We studied the prevalence of B. burgdorferi and the agent of HGE among questing nymphal and adult I. scapularis of the same generation, in natural foci with concurrent circulation of both pathogens in Connecticut. In 1996, we collected ticks at two study sites—Bridgeport and Woodbridge—approximately 30 km apart. In 1997, we collected ticks at the Bridgeport site only; ticks feeding on white-footed mice and from vegetation were collected and flagged in June (nymphs) and October (adults). Mice were trapped in Sherman live-traps twice per month from June through August and were held for several days in the laboratory in individual wire-mesh cages over water to allow all naturally attached ticks to feed to repletion. While in the laboratory, mice were provided with food and drinking water ad libitum. Engorged ticks were collected daily. A serum sample was collected from each mouse before release at the capture site.

Serum samples from 121 mice were tested for specific antibodies to the agent of HGE by indirect immunofluorescence assay (IFA) (Aquila Biopharmaceuticals, Worcester, MA). Antigen derived from human promyelocyte cell culture (HL-60) infected with the agent of HGE obtained from Westchester County, New York. Sera were screened at a dilution of 1:40 in 1X phosphate-buffered saline (pH 7.4). Several studies examined the specificity of IFA for the agent of HGE (including an assay involving the antigen produced by Aquila Biopharmaceuticals) and found no considerable serologic cross-reactivity between the agent of HGE and rickettsial organisms outside the E. phagocytophila group at dilutions 1:16 and higher (8,20,21). Thus, screening samples at 1:40 dilution ensures that sera testing HGE-positive were from mice actually exposed to that agent.

Host-seeking nymphal and adult I. scapularis collected from vegetation were tested individually by polymerase chain reaction (PCR) for infection with B. burgdorferi and the agent of HGE. Engorged ticks were allowed to molt to the next stage and were identified by species. I. scapularis nymphs derived from mouse-fed larvae were tested in pools—one pool (up to 10 ticks) per mouse—to assess the infectivity of individual mice for feeding larvae. Adult I. scapularis ticks derived from mouse-fed nymphs were tested individually, and the prevalence of each infection among these ticks was compared with the prevalence of each infection among questing adult ticks collected from vegetation at the same site.

For PCR testing, individual adult or nymphal ticks, or pools of nymphs, were placed in sterile 1.5 cc plastic vials, deep-frozen in liquid nitrogen, ground with a sterile plastic pestle, and resuspended in 50 ml of Tris-EDTA buffer. DNA was extracted from samples by using the IsoQuick Nucleic Acid Extraction Kit (ORCA Research Inc., Bothell, WA) to maximize sensitivity (22). Briefly, guanidine thiocyanate, a proprietary extraction matrix, and sodium dodecyl sulfate solution were added to a suspension, and the mixture was incubated at 65°C for 10 min. After separation of phases by centrifugation, DNA was precipitated with sodium acetate and isopropanol and washed with 70% ethanol. The final DNA pellet was resuspended in 50 ml of RNase-free water, and a 2.5-ml aliquot was used for each PCR. Primers EHR521 (5'-TGT AGG CGG TTC GGT AAG TTA AAG-3') and EHR747 (5'-GCA CTC ATC GTT TAC AGC GTG-3') were used to amplify a 247-bp fragment of 16S rDNA from the agent of HGE (6). Primers FLA297 (5'-CGG CAC ATA TTC AGA TGC AGA CAG-3') and FLA652 (5'-CCT GTT GAA CAC CCT CTT GAA CC-3') developed in the laboratory of Dr. Erol Fikrig (Yale School of Medicine) were used to amplify a 378-bp fragment of the flagellin gene of B. burgdorferi. The amplification products were visualized in 2% agarose gels.

The prevalence of B. burgdorferi infection in both questing nymphal and adult I. scapularis was similar between the two study sites in 1996 and remained stable for 2 consecutive years at the Bridgeport site (Table 1). Within a generation, the proportion of Borrelia-infected ticks increased less than twofold from nymphal (32% to 33%) to adult stage (52% to 56%) at both sites and in both years.

Prevalence of ehrlichial infection in I. scapularis nymphs was also similar at the two study sites and between years at the Bridgeport site (Table 1), while in questing adult ticks, ehrlichial prevalence varied. In 1996, the prevalence of the agent of HGE in adult ticks at the Bridgeport site (12.5%) was higher than at the Woodbridge site (8.3%), although not significantly (p = 0.11). The proportion of adult ticks infected with the agent of HGE in Bridgeport was significantly higher in 1997 than in the previous year (p = 1.44x10^-7). Within the same generation, the proportion of Ehrlichia-infected ticks increased fivefold in Woodbridge in 1996 and 10.4- to 10.6-fold in Bridgeport in 1996 and 1997, respectively.

An average of 0.7 engorged I. scapularis nymphs (0 to 7) and 16.7 (0 to 113) engorged I. scapularis larvae were collected per mouse. The highest mean density (± standard error) of nymphal infestation in P. leucopus (1.3±0.2) was recorded in late June, with mean larval density peaking in late August (34.6±1.7). Overall, 113 of 121 mice were infested with either nymphal or larval I. scapularis. Of 40 mice with nymphs, 32 (80.0%) produced adult ticks infected with B. burgdorferi, and 7 (17.5%) yielded ticks infected with the ehrlichial agent. Of 108 mice infested with I. scapularis larvae, 56 (51.4%) produced B. burgdorferi-infected nymphal ticks, and 20 (18.4%) produced nymphs infected with the agent of HGE. Of the 108 mice, 13 (11.9%) infected feeding ticks with both pathogens. Prevalence of infectivity in mice did not differ by month.

