This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Tsukahara, M.
Right arrow Articles by Uchida, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tsukahara, M.
Right arrow Articles by Uchida, M.

 Previous Article  |  Next Article 

Journal of Clinical Microbiology, May 2000, p. 1990-1991, Vol. 38, No. 5
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.

Bartonella henselae Infection as a Cause of Fever of Unknown Origin

Masato Tsukahara,1,* Hidehiro Tsuneoka,2 Hidechika Iino,1 Ichiro Murano,3 Hirohiko Takahashi,4 and Masashi Uchida5

School of Allied Health Sciences, Yamaguchi University,1 Department of Clinical Laboratory, Kohseiren Nagato Hospital,2 Department of Pediatrics, Yamaguchi Prefectural Hospital,3 Department of Pediatrics, Onoda City Hospital,4 and Department of Pediatrics, Tokuyama Central Hospital,5 Yamaguchi-Ken, Japan

Received 12 October 1999/Returned for modification 18 January 2000/Accepted 8 February 2000


    ABSTRACT
Top
Abstract
Text
References

Fourteen of 41 patients (34%) with a serological diagnosis of Bartonella henselae infection were found to have prolonged fever or fever of unknown origin, suggesting that generalized systemic B. henselae infection is not rare in immunocompetent healthy individuals.


    TEXT
Top
Abstract
Text
References

The clinical spectrum of Bartonella henselae infection varies, ranging from classic cat scratch disease with only lymphadenopathy to severe systemic disease. In general, immunocompetent individuals tend to develop classic cat scratch disease, while immunocompromised individuals tend to have systemic disease (1). We report the prevalence of systemic B. henselae infection among otherwise healthy individuals.

Between 9 July 1996 and 7 January 1999, a total of 119 patients (80 children and 39 adults) suspected of having cat scratch disease because of either lymphadenopathy or fever of unknown origin and pet ownership were referred to us for serological diagnosis. All the patients had no underlying diseases. Sera from 33 hospitals located in central and southwestern areas of Japan were included in this study, and referring doctors included pediatricians, physicians, surgeons, otolaryngologists, ophthalmologists, dentists, radiologists, and pathologists. Serological diagnosis using the indirect fluorescent-antibody (IFA) method (4, 6) was made on the basis of either elevated titers of immunoglobulin M (IgM) (>= 1:20) or IgG (>= 1:256) antibodies or a fourfold rise in IgG titer between acute- and convalescent-phase sera. The sensitivity and specificity of our IFA method were 87 and 97.7%, respectively.

The 119 patients were categorized into four groups by clinical features (Table 1). Group 1 included patients with regional lymphadenopathy and mild symptoms, with no fever or a fever lasting less than 7 days, indicating classic cat scratch disease. Group 2 included patients with regional lymphadenopathy and a prolonged fever, lasting more than 7 days. Group 3 included patients without lymphadenopathy and with a fever lasting less than 7 days. Group 4 included patients without lymphadenopathy and with a fever lasting more than 7 days. The numbers of patients in the groups were 90, 16, 2, and 11, respectively. There were no differences between the groups in terms of age, sex, or exposures to cats.

                              
View this table:
[in this window]
[in a new window]
 
TABLE 1.   Clinical and laboratory findings for 119 patients

Of the 119 patients, 41 (31 children and 10 adults) were serologically positive for B. henselae, whereas 78 were serologically negative. Out of the 41 patients who tested positive for IFA, 27 (18 children and 9 adults) were from group 1, 6 (all children) were from group 2, and 8 (7 children and 1 adult) were from group 4.

Table 2 summarizes the clinical features for the 14 patients from groups 2 and 4 (fever lasting more than 7 days) who tested positive for IFA. The maximum temperature of these patients ranged from 39.0 to 40.5°C. Despite a prolonged fever, they were otherwise in good condition. It is noteworthy that 8 (7 children) of the 14 patients had no lymph node swelling, even though they had a prolonged fever, lasting from 7 to 25 days. Of these eight, three had hepatic granuloma and/or splenic granuloma. By using PCR analysis (5), we were able to confirm that one patient had septicemia, whereas we could not confirm septicemia for three patients. The other six patients had regional lymphadenopathy accompanied by a prolonged fever, lasting from 9 to 30 days, and PCR analysis confirmed septicemia in one patient.

