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Tularemia in Alaska, 1938 - 2010
Acta Veterinaria Scandinavicavolume 53, Article number: 61 (2011)
Tularemia is a serious, potentially life threatening zoonotic disease. The causative agent, Francisella tularensis, is ubiquitous in the Northern hemisphere, including Alaska, where it was first isolated from a rabbit tick (Haemophysalis leporis-palustris) in 1938. Since then, F. tularensis has been isolated from wildlife and humans throughout the state. Serologic surveys have found measurable antibodies with prevalence ranging from < 1% to 50% and 4% to 18% for selected populations of wildlife species and humans, respectively. We reviewed and summarized known literature on tularemia surveillance in Alaska and summarized the epidemiological information on human cases reported to public health officials. Additionally, available F. tularensis isolates from Alaska were analyzed using canonical SNPs and a multi-locus variable-number tandem repeats (VNTR) analysis (MLVA) system. The results show that both F. t. tularensis and F. t. holarctica are present in Alaska and that subtype A.I, the most virulent type, is responsible for most recently reported human clinical cases in the state.
Tularemia is a serious and potentially life threatening zoonotic disease caused by the Gram-negative bacterium Francisella tularensis. Due to its high virulence and zoonotic potential, F. tularensis is listed as a category A select bioterrorism agent. F. tularensis has been weaponized in the past by the United States, Japan, the former USSR, and potentially other countries . The organism was first isolated from a ground squirrel in 1911 in Tulare County, CA. It was named Bacterium tularense, was later reclassified as Pasteurella tularense, and finally, in 1966, was named Francisella tularensis after Edward Francis. Descriptions of a plague-like disease now considered to be tularemia predate this first isolation, going as far back as 1818 in Japan . The first laboratory-confirmed human case was reported in 1914 . Since then F. tularensis has been isolated from more than 250 host species .
F. tularensis is ubiquitous in the Northern hemisphere and currently there are four recognized subspecies. F. tularensis subsp. tularensis (type A) is the most virulent of subspecies and is found throughout North America. F. tularensis subsp. holarctica (type B) is less virulent and is found throughout the Northern hemisphere. The distinction between type A and B tularemia was first made in the middle of the 20th century . Type A is divided into types A.I and A.II, and A.I is still further divided into types A.Ia and A.Ib. In a review of isolates collected in the US over 40 years, the highest human mortality rate was associated with type A.Ib (12/49 or 24%), followed by type B (8/108 or 7%), type A.Ia (2/55 or 4%), and finally, type A.II (0/53 or 0%). The third subspecies, F. tularensis subsp. mediasiatica is virulent and has been isolated in central Asia. Finally, many consider F. tularensis subsp. novicida to be a fourth subspecies of F. tularensis based on genetics and biochemical requirements , though this classification is still disputed [8, 9]. F. tularensis subsp novicida is generally avirulent in humans and is distributed globally [2, 10].
The disease caused by F. tularensis depends on the route of entry. Ulceroglandular tularemia, the most common form of disease, results from exposure through the skin (either preexisting wound or arthropod bite). This form results in an ulcer at the site of infection followed by lymphadenopathy. Pneumonic tularemia, the most serious form of disease, results from inhalation of aerosolized bacteria. Other forms of the disease include oculoglandular (exposure via the eye), oropharyngeal (ingestion), and typhoidal tularemia (systemic infection without a primary ulcer).
Here we review the history of tularemia in both wildlife and humans in the state of Alaska. We also report on the genetic characterization of recent Alaskan F. tularensis human and animal isolates using canonical SNPs (canSNPs) and multi-locus variable tandem repeat (VNTR) analysis (MLVA).
Tularemia in wildlife in Alaska
In Alaska, F. tularensis was first isolated from a rabbit tick (Haemophysalis leporis-palustris) removed from a varying hare (Lepus americanus) near Fairbanks in 1938 . The isolated strain was virulent in both guinea pigs and rabbits, resulting in enlarged spleens and areas of focal necrosis in both the spleens and livers. The high virulence in both species suggests that the isolate may have been type A. Later, an additional two virulent and likely type A isolates were obtained when suspensions of ground ticks removed from two healthy hares were inoculated into guinea pigs [12, 13]. Isolates collected from subsequent animals indicated the presence of a less virulent type, likely type B. The first of these was an isolate obtained from ticks collected from willow ptarmigan (Lagopus lagopus) in the Fairbanks area in 1959 . Voles sampled during the summer of 1963 on the Alaska Peninsula revealed a large number with splenomegaly and resulted in the isolation of another less virulent isolate . During the summer of 1971 in the Fairbanks area, 10 of 24 hares had enlarged spleens from which F. tularensis was isolated . This isolate was compared to the vole isolate from 1963  and shown to be significantly more virulent in challenge studies, further supporting the coexistence of type A and B strains in Alaska  (Table 1).
