6.
J Vet Med Sci ; 75(9): 1201-7, 2013.
Article in English | MEDLINE | ID: mdl-23665530

ABSTRACT

Lyme disease Borrelia spp. are transmitted by Ixodes ticks, and more than 10 species of borreliae have been identified around the world. Recently, another Borrelia sp. has been reported in Asia (Japan, Korea, China, Taiwan and Thailand) as Borrelia valaisiana-related sp. In the present study, we obtained and genetically characterized 19 B. valaisiana-related sp. strains from mammals and ticks. Genetic analyses showed that the Borrelia strains were distinct from B. valaisiana found in Europe. Multilocus sequence typing revealed that these Borrelia isolates formed a monophyletic group with B. yangtze strains in China. Some of the strains were isolated from the bladders of small mammals, and also two strains were experimentally confirmed to be infectious in C3H/HeN mice. We observed that the Borrelia sp. was maintained in the Ixodes granulatus tick after molting. These results suggested that small mammals and I. granulatus were possible reservoir hosts and the vector tick for the Borrelia sp., respectively. B. valaisiana, originally found in Europe, was transmitted mainly by I. ricinus, and birds were mainly thought to be reservoir hosts. Our results suggested that Japanese isolates of B. yangtze (formerly B. valaisiana-related sp.) were distinguishable from B. valaisiana according to the reservoir host and its vector tick. In this study, we also deposited borrelia strain Okinawa-CW62 into bioresource centers as a reference strain of B. yangtze(=DSM 24625, JCM 17189).


Subject(s)
Arachnid Vectors/microbiology , Borrelia/genetics , Disease Reservoirs/microbiology , Ixodes/microbiology , Rodentia/microbiology , Animals , Comparative Genomic Hybridization , Japan , Mice , Multilocus Sequence Typing , Phylogeny , Species Specificity
7.
J Vet Med Sci ; 75(5): 643-8, 2013.
Article in English | MEDLINE | ID: mdl-23238428

ABSTRACT

Mycoplasma haemomuris is a causative organism of infectious anemia or splenomegaly in rodents. Here, we report two distinct genetic groups among M. haemomuris strains detected from rats and mice, respectively, by examining the nucleotide sequences of the 16S-23S rRNA intergenic transcribed spacer region that has been shown to be a stable genetic marker for mycoplasma species. Our results may reveal host-tropism of each cluster of M. haemomuris strains, and suggest an idea to distinguish M. haemomuris into two different genetic clusters.


Subject(s)
Genetic Variation , Host Specificity/genetics , Mycoplasma/classification , Mycoplasma/genetics , Phylogeny , Animals , Base Pairing , Base Sequence , Cluster Analysis , DNA Primers/genetics , DNA, Intergenic/genetics , Japan , Mice , Models, Genetic , Molecular Sequence Data , RNA, Ribosomal/genetics , Rats , Sequence Alignment , Sequence Analysis, DNA
8.
Ticks Tick Borne Dis ; 3(4): 259-61, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22910061

ABSTRACT

A novel relapsing fever Borrelia sp. was found in Amblyomma geoemydae in Japan. The novel Borrelia sp. was phylogenetically related to the hard (ixodid) tick-borne relapsing fever Borrelia spp. Borrelia miyamotoi and B. lonestari. The novel relapsing fever Borrelia sp. was detected in 39 A. geoemydae (39/274: 14.2%), of which 14 (14/274: 5.1%) were co-infected with the novel relapsing fever Borrelia sp. and Borrelia sp. tAG, one of the reptile-associated borreliae. Transstadial transmission of the novel relapsing fever Borrelia sp. occurred in the tick midgut and the salivary glands, although Borrelia sp. tAG was only detected in the tick midgut. The difference of the borrelial niche in molted ticks might be associated with borrelial characterization.


