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Research Article
1 April 2001

Molecular Evidence of Bartonella spp. in Questing Adult Ixodes pacificus Ticks in California


Ticks are the vectors of many zoonotic diseases in the United States, including Lyme disease, human monocytic and granulocytic ehrlichioses, and Rocky Mountain spotted fever. Most knownBartonella species are arthropod borne. Therefore, it is important to determine if some Bartonella species, which are emerging pathogens, could be carried or transmitted by ticks. In this study, adult Ixodes pacificus ticks were collected by flagging vegetation in three sites in Santa Clara County, Calif. PCR-restriction fragment length polymorphism and partial sequencing of 273 bp of the gltA gene were applied forBartonella identification. Twenty-nine (19.2%) of 151 individually tested ticks were PCR positive for Bartonella. Male ticks were more likely to be infected with Bartonellathan female ticks (26 versus 12%, P = 0.05). None of the nine ticks collected at Baird Ranch was PCR positive forBartonella. However, 7 (50%) of 14 ticks from Red Fern Ranch and 22 (17%) of 128 ticks from the Windy Hill Open Space Reserve were infected with Bartonella. In these infected ticks, molecular analysis showed a variety of Bartonella strains, which were closely related to a cattle Bartonella strain and to several known human-pathogenic Bartonella species and subspecies: Bartonella henselae, B. quintana, B. washoensis, and B. vinsonii subsp.berkhoffii. These findings indicate that I. pacificus ticks may play an important role inBartonella transmission among animals and humans.
Bartonella spp. are emerging pathogens, as new Bartonella species have been identified in humans and a wide range of mammals in recent years (5, 17, 18, 20-23, 27, 28; B. B. Chomel, R. W. Kasten, C. C. Chang, K. Yamamoto, R. Heller, S. Maruyama, H. Ueno, D. Simpson, S. S. Swift, Y. Piemont, and N. C. Pedersen, Abstr. Int. Conf. Emerg. Infect. Dis., p. 21.10, 1998; R. Heller, M. Kubina, G. Delacour, I. Mahoudeau, F. Lamarque, M. Artois, H. Monteil, B. Jaulhac, and Y. Piemont, Abstr. 97th Gen. Meet. Am. Soc. Microbiol., abstr. B-505, p. 115, 1997; R. Heller, M. Kubina, G. Delacour, F. Lamarque, G. Van Laere, R. Kasten, B. Chomel, and Y. Piemont, Abstr. Int. Conf. Emerg. Infect. Dis., p. 21.18, 1998). SeveralBartonella species and subspecies are important human pathogens that cause a variety of clinical syndromes, and mostBartonella organisms are arthropod borne. Bartonella bacilliformis is the agent of Carrión's disease, which is mainly found in the Andes mountains, and is transmitted by sand flies (3). B. bacilliformis infection is characterized by a biphasic process. The acute form of the infection, Oroya fever, causes severe and life-threatening hemolytic anemia, and the chronic form, verruga peruana, results in vascular proliferative lesions of the skin (12). B. quintana, the agent of trench fever, is transmitted by the human body louse (36). B. quintana was also identified as one of two agents causing bacillary angiomatosis (26). In urban centers, human cases of this infection were recently observed in homeless people and alcohol abusers. Cat scratch disease (CSD), caused by B. henselae, is an important zoonosis with cats serving as the major reservoir (25) and cat fleas (Ctenocephalides felis) as the vector (16). Although CSD is usually a self-limiting disease in immunocompetent patients, atypical forms of this infection can occur, such as Parinaud's oculoglandular syndrome, encephalopathy, osteomyelitis, or endocarditis (1). In immunocompromised patients, B. henselae is the other causative agent of bacillary angiomatosis (40). B. vinsoniisubsp. berkhoffii infection was reported in several canine endocarditis cases (7, 10) and recently in one human endocarditis case (41). Based on a seroepidemiological study (38), B. vinsonii subsp.berkhoffii infection has been suggested to be tick transmitted. Recently, new human pathogenic Bartonellastrains have been identified, but their vectors remain unknown. For example, B. grahamii was associated with one human case of neuroretinitis (24), but the mode of transmission was not identified. A human patient with fever and neurological signs was infected with a novel strain, B. vinsonii subsp.arupensis, possibly from a rodent source (22, 45). Furthermore, in Washoe County, Nev., a human case of myocarditis was related to a new Bartonella organism,B. washoensis. Rodents were determined to be the likely reservoir (9).
Ticks are the vectors of many zoonotic diseases in the United States, including Lyme disease, human monocytic and granulocytic ehrlichioses, and Rocky Mountain spotted fever. Various Bartonella species have been isolated from small rodents (4, 5, 17, 18, 20-22, 28). Natural coinfection of Bartonella species andBorrelia burgdorferi has also been demonstrated in wild-caught mice (22). Because these small mammals usually serve as a blood source for larval and nymphal ticks, it is of great interest to determine if certain Bartonella organisms could be tick borne. In order to investigate the possible transmission ofBartonella organisms by ticks, it is important to first demonstrate the presence of Bartonella in questing adult ticks from a natural environment. Therefore, the objective of this study was to determine if Bartonella organisms could be detected in questing adult ticks collected by flagging vegetation. The tick species carrying Bartonella is likely to be I. pacificus, since it is a very common tick species in California and the known vector for Borrelia burgdorferi. As a follow-up to previous epidemiological studies of Bartonellain coyotes from California (13, 15), I. pacificus ticks were collected from Santa Clara County, Calif., where Bartonella infection is enzootic in coyotes.
(Part of this research has been presented at the International Conference on Emerging Infectious Diseases, 16 to 19 July 2000, Atlanta, Ga.)


