Isolation of Candidatus Bartonella melophagi from Human Blood

Candidatus Bartonella melophagi was isolated by blood culture from 2 women, 1 of whom was co-infected with B. henselae. Partial 16S rRNA, RNA polymerase B, and citrate synthase genes and 16S–23S internal transcribed spacer sequences indicated that human isolates were similar to Candidatus B. melophagi.

During the next 2 years, these symptoms persisted, along with exertional chest pains, a previously undiagnosed ausculted II to III/VI holosystolic murmur, headaches, diffi culty speaking, diffi culty sleeping, weakness involving the arms, joint pain, and facial tremors. No abnormalities were shown on an electrocardiogram. An echocardiogram identifi ed mildly thickened aortic and mitral valve leafl ets, mild aortic insuffi ciency, and mild mitral regurgitation.
After the acute illness, the woman reported cycles of illness every 3 to 4 weeks. Results of numerous complete blood counts were normal, with the exception of persistently low neutrophil counts of 2,000-2,500 neutrophils/μL. All serum biochemical parameters remained within normal reference ranges during the 2-year illness. Borrelia burgdorferi C6 peptide and immunoglobulin (Ig) M and IgG antibodies to Babesia microti were not detected. Results of PCRs specifi c for Anaplasma phagocytophilum, B. microti, and B. burgdorferi were negative. Oral antimicrobial drugs resulted in transient improvement; however, symptoms returned within days after the use of these drugs was stopped. Blood culture resulted in the detection of Candidatus B. melophagi and isolation of B. henselae. Her serum was not reactive with B. henselae or B. vinsonii subsp. berkhoffi i antigens.
Treatment with rifampin and azithromycin, started in January 2006, resulted in some overall improvement in symptoms. Cefuroxime was added in February, and the combination resulted in substantial improvement, after which the drugs were selectively withdrawn. For 15 years before the onset of illness, this person had worked as an animal shelter manager in West Virginia and as a veterinary offi ce manager in Virginia. Animal contact was minimal, but she had been bitten by fl eas and mosquitoes. Travel history was limited to the eastern and central United States.
Patient 2 was a 65-year-old woman whose condition had been diagnosed as pericarditis of undetermined etiology in September 2004. Six months later, because of residual fatigue and muscle weakness in the arms and legs, mostly on her right side, a blood sample was cultured in Bartonella alpha proteobacteria growth medium (BAPGM).
The woman lived on a farm in southern California with her husband and managed a large animal sanctuary that also housed ≈100 cats and ≈100 dogs. She had resided in southern California for 50 years but occasionally traveled to the southeastern United States and other countries. She was directly involved in daily care of animals and had exposure to pet cattle and sheep, wolf hybrids, lamas, emus, pigs, horses, and numerous pet bird species. Bites and scratches were a daily occurrence, and exposure to cattle and sheep occurred at least weekly. In addition, the woman We used BAPGM and other published blood culture methods to test blood samples from both women (2,8,9). Candidatus B. melophagi DNA was amplifi ed directly from blood of patient 2, and from the respective BAPGM enrichment cultures and 14-day subculture colonies from both patients. Sequence analysis of respective colony isolates showed B. henselae (internal transcribed spacer [ITS] sequence identical to Houston 1 strain, data not shown) and Candidatus B. melophagi from patient 1 and Candidatus B. melophagi (isolate 05-HO-1) from patient 2. Both isolates were composed of extremely small gram-negative bacilli consistent with Bartonella spp. Sequence analyses for both isolates are summarized in the Table. Unfortunately, attempts to separate B. henselae and Candidatus B. melophagi colonies from the sample of patient 1 by serial passage were unsuccessful. Bartonella sp. DNA was not amplifi ed from an uninoculated BAPGM control culture or from sheep blood used as a supplement. Flagella, as visualized in the Candidatus B. melophagi strain K-2C isolated from sheep blood (Figure), were not visualized in the human 05-HO-2 strain by transmission electron microscopy.

Conclusions
Based on 16S rRNA, citrate synthase and RNA polymerase B genes, and the 16S-23S ITS region, the bacteria detected in these woman was most likely Candidatus B. melophagi, which was recently isolated from sheep blood and sheep keds (10; M. Kosoy, unpub. data). ITS sequences were nearly identical to those of Wolbachia melophagi de-tected in a tick removed from sheep in Peru (11). Similar to electron micrographs of the Bartonella sp. isolated from sheep blood (1), no fl agella were observed by transmission electron microscopy of the 05-HO-1 human isolate, whereas the sheep ked isolate contains fl agella. Because both women had had frequent contact with numerous domestic and wild animals and potential insect vectors, the route of transmission is unknown.
The clinical relevance of Candidatus B. melophagi infection in these women remains to be established. Efforts to passage Candidatus B. melophagi in our laboratory and others (D.A. Bemis, 10) have not been successful. Therefore, development of a serologic assay was not pursued. Nonspecifi c abnormalities, including diffi culty sleeping, muscle weakness, joint pain, and facial tremors, have been reported in association with isolation of B. henselae and B. vinsonii subsp. berkhoffi i (2,12). Pericardial or pleural effusions are infrequent complications of B. henselae infection in association with classical cat-scratch disease (13,14).
Before the report of Candidatus B. melophagi in commercial sheep blood sources in 2007 (10), sheep blood was used as a BAPGM supplement in our laboratory. With the exception of these 2 patients, Candidatus B. melophagi was never detected by PCR in >2,250 BAPGM enrichment blood cultures or subculture isolates obtained from animals or humans. In addition, Candidatus B. melophagi DNA was never amplifi ed from >250 BAPGM uninoculated BAPGM enrichment control cultures, and bacterial colonies were never observed after subculture. Beginning in 2007, we also found that some batches of commercial sheep blood contained Candidatus B. melophagi DNA. Therefore, we no longer use blood as a BAPGM supplement. Recently, BAPGM was used to facilitate isolation of B. tamiae from human patients in Thailand (7), and another laboratory has published data supporting the utility of insect cell culture media for growing Bartonella spp. (15).