Subject(s)
Borrelia/classification , Borrelia/genetics , Ixodidae/microbiology , Salivary Glands/microbiology , Animals , Female , Larva , Male , Molting , Nymph
9.
Parasitol Int ; 61(3): 431-6, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22387862

ABSTRACT

We conducted a pilot survey of genetic variation of A. cantonensis using small subunit (SSU) ribosomal (r) RNA and mitochondrial cytochrome c oxidase subunit I (coxI) gene sequences. Two distinct SSU genotypes (G1 and G2) were identified among 17 individual A. cantonensis worms from 17 different geographical localities in Japan, Mainland China, Taiwan, and Thailand. The partial coxI sequences were determined for 83 worms from 18 different geographical localities from Japan, Mainland China, Taiwan, and Thailand. Phylogenetic analysis showed eight distinct coxI haplotypes (ac1 to ac8). In 16 out of 18 localities, only a single coxI haplotype was found. However, in two localities, two coxI haplotypes coexisted. The common haplotypes found were: haplotype ac1 (Tokyo, Chiba, Kanagawa, Amamioshima Island, and Taichung), haplotype ac2 (Ishikawa, Shenzhen, and Lianjiang), haplotype ac5 (the Okinawa and the Ogasawara Islands), and haplotype ac7 (Miyagi, Aichi, and Kanagawa). Each of these regions is separated from the others by high mountain ranges or oceans. In addition, the lower genetic variation and particular geographical distribution of A. cantonensis in each location could indicate a founder effect, which may have resulted from multiple independent origins, and suggests that haplotypes migrated from endemic areas via human-related transportation.


Subject(s)
Angiostrongylus cantonensis/classification , DNA, Helminth/genetics , Phylogeny , Angiostrongylus cantonensis/genetics , Angiostrongylus cantonensis/isolation & purification , Animals , Base Sequence , China , Electron Transport Complex IV/genetics , Genetic Variation , Haplotypes , Japan , Molecular Sequence Data , Phylogeography , Pilot Projects , Rats/parasitology , Ribosome Subunits, Small/genetics , Sequence Analysis, DNA , Taiwan , Thailand
11.
Ticks Tick Borne Dis ; 2(2): 94-8, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21771542

ABSTRACT

We demonstrated the presence of the agent of human granulocytic anaplasmosis (HGA), Anaplasma phagocytophilum, and the agent of Lyme borreliosis, Borrelia burgdorferi sensu lato, in north-western Turkey. A total of 241 questing Ixodes ricinus adult ticks were sampled by flagging from recreational parks of the Asiatic and European sides of the heavily populated Istanbul metropolitan area and rural forests of Kirklareli located in the Thrace region in 2008. Both tick-borne pathogens were detected and identified by PCR and DNA sequencing analysis. A. phagocytophilum infection rates were 2.7% in Istanbul and 17.5% in the Kirklareli area. B. burgdorferi sensu lato infection rates were 38.7% in Istanbul and 11.4% in the Kirklareli area. Only 3 of 241 ticks were coinfected with A. phagocytophilum and B. burgdorferi sensu lato.


Subject(s)
Anaplasma phagocytophilum/isolation & purification , Arachnid Vectors/microbiology , Borrelia burgdorferi/isolation & purification , Ixodes/microbiology , Anaplasma phagocytophilum/genetics , Animals , Borrelia burgdorferi/genetics , Phylogeny , RNA, Ribosomal, 16S/genetics , Turkey
12.
Environ Microbiol Rep ; 3(5): 632-7, 2011 Oct.
Article in English | MEDLINE | ID: mdl-23761345

ABSTRACT

The genus Borrelia is arthropod-borne infectious agents in vertebrates, and is classified into Lyme disease (LD) Borrelia spp. and Relapsing fever (RF) Borrelia spp. In addition to these Borrelia groups, we recently reported reptile-associated (REP) Borrelia spp. from reptiles and from hard-bodied ticks, which probably transmitted the REP Borrelia spp. In this study, we investigated the presence of REP Borrelia sp. in moulted ticks, and found that trans-stadial transmission of REP Borrelia sp. occurred in the midgut, while it was observed that REP Borrelia sp. entered the salivary gland during blood-feeding. This characteristic is also found in LD Borrelia spp., which are also transmitted by hard-bodied ticks. Although phylogenetic analysis demonstrated that REP Borrelia spp. are similar to RF Borrelia spp., the ecology of the spirochaetes within the vector ticks is different for REP Borrelia spp. and RF Borrelia spp. Elucidation of the evolutionary history of the genus Borrelia and its adaptation to ticks promises to be of great interest to researchers of vector-borne microorganisms.