Though few isolates have been obtained, serological surveys for tularemia conducted between 1964 and 2000 have indicated the presence of F. tularensis among a wide variety of wildlife species and across a wide geographic area in Alaska. Seropositive animals (titer ≥ 1:20) in these surveys included various rodents and hares, birds and large predators (Table 2). Of those titers reported, the range was 1:20 - 1:320 [14, 17–20]. These serology results are consistent with the wide number of species in which F. tularensis has been found , but revealed few clues as to the important reservoir(s) for F. tularensis in Alaska. Of note, however, were two studies by Zarnke et al. [19, 20], which found that positive tularemia serology peaks in predators followed peaks in snowshoe hare populations, suggesting the possibility of a hare reservoir. In addition, F. tularensis DNA was found in 30% of > 2500 mosquitoes in Alaska, suggesting the possibility of an arthropod reservoir as well .
History of human tularemia in Alaska
The first possible case of human tularemia in Alaska was reported in 1938 in a 62-year-old man from Wiseman, north of the Arctic Circle. The patient exhibited symptoms of ulceroglandular tularemia and was hospitalized for 2 months, though there was no laboratory confirmation of tularemia . In 1946, a 31-year-old male from Northway (interior Alaska) with a history of skinning muskrats became the first laboratory-confirmed case by serology (titer 1:1280). His symptoms were headache, orbital pain, general aches and fever followed by development of swollen lymph nodes. The patient also reported that an ulcerated lesion had been present on his left middle finger for about one week. However, no isolate was cultured . The first culture positive human infection occurred in 1974 in a 42-year-old laboratory worker with pneumonia whose pleural fluid yielded an isolate of F. tularensis .
Following the diagnosis of these initial cases of tularemia, surveillance projects were conducted throughout the state. The first of these occurred between 1954 and 1957 and involved 816 skin tests of inhabitants of Alaskan villages, of which 64 (8%) were positive, with 50 - 59 year olds having the highest incidence by age group . The highest incidence was found in central Alaska, between Minto and Kaltag and as far north as Hughes, corresponding with the rich trapping areas in central Alaska. Following this initial surveillance, two additional surveys of Alaska Natives were completed. First, in the 1960s, serological surveys of 793 Aleut, Indian and Eskimo men showed an overall detection rate of 18% (139 of 793), with titers ranging from 1:20 to 1:640. A second survey involved skin tests on a subset of 115 (15%) of these Alaska Natives. Fifty-one (44%) of the 115 had positive skin tests, 43 (84%) of which also had detectable titers in the first survey, indicating a high correlation between skin test and titer results. Following these results, questionnaires were completed to determine if clinical disease resembling tularemia had been present. No difference in either total illness or tularemia-like illness was found between seropositive and seronegative groups, suggesting that the tularemia present in Alaska Natives may be of a less virulent type .
A final survey of Alaska Natives was completed in 1974. In this study, there were 4% (29 of 810) and 7% (28 of 402) positive titer rates (≥ 1:80, range 1:80-1:1280) in southwestern and east central Alaska, respectively. In addition, two seroconversions in children were documented (both > 4-fold increase in titer), with one child reporting a rash at around the time of the rise in titer and the other exhibiting no signs of disease. Similar to the previous surveys, no cases of tularemia-like illness were described in the villages studied, again suggesting that the tularemia present in these villagers was due to a less virulent type, that the route of infection favors asymptomatic disease or that Alaska Natives have developed resistance .
In 1993, two human cases related to housecats occurred in Fairbanks. One patient was a 44-year-old man who had been bitten on the thumb by his cat three and a half weeks prior to admission. Prior to the man's illness, his cat had been seen by a veterinarian and treated with antibiotics for an unknown febrile illness. The second patient was a 42-year-old veterinarian who presented with similar symptoms. The veterinarian had treated several cats with tularemia during the two-month period prior to his illness. Both human cases resolved with appropriate antibiotics .
Following the above housecat-associated cases, a serological survey of veterinarians was done in the Fairbanks area; two of 14 veterinarians (14%) had positive titers (≥ 1:80) for tularemia. Questionnaires sent to Fairbanks physicians and veterinarians indicated that 54% (15/28) and 92% (11/12), respectively, were aware that tularemia was prevalent in local wildlife. In addition, nine veterinarians had treated local domestic cats or dogs for suspected tularemia, indicating that household pets can pose a significant source for human infection .