Tick collection.

The sample size (n) of ticks to be tested in this study was calculated based on the following formula: (1 − prevalence of infection in ticks)n = (1 − percentage of confidence). It was assumed that the prevalence of Bartonella in ticks from this area should be low, as the prevalence for Borrelia burgdorferi infection inI. pacificus from California has been reported to be approximately 2% (29, 32). Therefore, the collection of 150 ticks was required for a 95% confidence of finding at least oneBartonella-positive tick. A total of 151 I. pacificus adult ticks was captured by flagging vegetation from areas in Santa Clara County, Calif.: Red Fern Ranch (14 ticks), Baird Ranch (9 ticks), and Windy Hill Open Space Reserve (128 ticks). Collection and identification of tick species were carried out by the Vector Control Section, Wildlife Unit, Santa Clara County Department of Health Services, from December 1998 to January 1999. After collection, ticks were stored at −70°C until DNA extraction was performed.

DNA extraction from ticks.

DNA extraction using the DNeasy tissue kit (Qiagen, Hilden, Germany) was performed by following the manufacturer's instructions, with minor modifications. Before extraction, ticks were individually put in 1.5-ml microtubes containing 1 ml of 70% ethanol solution for 1 min and briefly rinsed with sterile water. Each tick was then transferred to a clean microtube and macerated in 180 μl of Buffer ATL (Qiagen). After addition of 20 μl of proteinase K (18 mg/ml) (Qiagen), samples were incubated in a 50°C water bath overnight for complete lysis of soft tissues inside the ticks. The lysed samples were treated with 20 μl of RNase A (10 mg/ml) for 2 min at room temperature and then incubated at 70°C for 10 min after addition of 200 μl of Buffer AL (Qiagen). To inactivate potential infectious agents, samples were then heated at 95°C for 15 min. The following steps of DNA extraction were performed according to the manufacturer's instructions.

PCR-RFLP procedures.

