Hypersensitivity to ticks and lyme disease risk.
Although many residents of Lyme disease-endemic regions describe frequent exposure to ticks, relatively few become infected by the causative spirochetal agent, Borrelia burgdorferi (1-4). This disparity reflects both a relative paucity of spirochetal infection in vector ticks and the limited number of people actually bitten by ticks (5-6). Other variables that might restrict Lyme disease incidence include prompt removal of attached ticks before the pathogen is transmitted and acquired immunity to the salivary proteins of these ticks, the spirochetal pathogen, or both (7-11). Repeated exposure to tick bites has been associated with developing cutaneous hypersensitivity, which results in persistent itch and local swelling at the site of tick attachment (12-13). Itching provides an early sign of tick bite and may facilitate removal of the attached tick before the pathogen can be transmitted. Additional inflammatory reaction to tick salivary proteins also may help prevent transmission (10-11). The epidemiologic relevance of host immunity to tick bite for preventing Lyme disease remains unknown.
Acquired immunity to vector ticks may limit the incidence of Lyme disease by protecting persons who have been previously exposed to bites of vector ticks. Accordingly, we determined whether cutaneous hypersensitivity against tick antigens increases with the frequency of tick exposure and whether such reactivity protects against Lyme disease. In particular, we determined whether residents of Block Island, Rhode Island, who experienced itching associated with attached ticks have fewer episodes of Lyme disease than those who report no episodes of itching associated with tick attachment.
Study Site and Sampling Procedures
Block Island is located 15 km from the New England mainland, and Lyme disease is highly endemic there. Beginning in 1991, we invited all residents to participate in a serosurvey twice yearly (during October and April). We sought to identify all cases of infection due to B. burgdorferi among serosurvey participants with the help of the staff" of the Block Island Medical Center, the sole medical facility on the island, and by a dedicated research nurse (3). Borrelial infections were identified among members of the study cohort who visited the medical center for an acute tickborne illness or who seroconverted against borrelial antigen during the study period. Written informed consent was obtained from all adult study participants and from the parents or legal guardians of minors, in accordance with human experimentation guidelines approved by the institutional review boards at Connecticut Children's Medical Center and the Harvard School of Public Health.
At the serosurvey visit, participants submitted a blood sample and responded to a questionnaire about tick bites, use of protective measures, exposure factors, and symptoms of tickborne illness during the previous year (Figure 1). Specifically, they were asked if they had experienced a tick bite in the previous year and whether their tick bites produced itch. A medical history, physical examination, and specific Lyme disease laboratory tests were performed on all symptomatic participants at the time of suspected Lyme disease illness and 4-6 weeks later. A medical history was repeated at least every 3 months until the participants became asymptomatic. Ixodes scapularis ticks (I. dammini) were collected in May through October from 1991 through 2000 by flagging at diverse sites on the island. Ticks were analyzed for B. burgdorferi by polymerase chain reaction (PCR).
PCR Assay for Spirochete DNA
Whole blood samples were analyzed and processed by personnel blinded to the clinical status of the donor, as previously described (14). DNA extraction was performed on blood from Lyme disease patients and on Ixodes ticks with a commercially available kit (IsoQuick Nucleic Acid Extraction Kit, ORCA Research, Bothell, WA) (14,15). A 294-bp portion of the B. burgdorferi OspA gene was targeted for amplification by using a previously described PCR protocol (14,15).
Assays for Antispirochetal Antibody
Serologic evidence of exposure to the Lyme disease spirochete was detected by enzyme-linked immunosorbent assay (16). A reactive serum was defined as one with a positive reaction at a dilution [less than or equal to] 1:320. All borderline or reactive sera were further characterized by immunoblot (16,17). Specimens were considered positive if the immunoglobulin (Ig) G immunoblot contained [less than or equal to] 5 of the 10 most common B. burgdorferi-specific bands (17).