Epidemiology of reported human cases in Alaska 1946-2010
Between 1946 and 2010, a total of 38 cases of tularemia were known to public health authorities in Alaska, with 9 cases in the Fairbanks-Steese area between 1946 and 1953  and an additional 29 cases from throughout the entire state between 1972 and 2009. Of the 38 reported cases, 23 were laboratory confirmed, with detailed laboratory data available for 19 of those 23. Of these 19, 10 had four-fold changes in paired titers, 7 had positive cultures for F tularensis, 1 had a positive lymph node stain and 1 had a single high titer along with clinical and epidemiological evidence. Seventy-three percent (22 of 30) of the patients were male with a median age of 39 years (range of 15-59 years). Seventy-one percent (27 of 38) were white and 16% (6 of 38) were of unknown race. Most (69%, 20 of 29) had illness onsets between June and August. Geographically, 68% (26 of 38) were exposed in central eastern Alaska, 21% (8 of 38) in the greater Anchorage area, 5% (2 of 38) in northwestern Alaska, 3% (1 of 38) in Southeastern Alaska and 3% (1 of 38) were exposed out-of-state. Ulceroglandular tularemia was most common (70%, 19 of 27), followed by typhoidal (11%, 3 of 27) and pneumonic (7%, 2 of 27) tularemia. None of the cases were fatal. Of those case-patients with detailed exposure histories, 79% (19 of 24) had direct contact with animals and 84% (16 of 19) of those had contact with a known wildlife reservoir (Figure 1). The remaining 16% (3 of 19) had had contact with domestic animals (one cat bite and two dogs known to have killed hares).
Molecular subtyping of recent F. tularensis isolates
We subtyped DNAs from eight recent (2003-2009) F. tularensis isolates (6 hare and 2 human) obtained by the public health laboratory of Alaska from interior Alaska and an additional four Alaskan DNAs (3 human and 1 rodent) available in Northern Arizona University's F. tularensis DNA collection to determine if the presumed coexistence of types A and B in Alaska could be confirmed. We first subtyped the isolate DNAs using a set of canSNPs described by Vogler et al.  to identify the major F. tularensis subclades found in Alaska. We then subtyped the isolate DNAs using the MLVA system described by Vogler et. al.  in order to identify additional variation among the isolates.
The canSNP analysis identified 10 isolates as type A.I (6 hares, 1 rodent, 3 human), one as type A.II (human), and one as type B (human) (Figure 2). The canSNP assays further placed the type A.I isolates into subclade A.I.Br.001/002, the type A.II isolate into subclade A.II.Br.006/007 and the type B isolate into subclade B.Br.OR96-0246. This built upon a previous global analysis of F. tularensis, which had identified a single subclade A.I.Br.001/002 isolate (also included in this study) in Alaska . This genetic analysis confirmed the previous virulence studies that had suggested the coexistence of types A and B in Alaska. Indeed, this analysis revealed an even greater level of genetic diversity than previously suspected, in that members of three major genetic groups were found to be present. The fact that most of these isolates were type A.I is likely related to the greater virulence of this genetic group  and thus the greater likelihood of severe disease and resultant opportunities for obtaining isolates through the public health system. However it is also possible that different strains are distributed differently throughout the environment, or that the reservoirs are distributed differently. It is probable that types B and A.II are present in much higher proportions in the wild than is indicated by this analysis. By relying on clinical isolates for genetic analysis we are limited to strains that are more likely to cause disease. Intensive sampling efforts would be needed to obtain more isolates from wildlife or people in the state.
The MLVA analysis revealed additional genetic diversity among the Alaskan isolates. Specifically, a neighbor-joining analysis based on MLVA data for the Alaskan isolates and an additional 34 A.I.Br.001/002 isolates revealed that the Alaskan subclade A.I.Br.001/002 isolates did not form a monophyletic group. Rather, they were scattered amongst subclade A.I.Br.001/002 isolates from diverse North American geographic locations (Figure 2), indicating a relatively high level of genetic diversity within this subclade in Alaska. This relatively high level of genetic diversity suggests either multiple introductions of F. tularensis to Alaska, a long history of F. tularensis in Alaska with ample time for diversification and possible transfers to other geographic locations, or a combination of the two. However, it is important to note that such high levels of genetic diversity within a single geographic location are not unique to Alaska, having been observed elsewhere in North America . Additional whole genome sequencing, SNP discovery and SNP screening as well as increased sampling will likely be needed to determine the origins and spread of F. tularensis in North America as a whole and Alaska specifically.