PCR amplification was performed withBartonella-specific primers of the citrate synthase (gltA) gene as previously described (14). Undiluted DNA and a 1:5 dilution of the extracted DNA from each macerated tick were used as DNA templates. The PCR-amplified products were verified by gel electrophoresis for the appearance of an approximately 400-bp fragment of the gltA gene. If extra bands were observed, further purification of the 400-bp band of thegltA gene was conducted. A small piece of the agarose at the position of 400 bp was cut from the agarose gel with a sterile tip through UV-light visualization, mixed with 50 μl of sterile water in a 1.5-ml microtube, and melted at 100°C for 10 min. The final product, kept at 50°C, was used as the template for a secondary PCR.B. vinsonii subsp. berkhoffii DNA was added to aBartonella PCR-negative I. pacificus extract as a positive control. A negative control was made by using sterile water instead of template DNA. In order to prevent laboratory contamination, different isolated areas were used for DNA extraction and PCR preparation. Disposable sterile vials and filter tips were used for DNA extraction and PCR reagent preparation. The PCR chamber was used only for the preparation of PCR reagents and not for the isolation or subculture of Bartonella spp. To minimize bacterial contamination in the laboratory, all isolations were performed in a safety class II hood cabinet. The positive control of B. vinsonii subsp. berkhoffii was systematically prepared last, to prevent possible cross contamination with the tested samples. The final purified PCR product of the gltA gene was then used for PCR-restriction fragment length polymorphism (PCR-RFLP) and further sequencing analyses. TaqI (Promega, Madison, Wis.),HhaI (New England Biolabs, Beverly, Mass.), andMseI (New England Biolabs) restriction endonucleases were used for PCR-RFLP analysis of the gltA gene. The digestion conditions used were those recommended by the enzymes' manufacturers. Banding patterns were compared to the profiles of B. henselae Houston-1 (ATCC 49882), B. clarridgeiae (ATCC 700095), B. quintana (ATCC VR-358), B. bacilliformis (ATCC 35686), B. elizabethae (ATCC 49927), Bartonella strain cattle-1 (University of California, Davis), B. vinsonii subsp. vinsonii(ATCC VR-152), and B. vinsonii subsp. berkhoffii(ATCC 51672).

DNA sequencing.

All PCR-positive tick samples were sequenced for the gltA gene as previously described (14). First, the BLASTN program of the GCG software (Wisconsin Sequence Analysis Package, version 10; Genetics Computer Group) was applied to determine the bacterial species and subspecies closest to the sequencing results of the Bartonella-positive tick samples, based on the DNA sequence similarity of 273 bp of the gltAgene. Then, the GAP program was used for sequence alignments and determination of the percentage of DNA similarity between the sequences of the gltA gene for a Bartonella-positive tick sample and the closest bacterial species and subspecies. The EMBL-GenBank accession numbers for the citrate synthase gene sequences of the strains used for the sequence comparisons were as follows:B. vinsonii subsp. berkhoffii,U28075 ; B. henselae Houston-1, L38987 ; B. quintana,Z70014 ;B. washoensis,AF050108 ; and Bartonella strain cattle-1, AF228768 .

Statistical analysis.

The data were tabulated by SAS, version 6.12, and then analyzed by Epi-Info, version 6.03. The chi-square test for homogeneity was used to evaluate the association between the infection and a categorized factor (i.e., gender of ticks), and P values were calculated with the Yates corrected method.