13.
Microbiol Immunol ; 53(2): 101-6, 2009 Feb.
Article in English | MEDLINE | ID: mdl-19291093

ABSTRACT

Ehrlichia-specific DNA fragments of Ehrlichia omp-1 and groEL genes were found in two I. granulatus ticks which had been collected from wild small mammals in a subtropical zone in Japan. The DNA sequences of groEL and 16SrDNA of the suspected Ehrlichia were clustered into a group of E. chaffeensis, E. muris, and Ehrlichia sp. HF565 found in I. ovatus, but were distinctly different. Therefore the Ehrlichia strain was designated as a novel Ehrlichia sp. 360. The Ehrlichia sp. 360 was detected in I. granulatus but not in any other ticks. This suggests that I. granulatus is a probable vector of Ehrlichia sp. 360 in Japan.


Subject(s)
Ehrlichia/genetics , Ixodes/microbiology , Animals , DNA, Bacterial/genetics , Ehrlichia/classification , Ehrlichia/isolation & purification , Japan , Phylogeny , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA
15.
Appl Environ Microbiol ; 74(16): 5086-92, 2008 Aug.
Article in English | MEDLINE | ID: mdl-18606803

ABSTRACT

Here, we describe for the first time the prevalence and genetic properties of Bartonella organisms in wild rodents in Japan. We captured 685 wild rodents throughout Japan (in 12 prefectures) and successfully isolated Bartonella organisms from 176 of the 685 rodents (isolation rate, 25.7%). Those Bartonella isolates were all obtained from the rodents captured in suburban areas (rate, 51.8%), but no organism was isolated from the animals captured in city areas. Sequence analysis of rpoB and gltA revealed that the Bartonella isolates obtained were classified into eight genetic groups, comprising isolates closely related to B. grahamii (A-I group), B. tribocorum and B. elizabethae (B-J group), B. tribocorum and B. rattimassiliensis (C-K group), B. rattimassiliensis (D-L group), B. phoceensis (F-N group), B. taylorii (G-O group), and probably two additional novel Bartonella species groups (E-M and H-P). B. grahamii, which is one of the potential causative agents of human neuroretinitis, was found to be predominant in Japanese rodents. In terms of the relationships between these Bartonella genetic groups and their rodent species, (i) the A-I, E-M, and H-P groups appear to be associated with Apodemus speciosus and Apodemus argenteus; (ii) the C-K, D-L, and F-N groups are likely implicated in Rattus rattus; (iii) the B-J group seems to be involved in Apodemus mice and R. rattus; and (iv) the G-O group is probably associated with A. speciosus and Clethrionomys voles. Furthermore, dual infections with two different genetic groups of bartonellae were found in A. speciosus and R. rattus. These findings suggest that the rodent in Japan might serve as a reservoir of zoonotic Bartonella infection.


Subject(s)
Bartonella Infections/veterinary , Bartonella/genetics , Disease Reservoirs/microbiology , Genetic Variation , Rodent Diseases/microbiology , Animals , Arvicolinae/microbiology , Bacterial Typing Techniques , Bartonella/classification , Bartonella/isolation & purification , Bartonella Infections/epidemiology , Bartonella Infections/microbiology , DNA, Bacterial/genetics , Japan/epidemiology , Mice , Phylogeny , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length , Rats , Rodent Diseases/epidemiology , Sequence Analysis, DNA
17.
Int J Med Microbiol ; 294(7): 455-64, 2005 Jan.
Article in English | MEDLINE | ID: mdl-15715174

