Volume 29, Number 4—April 2023
Retrospective Screening of Clinical Samples for Monkeypox Virus DNA, California, USA, 2022
We retrospectively screened oropharyngeal and rectal swab samples originally collected in California, USA, for Chlamydia trachomatis and Neisseria gonorrhoeae testing for the presence of monkeypox virus DNA. Among 206 patients screened, 17 (8%) had samples with detectable viral DNA. Monkeypox virus testing from mucosal sites should be considered for at-risk patients.
Monkeypox virus (MPXV) is an enveloped, double-stranded DNA virus in the family Poxvirus, genus Orthopoxvirus, and is related to variola, the causative agent of smallpox. In 2022, MPXV transmission caused a large global mpox disease outbreak that disproportionately affected male persons who identified as gay, bisexual, and men who have sex with men (MSM) and persons who identified as transgender (1). The clinical manifestations of MPXV infection also evolved from prior outbreaks; more patients in 2022 had anogenital rash and proctitis, rather than disseminated cutaneous lesions (1). During prior mpox outbreaks, asymptomatic or subclinical MPXV infection was thought to be rare, but evidence from the 2022 outbreak suggests that infected patients can have minimal symptoms (2,3). To identify persons with subclinical MPXV infection, we retrospectively analyzed oropharyngeal and rectal swab samples submitted for Chlamydia trachomatis and Neisseria gonorrhoeae (CT/NG) testing at a tertiary academic medical center.
Swab samples were collected at Stanford Health Care by using the Aptima Multitest Swab Specimen Collection Kit for the Aptima Combo 2 Assay (Hologic, https://www.hologic.com). We included all samples collected during July 7–September 6, 2022 that had sufficient residual volume. The study was approved by the Stanford University institutional review board (protocol no. 66786).
We extracted total nucleic acids from 300 μL of Aptima Specimen Transport Medium (Hologic) by using the Chemagic instrument (PerkinElmer, https://www.perkinelmer.com), according to the manufacturer’s recommendations. To test for MPXV DNA, we used 2 laboratory-developed quantitative PCR (qPCR) assays modified from Centers for Disease Control and Prevention published assays (4,5). The first qPCR targeted viral DNA polymerase sequence conserved throughout nonvariola orthopoxviruses, including MPXV. The second qPCR targeted the viral tumor necrosis factor (TNF) receptor sequence specific for MPXV clade II (formerly West African clade). We performed qPCR reactions as previously described (6), except we used the CFX96 thermal cycler (Bio-Rad, https://www.bio-rad.com). We tested all specimens with both qPCR assays and interpreted samples with concordant MPXV as mpox-positive and samples without detected MPXV as mpox-negative. When there was discordance between viral DNA polymerase and the viral TNF receptor targets, we repeated both reactions from the eluate and interpreted the sample as positive only if MPXV was reproducibly detected. We excluded 3 concordant negative samples in which the internal control (β-globin gene) failed in one or both reactions.
A total of 347 swab samples submitted for CT/NG testing from 206 patients met the inclusion criteria: 195 (56%) oropharyngeal and 152 (44%) rectal swab specimens. Patients ranged in age from 7 days–77 years (mean 35 years). Most (176/206; 85%) patients were male; 1 patient was assigned male at birth but identified as genderqueer. Twelve patients in this cohort had known MPXV infection diagnosed via lesion qPCR.
Overall, we detected viral DNA in 24/347 (7%) samples, including 11/195 oropharyngeal and 13/152 rectal swab specimens, representing 17/206 (8%) patients (Figure). Among 17 patients who tested MPXV-positive, 6 (35%) had received an mpox vaccine. No patients received a vaccine >14 (range 4–12) days before their positive test. Of 12 persons with known mpox who underwent CT/NG testing, 11 (91.7%) had detectable MPXV DNA from swab samples, comprising 16 positive samples. Six patients without lesions or diagnosed mpox had detectable MPXV DNA from CT/NG swabs, comprising 8 positive samples (Table). Of those patients, 3 (50%) were asymptomatic and 3 (50%) symptomatic; 2 had proctitis and 1 had pharyngitis. Like patients with known mpox, all 6 patients with newly diagnosed mpox were MSM. In addition, 50% (3/6) of patients with new mpox diagnoses were co-infected with another sexually transmitted infection compared with 42% (5/12) of patients with known MPXV infections, 33% (2/6) were HIV-positive (vs. 42%; 5/12), and 33% (2/6) were on HIV preexposure prophylaxis (vs. 58%, 7/12).
Our findings demonstrate that patients without cutaneous lesions can be MPXV-positive, which is consistent with observations reported in similarly designed studies in Europe (7,8). Occult infection with oropharyngeal and rectal viral shedding might have contributed to the scale of the 2022 mpox outbreak, which spread through sexual networks. All but 1 patient with known MPXV infection in our cohort had detectable viral DNA in oropharyngeal or rectal swab samples, suggesting that the new infections we detected are likely true positives. Furthermore, all newly identified mpox patients in our study had >1 sample for which both qPCR targets were detected.
Current MPXV tests cleared for emergency use are indicated only for use on lesion samples (9). Further studies are needed to characterize viral shedding dynamics, particularly related to symptom onset and duration of infectivity. As data demonstrating mucosal viral shedding in mpox emerge, expanding testing to allow broader sample collection and expedite diagnostic validation of samples from various anatomic sites will be crucial.
In conclusion, during the ongoing mpox outbreak, clinicians should consider oropharyngeal and rectal MPXV qPCR testing for at-risk patients with pharyngitis or proctitis. In addition, asymptomatic screening in high-risk populations might be warranted if community prevalence is high or rising.
Dr. Contag is an infectious diseases fellow at Stanford University, Stanford, California, USA. Her primary research interests are emerging and reemerging infectious diseases and the management of critical illness in low-resource settings.
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TableCite This Article
Original Publication Date: March 14, 2023
Table of Contents – Volume 29, Number 4—April 2023
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Please use the form below to submit correspondence to the authors or contact them at the following address:
Caitlin Contag, Stanford University, Department of Medicine, Division of Infectious Diseases and Geographic Medicine, 300 Pasteur Dr, L-134, Stanford, CA 94305, USA