Twenty-nine (19.2%) of 151 individually processed adult ticks tested were PCR positive for Bartonella (Table1). None of the ticks collected from Baird Ranch was PCR positive for Bartonella. However, 7 (50%) of 14 ticks from Red Fern Ranch and 22 (17%) of 128 ticks from the Windy Hill Open Space Reserve were infected withBartonella. Overall, male ticks were more likely to be infected with Bartonella than female ticks (26 versus 12%, P = 0.05 ). After stratification by tick collection location, an even distribution of Bartonella infection was observed in male and female ticks from Red Fern Ranch. However, for ticks from the Windy Hill Open Space Reserve, male ticks were more likely to be Bartonella PCR positive than female ticks (P < 0.05) .
Table 1.
Table 1. Epidemiological characteristics of Bartonellainfection in Ixodes pacificus adult ticks from Santa Clara County
OriginSex% of ticks withBartonella infection (no. PCR positive/total no. tested)
Baird RanchMale0 (0/4)
 Female0 (0/5)
Red Fern RanchMale42.9 (3/7)
 Female57.1 (4/7)
Windy Hill Open Space ReserveMale25.8 (17/66)
Female8.1 (5/62)
Total 19.2 (29/151)
After PCR-RFLP analysis for Bartonella species identification with three different endonucleases, three ticks (ticks 4, 5, and 12) collected at Red Fern Ranch were found to be infected with a Bartonella-like strain, for which the digestion profile was similar to that of B. quintana (Table2 and Fig.1). The partial sequence analysis of thegltA gene showed that the closest related sequence was in the B. quintana Fuller strain, with a DNA similarity ranging from 97.8 to 100% (Table 2). The PCR-RFLP profiles of theBartonella-like strains from six ticks (ticks 15, 17, 22, 34, 74, and 80) collected at the Windy Hill Open Space Reserve were identical to the profile of B. henselae (Table 2 and Fig.1). The nucleotide sequences of the partial gltA gene of these six samples showed a 97.4 to 100.0% sequence similarity to thegltA sequence of the B. henselae Houston-1 strain (Table 2). A profile similar to that of a cattle Bartonellastrain (13) was identified in five ticks (ticks 63, 73, 75, 81, and 93) collected at the Windy Hill Open Space Reserve, including one tick (tick 75) with a mixed profile of B. henselae and Bartonella cattle-1 strains (Table 2 and Fig. 1). All of these strains showed very high percentages of DNA similarity compared to the cattle Bartonella strain, ranging from 99.3 to 99.6% (Table 2). One tick (tick 70) was infected with aBartonella-like strain closely related to B. vinsonii subsp. berkhoffii, based on a 98.9% nucleotide similarity by partial sequence analysis of thegltA gene (Table 2). However, the PCR-RFLP profile of this tick extract showed a mixed PCR-RFLP profile of B. vinsoniisubsp. berkhoffii and B. henselae (Table 2 and Fig. 1). There were three ticks (ticks 143, 146, and 147) infected withBartonella-like strains with previously unrecognized PCR-RFLP profiles (Table 2 and Fig. 1) compared to the availableBartonella type strains tested. After sequence comparisons of the partial gltA gene, these strains were determined to be closely related to B. washoensis (DNA similarity from 99.3 to 100.0%) (Table 2). Based on the partial sequences of thegltA gene, all strains obtained from the PCR-positive ticks were significantly different from Rickettsia prowazekii (DNA similarity of <70%), a species closely related toBartonella spp., and from Coxiella burnetii (DNA similarity of <70%). In the 11 remaining Bartonella-PCR positive ticks, despite a PCR-RFLP profile suggestive ofBartonella coinfection, partial sequencing analysis was inconclusive.
Table 2.
Table 2. PCR-RFLP and partial sequencing analyses of thegltA gene for Bartonella species identification in 18 infected ticks
OriginTickPCR-RFLP profileaClosest Bartonellaspecies (% DNA similarity based on 273 bp of the gltAgene)
Red Fern Ranch4B. quintana-likeB. quintana (97.8)
 5B. quintana-likeB. quintana(99.6)
 12B. quintana-likeB. quintana (100.0)
Windy Hill Open Space Reserve15B. henselae-likeB. henselae(99.6)
17B. henselae-likeB. henselae(98.5)
 22B. henselae-likeB. henselae (99.3)
 34B. henselae-likeB. henselae (97.4)
 63Bartonella strain cattle-1-likeBartonella strain cattle-1 (99.6)
 70Mixed type of B. henselae and B. vinsonii subsp. berkhoffiiB. vinsonii subsp.berkhoffii (98.9)
 73Bartonella strain cattle-1-likeBartonella strain cattle-1 (99.3)
 74B. henselae-likeB. henselae(98.9)
 75Mixed type of B. henselae andBartonella cattle-1 strainBartonella strain cattle-1 (99.6)
 80B. henselae-likeB. henselae (100.0)
 81Bartonella strain cattle-1-likeBartonella strain cattle-1 (99.6)
 93Bartonella strain cattle-1-likeBartonella strain cattle-1 (99.3)
 143Unrecognized typeB. washoensis (99.3)
 146Unrecognized typeB. washoensis (100.0)
 147Unrecognized typeB. washoensis(100.0)
PCR-RFLP profile of B. quintana: 310-bp band with TaqI digestion, 400-bp band with HhaI digestion, and 150- and 200-bp bands afterMseI digestion. PCR-RFLP profile of B. henselae: 90-, 150-, and 190-bp bands with TaqI digestion, 190- and 220-bp bands with HhaI digestion, and 150- and 200-bp bands with MseI digestion. PCR-RFLP profile ofBartonella strain cattle-1: 150-and 250-bp bands withTaqI digestion, 400-bp band with HhaI digestion, and 140- and 200-bp bands with MseI digestion. PCR-RFLP profile of the mixed type of B. henselae and B. vinsonii subsp. berkhoffii: 90-, 150-, and 190-bp bands with TaqI digestion, 190-, 220-, and 400-bp bands withHhaI digestion, and 80-, 150-, 200-, and 210-bp bands withMseI digestion. PCR-RFLP profile of the mixed type ofB. henselae and Bartonella strain cattle-1: 90-, 150-, 190-, and 250-bp bands with TaqI digestion, 190-, 220-, and 400-bp bands with HhaI digestion, and 140- and 200-bp bands with MseI digestion.
Fig. 1.
Fig. 1. PCR-RFLP of the gltA gene of tick samples. Assays were performed by digestion with TaqI,HhaI, and MseI. Lane M, 100-bp molecular size ladder; lanes 1, 11, and 21, tick 22; lanes 2, 12, and 22, tick 70; lanes 3, 13, and 23, tick 75; lanes 4, 14, and 24, tick 81; lanes 5, 15, and 25, tick 12; lanes 6, 16, and 26, tick 143; lanes 7, 17, and 27, B. henselae; lanes 8, 18, and 28, B. vinsoniisubsp. berkhoffii; lanes 9, 19, and 29,Bartonella strain cattle-1; lanes 10, 20, and 30, B. quintana.


