We conducted the study among patients who visited Inha University Hospital, a tertiary hospital in Incheon, South Korea, during 2009–2016. From these patients, we isolated 5 cases in which B. henselae was identified from cultures of blood or bone marrow (Table 1).

Case-patient 1 (IIBC1301) was a 22-year-old man hospitalized for left inguinal lymphadenopathy that had started 10 days earlier. His body temperature was 38.5°C, and he had rashes that started on the palms and soles and subsequently spread to his entire body. B. henselae was isolated from the blood that was cultured on the second day of hospitalization.

Case-patient 2 (IIBC1302) was a 40-year-old woman hospitalized for fever and myalgia, symptoms that had lasted for 1 month. The patient had an erythematous papular rash on her face and extremities and tenderness in her abdomen. Computed tomography (CT) of the abdomen showed chronic cholecystitis; therefore, levofloxacin and metronidazole were prescribed (Technical Appendix Figure, panel A). B. henselae was identified from cultures of blood obtained on the first day of the hospitalization. The patient had not raised any animals. After discharge, the patient experienced continuous fever, poor oral intake, and weight loss. Reevaluation showed centrilobular ground-glass opacity in both lung fields on chest CT and growth of Mycobacterium tuberculosis on sputum acid-fast bacilli culture (Technical Appendix Figure, panel B). A pulmonary tuberculosis infection was diagnosed and treated with antituberculosis medication.

Case-patient 3 (IIBC1303) was a 52-year-old woman hospitalized for fever and left flank pain; her symptoms had persisted for 1 month. She also reported right-side neck swelling and pain at neck levels II, III, and VA. B. henselae was isolated from cultures of blood collected on the 16th day of hospitalization. She had no contact with animals.

Case-patient 4 (IIBC1304) was a 42-year-old man we previously reported (5) whose main complaints were fever, rash, and arthralgia. B. henselae was isolated from a bone marrow sample. The patient had no contact with or experience in raising pets.

Case-patient 5 (IIBC1305), also previously published (4), was a 73-year-old woman who had B. henselae isolated from her blood. She also did not have any contact with animals.

Bartonella species can be grown by blood agar–based culture systems. However, it is difficult to culture them this way because the growth of bacterial cells is slow, and obtaining colonies on the agar plate takes a long time. On the other hand, Bartonella species grow more rapidly with cell culture–based systems (6). For testing of these patients, we grew ECV304 cells in M199 media containing 10% heat-inactivated fetal bovine serum and inoculated 1 mL of whole blood or other samples from the patients onto the cells. After 24 hours, we washed the cells with Dulbecco’s phosphate-buffered saline and maintained them in M199 media. We performed an immunofluorescence assay (IFA) with the patient’s own serum (1:40 diluted) every week after the inoculation. When the growth of bacteria was observed, we scraped all cultured cells from the T25 flask. We then reinoculated 1 mL of infected ECV304 cells onto uninfected ECV304 cells in a T75 flask for expansion of bacterial cells.

Figure

Figure. Phylogenetic tree of 5 Bartonella henselae clinical isolates from patients in South Korea (black dots) and closely related species based on 16S rRNA gene sequences. Database accession numbers are provided for...

To identify the bacterial isolates, we amplified and sequenced the 16S rRNA gene (7). The pathogens cultured from the specimens showed the highest sequence similarities with B. henselae Houston-1 strain (GenBank accession nos. KY773227, KY773228, KY773229, KY773290, and KY885188). The similarity was >99% (Figure) (8,9). IFA results using a commercial Bartonella IFA IgG kit (FOCUS Diagnostics, DiaSorin Molecular, Cypress, CA, USA) also showed positive results for all patients’ serum samples; titers ranged from 1:40 to 1:1,280 (Table 1). We also performed multilocus sequence typing to determine the genotypes of B. henselae isolates (10) and found that all isolates belonged to sequence type 1 (Table 2).

We cultured B. henselae isolates from clinical samples and compared characteristics of 5 patients: 3 new cases and 2 previously reported cases from which B. henselae was isolated (Table 2). Because of the diverse manifestations of B. henselae infection, the symptoms were similar to those of other bacterial infections. B. henselae infections in 3 patients were initially misdiagnosed as other diseases: sexually transmitted disease (case-patient 1), enteric fever-like syndrome (case-patient 2), and acute pyelonephritis (case-patient 3). The diagnosis of B. henselae infection was made even more difficult because none of these 5 patients reported a history of raising cats. However, the absence of contact with animals should not preclude infection; even though B. henselae infection is ususally related to cat scratches or bites, it may also occur without animal contacts (5). It is also noteworthy that the patient described in case 2 was co-infected with pulmonary tuberculosis. Co-infection with B. henselae and Mycoplasma spp. has also been reported in previous studies (11,12). Co-infection with other bacteria suggests that infection with Bartonella species may weaken the host’s immune system, leaving the host vulnerable to secondary infections. In addition, these co-infections may cause difficulty in diagnosing Bartonella infection.

Multilocus sequence typing indicated that all isolates from this study belonged to B. henselae sequence type 1. This result is consistent with previous studies, which showed relatively less diversity among human strains than among the feline reservoir (10,13).

In summary, the clinical features of B. henselae infection are diverse and nonspecific, which could initially lead to misdiagnosis as other diseases. Physicians and patients should consider that Bartonella infection presents various clinical symptoms and might be a common cause of fever of unknown origin, irrespective of exposure to cats. Once Bartonella infection is suspected, cell culture should be considered to confirm the diagnosis.