Volume 19, Number 11—November 2013
Mayaro Virus Infection, Amazon Basin Region, Peru, 2010–2013
During 2010–2013, we recruited 16 persons with confirmed Mayaro virus infection in the Peruvian Amazon to prospectively follow clinical symptoms and serologic response over a 12-month period. Mayaro virus infection caused long-term arthralgia in more than half, similar to reports of other arthritogenic alphaviruses.
Since the discovery of Mayaro virus (MAYV) in Trinidad in 1954, the etiologic agent of Mayaro fever has been identified in French Guiana, Suriname, Venezuela, Peru, Bolivia, and Brazil (1–9). The presumed primary vectors, Haemagogus mosquitoes, inhabit rural settings and tree canopies, a factor that may explain the relative paucity of cases and restricted endemicity. However, Aedes aegypti mosquitoes have been shown to be competent vectors of MAYV in the laboratory (10), suggesting that an urban-dwelling arthropod could be a vector of this virus over a wider scale. MAYV infection has been demonstrated in tourists returning from the Amazon region, highlighting not only the need to consider MAYV in febrile returned travelers, but also a possible role in global transmission (11).
Incapacitating chronic joint pain has been described with other arthritogenic alphaviruses (12), but little is known about the prognosis and serologic response over long periods after MAYV infection. Therefore, we conducted a prospective 1-year longitudinal study to determine the clinical manifestations and to describe the serologic response among humans with Mayaro fever in the Peruvian Amazon Basin.
Persons identified for this cohort were recruited in a passive febrile surveillance study in 15 health centers in 4 Peruvian cities: Iquitos, Yurimaguas, Chanchamayo, and Puerto Maldonado (Figure 1). Persons meeting the following criteria were recruited: age >5 years, oral/tympanic temperature >38°C (or axillary >37.5°C), and no obvious focus of infection. Written consent was obtained from all adults and from a parent or guardian for participants <18 years of age; participants 8–17 years of age also provided written assent. The surveillance period of this study was December 6, 2010–April 30, 2012. Follow-up appointments continued for another year, through April 5, 2013. The institutional review boards of the US Naval Medical Research Unit No. 6 and the Peruvian Ministry of Health approved the protocol.
Compared with the day of the visit for acute illness (acute-phase visit), follow-up evaluations occurred at 20 (SD) days (±10 days), 3 months (±10 days), 6 months (±15 days), and 12 months (±30 days). At the acute-phase visit and at all follow-up visits, a blood sample was obtained.
For every participant, we attempted to determine the cause of infection by testing acute-phase serum for virus in Ae. albopictus (C6/36) and African green monkey kidney (Vero 76) cell culture (with immunofluorescence assay) and for viral nucleic acid by reverse transcription PCR (RT-PCR). Capture IgM and IgG ELISAs were performed at 1:100 dilution on the acute-phase and all follow-up samples to evaluate antibody responses to MAYV and other endemic arboviruses (i.e., Venezuelan equine encephalitis, Oropouche, group C, Guaroa, and dengue viruses) (6). Samples with detectable IgM or IgG were serially diluted and retested. Seroconversion was defined as a >4-fold increase in IgM titer between the acute-phase visit and the second visit. A Mayaro fever case was defined as IgM seroconversion or virus detected by isolation or by RT-PCR. In addition, we collected throat swabs from participants with pharyngeal erythema at the acute-phase visit and urine samples from the 3-month follow-up visit to determine the presence of MAYV with RT-PCR (13).
Of 2,094 febrile participants enrolled, 16 (0.8%) had Mayaro fever (Table 1). Of the 16 persons with Mayaro fever, 11 had MAYV isolated by the cell culture assays (11 in both Vero 76 and C6/36), 13 were MAYV positive by RT-PCR, and all had IgM ELISA seroconversion between the acute-phase and 20-day follow-up visits (Table 1). In all 16 participants, no IgM ELISA seroconversion occurred for endemic non-alphavirus viruses (i.e., Oropouche, group C, Guaroa, and dengue viruses). Four participants demonstrated IgM ELISA seroconversion against another alphavirus, Venezuelan equine encephalitis virus, but these 4 all had MAYV identified by immunofluorescence assay and by RT-PCR. Using RT-PCR, we did not detect MAYV in 2 acute visit throat swabs, any second-visit (20-day) serum samples, and any third-visit (3-month) urine samples.
