A total of 615 serum samples were obtained from 408 persons in Japan who had confirmed Lyme disease or unconfirmed, clinically suspected Lyme disease and used to detect B. miyamotoi DNA. The serum archive was established during 2008–2013 at the National Institute of Infectious Diseases (Tokyo, Japan). Use of human samples was approved by the ethical committee of the National Institute of Infectious Diseases for medical research with humans (approval no. 360; July 2, 2012).

All serum samples were centrifuged (15,000 × g for 10 min), and sediments were used for DNA extraction. DNA extraction was performed by using the DNeasy Blood and Tissue Kit (QIAGEN, Hilden, Germany) according to the manufacturer’s instructions with minor modification (the extraction column was incubated for 10 min at 70°C before DNA was collected).

For detection of B. miyamotoi DNA, real-time PCR was performed with primers and probes described by Barbour et al. (8). The reaction was performed in a 25-μL volume in single tubes with 1 µmol/L of each primer and 0.25 µmol/L of each probe. The PCR was conducted on a 7000 Real Time PCR Apparatus (Applied Biosystems, Foster City, CA, USA), and conditions were 42 cycles at 95°C for 5 s and 60°C for 31 s. For confirmation of positive samples, a flaB gene nested PCR and sequencing of amplicons were performed as described (9).

The number of copies of DNA in patient serum samples was estimated by quantitative PCR (qPCR). Plasmid pBMrrs1 that contained part of the 16S rRNA gene for B. miyamotoi strain HT31 was prepared as described (9) and was used as a quantitative control.

A recombinant B. miyamotoi glycerophosphoryl diester phosphodiesterase (GlpQ) was used for serologic testing. The GlpQ gene (glpQ) of B. miyamotoi strain HT31 was cloned into plasmid vector pET-19b (Merck KGaA, Darmstadt, Germany). His-tagged GlpQ was subsequently expressed in Escherichia coli Rossetta strain (Merck KGaA) by using MagicMedia (Life Technologies, Carlsbad, CA, USA). Western blotting for detection of antibodies against GlpQ in patient serum was performed as described (10). Our retrospective investigation identified 2 cases of B. miyamotoi infection.

Case-patient 1 was a previously healthy, 72-year-old woman who lived in Hokkaido, Japan. The patient reported no history of foreign travel. Myalgia and anorexia developed on July 23, 2011, and she was hospitalized on July 25, at which time she had a fever of 39°C. Physical examination showed erythema migrans, and the patient confirmed that she had been bitten by a tick 10 days earlier.

Laboratory tests on July 25 showed increased levels of C-reactive protein (44 mg/L), alanine aminotransferase (94 IU/mL), and aspartate aminotransferase (90 IU/ml). The procalcitonin level was ≥0.05 ng/mL, as determined by using a PCT-Q Test (Brahms GmbH, Hennigsdorf, Germany). The leukocyte count was 3,900 cells/μL (87% neutrophils), and a left shift was observed. Erythrocyte and platelet counts were within reference ranges. The patient was given a clinical diagnosis of acute Lyme disease because of typical erythema migrans and a history of a tick bite. The patient was treated with minocycline (100 mg/day for 5 days). Symptoms improved rapidly, and she was discharged from the hospital on July 30.

Borrelial DNA was detected in a serum sample obtained on July 25 by 16S rRNA gene–based-real time qPCR and a flaB gene–specific nested PCR. Sequencing of a flaB PCR amplicon (294 bp) indicated that the infectious borreliae was B. miyamotoi (GenBank accession no. AB921566) because the sequence was identical to that of B. miyamotoi HT31 (GenBank accession no. D43777). The number of copies of the Borrelia genome in serum was estimated to be 7.2 × 10³ copies/mL by qPCR.

Figure

Figure. Immunoblot analysis of serum reactivity to antigens of Borrelia miyamotoi and Lyme disease borreliae, JapanSerum samples obtained from 2 patients were examinedFor case-patient 1, acute-phase serum obtained on July 25, 2011,...

The level of IgM against GlpQ was increased in a convalescent-phase serum sample obtained on August 10 (Figure, panel A). We also found that antibody levels were increased in convalescent-phase serum by conducting immunoblot analysis with a whole cell lysate of B. miyamotoi strain MYK3 (Figure, panel B).

Case-patient 2 was a previously healthy 37-year-old man who lived in Hokkaido, Japan. The patient reported no history of foreign travel. The patient was bitten by a tick on May 28, 2013, and was subsequently hospitalized on June 11, at which time he had a fever of 39.8°C and erythema migrans at the site of the tick bite. The patient was given a clinical diagnosis of acute Lyme disease and erythema migrans. The patient was treated with ceftriaxone (1 g/day for 7 days). Symptoms improved rapidly, and treatment was administrated until July 17 in the outpatient setting.

Borrelial DNA was detected from a serum sample obtained on June 11 by qPCR and nested flaB PCR. Sequencing of the flaB PCR amplicon (294 bp) confirmed B. miyamotoi (GenBank accession no. AB921567) infection in the patient because the sequence was identical to B. miyamotoi HT31 (GenBank accession no. D43777). The number of copies of the borrelia genome in serum was estimated to 2.8 × 10⁴ copies/mL by qPCR. Antibodies against GlpQ were not detected in serum obtained on June 11 (Figure, panel A).

Serologic analysis with a commercial kit for IgM (RecomLine Borrelia IgG/IgM; Mikrogen, Neuried, Germany) (Figure, panel C) showed that serum from these 2 patients reacted with several antigens of Lyme disease borreliae (Figure, panel C). Convalescent-phase serum from case-patient 1 reacted to P100 from B. afzelii, VlsE from various Borrelia species, P41 from B. burgdorferi sensu stricto, and OspC from B. afzelii and B. garinii. Acute-phase serum from case-patient 2 reacted with OspC for all Borrelia species included in the kit. However, the commercial serologic test used does not provide enough evidence to determine whether these 2 patients were co-infected with Lyme disease borreliae because antigenic difference between B. miyamotoi and B. burgdorferi sensu lato have not been investigated.

Platonov et al. (1) reported that I. persulcatus ticks are a transmission vector for B. miyamotoi and Lyme disease borreliae in Russia. This tick species is also ubiquitous in Hokkaido, Japan, and host-seeking behavior of adult ticks is active during spring–late summer. Humans in Hokkaido are bitten most often by I. persulcatus ticks, and Lyme disease borrelia is transmitted to humans mainly through the bite of the adult tick (11). Although the causative tick species was not identified for the 2 case-patients, circumstantial evidence suggests that I. persulcatus ticks are a main transmission vector for B. miyamotoi in Hokkaido, as shown in Russia (1).

Emerging relapsing fever caused by B. miyamotoi has been identified in Russia, North America, and Europe, and B. miyamotoi-related meningoencephalitis has been reported in the United States and the Netherlands. Our study indicates that a human health threat from emerging relapsing fever is present in Japan. For risk analysis of this emerging relapsing fever, epidemiologic surveys (e.g., determining infection rates of host-seeking ticks of the I. persulcatus species complex in various locations in Japan) and improvement of serologic diagnostic systems (especially early diagnosis) should be considered.