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Volume 31, Number 4—April 2025
Research Letter

Coxiella burnetii Infections Identified by Molecular Methods, United States, 2006–2023

Author affiliation: Centers for Disease Control and Prevention, Atlanta, Georgia, USA (C.K. Maki, J.S. Salzer, N. Bestul, G.J. Kersh, D.W. McCormick); Oak Ridge Institute for Science and Education, Oak Ridge, Tennessee, USA (C.K. Maki); University of Washington, Seattle, Washington, USA (T.T. Truong, B.T. Cookson, S.J. Salipante, J.A. Lieberman)

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Abstract

We identified 34 patients with Coxiella burnetii infection using PCR; 31 (86%) cases were diagnosed from cardiac specimens. Nearly half (15/31, 48%) of those cases were not reported to any channel of national disease surveillance, indicating substantial underreporting for diseases identified using molecular methods at noncommercial laboratories.

Coxiella burnetii bacteria, the etiologic agent of Q fever, can cause nationally notifiable acute or chronic infection in humans (1). In accordance with the Council for State and Territorial Epidemiologists case definition published in 2008 (2), confirmed cases must meet clinical criteria and have either confirmatory laboratory evidence via paired serology or molecular methods, including PCR, or a confirmed epidemiologic link (3). Probable cases are those with clinically compatible symptoms and presumptive laboratory evidence (3). Suspected cases are those reported to local and state health departments by clinicians and laboratories where health department staff classify cases as confirmed or probable and report to US Centers for Disease Control and Prevention through the National Notifiable Diseases Surveillance System (NNDSS) using a standardized case report form (CRF). During 2008–2019, an annual average of 131 acute and 30 chronic cases were reported to CDC (4). Although PCR is a useful diagnostic modality for Q fever, it is not clear if cases identified using molecular methods at noncommercial laboratories are captured in national surveillance data (3,5).

We searched the laboratory information system for specimens submitted to the University of Washington Medicine Molecular Microbiology clinical diagnostic reference laboratory (UWMMD) with C. burnetii identified by broad-range bacterial PCR assay (6) or 16S amplicon next-generation sequencing (7). Acceptable specimen types were fresh-frozen tissue, body fluids other than blood, and formalin-fixed paraffin-embedded tissue. We obtained information on specimen type, patient age and sex, date of specimen collection, and submission state for 35 specimens from 34 patients. We attempted to match those patients to CRFs reported to CDC (3) by using patient age at time of specimen collection, sex, test result date, state from which the specimen was submitted, and specimen type information. We also matched using NNDSS data based on age and state of residence; those matches were not considered as strong as the CRF matching because NNDSS data do not include laboratory results. We performed descriptive statistical computations using R Studio 2023.06.1 (Posit, http://www.rstudio.com). The University of Washington Institutional Review Board approved the study (IRB; approval no. STUDY00013877); the study was exempt from IRB requirements, in accordance with CDC policies and procedures.

Median age of 34 identified patients was 62.5 (range 23–79) years; 19 (56%) were male and 15 (44%) were female (Table 1). The most common states for specimen collection were California (9 [27%]), Washington (7 [21%]), and Oregon (2 [6%]). Most (30/35 [86%]) specimens were cardiac tissue involving the aortic or mitral valves (23/30 [77%]). Eight (27%) specimens were prosthetic valves.

Matching was not possible for 3 patients because surveillance data from 2023 were not submitted to CDC at the time of this investigation. Of the 16 (52%) patients reported in surveillance data, 3 (10%) had data via CRF alone, 8 (26%) had data via NNDSS alone, and 5 (16%) had data through both sources (Table 2). Among 31 patients with invasive C. burnetii infections identified during 2006–2023 using molecular methods, 48% had no surveillance data submitted to either reporting channel. That finding suggests that Q fever cases identified using molecular methods are not adequately captured in routine public health surveillance. Previous studies have detailed substantial underreporting of both acute and chronic Q fever in the United States (8,9). The lack of reporting of nearly half of those tissue invasive infections identified using molecular methods is especially concerning because invasive cases are likely to be more severe (8).

Testing laboratories are responsible for notifying local or state public health departments of positive cases. However, C. burnetii molecular testing on invasive tissue infections is typically performed at specialized referral laboratories that may be outside of the patient’s state of residence. Consistent with state policies that require reporting to the local public health jurisdiction, out-of-state referral laboratories do not routinely report back to the patient’s public health department; the clinician who ordered testing or the local clinic laboratory are typically required to report to the patient’s home state.

C. burnetii was identified in cardiac specimens among most (86%) patients in this cohort. Endocarditis accounts for 60%–78% of chronic Q fever cases globally (3), and patients with previous valvulopathy or with prosthetic valves are at increased risk (2,10). The higher proportion of endocarditis identified in this case series likely reflects referral practices from submitting institutions, particularly the common use of molecular testing in cases of suspected culture-negative endocarditis. We also observed bias in referral practices in the geographic skew to the West Coast, given UWMMD’s location in Washington.

In summary, our findings suggest substantial underreporting of C. burnetii cases identified through molecular methods as well as the need to create mechanisms that streamline reporting notifiable conditions from laboratories outside a patient’s home public health jurisdiction. Lack of clinician knowledge on reporting protocols, combined with miscommunication between healthcare providers, hospital laboratories, and state and local health departments, might contribute to the underreporting of C. burnetii infection we observed.

Ms. Maki is an ORISE fellow in the Rickettsial Zoonoses Branch in the Division of Vector-Borne Diseases, National Center for Emerging and Zoonotic Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia. Her primary interests are zoonotic disease transmission and One Health.

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Acknowledgment

This project was supported in part by an appointment to the Research Participation Program at the Centers for Disease Control and Prevention administered by the Oak Ridge Institute for Science and Education through an interagency agreement between the US Department of Energy and the Centers for Disease Control and Prevention.

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References

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  3. Anderson  A, Bijlmer  H, Fournier  PE, Graves  S, Hartzell  J, Kersh  GJ, et al. Diagnosis and management of Q fever—United States, 2013: recommendations from CDC and the Q Fever Working Group. MMWR Recomm Rep. 2013;62(RR-03):130.PubMedGoogle Scholar
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Tables

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Suggested citation for this article: Maki CK, Truong TT, Salzer JS, Bestul N, Cookson BT, Kersh GJ, et al. Coxiella burnetii infections identified by molecular methods, United States, 2006–2023. Emerg Infect Dis. 2025 Apr [date cited]. https://doi.org/10.3201/eid3104.241214

DOI: 10.3201/eid3104.241214

Original Publication Date: March 12, 2025

1These senior authors contributed equally to this article.

Table of Contents – Volume 31, Number 4—April 2025

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David McCormick, Centers for Disease Control and Prevention, 1600 Clifton Rd NE, MS H16-2, Atlanta, GA 30329-4018, USA

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Page created: February 28, 2025
Page updated: March 12, 2025
Page reviewed: March 12, 2025
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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