Reemerging murine typhus, Japan.
On May 4, 2003, a 56-year-old man living in Tokushima, Japan, sought medical care; he had a temperature of 39.1[degrees]C and exanthema on the trunk and the upper limbs. No surface lymph nodes were palpable. He was treated with lincomycin and cefditoren pivoxil with no improvement. On day 3, the patient informed caregivers that he had been in a bamboo grove on days 1 and 11 before the onset of symptoms. C-reactive protein of the serum sample collected on day 3 was positive (= 7.6 mg/dL). From this finding, spotted fever was suspected; the disease is endemic in Tokushima. On day 4, the exanthema had spread systemically, and treatment with minocycline was started, which led to a gradual decrease in fever and rashes. The patient was admitted to the Tokushima University Hospital on day 6 of the illness for diagnosis and further treatment.
Serum samples were collected from the patient on days 5, 6, 9, 20, and 34. Indirect immunoperoxidase tests on the serum samples for tsutsugamushi disease, spotted fever, murine typhus, and Q fever on day 5 of the illness were negative for immunoglobulin (Ig) G and IgM antibodies (<1:40). Weil-Felix tests on the serum samples on days 5 and 9 of the illness were negative for OX2, OX19, and OXK. Indirect immunofluorescence of the serum samples on days 6, 9, 20, and 34 of the illness was conducted by using strains 18 and Wilmington of R. typhi, and the strain Breinl of R. prowazekii as typhus group rickettsiae; and the strain YH of R.japonica, the strain Malish 7 of R. conorii, and the strain Tick of R. montanensis as the spotted fever group rickettsiae. All serum samples tested for the rickettsiae showed an IgM titer of 1:20. On the other hand, the IgM titers of these serum samples, to the Orientia tsutsugamushi were <1:20. For the IgG antibodies of these serum, spotted fever group rickettsiae were negative (<1:20). However, the typhus group rickettsiae were positive for IgG antibodies. Among the typhus group rickettsiae, strain 18 of R. typhi had the highest elevated titers. The titers to the sera on days 6, 9, 20, and 34 of illness were 1:80, 1:160, 1:160, and 1:80, respectively. Another strain of R..typhi, the strain Wilmington, had lower titers of 1:40, 1:80, 1:80, and 1:40, on days 6, 9, 20, and 34 of the illness, respectively. This could have occurred because strain 18 may be a closer antigenic relation of the causative agent than is the strain Wilmington. R. prowazekii demonstrated the lowest IgG titers among typhus group rickettsiae for these serum samples, <1:20, 1:20, 1:40, and 1:20, on days 6, 9, 20, and 34 of the illness, respectively. These results suggested that the disease was murine typhus.
To demonstrate more detailed antigenic reactivity, Western immunoblotting of rickettsiae was conducted by using a serum specimen from day 20. All of the rickettsiae were reactive to the serum to various extents. The serum reacted to the ladder-like lipopolysaccharide of R. typhi and R. prowazekii; the antigenicity of rickettsial lipopolysaccharide is groupspecific. As expected from the immunofluorescence data, no reaction was demonstrated to the lipopolysaccharide of spotted fever group rickettsiae, R. japonica and R. montanensis, although trace cross-reactivity, mainly to rOmpB, was shown. Thus, typhus group rickettsiosis was suspected for this case on the basis of these data. Compared to the trace reaction of spotted fever group rickettsiae to rOmpB, a stronger, but still weak, reaction was detected to the heat-labile state of rOmpB of R. prowazekii and an extremely strong reaction was demonstrated to the heat-labile and heat-stable states of rOmpB of R. typhi. These results strongly suggested that the disease was murine typhus.
To confirm this diagnosis, we conducted absorption tests as described previously (10). The patient serum collected on day 20 showed complete absorption by the homologous antigen, the purified R. typhi strain 18, demonstrating no reaction to R. typhi or to R. prowazekii by immunofluorescence. However, the serum showed incomplete absorption by the heterologous antigen, the purified R. prowazekii, demonstrating no reactivity to R. prowazekii but some reactivity to R. typhi. These tests confirmed the diagnosis of murine typhus.
Murine typhus has never been reported in Japan after the 1950s, except for the three suspected cases and this case. Although other undiagnosed cases may have occurred, they appear to be few; many febrile cases of exanthema have been examined for various rickettsioses, especially after spotted lever was diagnosed in Japan in 1984. Murine typhus may have reemerged because of the recent increase of black rats, Rattus rattus, in Japan. This patient mentioned that he had captured a rat and disposed of the carcass about a week before the onset of symptoms. Infection could have resulted at that time from contamination with feces of infected fleas such as the oriental rat flea, Xenopsylla cheopis. Historical review indicates that this is the first complete serologic diagnosis of a murine typhus case in Japan.
We thank Akio Adachi for his valuable suggestions.
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Address for correspondence: Tsuneo Uchiyama, Department of Virology, University of Tokushima Graduate School of Medicine, Kuramoto 3-18-15, Tokushima 770-8503, Japan; fax: +81-88-633-7080; email: firstname.lastname@example.org
Satoshi Sakaguchi, * Ichiki Sato, ([dagger]) Hiroaki Muguruma, * Hiroaki Kawano, * Yoshito Kusuhara, * Seiji Yano, * Saburo Sone, * and Tsuneo Uchiyama *
* The University of Tokushima Graduate School of Medicine, Tokushima, Japan; and [dagger]Sato Clinic, Tokushima, Japan
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|Publication:||Emerging Infectious Diseases|
|Date:||May 1, 2004|
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