ABSTRACT

The relationships between Borrelia species and the vector ticks, Ixodes persulcatus and Ixodes ricinus were examined in a molecular epidemiological study. We conducted a survey in the Moscow region which is a sympatric region for both species of tick. We examined 630 unfed I. ricinus and I. persulcatus, ticks collected from four different regions around Moscow within an area of 250 km2. Eighty-four ticks were culture positive (13.3%) and the prevalence rate varied in each region from 5.7% to 42.3%. No difference was found between the total prevalence rate for both species. Eight Borrelia afzelii-like variant isolates from I. ricinus and Clethrionomys glareolus were identified as B. afzelii by flagellin gene and 16S rDNA sequence analyses. Most isolates from I. ricinus were identified as Borrelia garinii type 20047 and B. afzelii. Two isolates were identified as Borrelia burgdorferi sensu stricto (s.s.) and Borrelia valaisiana, respectively, but no B. garinii type NT29 was found. In contrast, isolates from I. persulcatus were identified as both types 20047 and NT29 of B. garinii, and B. afzelii. No B. burgdorferi s.s. isolate was found among isolates from I. persulcatus.


Subject(s)
Arvicolinae/microbiology , Borrelia burgdorferi Group/classification , Ixodes/microbiology , Lyme Disease/veterinary , Rodent Diseases/microbiology , Animals , Arachnid Vectors/microbiology , Base Sequence , Borrelia burgdorferi Group/genetics , Borrelia burgdorferi Group/isolation & purification , DNA, Bacterial/analysis , DNA, Ribosomal/analysis , DNA, Ribosomal Spacer/analysis , Flagellin/genetics , Ixodes/classification , Lyme Disease/microbiology , Molecular Sequence Data , Moscow , Phylogeny , Polymorphism, Restriction Fragment Length , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA , Species Specificity
18.
J Parasitol ; 91(5): 1116-21, 2005 Oct.
Article in English | MEDLINE | ID: mdl-16419757

ABSTRACT

The large intestine of a rat has been neglected almost completely as a site of Strongyloides sp. infection. We reported that adult Strongyloides ratti remained in the large intestine for more than 80 days, producing more number of infective larvae than small intestine adults, and therefore hypothesized that parasitism in this site could be a survival strategy. In wild rats, however, no study has focused on large intestine infections of Strongyloides. The present study revealed that 32.4% of 68 wild rats, Rattus norvegicus, had the infection of S. ratti in the large intestine, with an average of 4.7 worms. These worms harbored normal eggs in the uterus. In a laboratory experiment with S. ratti and Wister rats, daily output of infective larvae by 4.7 females in the large intestine was estimated to be 4,638.4, suggesting that a few parasites could play a role in the parasite transmission. Five species of nematode found in the wild rats showed seasonality in infection intensity, with highest intensities in March-May. The number of S. ratti in the large intestine was also highest in these months.


Subject(s)
Intestinal Diseases, Parasitic/veterinary , Intestine, Large/parasitology , Rats/parasitology , Rodent Diseases/parasitology , Strongyloides ratti/isolation & purification , Strongyloidiasis/veterinary , Animals , Animals, Wild , Ascaridida/isolation & purification , Ascaridida Infections/epidemiology , Ascaridida Infections/parasitology , Ascaridida Infections/veterinary , Female , Intestinal Diseases, Parasitic/epidemiology , Intestinal Diseases, Parasitic/parasitology , Japan/epidemiology , Male , Nippostrongylus/isolation & purification , Prevalence , Rodent Diseases/epidemiology , Seasons , Strongylida Infections/epidemiology , Strongylida Infections/parasitology , Strongylida Infections/veterinary , Strongyloidiasis/epidemiology , Strongyloidiasis/parasitology
19.
Int J Syst Evol Microbiol ; 54(Pt 5): 1649-1652, 2004 Sep.
Article in English | MEDLINE | ID: mdl-15388724