Interestingly, though there was no obvious geographic separation among the different Alaskan subclade A.I.Br.001/002 MLVA genotypes as they were all collected from Interior Alaska, the single Alaskan type A.II isolate was geographically separated from the other Alaskan isolates. The type A.II isolate (human) was isolated from the Matanuska Susitna Valley whereas most of the other isolates were from interior Alaska, where most tularemia cases occur. These two regions are separated by the Alaska Range, which might serve as a geographic barrier separating type A.II F. tularensis from other F. tularensis genetic types in Alaska. However, this hypothesis would need to be confirmed by genotyping more isolates from both geographic regions.
We have reviewed a history of F. tularensis in Alaska, beginning with its first isolation in a group of hare ticks in 1938 and progressing to its molecular characterization in 2011. Only limited studies have taken place within the state, there is still much to be learned about the ecology and epidemiology of tularemia, particularly in northern climates where it is endemic. We still do not know the reservoir in Alaska, though it is suspected to be hares or muskrats. We also do not know the prevalence of tularemia in most of the wildlife in the state. Overall the presented work suggests the need for renewed serological surveillance in both wildlife and humans to assess possible changes in Francisella prevalence in a rapidly changing Arctic. The current distribution of tularemia in Alaska is not well understood. While most cases are reported from Interior Alaska, while distribution of cases in wildlife or subclinical human cases is not known. In addition more molecular work is warranted to better understand the strains circulating in Alaska and assess potential for human infection associated with different host species. Transstadial transmission of tularemia should be addressed similar to work done in Sweden . These steps will further increase our understanding of tularemia in Alaska and can guide public health surveillance and intervention.
Oyston PCF, Sjostedt A, Titball RW: Tularemia: bioterrorism defense renews interest in Francisella tularensis. Nat Rev Microbiol. 2004, 2: 967-978. 10.1038/nrmicro1045.
Sjostedt A: Tularemia: history, epidemiology, pathogen physiology, and clinical manifestations. Ann NY Acad Sci. 2007, 1105: 1-29. 10.1196/annals.1409.009.
Hopla CE: The ecology of tularemia. Adv Vet Sci Comp Med. 1974, 18: 25-53.
Abd H, Johansson T, Golovliov I, Sandstrom G, Forsman M: Survival and growth of Francisella tularensis in Acanthamoeba castellanii. Appl Environ Microbiol. 2003, 69: 600-606. 10.1128/AEM.69.1.600-606.2003.
Olsulfiev NG, Emelyanova OS, Dunayeva TN: Comparative study of strains of B. tularense in the old and new world and their taxonomy. J Hyg Epidemiol Microbiol Immunol. 1959, 3: 138-149.
Kugeler KJ, Mead PS, Janusz J, Staples JE, Kubota KA, Chalcraft LG, Petersen JM: Molecular Epidemiology of Francisella tularensis in the United States. Clin Infect Dis. 2009, 48: 863-870. 10.1086/597261.
Huber B, Escudero R, Busse HJ, Seibold E, Scholz HC, Anda P, Kampfer P, Splettstoesser WD: Description of Francisella hispaniensis sp. nov., isolated from human blood, reclassification of Francisella novicida comb. nov. and emended description of the genus Francisella. Int J Syst Evol Micr. 2010, 60: 1887-1896. 10.1099/ijs.0.015941-0.
Busse HJ, Huber B, Anda P, Escudero R, Scholz HC, Seibold E, Splettstoesser E, Kampfer P: Objections to the transfer of Francisella novicida to the subspecies rank of Francisella tularensis - response to Johansson et al. Int J Syst Evol Micr. 2010, 60: 1718-1720.
Johansson A, Celli J, Conlan W, Elkins K, Forsman M, Keim PS, Larsson P, Manoil C, Nano FE, Petersen JM, Sjostedt A: Objections to the transfer of Francisella novicida to the subspecies rank of Francisella tularensis. Int J Syst Evol Micr. 2010, 60: 1717-1718. 10.1099/ijs.0.022830-0.
Keim P, Johansson A, Wagner DM: Molecular Epidemiology, Evolution, and Ecology of Francisella. Ann NY Acad Sci. 2007, 1105: 30-66. 10.1196/annals.1409.011.
Philip CB, Parker RR: Occurence of tularemia in the rabbit tick (Haemaphysalis leporis-palustris) in Alaska. Pub Health Rep. 1938, 53: 574-575. 10.2307/4582509.
Philip CB, Hull GD, Geary JM: Notes on the Rabbit Tick, Haemaphysalis leporis-palustris (Packard), and Tularemia in Central Alaska. J Parasitol. 1954, 484-485.