To include both symptomatic and asymptomatic cases of Lyme disease, diagnosis of newly acquired B. burgdorferi infection during the course of the study required one of the following: 1) a physician diagnosis of erythema migrans consisting of an expanding, ringlike erythematous rash at least 5 cm in diameter; 2) influenzalike symptoms consistent with Lyme disease and laboratory evidence of recent infection; 3) seroconversion from an initial nonreactive serum to a subsequent reactive serum that contained anti-B, burgdorferi antibody. The influenzalike symptoms of Lyme disease include fever, chills, sweats, fatigue, headache, or myalgia. Laboratory evidence of recent infection included either amplification of B. burgdorferi DNA in blood by PCR, seroconversion, or a 4-fold rise in antiB. burgdorferi antibody in paired acute-phase and convalescent-phase sera.
Predicted and Observed Lyme Disease Rates
A simple model of Lyme disease transmission would calculate the rate of Lyme disease infection as the product of 2 main factors: the proportion of persons who report being bitten by deer ticks and the proportion of these ticks infected by B. burgdolferi. We calculated the yearly incidence of Lyme disease by determining the number of serosurvey participants who met the Lyme disease case definition each year in relation to the number of participants enrolled each year. By comparing the projected incidence using the Lyme disease transmission model to actual incidence of Lyme disease, we could assess the overall importance of factors missing from the basic model, such as the effects of inflammatory reactions against tick salivary proteins and acquired immunity to the spirochetal pathogen.
All statistical calculations were performed with JMP 5.1 (SAS Institute, Cary, NC). To estimate the study sample frequency of tick bite and tick-associated itch, we averaged the individual reports of tick bite and tick-associated itch among study participants each year. To determine yearly Lyme disease incidence, we compared the number of new cases of Lyme disease each year to the total number of study participants who had enrolled in the study up to that time. To create 10-year individual measures, reports of tick bite and itch were summed across all visits for each participant. The results were analyzed with descriptive statistics (mean, proportion, and confidence intervals with 5% error). Bivariate logistic regression was used to estimate probability of itch for increasing tick bites. The relative contribution of risk factors to the acquisition of Lyme disease was evaluated from multiple logistic regression models to calculate odds ratios with associated confidence limits. The predicted probability of acquiring Lyme disease was estimated for significant risk factors.
A total of 1,669 residents of Block Island, most of the island population, enrolled in our study from 1991 to 2000. We excluded those participants who did not report spending at least 1 month on the island during May through October, which resulted in a sample of 1,490. The mean age of the sample was 43 years (95% CI 42.2-44.1) and approximately half (51%) were female.
We determined how frequently the 1,490 persons in our sample recalled a deer tick bite. Each year an average of 27% (95% CI 23%-31%) of the study participants reported [less than or equal to] 1 tick bite during the prior year (range 20%-37%). An average of 17% (95% CI 13%-21%) of study participants reported itch associated with tick bite (Figure 2).
[FIGURE 2 OMITTED]
We then determined the prevalence of B. burgdorferi infection in nymphal deer ticks that contained B. burgdorferi DNA and that were swept from vegetation on Block Island throughout the course of this study. Of 135 such ticks tested, 23% (95% CI 20%-26%) contained amplifiable B. burgdorferi DNA. We therefore predicted that the maximum yearly incidence of Lyme disease would be 6.2% (95% CI 4.6%-8.1%) (27% with tick bite x 23% of ticks infected).
We next calculated yearly incidence rate of new Lyme disease cases among study participants from 1991 to 2000. The average incidence was 1.74% (95% CI 1.1%-2.4%) (Table). Thus, the predicted incidence of Lyme disease using the basic model (95% CI 4.6%-8.1%) was 3%-6% greater than the observed incidence. This difference would not be expected due to chance.
We next determined whether increasing exposure to ticks increases the probability of tick-associated itch. This analysis was limited to participants whose sera displayed no evidence of tickborne illness before study entry, who had >1 serosurvey visit, and who were >2 years of age. Among these 610 participants, 52% reported at least 1 tick bite (mean 2.2, 95% CI 2.0-2.4), and 32% reported itch with any tick bite. The probability of itch doubled as the number of reported tick bites increased from 1 to 2 (21% to 46%, respectively) and doubled again from 2 to 4 reported bites (46% to 97%, respectively; linear trend p < 0.001).