ABSTRACT

Previously, a novel, fast-growing spirochaete was isolated from the hard tick Hyalomma aegyptium, which infests tortoises (Testudo graeca), by using Barbour-Stoenner-Kelly (BSK) II medium; the tick samples were taken from the Istanbul area in northwestern Turkey [Güner et al. (2003). Microbiology 149, 2539-2544]. Here is presented a detailed characterization of the spirochaete. Electron microscopy revealed that strain IST7T is morphologically similar to other spirochaetes of the genus Borrelia and possesses 15 to 16 flagellae that emerge from both polar regions. PFGE analysis revealed the genome to comprise a linear chromosome of approximately 1 Mb; two large linear plasmids of approximately 145 and 140 kb, and several small plasmids ranging from 50 to 20 kb in size were also found. The 16S rRNA gene sequence of this Borrelia isolate exhibited 99.4 to 99.8 % identity with other strains isolated from H. aegyptium and less than 99 % similarity with those of other Borrelia species. A phylogenetic tree, generated from 16S rRNA gene sequences, demonstrated that the spirochaete isolates from H. aegyptium clustered together and branched off from both Lyme-disease-related and relapsing-fever-associated Borrelia species. A single copy of the rrs gene was detected in the genome of strain IST7T by Southern hybridization. DNA-DNA hybridization results showed that strain IST7T was distinct from Lyme-disease-related Borrelia, Borrelia burgdorferi and the relapsing-fever-associated species Borrelia hermsii. The G+C content of strain IST7T is 30.0 mol%. From these genetic features, a novel Borrelia species, Borrelia turcica sp. nov., is proposed; the type strain is IST7T (= JCM 11958T = DSM 16138T).


Subject(s)
Borrelia/classification , Borrelia/isolation & purification , Ixodidae/microbiology , Animals , Base Composition , Blotting, Southwestern , Borrelia/genetics , Borrelia/ultrastructure , DNA Fingerprinting , DNA, Bacterial/analysis , DNA, Bacterial/chemistry , DNA, Bacterial/isolation & purification , DNA, Ribosomal/chemistry , DNA, Ribosomal/isolation & purification , Electrophoresis, Gel, Pulsed-Field , Flagella , Genes, rRNA , Microscopy, Electron , Molecular Sequence Data , Nucleic Acid Hybridization , Phylogeny , Plasmids/analysis , RNA, Bacterial/genetics , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA , Tick Infestations/veterinary , Turkey , Turtles/parasitology
20.
J Med Microbiol ; 53(Pt 5): 421-426, 2004 May.
Article in English | MEDLINE | ID: mdl-15096552

ABSTRACT

In 2000 and 2001, a survey was conducted of Borrelia isolated from various mammals in the southernmost islands of Japan, including Okinawa (main island), Izena, Iriomote and Ishigaki. Isolates obtained from the ear tissues of Suncus murinus (10 isolates), Mus calori (four isolates), Rattus norvegicus (one isolate) and Crocidura watasei (one isolate), were characterized by RFLP of the 5S-23S rDNA intergenic spacer and sequence analysis of the intergenic spacer, 16S rDNA and flagellin gene. While these isolates showed identical RFLPs to Borrelia valaisiana found in Korea, Taiwan and the southern and central parts of China, their RFLP patterns differed from those of B. valaisiana found in European countries, and strain Am501 isolated from Ixodes columnae in Japan. It was found that these isolates clustered with each other on a phylogenetic tree based on flagellin gene and 16S rDNA sequences, but were relatively divergent from the European B. valaisiana and strain Am501. These findings suggest that these isolates found in East Asia should be classified as a new genomospecies of Borrelia burgdorferi sensu lato.


Subject(s)
Borrelia burgdorferi Group/classification , Borrelia burgdorferi Group/genetics , Lyme Disease/veterinary , Mammals/microbiology , Animals , Borrelia burgdorferi Group/isolation & purification , DNA, Ribosomal Spacer/analysis , Flagellin/genetics , Genome, Bacterial , Japan , Lyme Disease/microbiology , Molecular Sequence Data , Phylogeny , Polymorphism, Restriction Fragment Length , RNA, Ribosomal, 16S/genetics , Rats , Sequence Analysis, DNA
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