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Synopses The Human Ehrlichioses in the United StatesJennifer H. McQuiston, Christopher D. Paddock,
Robert C. Holman, and James E. Childs
First recognized in the United States in 1986, the human ehrlichioses are considered emerging zoonotic diseases. Two etiologically and epidemiologically distinct forms of illness are recognized: human monocytic ehrlichiosis (HME), caused by Ehrlichia chaffeensis (1), and human granulocytic ehrlichiosis (HGE), caused by an agent similar or identical to the veterinary pathogens E. equi and E. phagocytophila (2). A third species, E. ewingii, can also cause human illness (3). The bacteria that cause ehrlichiosis are transmitted to humans through the bite of infected ticks, which acquire the agents after feeding on infected animal reservoirs.
During infection, ehrlichiae form distinctive membrane-bound, intracytoplasmic bacterial aggregates (morulae) in white blood cells. HME is characterized by morulae in monocytes, HGE by morulae in granulocytes. Clinically, HME and HGE are nearly indistinguishable and are characterized by one or more of the following symptoms: fever, headache, myalgia, thrombocytopenia, leukopenia, and elevated liver enzyme levels (4-8). A rash occurs in approximately one third of patients with HME (8) but is less common in patients with HGE (4,9). Most cases of ehrlichiosis are characterized by mild illness. However, complications such as adult respiratory distress syndrome, renal failure, neurologic disorders, and disseminated intravascular coagulation can occur (6,10). Case-fatality ratios are as high as 5% for HME and 10% for HGE (10), although more serious cases are probably overrepresented in these estimates. Other studies have reported case-fatality ratios of <5% for these diseases (4,7). HME and HGE are most often diagnosed by indirect immunofluorescence assay (IFA), although polymerase chain reaction (PCR) assays are increasingly used (11). A confirmed case is defined as a fourfold change in antibody titer by IFA in acute- and convalescent-phase serum samples, PCR amplification of ehrlichial DNA from a clinical sample, or detection of intraleukocytic morulae and a single IFA titer of > 64. A probable case is defined as a single IFA titer of > 64 or the presence of morulae within infected leukocytes. Laboratory data are only used to support clinical suspicion; the designation of a confirmed or probable case of ehrlichiosis is interpreted in the context of compatible illness (11). The public health importance of the ehrlichioses has not been well defined, largely because these diseases are newly recognized. Because ehrlichiae are present in blood, concerns have been raised about the risk for perinatal and blood-transfusion transmission (12,13). Ehrlichiae are susceptible to tetracyclines, so rapid and effective treatment is possible (8). However, the nonspecific signs and symptoms of these diseases may interfere with timely clinical diagnosis. Ehrlichial infections can be life-threatening. Raising disease awareness and educating physicians and the public about clinical manifestations and proper treatment are indicated. A national ehrlichiosis surveillance program does not exist, so national incidence rates have not been determined because of wide variability in state surveillance activities. The Council of State and Territorial Epidemiologists recommended that human ehrlichiosis be made nationally notifiable in 1998, but many states do not have a system for surveillance and do not test for ehrlichiosis in state diagnostic laboratories. We summarize the scope of state-supported surveillance efforts and present data on ehrlichiosis cases reported to state health departments from 1986 through 1997. In addition, we include data on ehrlichiosis cases diagnosed by serologic testing at the Centers for Disease Control and Prevention (CDC).
Reported Ehrlichiosis Cases in the United StatesFrom 1986 through 1997, 1,223 ehrlichiosis cases were reported by 30 state health departments in the United States. Data were reported from 19 states that considered ehrlichiosis notifiable as of August 1998, five that routinely collected information on cases, and six that occasionally received reports of ehrlichiosis cases (Appendix I) (14-17). For states where ehrlichiosis was not notifiable, the designation routine reporting versus occasional reporting was based on the completeness of data provided. Because some states did not differentiate between probable and confirmed cases in their records, both categories were considered cases for the purposes of this report. Of the 1,223 reported ehrlichiosis cases, 742 (60.7%) were categorized as HME, 449 (36.7%) as HGE, and 32 (2.6%) as not ascribed to a specific ehrlichial agent. Using data from 20 states that reported information on deaths, we found case-fatality ratios of 2.7% (8 of 299) for HME and 0.7% (3 of 448) for HGE. HME and HGE IncidenceData provided through 1997 were used to calculate state-specific average annual incidence rates for 16 of the 19 states that considered ehrlichiosis notifiable and the five states that routinely collected surveillance data (Table). Although Missouri, South Carolina, and Tennessee considered ehrlichiosis notifiable, average annual incidence rates could not be calculated because these states did not differentiate between HME and HGE. Average annual incidence per one million population was calculated by dividing the number of reported cases by the number of years a state collected data (Table). When possible, average annual incidence by county was determined for HME and HGE (Figures 1-2) (15,17).
