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Published on: August 31, 2013
Bartonella henselae is usually not viable in lymph nodes of patients with cat scratch disease
Insights
Bartonella henselae, the cause of cat scratch disease (CSD), is rarely viable in patient lymph nodes. This study found that most lymph nodes with B. henselae DNA showed no signs of active infection.
Area of Science:
- Infectious Diseases
- Microbiology
- Pathology
Background:
- Bartonella henselae is the primary cause of cat scratch disease (CSD), a common condition leading to lymphadenitis in children and adults.
- Isolation rates of B. henselae from CSD patient lymph nodes are notably low, suggesting challenges in detecting active infection.
Purpose of the Study:
- To assess the viability of Bartonella henselae within lymph node biopsy samples from patients diagnosed with CSD.
- To investigate the discrepancy between the presence of B. henselae DNA and active bacterial presence in CSD lymphadenitis.
Main Methods:
- Analysis of 87 lymph node biopsy samples from CSD patients using reverse transcription-quantitative polymerase chain reaction (RT-qPCR) to detect B. henselae RNA.
- Complementary diagnostic methods included bacterial cultures, histological analysis, and fluorescence in situ hybridization (FISH).
Main Results:
- Only 8% (9 out of 87) of lymph nodes positive for B. henselae DNA also showed detectable B. henselae RNA, indicating low viability.
- No significant difference in threshold cycle (CT) values was observed between RNA-positive and RNA-negative samples.
- Cultures, histology, and FISH assays were negative across all tested samples, further supporting limited bacterial viability.
Conclusions:
- Bartonella henselae demonstrates limited or no viability in the majority of lymph nodes from patients presenting with cat scratch disease.
- The presence of B. henselae DNA in lymph nodes does not reliably indicate active bacterial infection or viability in CSD cases.
Abstract:
Bartonella henselae, the agent of cat scratch disease (CSD), appears to be a common organism responsible for lymphadenitis in both adults and children. There is a very low isolation rate for B. henselae from lymph nodes of patients with CSD. Our objective was to evaluate B. henselae viability in a large series of lymph nodes from patients with CSD. From January to November 2016, we analyzed lymph node biopsy samples from patients diagnosed with CSD. We used reverse transcription-quantitative polymerase chain reaction (RT-qPCR) to detect B. henselae RNA, as well as cultures, histological analyses, and fluorescence in situ hybridization (FISH). We tested 87 lymph nodes positive for B. henselae DNA but only 8 (9%) presented with B. henselae RNA. We did not find a significant difference for the pap threshold cycle (CT) values between RNA-positive and RNA-negative lymph nodes (p = 0.5). Cultures, histological analyses, and FISH were negative for all the tested samples. We provide evidence that B. henselae are not or are rarely viable in most cases in the lymph nodes of patients with CSD.
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