Finally, we tested the hypothesis that tick-associated itching is associated with decreased risk of Lyme disease. The acquisition of Lyme disease increased from 15% to 25% to 31% among participants who reported no itch, 1 episode of tick-associated itch, and 2 reports of itch, respectively. In contrast, the frequency of Lyme disease decreased to 13% in participants who reported 3 episodes of tick-associated itch and 10% in those with [less than or equal to] 4 such reports. We used a multiple logistic regression model to estimate the likelihood of acquiring Lyme disease for participants reporting none to 1, 2, and [less than or equal to] 3 reports of itch, controlling for number of study visits and reports of tick bite. Consistent with the bivariate analysis, the risk of acquiring Lyme disease was higher for 1 report of itch (OR 2.7, 95% CI 0.4-2.3), and decreased among those who reported itch at [less than or equal to] 3 study visits (range 3 12, OR 0.18, 95% CI 0.05-0.5) (Figure 3). Confining the analysis to only those who had Lyme disease illness by omitting participants whose evidence of Lyme disease was by seroconversion alone did not alter the inverse relationship between itch and developing Lyme disease. Persons who consistently report itching in association with tick bites are less likely to experience an episode of Lyme disease than do those who fail to react against tick bite.
[FIGURE 3 OMITTED]
These observations suggest that residents of disease-endemic sites who experience persistent tick-associated itch are less likely to develop Lyme disease than are those who do not experience this reaction. Itch was reported at the site of tick bite, and the frequency of itch increases as the number of reported tick bites increase, which strongly suggests that tick-associated itch is linked to an acquired cutaneous hypersensitivity response. Such a relationship has definitively been established in the case of I. ricinis, the European analog of the North American deer tick. After having been bitten by these ticks repeatedly, persons experience both immediate and delayed cutaneous hypersensitivity reactions. They express tick-specific IgE antibodies, as well as dermal and perivascular infiltrates of CD8+ T lymphocytes and Langerhans' cells (13). Additional studies of other tick species also suggest that tick-associated itch is mediated by tick-specific antibody or cellular infiltration (12,18,19). People in our study who reported a single episode of tick-associated itch were more likely to acquire Lyme disease than those who did not report itch, probably because tick-associated itch is a marker for tick exposure. In contrast, persons who had repeated tick-associated itch were protected from developing Lyme disease. We are confident, therefore, that the people in our study who described repeated episodes of tick-associated itching were experiencing cutaneous hypersensitivity and that this immune reaction protected them from acquiring Lyme disease.
The antitick immune response that protects people from acquiring Lyme disease might act through any of several effector mechanisms. A heightened awareness by a person of an attached tick would result in the removal of the potentially infecting tick before pathogen transmission could occur. Because vector ticks must remain attached for at least 2 days before spirochetes are transmitted, prompt tick removal should prevent spirochetal infection (8,20). Vector ticks generally are removed by persons within such a time period (21-23). Alternatively, immunity against tick salivary antigens might interfere with pathogen transmission independent of early host recognition and removal of ticks. Indeed, preexposure of mice and guinea pigs to uninfected ticks prevents Lyme disease after challenge by spirochete-infected ticks using infestation conditions that prevent removal of feeding ticks by host grooming (24,25). Ticks feeding on such immune hosts detach sooner and retain less host material than do ticks feeding on nonimmune hosts. Although natural hosts, such as Peromyscus leucopus, do not develop robust antitick immunity, inbred strains of mice and guinea pigs become immune to the salivary antigens secreted by feeding ticks (10,26,27). This immunity results in reduced volume of engorgement, abnormal blood meal composition, prolonged feeding, and frequently death of the tick (10,27). Antitick immunity may specifically neutralize some components of tick saliva that ensure successful feeding and facilitate pathogen transmission, such as vasodilators, anticoagulants, and immunosuppressors (10,11,28). Prevention of B. burgdorferi transmission in guinea pigs is associated with antivector antibody (25). Persons who experience frequent deer tick bites produce an array of specific antitick antibodies (29-31). Cell-mediated immune factors against tickderived antigen might similarly play a role in developing cutaneous hypersensitivity and protect against infection (13,19). A strong delayed cutaneous hypersensitivity response to sandfly bites in persons has been correlated with reduced transmission of leishmanial parasites (32,33). An array of antitick immune reactions may prevent Lyme disease and other tickborne diseases.