Most HME cases were reported from the southeastern and southcentral areas of the United States (Table, Figure 1). The highest reported average annual incidence rates of HME were in Arkansas (5.53 per million), North Carolina (4.72 per million), Missouri (3.05 per million), and Oklahoma (2.90 per million). In contrast, the highest reported average annual incidence rates of HGE were in the northeastern and upper midwestern areas of the United StatesConnecticut (15.90 per million), Wisconsin (8.79 per million), Minnesota (3.90 per million), and New York (2.68 per million) (Figure 2). The county reporting the highest average annual incidence of HME was Searcy, Arkansas (64.80 per million), and the county with the highest annual incidence of HGE was Jackson, Wisconsin (521.68 per million). These incidence rates follow the expected geographic distribution of tick vectors for each type of ehrlichiosis. E. chaffeensis is primarily transmitted by the lone star tick (Amblyomma americanum), which is common in the southeastern United States (19). The black-legged tick (Ixodes scapularis) transmits the causative agent of HGE in the northeastern United States (20,21) and the western black-legged tick (I. pacificus) in the western coastal United States (22). Reporting TrendsThe annual number of ehrlichiosis cases reported by the state health departments was calculated with data from 18 states that considered ehrlichiosis notifiable as of August 1998 (yearly summaries were not available for Missouri) and the five additional states that routinely collected information on ehrlichiosis cases (Figure 3). The annual number of reported ehrlichiosis cases increased sharply, from 69 in 1994 to 364 in 1997. This increase may be explained by the addition of ehrlichiosis as a notifiable disease in 10 states during this same 4-year interval, the discovery of HGE in 1994, increased availability of diagnostic tests, and increased awareness of ehrlichiosis.
Ehrlichioses Cases Diagnosed at CDCAt CDC, antigen from E. chaffeensis, Arkansas strain, is used to diagnose HME by IFA. Before E. chaffeensis was isolated in 1991, E. canis was used as a surrogate antigen (23). During 1995 to 1996, antigen from E. equi obtained from infected horse neutrophils was used, but cases submitted to CDC after 1996 were diagnosed by IFA using cell culture杁erived antigen from the HGE agent (24). Antibody from patients with ehrlichial infection may cross-react with both E. chaffeensis and the HGE agent (24,25). For patients with significant antibody titers to both Ehrlichia species, the causative agent is assumed to be the one with a fourfold or greater change in antibody titer between paired serum samples. If both agents show a fourfold difference, the one with the highest titer is considered the causative agent. If neither shows a fourfold difference, the causative agent is usually not ascribed to a specific ehrlichial species (25). Of 827 probable and confirmed ehrlichiosis cases diagnosed by IFA from serum or plasma specimens submitted to CDC through the end of 1997, 754 were HME, 44 were HGE, and 29 could not be differentiated because of antibody cross-reactivity. The geographic distribution was widespread (Figures 4, 5), and cases of ehrlichiosis were diagnosed from every state except North Dakota and South Dakota (Appendix 2). Imported disease acquired by travel to disease-endemic areas may explain cases reported from states without the recognized tick vectors, including Hawaii and Alaska. Because information about clinical manifestations was not always provided with specimens, whether all cases had compatible clinical illness is unknown. Of 754 HME cases, 423 (56.1%) were classified as probable and 331 (43.9%) as confirmed on the basis of serologic criteria established by CSTE and CDC (11). In contrast, of 44 HGE cases, 39 (88.6%) were classified as probable and 5 (11.4%) as confirmed. Conclusions
