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Bartonella Species Antibodies (IgG, IgM) with Reflex to Titers

Test Summary

This antibody panel helps diagnose infections with Bartonella henselae and Bartonella quintana. This panel includes IgM and IgG antibodies with reflexes to titers for positive results.

B henselae causes cat scratch disease, a self-limiting bacterial infection transmitted via exposure to cats or cat fleas. B quintana causes trench fever, a febrile bacteremic illness transmitted via body lice. B henselae and B quintana are the 2 Bartonella species that most frequently cause blood culture-negative endocarditis. In immunocompromised individuals, infections with B henselae and B quintana may present as bacillary angiomatosis, a vasculoproliferative disease of the skin [1-4].

Because of the fastidious nature of B henselae and B quintana, recovery of these bacteria is rarely successful, especially from blood. Serology is commonly used for diagnosing Bartonella infections [1,3]. Confirmation of recent or current infection with either B henselae or B quintana may require testing of serial specimens to demonstrate a 4-fold increase of IgG titers or the presence of IgM. A B henselae or B quintana IgG titer of 1:800 has been proposed as a major criterion for diagnosing Bartonella endocarditis [4].

IgG cross-reactivity between B henselae and B quintana often occurs [1,3]. Qualitative real-time polymerase chain reaction is a highly specific and sensitive method to detect the presence of Bartonella species DNA in clinical specimens and can differentiate between B henselae and B quintana.

The results of this test should be interpreted in the context of pertinent clinical history and physical examination findings.

References
1. Dumler JS, et al. Bartonella. In: Carroll KC, et al, eds. Manual of Clinical Microbiology. 12th ed. ASM Press; 2019. https://www.clinmicronow.org/doi/book/10.1128/9781683670438.MCM.ch50
2. Centers for Disease Control and Prevention. Bartonella infection (cat scratch disease, trench fever, and Carrion's disease). Last reviewed December 18, 2019. Accessed January 28, 2022. https://www.cdc.gov/bartonella/clinicians/index.html
3. Miller JM, et al. Clin Infect Dis. 2018;67(6):813-816.
4. Okaro U, et al. Clin Microbiol Rev. 2017;30(3):709-746.

Aliases

  • N/A

Specimen Collection

Special Instructions

N/A

Preferred Specimen

1 mL serum

Minimum Volume

0.2 mL

Instructions

N/A

Patient Preparation

N/A

Storage

N/A

Transport Temperature

Room temperature

Specimen Stability

  • Room temperature: 7 days
  • Refrigerated: 14 days
  • Frozen: 30 days

Limitations

B. quintana and B. henselae as well as chlamydia species and Coxiella burnetii may cross-react and produce false-positive results.

Other Acceptable Specimens

N/A

Unacceptable Specimens

Gross hemolysis • Grossly lipemic • Grossly Icteric

Order Code

BARTSP

EPIC (Premier) Code

LAB3775

Includes

Bartonella henselae Antibodies (IgG, IgM) with Reflex to Titers
Bartonella quintana Antibodies (IgG, IgM) with Reflex to Titers

If B. henselae (IgG) Screen is positive, then B. henselae (IgG) titer will be performed at an additional charge (CPT code(s): 86611).
If B. henselae (IgM) Screen is positive, then B. henselae (IgM) titer will be performed at an additional charge (CPT code(s): 86611).

If B. quintana (IgG) Screen is positive, then B. quintana (IgG) titer will be performed at an additional charge (CPT code(s): 86611).
If B. quintana (IgM) Screen is positive, then B. quintana (IgM) titer will be performed at an additional charge (CPT code(s): 86611).

CPT Code

  • 86611 (x4)

Billing Code

  • 670576

CPT Statement

Methodology

Immunofluorescence Assay (IFA)

FDA Status

This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by the U.S. Food and Drug Administration. The FDA has determined that such clearance or approval is not necessary. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.

Physician Attestation of Informed Consent

N/A

Testing Laboratory

Quest Diagnostics Nichols Institute
14225 Newbrook Drive
Chantilly VA, 20153

Department

Reference Testing

Reference Range

B. henselae (IgG) Screen Negative
B. quintana (IgG) Screen Negative
B. henselae (IgM) Screen Negative
B. quintana (IgM) Screen Negative

Setup Schedule / Expected Turnaround Time

Monday - Saturday morning; Report available: 1 day

Specimen Collection

Special Instructions

N/A

Preferred Specimen

1 mL serum

Minimum Volume

0.2 mL

Instructions

N/A

Patient Preparation

N/A

Storage

N/A

Transport Temperature

Room temperature

Specimen Stability

  • Room temperature: 7 days
  • Refrigerated: 14 days
  • Frozen: 30 days

Limitations

B. quintana and B. henselae as well as chlamydia species and Coxiella burnetii may cross-react and produce false-positive results.

Other Acceptable Specimens

N/A

Unacceptable Specimens

Gross hemolysis • Grossly lipemic • Grossly Icteric

Billing

CPT Code

  • 86611 (x4)

Billing Code

  • 670576

CPT Statement

Result Information

Methodology

Immunofluorescence Assay (IFA)

Testing Laboratory

N/A

Reference Range

B. henselae (IgG) Screen Negative
B. quintana (IgG) Screen Negative
B. henselae (IgM) Screen Negative
B. quintana (IgM) Screen Negative

Setup Schedule / Expected Turnaround Time

Monday - Saturday morning; Report available: 1 day