Antibodies Reactive to Rickettsia rickettsii Among Children Living in the Southeast and South Central Regions of the United States FREE

EMERGING TICK-BORNE diseases represent a particular problem for pediatricians because the habitats of children and ticks increasingly converge.¹ In fact, Rocky Mountain spotted fever (RMSF), a prototypical tick-borne rickettsiosis caused by Rickettsia rickettsii, occurs most commonly in children aged 5 to 9 years.² Unfortunately, early recognition of the disease can be impeded by the overlap of symptoms such as fever, headache, myalgia, and rash with common benign viral syndromes.³ This can lead to delayed empirical antibiotic therapy and increased mortality.^4- 7

Although RMSF is the most common fatal tick-borne disease in the United States, it remains relatively rare. From 1993 to 1996, only 1253 cases were reported to the Centers for Disease Control and Prevention, for an average annual incidence of 2.2 per million.² Human contact with ticks, however, is undoubtedly common, and in regions where the prevalence of R rickettsii–infected ticks may be high,⁸ such contact is likely to lead to exposure and infection. The discrepancy between the number of reported cases and the number of probable exposures has led to the suggestion that many cases of RMSF are self-limited and subclinical or misdiagnosed.^9- 14

The present study is, to our knowledge, the largest and most geographically extensive serosurvey of rickettsial infection in children in the United States. Even if one uses the most stringent criteria to define seropositive individuals, the results suggest widespread infection with R rickettsii or related spotted-fever group rickettsia.

Details of the study population have been published.¹⁵ Briefly, residual serum or plasma from patients who had their blood drawn for any reason was collected at each of 7 pediatric centers. These specimens were considered waste, and since they were anonymously linked to demographic data, the need for informed consent was waived at each institution. A total of 1999 subjects (1015 boys) aged 1 to 17 years of age were studied from the following sites: Winston-Salem, NC (n = 312); Louisville, Ky (n = 300); Nashville, Tenn (n = 299); Memphis, Tenn (n = 302); Little Rock, Ark (n = 296); Kansas City, Mo (n = 194); and Oklahoma City, Okla (n = 296). The age distribution was skewed toward older patients, because they have more residual serum after clinical tests are performed. Sites differed with respect to subject age, racial distribution, the proportion living in an urban setting, and the source of specimens (hospital admission, emergency department visit, or other outpatient visit).¹⁵

Specimens were tested for antibodies to R rickettsii using an indirect fluorescence antibody assay (IFA) (PanBio InDx, Inc, Baltimore, Md). Each slide had 12 wells containing fixed whole Vero cells infected with R rickettsii (Sheila Smith strain).For screening, serum samples stored at −20°C were thawed,centrifuged at 1730g for 10 minutes at 4°C, and diluted 1:64 in phosphate-buffered saline (PBS; pH, 7.4); 20 µL was thenpipetted onto each well. Slides were incubated in a moistchamber at room temperature for 30 minutes, after which theywere rinsed with PBS, washed in PBS for 10 minutes, and rinsed again with distilled water. Slides were then air-dried, and the wells were reacted with 20 µL of fluorescein isothiocyanate–conjugated polyclonal goat antiserum reactive with human IgG heavy and light chains diluted 1:100 in PBS with eriochrome black counterstain. After 30 minutes in a moist chamber at room temperature, slides were rinsed and washed with PBS, overlaid with 80% glycerol in PBS (pH, 8.0) and a cover slip, and observed using epifluorescence microscopy at a magnification of ×400. Results were determined to be positive if the specimens showed readily identifiable apple green fluorescing coccobacillary organisms. Specimens that were positive at the screening dilution were retested at dilutions of 1:64, 1:128, and 1:256 to determine the antibody titer. Positive and negative control serum samples were run with each assay.

All slides were read independently by 2 individuals (G.S.M. and G.G.S.) who were masked to information about the specimens (except site of origin). Disagreements were resolved by consensus after reexamination of the slides. To monitor for problems in specimen shipping, handling, and storage and to assess the accuracy of signal detection, 4 vials of control serum (shipping controls) were randomly included in the sequence of patient specimens from each site; 2 were from a patient with RMSF who was seropositive for antibodies to R rickettsii, and 2 were from a seronegative individual. All serum samples were also tested for Ehrlichia chaffeensis and Rickettsia typhi antibody as previously described.^15- 16

Most studies of R rickettsii seroprevalence have used IFA cutoff titers of at least 64 to define positive specimens,^9- 14 and the Centers for Disease Control and Prevention case definition¹⁷ considers a single titer of this magnitude to be supportive of infection in the proper clinical context. Because standards for interpreting IFA results in seroepidemiological studies do not exist, the present data were analyzed at 3 different cutoff titers (≥64, ≥128, and ≥256) that represent increasing levels of stringency and specificity for R rickettsii infection.