Although a few state health departments have published information on local ehrlichiosis surveillance (14-17,26-28), comprehensive national surveillance data had not been collected until this review. This review further defines the public health problem posed by the ehrlichioses in the United States. These diseases have incidence rates comparable with or exceeding those of Rocky Mountain spotted fever in some states (29). These state-reported data have several limitations. State health departments provided information on ehrlichiosis cases in different ways. For example, some states provided only data compiled after ehrlichiosis became notifiable, while others provided information as far back as data were available. The ehrlichiosis cases in this article represent a compilation of existing (albeit incomplete) surveillance datasets and probably underestimate the true prevalence of the disease in the United States. Moreover, the accuracy of HME and HGE case-fatality ratios presented here is uncertain. The number of deaths may be underreported because diagnosis of ehrlichiosis requires laboratory confirmation. However, serious or complicated cases, more likely to end in death, are more likely to be investigated and reported to state health departments. The case-fatality ratios described in this article are compatible with findings from other studies (4,7). Finally, the state-reported data include some cases from areas where ehrlichiosis is not commonly diagnosed. For example, a single case of HME was reported from Arizona, although the recognized distribution of the lone star tick does not include this state. Ehrlichiosis cases are usually reported from the patient's county and state of residence at the time of diagnosis; however, ehrlichiosis may be acquired during travel to an area with Ehrlichia-infected ticks. Imported cases of ehrlichiosis in states where the disease is not common or tick vectors are absent underscores the need to consider this diagnosis even in areas of low risk.
Diagnostic serologic testing has been offered at CDC since 1986 for HME, and since 1995 for HGE. Records show that from 1986 through 1997 more than 800 ehrlichiosis cases were diagnosed from 48 states. This finding contrasts sharply with state-reported surveillance data, which identified specific geographic regions where ehrlichiosis was most likely to occur. The number of cases diagnosed at CDC from each state may not accurately reflect expected regional incidence patterns; for example, states with public health laboratories that offer in-house diagnostic tests or states that frequently use commercial laboratories may be less likely to submit samples to CDC for testing. Some cases of ehrlichiosis diagnosed at CDC may also have been reported by state surveillance systems; these reporting systems cannot be regarded as mutually exclusive. The numbers of serologically diagnosed cases of ehrlichiosis reported here may differ from numbers published in other CDC reports because other reports include samples obtained for specific studies (7), whereas most of the cases in this report were submitted for routine diagnostic tests. As of August 1998, only 19 states considered ehrlichiosis notifiable, and fewer than one fourth of state health departments offered in-house diagnostic assays for HME or HGE. Average annual incidence rates, an important indicator of disease prevalence, could be calculated for only 21 states. These data underscore the need for better nationwide surveillance of ehrlichiosis. |
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AcknowledgmentsWe thank the state health departments for sharing these data and gratefully acknowledge the contributions of Bob England, Thomas McChesney, Dennis Berry, Thomas Tsang, Mark Starr, David Schnurr, John Poppy, Jim Meek, Cathy Rebmann, Lisa Conti, Valerie Mock, Jeff Chapman, Mike Loeffelholz, Carl Langkop, Robert Teclaw, Pam Judson, Mike Auslander, Louise McFarland, Mike McGuill, David Blythe, Linda Traviti, Jeff Beckett, Mary Grace Stobierski, Sheril Arndt, Dave Neitzel, Mary Currier, Melissa Johnson, Faye Sorhage, Lorna Lynch, Paul Edistat, Philip Kurpiel, Susan Wong, Todd McPherson, Leslie Wolf, Mike Crutcher, Maria Moll, Ted Donnelly, Ted LeBlanc, Steve McLaughlin, Robert Taylor, Jerry Hindman, Julie Rawlings, Farah Babakhani, Les Branch, John Kobayashi, Jim Kazmierczak, and Ed Belongia. We thank Joseph Singleton for help in collecting data on confirmed and probable ehrlichiosis cases diagnosed at CDC. Dr. McQuiston, a veterinarian, is serving as an Officer in the Epidemic Intelligence Service, Centers for Disease Control and Prevention. Her research focuses on the epidemiologic investigation of several zoonotic pathogens, including rabies virus, ehrlichioses, and Rickettsia rickettsii. Address for correspondence: J.E. Childs, Centers for Disease Control and Prevention, Mail Stop G13, 1600 Clifton Road, Atlanta, GA 30333, USA; fax: 404-639-2778; e-mail: jfc5@cdc.gov. References
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