Our analysis incorporates several potentially confounding assumptions. Although our estimate of the prevalence of spirochetal infection in vector ticks is based on a small sample of ticks, this rate is consistent with that derived in other parts of southern New England at approximately the same time (5,6). Although our study participants live on Block Island where deer ticks predominate, some of our participants may have been bitten by other kinds of ticks or been bitten by ticks off the island. While approximately a quarter of our participants reported a tick bite, previous studies have shown that persons are often unaware that they have been bitten. From a third to three fourths of patients with Lyme disease cannot recall having been bitten by a tick (6,34-36). Assuming that a similar percentage of our study participants were unaware of a previous tick bite, the tick bite prevalence on Block Island would have varied from half to all of our participants. A tick bite prevalence of 71% was reported at another site where Lyme disease is highly endemic (37). Any underestimate of the frequency of tick attachment would increase the likelihood that other factors, including antitick immunity, help limit the incidence of Lyme disease. Finally, our predicted Lyme disease incidence assumes that people are bitten only once in any year. An increase in yearly tick bite frequency among persons would increase the likelihood that the tick bite is from an infected tick, thus similarly increasing the difference between predicted and observed incidence rates. We believe that none of these assumptions is notably confounding.
Several factors help prevent Lyme disease in persons who live in disease-endemic regions. These factors include the paucity of ticks that are infected with the Lyme spirochete, the limited number of persons who are bitten by ticks, acquired immunity against the spirochetal pathogen, and the immune reaction to ticks that develops in the course of tick attachment. Persons who express an immune reaction against the vector tick appear to acquire Lyme disease less frequently than do those who experience no such immune reaction. The protective effect of the immune response to tick salivary protein against the agent of Lyme disease in persons suggests that a tick protein-based vaccine might be developed that would protect against infection by the agent of Lyme disease and possibly other tickborne infections.
Table. Yearly incidence of Lyme disease among Block Island study cohort, 1991-2000 * No. (%) with first Year No. participants episode of Lyme disease 1991 731 25 (3.4) 1992 824 27 (3.3) 1993 933 17 (1.8) 1994 1,038 23 (2.2) 1995 1,114 15 (1.4) 1996 1,169 15 (1.3) 1997 1,246 5 (0.4) 1998 1,325 18 (1.4) 1999 1,432 14 (1.0) 2000 1,490 19 (1.3) * 10-year average = 1.74 (95% confidence interval 1.1-2.4).
We thank Jean and Bill Crawford, Dorothy and Norman Dahl, Betty Fitzpatrick, Nancy and Malcolm Greenaway, Barbara Hobe, Ruth and Carl Kaufmann, Gerald Lange, Florence Lentz, Claire and Stephen McQueeny, Frankie and Gordon Smith, and Martha and William Wilson for help in acquisition of data and Claudia Alford for assistance in manuscript preparation.
This work was supported in part by grants from the National Institutes of Health: AI 42402 (Dr. Krause), AI 37993 and AI 39002 (Dr. Telford), AI 19693 (Dr. Spielman), and the University of Connecticut Health Center General Clinical Research Center (MO 1RR06192).
(1.) Falco RC, Fish D. A survey of tick bites acquired in a Lyme disease endemic area in southern New York State. Ann N Y Acad Sci. 1988;539:456-7.
(2.) Campbell GL, Fritz CL, Fish D, Nowakowski J, Nadelman RB, Wormser GP. Estimation of the incidence of Lyme disease. Am J Epidemiol. 1991:148:1018-26.
(3.) Krause PJ, McKay K, Gadbaw J, Christianson D. Closter E, Lepore T. el al. Increasing health burden of human babesiosis in endemic sites. Am J Trop Med Hyg. 2003;68:431-6.
(4.) Spichnan A, Wilson ME, Levine JK Piesman J. Ecology of Ixodes dammini-borne human babesiosis and Lyme disease. Annu Rev Entomol. 1985;30:439-60.
(5.) Piesman J. Mather TN, Yelford SR, Spielman A. Concurrent Borrelia burgdorferi and Babesia microti infection in nymphal Ixodes dammini. J Clin Microbiol. 1986;24:446-7.
(6.) Stafford KC. Cartter ML, Magnarelli LA, Ertel Ski, Mshar PA. Temporal correlations between tick abundance and prevalence of ticks infected with Borrelia burgdorferi and increasing incidence of Lyme disease. J Clin Microbiol. 1998;36:1240-4.
