Spotted-Fever Group Rickettsia in Dermacentor variabilis, Maryland

Three-hundred ninety-two adult Dermacentor variabilis were collected from six Maryland counties during the spring, summer, and fall of 2002. Infection prevalence for spotted fever group Rickettsia was 3.8%, as determined by polymerase chain reaction. Single strand conformational polymorphism (SSCP) analysis followed by sequencing indicated that all infections represented a single rickettsial taxon, Rickettsia montanensis.

areas become better understood, determining the relationship between the rickettsiae involved in human disease and those isolated from vector ticks and mammal and tick reservoirs may be necessary.
Differentiating the tick-borne SFG Rickettsia before the 1990s depended largely on culture and epitope recognition techniques, such as immunoflourescence and agglutination tests and mouse serotyping with monoclonal antibodies. Genotypic studies of rickettsiae conducted during the 1990s led to two rickettsial genes that can be used to identify rickettsial infections: citrate synthase (gltA) and rOmpA (9). Citrate synthase encodes the first enzyme of the tricarboxylic acid cycle and is highly conserved among all Rickettsia species, serving as a polymerase chain reaction (PCR) target to identify any rickettsial infection. rOmpA encodes a surface-expressed protein of SFG-rickettsiae that is important for adhesion to host cells (10). Only SFG Rickettsia contain the rOmpA gene (11) (12). Modifying the existing extraction procedure involved an additional phenol:chloroform:isoamyl alcohol (25:24:1) extraction step to further stabilize the extracted DNA. Tick extractions were screened by PCR for evidence of infection with Rickettsia by using primers specific to the Rickettsia citrate synthase gene (9). The Rickettsia infection rate was 6.1% (24/392, 95% confidence interval [CI] 4.0%-9.0%). All Rickettsia-positive tick extractions were subsequently screened by PCR for SFG Rickettsia by using primers for the rOmpA gene of SFG-Rickettsia (9). The prevalence of SFG Rickettsia infection was 3.8% (15/392, 95% CI 2.2%-6.2%). Single strand conformational polymorphism (SSCP) banding patterns were identical for all tick-derived rOmpA PCR amplicons. Similarly, SSCP banding patterns of the tickderived citrate synthase amplicons for the SFG-Rickettsia-positive samples were monomorphic. These results suggest that these tick infections represent a single DISPATCHES SFG Rickettsia taxon (13). Citrate synthase and rOmpA PCR products from three ticks were sequenced with the citrate synthase and shortened rOmpA PCR primers, respectively. Sequences of each respective gene fragment derived from these ticks were identical and confirm the SSCP findings (GenBank accession no.: gltA, AY548828-AY548830, rOmpA, AY543681-AY543683). The derived sequences were also compared to rickettsiae sequences in the public domain and were identical to those derived from R. montanensis from D. andersoni (GenBank accession no. RMU55823 rOmpA and RMU74756 gltA).
Prevalence estimates were reported as percentages with exact 95% CI based on the binomial distribution. Fisher exact test was used to compare infection prevalence across the strata of selected characteristics. The association between each characteristic and the prevalence of infection was quantified as odds ratios (OR), calculated with logistic regression or exact methods for categorical data when the data were highly unbalanced. All statistical analyses were performed with STATA (version 7.0; Stata Corporation, College Station, TX) or StatXact (version 5.0.3; Cytel Software Corporation, Cambridge, MA).
The variation in prevalence of Rickettsia-positive ticks across all counties was marginally significant (p = 0.052), with a higher prevalence in St. Mary's County compared to all other counties (OR 5.1, 95% CI 0.5-27.2, p value = 0.08). However, only 13 ticks were collected from St. Mary's County, so this estimate was based on limited data. In contrast to the equivocal results for the geographic distribution of Rickettsia-positive ticks, temporal heterogeneity was evident, as the prevalence of Rickettsia-positive ticks varied significantly with month of collection (p = 0.007). Risk for infection was significantly elevated for any Rickettsia organism in ticks collected in July or August (OR 4.1, 95% CI 1.5-11.5) compared to those collected in April. Further analyses combining the data from the spring and early summer months showed that the risk for  infection with any Rickettsia organism in July or August was even higher (OR 4.7, 95% CI 2.0-11.3). The risk for infection with R. montanensis with the late summer months, compared to the spring and early summer months, was somewhat less but still approached statistical significance (OR 3.0, 95% CI 0.8-10.2, p value = 0.06). This observation may be an artifact of diminishing tick abundance later in the summer months.

Conclusions
The prevalence of SFG Rickettsia in D. variabilis estimated from this study (3.8%) was lower than that in previous reports from Maryland. However, in regions where RMSF is observed annually, prevalence estimates range widely, from 2% in Connecticut to 10% in Alabama, with intermediate prevalences in New York, Kentucky, Tennessee, and Arkansas (5). In addition, R. montanensis had not been previously recognized in Maryland. Most earlier studies of SFG Rickettsia infection prevalence did not identify the Rickettsia to the species level, although the SFG-positive samples were sometimes assumed to represent R. rickettsii. One study in Maryland in which 26 Rickettsia isolates were obtained from D. variabilis determined the species composition of the rickettsiae. Two isolates were R. rickettsii, 1 isolate was R. bellii (non-SFG), and 23 (88%) were identified as WB-8-2, a then-unnamed SFG-Rickettsia (5). Weller et al. performed a phylogenetic analysis and found WB-8-2 ("R. amblyommii") to be closely related to R. montanensis (14), although they can be differentiated by serotyping.
R. montanensis has been isolated from ticks in other eastern states. During the 1980s, Feng (3). Further, these researchers noted that R. rickettsii were not isolated from ticks collected in several Ohio counties where RMSF was considered endemic. These studies illustrate that the rickettsial composition and dynamics within the RMSF-endemic areas are complex and need to be addressed with greater scrutiny.
The role of SFG Rickettsia in human health is largely unknown, and many are considered to be nonpathogenic either because the bacteria have not been isolated from humans or they do not demonstrate pathogenicity in animal models. For example, R. montanensis is avirulent in guinea pigs but virulent in voles (15). These findings have led to caution when labeling rickettsiae as nonpathogenic (2). R. montanensis and other "nonpathogenic" SFG Rickettsia-infected ticks may also benefit human health by decreasing R. rickettsii in tick populations as a result of the "interference" phenomenon (15).
The findings of this study and others raise important questions. In 2000, a total of 495 cases of RMSF were reported to CDC and 4 deaths were attributed to spotted fever caused by Rickettsia rickettsii. The extent to which R. rickettsii is the agent responsible for reported cases of RMSF should be reevaluated, considering the number of studies completed in RMSF-endemic regions, including this one, that have found non-R. rickettsii as the predominant or only detectable SFG Rickettsia.
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