                              
View this table:
[in this window]
[in a new window]
 
TABLE 2.   Clinical features for patients with prolonged fever (>= 7 days)

B. henselae has been reported as a cause of fever with bacteremia or fever of unknown origin in both immunocompetent and immunocompromised hosts (2, 3, 7). Previous reports indicated that B. henselae infection may cause fever of unknown origin without regional lymphadenopathy or hepatosplenic involvement (2, 3, 7) and is one of most common infectious diseases in children (2). Our findings support previous reports and suggest that generalized systemic B. henselae infection is not rare in healthy individuals and that children seem to be more prone to develop a prolonged fever or fever of unknown origin.

If a patient with prolonged fever or fever of unknown origin, irrespective of lymphadenopathy, owns a pet, especially a cat or dog, or has a history of pet contact, the possibility of B. henselae infection should be considered.


    ACKNOWLEDGMENTS

We thank the referring doctors for allowing us to analyze blood samples from patients suspected of having cat scratch disease.


    FOOTNOTES

* Corresponding author. Mailing address: School of Allied Health Sciences, Yamaguchi University, Ube City, Yamaguchi-Ken 755, Japan. Phone: 81-836-22-2816. Fax: 81-836-22-2816. E-mail: masato{at}po.cc.yamaguchi-u.ac.jp.


    REFERENCES
Top
Abstract
Text
References

1. Anderson, B. E., and M. A. Neuman. 1997. Bartonella spp. as emerging human pathogens. Clin. Microbiol. Rev. 10:203-219[Abstract].
2. Jacobs, R. F., and G. E. Schutze. 1998. Bartonella henselae as a cause of prolonged fever and fever of unknown origin in children. Clin. Infect. Dis. 26:80-84[Medline].
3. Lucey, D., M. Dolan, C. W. Moss, M. Garcia, D. G. Hollis, S. Wegner, G. Morgan, R. Almeida, D. Leong, K. S. Greisen, D. F. Welch, and L. N. Slater. 1992. Relapsing illness due to Rochalimaea henselae in immunocompetent hosts: implication for therapy and new epidemiological associations. Clin. Infect. Dis. 14:683-688[Medline].
4. Regnery, R. L., J. G. Olson, B. A. Perkins, and W. Bibb. 1992. Serological response to "Rochalimaea henselae" antigen in suspected cat-scratch disease. Lancet 339:1443-1445[CrossRef][Medline].
5. Tsukahara, M., H. Tsuneoka, H. Iino, K. Ohno, and I. Murano. 1998. Bartonella henselae infection from a dog. Lancet 352:1682[CrossRef][Medline].
6. Tsuneoka, H., R. Fujii, K. Yamamoto, K. Fujisawa, M. Matsuda, H. Iino, and M. Tsukahara. 1998. Determination of anti-Bartonella henselae antibody by indirect fluorescence antibody test---comparison of two types of antigen: non-cocultivated B. henselae and cocultivated B. henselae with Vero cells. J. Jpn. Assoc. Infect. Dis. 72:801-807.
7. Welch, D. F., D. A. Pickett, L. N. Slater, A. G. Steigerwalt, and D. J. Brenner. 1992. Rochalimaea henselae sp. nov., a cause of septicemia, bacillary angiomatosis, and parenchymal bacillary peliosis. J. Clin. Microbiol. 30:275-280[Abstract/Free Full Text].


Journal of Clinical Microbiology, May 2000, p. 1990-1991, Vol. 38, No. 5
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Mexas, A. M., Hancock, S. I., Breitschwerdt, E. B. (2002). Bartonella henselae and Bartonella elizabethae as Potential Canine Pathogens. J. Clin. Microbiol. 40: 4670-4674 [Abstract] [Full Text]  

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Tsukahara, M.
Right arrow Articles by Uchida, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tsukahara, M.
Right arrow Articles by Uchida, M.