(7.) Stjernberg L, Berglund J. Risk of acquiring tick bites in south-eastern Sweden. Scand J Infect Dis. 2002;34:840-4.
(8.) Hayes EB, Piesman J. How can we prevent Lyme disease'? New Engl J Med. 2003;348:2424-30.
(9.) Salazar JC, Pope CD, Sellati TJ, Feder HM. Kiely TG, Dardick KR, et al. Coevolution of markers of innate and adaptive immunity in skin and peripheral blood of patients with erythema migrans. J Immunol. 2003;171:2660-70.
(10.) Wikel SK. Host immunity to ticks. Annu Rev Entomol. 1996:41:1-22.
(11.) Ribeiro JM, Francischetti MB. Role of arthropod saliva in blood feeding: sialome and post-sialome perspectives. Annu Rev Entomol. 2003;48:73-88.
(12.) Gauci M, Loh RKS, Stone BF, Thong YH. Allergic reactions to the Australian paralysis tick, Ixodes holocyclus: diagnostic evaluation by skin test and radioimmuneassay. Clin Exp Allergy. 1989:19:279-83.
(13.) Beaudouin E, Kanny G, Guerin B, Guerin L, Plenat F. Moneret-Vautrin DA. Unusual manifestations of hypersensitivity after a tick bite: report of two cases. Ann Allergy Asthma Immunol. 1997;79:43-6.
(14.) Persing DH, Rutledge BJ, Rys PN, Podzorski DS, Mitchell PD, Reed KD, et al. Target imbalance: disparity of Borrelia burgdorferi genetic material in synovial fluid from Lyme arthritis patients. J Infect Dis. 1994;169:668-72.
(15.) Rys PN. PCR detection of Borrelia burgdorferi. In: Persing DH, Smith TF. Tenover F, White JT, editors. Diagnostic molecular microbiology: principles and applications. Washington: American Society for Microbiology; 1993. p. 203-10.
(16.) Trevejo RT, Krause PJ, Schriefer ME. Dennis DT. Evaluation of twotest serodiagnostic method for Lyme disease in a seroepidemiologic study in an endemic area. Am J Trop Med Hyg. 2001;65:563-6.
(17.) Dressler F, Whalen JA, Reinhardt BN, Steere AC. Western blotting in the serodiagnosis of Lyme disease. J Infect Dis. 1993;167:392-400.
(18.) Acero S, Blanco R, Bartolome. An occupational anaphylaxis in a goatherd. Allergy. 2003;58:824-31.
(19.) Alexander JOD. The physiology of itch. Parasitol Today. 1986;2:345-51.
(20.) Piesman J. Dynamics of Borrelia burgdorferi transmission by nymphal Ixodes dammini ticks. J Infect Dis. 1993; 167:1082-5.
(21.) Falco RC, Fish D, Piesman J. Duration of tick bites in a Lyme disease-endemic area. Am J EpidemioI. 1996;143:187-92.
(22.) Sood SK. Salzman MB, Johnson BJB, Happ CM, Feig K, Carmody L, et al, Duration of tick attachment as a predictor of the risk of Lyme disease in an area in which Lyme disease is endemic. J Infect Dis. 1997:175:996-9.
(23.) Nadelman RB, Nowakowski J, Fish D, Falco RC, Freeman K, McKenna D, et al. Prophylaxis with single-dose doxycycline for the prevention of Lyme disease after an lxodes scapularis tick bite. New Engl J Med. 2001;345:79-84.
(24.) Wikel SK, Ramachandra RN, Bergman DK, Burkot, TR, Piesman J. Infestation with pathogen-free nymphs of the tick Ixodes scapularis induces host resistance to transmission of Borrelia burgdorferi by ticks. Infect Immun. 1997;65:335-8.
(25.) Nazario S, Das S, de Silva AM. Prevention of Borrelia burgdorferi transmission in guinea pigs by tick immunity. Am J Trop Med Hyg. 1998;58:780-5.
(26.) Richter D, Spielman A, Matuschka FR. Effect of prior exposure to noninfected ticks on susceptibility of mice to Lyme disease spirochetes. Appl Environ Microbiol. 1998;64:4596-9.