Of 121 mice trapped from June to August 1997 in Bridgeport and tested by IFA, 46 (38.0%) had antibodies against the agent of HGE. The relatively high sera dilution (1:40) used for screening allows the possibility that some samples with low antibody titers were missed and that an even higher proportion of the mouse population had actually been exposed to the agent of HGE.

The proportion of HGE-seropositive mice decreased from 47% (n = 49) in late June and July to 32% (n = 72) in August, perhaps because of a loss of antibody by mice over time, the recruitment of naive young mice into the population, or both. Of the 20 mice that produced nymphs infected with the agent of HGE, 17 were also seropositive. Evidently, these mice remained infectious for ticks, despite the presence of specific antibodies. The other three infectious mice were HGE-seronegative, which most likely indicated recent infection. Thus, only 18.4% of P. leucopus were capable of infecting ticks with the agent of HGE, although at least twice as many (as determined by IFA) had been exposed to this agent. Apparently, mice exposed to ticks infected with the agent of HGE may develop an immune response to the pathogen but not become infectious for xenodiagnostic ticks. These findings suggest that a high prevalence of the specific antibody against the agent of HGE in rodent populations does not necessary reflect the scope of rodents' involvement in transmitting the ehrlichial agent.

Prevalence of B. burgdorferi infection among adult ticks derived from mouse-fed nymphs was higher than among questing ticks collected from vegetation (p = 0.0051) (Table 2). Conversely, prevalence of infection with the agent of HGE in mouse-fed ticks was not quite half that of adult ticks collected from vegetation (p = 0.0022). Concurrent infection in mouse-fed ticks was also half that in adult ticks collected from vegetation (Table 2). The same trend was observed when prevalence of ehrlichial infection was compared among Borrelia-infected adult ticks. In the Borrelia-infected cohort collected from vegetation, 14 (25.5%) of 55 ticks were simultaneously infected with the agent of HGE, but in the cohort collected from mice, only 5 (10.2%) of 49 were simultaneously infected with the agent of HGE.

Mice that collect and feed many nymphs have a high probability of finding an infected tick and becoming infected. Mice that feed large numbers of ticks after infection would increase the rate of pathogen transmission. We tested the hypothesis that mice exposed to or currently infected with the agent of HGE are continuously infested with large numbers of ticks and thus are capable of increasing the prevalence of infection in a natural tick population. When we compared tick densities between mice infectious for ticks, mice seropositive for the agent of HGE, and mice without specific antibodies or infected ticks, nymphal and larval infestation densities did not differ significantly (Table 3).

Because nymphal I. scapularis naturally feed on vertebrate animals (small rodents, medium-sized and large mammals, birds, and reptiles) (23) that may vary in their ability to acquire and transmit a pathogen, the prevalence of infection in different portions of an adult tick population would differ depending on which host species the tick had fed on. Thus, the prevalence of infection for the tick population as a whole is an average resulting from contributions of individual host species. We compared average prevalence to the prevalence of infection in ticks derived from a particular host species to assess the relative contribution of that host species to amplification of a pathogen. For example, the prevalence of B. burgdorferi infection in mouse-fed ticks is considerably higher than the average prevalence of the infection in a general tick population, which suggests that the white-footed mouse is an important amplifying reservoir of B. burgdorferi. The prevalence of the agent of HGE in mouse-fed ticks is lower than the average, suggesting that the white-footed mouse is not as effective an amplifying reservoir for this agent as are other host species. An important contribution from non-Peromyscus host species that infects a large proportion of feeding nymphs with the agent of HGE appears necessary to account for the average prevalence of infection in host-seeking adult ticks.

The prevalence of B. burgdorferi infection in ticks increased less than twofold from nymphal to adult stage, while more than 50% of the white-footed mouse population was infected with B. burgdorferi and transmitted the pathogen to feeding ticks. At the same time, prevalence of infection with the agent of HGE in ticks regularly showed a 4.5- to 10.6-fold increase from nymphal stage to adult stage, although only 18% of mice were infectious for feeding ticks. This steep increase in prevalence of ehrlichial infection in ticks also suggests the involvement of other susceptible host species that maintain the natural transmission cycle of the agent of HGE at the observed level.

Dissimilarities between two pathogens—in the increase of infection in ticks from nymphal to adult stage and in prevalence of infection in the host-seeking population versus a subpopulation of mouse-fed ticks—suggest that natural cycles of the agents of Lyme disease and HGE differ. They involve the same vector-species, but the principal amplifying hosts for the two pathogens are not the same.

Although the white-footed mouse is susceptible to infection with both agents, this species alone cannot account for the observed prevalence of the agent of HGE in adult ticks. Our data suggest that most nymphal I. scapularis acquire the agent of HGE from non-Peromyscus hosts.