Besides fever, the most common symptoms affecting participants in the acute stage of MAYV infection were malaise, headache, arthralgia, myalgia, and retro-orbital pain. The prevalence of these and other nonjoint signs and symptoms at the acute-phase and follow-up visits are available in the Technical Appendix Table.
Although reports of joint pain waned in study participants by the second (20-day) visit, complaints increased at 3 months and persisted in 54% even after 12 months. Joints of the hand, wrist, elbow, feet, and knee were identified as problematic, whereas hip or axial joint pain was rare (Figure 2). The chronic joint pain often interfered with activities of daily living (Table 2).
This study demonstrated that persons with acute Mayaro fever often have many nonspecific symptoms but may continue to have chronic joint pain for at least 1 year after acute illness. Our study offers physicians valuable prognostic data to share with patients. It also indicates the need to consider MAYV infection in patients with seronegative arthritis (i.e., negative rheumatoid factor and antinuclear antibodies) in regions to which MAYV is endemic.
Previous reports have documented persistent joint pain after MAYV infection (2–5,9,11), although all of these were either solitary case reports or case series of <4 persons. By using follow-up periods ranging from 1 month to 12 months, most of these studies identified persistent symptoms in the fingers. Involvement of joints of the wrist, ankle, and knee also were mentioned, similar to the participants in our study.
Long-term manifestations of infection with other alphaviruses have been more robustly characterized, with persistent arthralgia being commonly described. Follow-up of chikungunya virus–infected patients on Réunion Island revealed that ≈60% had joint pain >3 years after acute illness that most often affected the fingers, wrists, knees, and ankles (14). Sindbis virus infection in a cohort in Finland resulted in persistent arthralgia lasting at least a year in half of those infected, with ankles, fingers, and wrists being most often affected (15). One caveat of our study and other studies is the difficulty in definitively attributing persistent arthralgia solely to viral infection, although our participants’ limitations in activities of daily living were all described as starting after their acute Mayaro fever illness.
IgM seroconversion occurred in all of the participants in our study that were identified with either isolation or RT-PCR, consistent with another report that noted the reliability of serology in detecting MAYV infection (9). In our study participants identified by serology, both RT-PCR and culture were more sensitive than what others have found for Sindbis virus infection, for which 1 study found sensitivities of 7% and 1%, respectively (15). However, RT-PCR and culture were negative in the only 2 participants in our study who had Mayaro fever after day 3 of symptoms, suggesting a narrow window when these assays may be effective.
No effective vaccine or antiviral agent exists for the arthritogenic alphaviruses, and treatment relies mainly on supportive modalities, such as nonsteroidal anti-inflammatory medications (12). Our results offer evidence that MAYV, similar to other alphaviruses, may cause protracted joint symptoms and provide further impetus to the development of more effective preventive and treatment strategies.
Dr Halsey is a board-certified infectious diseases physician, US Air Force officer, and Virology Department head at the US Naval Medical Research Unit No. 6 in Lima, Peru. His research interests include the clinical and epidemiologic aspects of flavivirus, alphavirus, and bunyavirus infections.
We thank Brett Forshey for his critical reading of this manuscript and Karen Campos and Yojani Aguilar for their assistance with field work and follow-up in Yurimaguas.
This work was supported by the Armed Forces Health Surveillance Center’s Global Emerging Infections Systems Research Program. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
The authors have declared that no competing interests exist. The corresponding author had full access to all data in the study and final responsibility for the decision to submit this publication.
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Table of Contents – Volume 19, Number 11—November 2013
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Eric S. Halsey, US Naval Medical Research Unit No. 6, 3230 Lima Pl, Washington, DC 20521-3230, USA