(27.) Brossard M, Wikel SK. Tick immunobiology. Parasitology. In press 2004.
(28.) Stebbings JH. Immediate hypersensitivity: A defense against arthropods. Perspect Biol Med. 1974;17:233-9.
(29.) Schwartz BS, Ribeiro JM, Goldstein MD. Anti-tick antibodies: an epidemiologic tool in Lyme disease research. Am J Epidemiol. 1990;132:58-66.
(30.) Schwartz BS, Nadelman RB, Fish D, Childs JE, Forseter G, Wormser G. Entomologic and demographic correlates of anti-tick saliva antibody in a prospective study of tick bite subjects in Westchester County, New York. Am J Trop Med Hyg. 1993;48:50-7.
(31.) Schwartz BS, Goldstein MD, Childs JE. Antibodies to Borrelia burgdorjeri and tick salivary gland proteins in New Jersey outdoor workers. Am J Pub Health. 1993;83:1746-8.
(32.) Valenzuela JG, Belkaid Y, Garfield MK, Mendez S, Kamhawi S, Rowton ED, et al. Toward a defined anti-Leishmania vaccine targeting vector antigens: characterization of a protective salivary protein. J Exp Med. 2001;194:331-42.
(33.) Gomes RB, Brodskyn C, de Oliveira CI, Costa J, Miranda JC, Caldas A, et al. Seroconvcrsion against Lutzomyia longipalpis saliva concurrent with the development of anti-Leishmania chagasi delayed-type hypersensitivity. J Infect Dis. 2002;186:1530-4.
(34.) Williams CL, Strobino B, Lee A, Curran AS, Benach JL, lnamdar S, et al. Lyme disease in childhood: clinical and epidemiologic features of ninety cases. Pediatr Infect Dis J. 1990;9:10-4.
(35.) Fahrer H, van der Linden SM, Sauvain MJ, Gem L, Zhioua E, Aeschlimann A. The prevalence and incidence of clinical and asymptomatic Lyme borreliosis in a population at risk. J Infect Dis. 1991;163:305-10.
(36.) Gerber MA, Shapiro ED, Burke GS, Parcells VJ, Bell GL and the Pediatric Lyme Disease Study Group. Lyme disease in children in southeastern Connecticut. New Engl J Med. 1996;335:1270-4.
(37.) Gustafson R, Forsgren, Gardulf A, Granstrom M, Svenungsson B. Clinical manifestations and antibody prevalence of Lyme borreliosis and tick-borne encephalitis in Sweden: a study in five endemic areas close to Stockholm. Scand J Infect Dis. 1993;25:595-603.
Georgine S. Burke, * ([dagger]) Stephen K. Wikel, ([dagger]) Andrew Spielman, ([double dagger]) Sam R. Telford, ([double dagger][section]) Kathleen McKay, * ([dagger]) Peter J. Krause, * ([dagger]) and the Tick-borne Infection Study Group (1)
* Connecticut Children's Medical Center, Hartford, Connecticut, USA; ([dagger]) University of Connecticut School of Medicine, Farmington, Connecticut, USA; ([double dagger]) Harvard University, Cambridge, Massachusetts, USA; and ([section]) Tufts University School of Veterinary Medicine, North Grafton, Massachusetts, USA
(1) Harvard University: Richard Pollack, Steven Tahan; Connecticut Children's Medical Center: Patricio Tomas, Diane Christianson; University of Connecticut School of Medicine: T.V. Rajan, Raymond Ryan, Feliciano Dias, Pamela Fall, Tracey Urso, Christine Abreu, Jonathan Covault; Block Island Medical Center: Peter Baute, Linda Closter, Janice Miller.
Address for correspondence: Peter J. Krause, Connecticut Children's Medical Center, 282 Washington St, Hartford, Connecticut 06117, USA; fax: 860-545-9371; email: Pkrause@ccmckids.org
Dr. Burke is director of research operations at Connecticut Children's Medical Center and assistant professor of pediatrics at the University of Connecticut School of Medicine. Her research interests include the epidemiology, pathogenesis, and clinical manifestations of tickborne infections.
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|Author:||Krause, Peter J.|
|Publication:||Emerging Infectious Diseases|
|Date:||Jan 1, 2005|
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