Data were stored and analyzed on a Macintosh G4 computer (Apple Computer, Inc, Cupertino, Calif) running OS-9.1 and StatView 5.0 (SAS Institute Inc, Cary, NC). Age was collapsed into the following 3 categories: 1 to 6 years; 7 to 12 years; and 13 to 17 years. The ZIP code of residence was demographically categorized as urban or nonurban on the basis of 1990 census data as previously described.¹⁵ Preliminary analyses sought bivariate associations between categorical variables using the χ² test (the χ² test for trend was used when age group was a variable); in all cases, expected cell frequencies were greater than 5. In the case of 2 × 2 tables, Fisher exact test was used. Because age was found to be a significant predictor of seropositivity, and because age distribution differed from site to site, seroprevalence rates were adjusted for age using the entire study population as the reference. Multiple logistic regression was performed by adding the following variables in sequence: site, age group, source, residence, and sex. For each variable, the element with the lowest seroprevalence rate was used as the reference level. Significance for all analyses was defined at a P level of .05.

In the initial screening, there were 1620 agreements as negative, 321 agreements as positive, and 58 discrepancies, for a κ of 0.9, indicating excellent interrater reliability. All shipping controls were correctly identified.

Overall, 12.0% of children had R rickettsii antibody titers of at least 64; 7.3%, at least 128; and 4.3%, at least 256. Figure 1 shows the strong relationship between age and seroprevalence. Reactive antibodies were detected at a titer of at least 64 in 4.2% of children aged 1 to 6 years, 13.9% of those aged 7 to 12 years, and 16.4% of those aged 13 to 17 years (P<.001). Similarly robust associations were seen at titers of at least 128 and at least 256 (P<.001 for each cutoff value). Remarkably, 6.4% of children aged 13 to 17 years had antibody titers of at least 256. Age-adjusted seroprevalence rates for each site are given in Figure 2. At titers of at least 64, 21.9% of children in Little Rock were positive compared with 3.5% in Louisville. At titers of at least 256, seroprevalence ranged from a high of 7.7% in Nashville to a low of 1.8% in Winston-Salem. Differences between groups were significant for each cutoff titer (P<.001).

As seen in Table 1, other bivariate associations with seropositivity were seen at various cutoff titers, including the source of the specimen and nonurban residence. However, after multiple logistic regression, the only strong independent predictors of seropositivity at each cutoff titer were site and age group (Table 2). Much weaker associations were seen between seropositivity and specimen origin in the emergency department, male sex, and nonurban residence.

No subjects with R rickettsii antibodies had R typhi antibodies (tested at a dilution of 1:64). However, as seen in Table 3, 31 (13.0%) of the 239 subjects with R rickettsii antibodies had E chaffeensis titers of 80, and 11 (4.6%) had E chaffeensis titers of at least 160 (7 subjects had high titers to both organisms). Of the 42 children with antibodies to both organisms, 17 were from Little Rock; 8, Nashville; 6, Winston-Salem; 5, Oklahoma City; 3, Kansas City; 2, Mitalicis; and 1, Louisville (P<.001). Three of these subjects were aged 1 to 6 years; 13, 7 to 12 years; and 26, 13 to 17 years (P<.001).

The present study suggests that exposure to R rickettsii or related rickettsiae is much more common than indicated by disease reports. At a cutoff titer of at least 64, approximately one fifth of children living in Little Rock and Nashville had antirickettsial antibodies. Even when the stringency of the analysis was increased by raising the cutoff titer to at least 256, more than 7% of children living in some areas were seropositive. At each cutoff titer, age was significantly related to seroprevalence, which is consistent with the expected accumulation of exposures over time at the population level and the persistence of antibody after infection.

Microimmunofluorescence slides for the diagnosis of RMSF have been in worldwide commercial distribution since the early 1980s. They constitute the standard for serodiagnosis of RMSF and have been used in numerous seroprevalence studies of RMSF^9- 14 and other spotted-fever group rickettsiae.^18- 20 The slides used in this study have been cleared by the US Food and Drug Administration for diagnostic use and have been used in previous seroprevalence studies.¹⁴ Nevertheless, immunofluorescence is not an ideal method for seroepidemiological studies because nonspecific staining can occur, as can cross-reactivity between spotted-fever group rickettsiae.²¹ In this regard, antibodies to some human rickettsial pathogens, including Rickettsia conorii (Mediterranean spotted fever), Rickettsia akari (rickettsialpox), Rickettsia sibirica (Siberian tick typhus), and Rickettsia australis (North Queensland tick typhus), would not be expected because these infections are geographically circumspect. Cross-reactions with typhus group rickettsiae are less likely, and indeed were not demonstrated here with R typhi. Some of the antibodies detected in this study may have been directed against other spotted-fever group rickettsiae not presently thought to be pathogenic, such as Rickettsia montanensis, Rickettsia belli, Rickettsia parkeri, Rickettsia peacockii, Rickettsia amblyommii, and Rickettsia rhipicephali.²²