Philip CB: Tularemia in Alaska. Proceedings of the sixth Pacific Science Congress of the Pacific Science Association: 24 July -12. 1939, 71-73. August ; Berkley
Hopla CE: Ecology and epidemiology research studies in Alaska: A report of field collections and laboratory diagnostic assay. Proj 1471. 1965, Univ Okla Res Instit, Norman Oklahoma
Rausch RL, Huntley BE, Bridgens JG: Notes on Pasteurella tularensis isolated from a vole, Microtus oeconomus Pallas, in Alaska. Can J Microbiol. 1969, 15: 47-55. 10.1139/m69-008.
Miller LG: Further studies on tularemia in Alaska: virulence and biochemical characteristics of indigenous strains. Can J Microbiol. 1974, 20: 1585-1590. 10.1139/m74-245.
Chomel BB, Kasten RW, Chappuis G, Soulier M, Kikuchi Y: Serological survey of selected canine viral pathogens and zoonoses in grizzly bears (Ursus arctos horribilis) and black bears (Ursus americanus) from Alaska. Rev Sci Tech Off Int Epiz. 1998, 17: 756-766.
Hopla CE: Ecology and Epidemiology Research Studies in Alaska: A Report of field collections and laboratory diagnostic assay. Univ Okla Res Instit, Norman Oklahoma. 1968
Zarnke RL, Ballard WB: Serologic survey for selected microbial pathogens of wolves in Alaska, 1975-1982. J Wildl Dis. 1987, 23: 77-85.
Zarnke RL, Ver Hoef JM, DeLong RA: Serologic survey for selected disease agents in wolves (Canis lupus) from Alaska and the Yukon Territory, 1984- 2000. J Wildl Dis. 2004, 40: 632-638.
Triebenbach AN, Vogl SJ, Lotspeich-Cole L, Sikes DS, Happ GM, Hueffer K: Detection of Francisella tularensis in Alaskan Mosquitos (Diptera: Culicidae) and Assessment of a Laboratory Model for Transmission. J Med Entomol. 2010, 47: 639-648. 10.1603/ME09192.
Williams R: Tularemia: first case to be reported in Alaska. Pub Health Rep. 1946, 61: 875-876. 10.2307/4585715.
Miller LG: Further studies on tularemia in Alaska: human tularemia. Can J Microbiol. 1974, 20: 1539-1544. 10.1139/m74-241.
Hopla CE: Epidemiology of Tularemia in Alaska. U.S.A.F. Arctic Aeromedical Laboratory Technical Report 59-1. 1960, 1-42.
Philip RN, Huntley B, Lackman DB, Comstock GW: Serologic and skin test evidence of tularemia infection among Alaskan Eskimos, Indians, and Aleuts. J Infect Dis. 1962, 110: 220-230. 10.1093/infdis/110.3.220.
Liles WC, Burger RJ: Tularemia from Domestic Cats. Western J Med. 1993, 158: 619-622.
Pauls FP: Data compiled for indoctrination of medical officers. Elmendorf Air Force Base, Alaska. 1953
Vogler AJ, Birdsell D, Price LB, Bowers JR, Beckstrom-Sternberg SM, Auerbach RK, Beckstrom-Sternberg JS, Johansson A, Clare A, Buchhagen JL, Petersen JM, Pearson T, Vaissaire J, Dempsey MP, Foxall P, Engelthaler DM, Wagner DM, Keim P: Phylogeography of Francisella tularensis: global expansion of a highly fit clone. J Bacteriol. 2009, 191: 2474-2484. 10.1128/JB.01786-08.
Vogler AJ, Birdsell D, Wagner DM, Keim P: An optimized, multiplexed multi- locus variable-number tandem repeat analysis system for genotyping Francisella tularensis. Lett Appl Microbiol. 2009, 48: 140-144. 10.1111/j.1472-765X.2008.02484.x.
Lundström JO, Andersson AC, Bäckman S, Schäfer ML, Forsman M, Thelaus J: Transstadial transmission of Francisella tularensis holarctica in mosquitoes, Sweden. Emerg Infect Dis. 2011, 17: 794-799.
CM Hansen and K Hueffer are supported by Grant Number RR016466 from the National Center for Research Resources (NCRR), a component of the National Institutes of Health (NIH). Its contents are solely the responsibility of the authors and do not necessarily represent the official view of NCRR or NIH. The authors want to thank Louisa Castrodale from the Section of Epidemiology, State of Alaska for providing epidemiological data from reported tularemia cases in Alaska.
The authors declare that they have no competing interests.
CH drafted the manuscript, AV DM and PK performed molecular analysis. KH conceived of the review and study. All authors have read and approved the final manuscript.