A significant number of children (42 [17.6%]) with R rickettsii antibodies also had antibodies to E chaffeensis. Since cross-reactions between these organisms are not appreciable, these children might have had an infection with each organism at some point in the past. Dual infections have been described.^23- 25 Children in the present study with dual seropositive findings were older and more likely to live in regions with the highest prevalence of both diseases.

Several biases may have been operative in the acquisition of this convenience sample.¹⁵ However, after controlling for all other variables, strong independent relationships persisted between seroprevalence and site and age. The association of seroprevalence with site generally fit the national distribution of reported cases of RMSF,² except for Winston-Salem, where the age-adjusted seroprevalence was unexpectedly low. North Carolina has the highest statewide disease-reporting rate in the country (23.0 per million) and records the largest number of deaths due to RMSF east of the Mississippi.⁷ Potential explanations for this discrepancy include the following:

It is counterintuitive that a strong association was not seen between nonurban residence and seroprevalence, although this was true for ehrlichiosis as well.¹⁵ Although the ZIP code demographic classification might have been inaccurate, and travel to rural areas by urban dwellers could have occurred, it seems more likely that foliage density and the proximity of animal hosts is a more relevant factor than is urbanizationper se.

Two earlier studies looked at R rickettsii eroprevalence in children; both were limited to sixth graders in one geographic region, and both used IFA assays with a cutoff titer of at least 64. The first study⁹ found a 1% seroprevalence rate among 508 children in Forsyth County, North Carolina, and the second¹¹ showed a 9% seroprevalence rate among 368 children living in Johnson and Tarrant counties in Texas. Other studies of various populations in North Carolina (this study included some children),¹⁰ Arkansas,¹³ and New York¹⁴ yielded seroprevalence estimates in the range of 4% to 10%. The present study supports these earlier observations and suggests that infection with R rickettsii or related rickettsiae is much more common than would be expected from passive case reporting. Most rickettsial infections may thus be subclinical or mild and self-limited.

The possibility that the IFA reactivity reported herein was not the result of R rickettsii infection makes the interpretation of diagnostic IFA assays in children with suspected RMSF problematic. For example, approximately one fifth of children living in Little Rock may be seropositive for R rickettsii. Therefore, patients with a viral syndrome characterized by fever, myalgia, headache, and rash could easily meet the Centers for Disease Control and Prevention case definition for probable RMSF,¹⁷ which requires a single R rickettsii IFA titer of at least 64 in the presence of a compatible clinical syndrome. This finding highlights the importance of performing acute and convalescent serology, polymerase chain reaction analysis, tissue immunofluorescence, or organism isolation for definitive diagnosis. Prospective studies of seroconversion, surveillance for incident disease, and the development of more specific serological reagents could answer many of the questions raised by this study.

Corresponding author and reprints: Gary S. Marshall, MD, Division of Pediatric Infectious Diseases,University of Louisville School of Medicine, 571 S Floyd St, Suite 321, Louisville, KY 40202 (e-mail: gsmars01@athena.louisville.edu).

Accepted for publication December 12, 2002.

This study was supported by grant 97-44 from the Alliant Community Trust Fund, Louisville, Ky.

We thank Ann Laible of the Epidemiology Section, Division of Public Health, North Carolina Department of Health and Human Services, Raleigh, and Ayo Ademoyero, MPH, of the Forsyth County Department of Public Health, Winston-Salem, NC.

Additional members of the Tick-Borne Infections in Children Study Group include Joan Antony, BS (PanBio InDx, Baltimore, Md); Michael Leonard, MD (Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tenn); and J. Stephen Dumler, MD (Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, Md).

Fewer than 1000 confirmed cases of Rocky Mountain spotted fever (RMSF) are reported to the Centers for Disease Control and Prevention, Atlanta, Ga, each year, yet previous serological studies suggest that rickettsial infection may be much more common. In this large, multicenter serosurvey, 12.0% of children were found to have antibodies reactive to Rickettsia rickettsii at titers of at least 64 and 4.3% at titers of at least 256. Age-adjusted seroprevalence rates at titers of at least 256 approached 8% in some areas. Widespread serological reactivity could be the result of unrecognized infection with R rickettsii or related rickettsiae and has implications for the interpretation of one-time diagnostic titers in children with suspected RMSF.