To demonstrate the role of ticks as vectors forBartonella in natural environments, questing ticks have to be examined. This approach has been successfully used for Lyme borreliosis and the agents of human ehrlichioses in I. pacificus ticks in western North America (29, 30, 32). The gltA gene was chosen for PCR-RFLP and partial sequencing analysis because this gene is more variable, and thus more discriminative for identifying Bartonella species and subspecies, than the more conserved 16S rRNA gene (6, 42). To our knowledge, this is the first report ofBartonella infections identified in questing I. pacificus adult ticks. Not only was a high prevalence (19.2%) ofBartonella infection observed in these ticks, but also partial sequences of several previously recognized humanBartonella pathogens, i.e., B. quintana, B. henselae, B. washoensis, and B. vinsonii subsp.berkhoffii, were also identified in these infected ticks. These results indicate that these human-pathogenicBartonella species or closely related species could be carried by I. pacificus ticks. However, it is unclear why male ticks were more likely to be PCR positive forBartonella than females. This finding will require further confirmation with a larger sample size of male and female ticks from various geographical areas.
Based on previous studies, a significant percentage of humanBartonella infections have occurred without exposure to known reservoirs or vectors. Up to 30% of human CSD patients may not have been scratched or bitten by cats (33), and 1% of human CSD patients do not have any known contact with animals (35). Although fleas are the main vectors for B. henselae among cats (16), ticks have been suspected to be the source of infection in a few human cases of B. henselae infection (34). An epidemiological study conducted by Zangwill et al. (46) showed that CSD patients were more likely to have found one tick on their bodies than were controls. In a recent outbreak of trench fever in Seattle, Wash., vectors other than lice were suspected in B. quintanatransmission because no association was found between body louse infestation and the infection in these human patients (44). In the southeastern United States, two cases ofB. quintana-associated central nervous system infection were reported for children with no known history of louse exposure, including one case of rural origin (39). Furthermore,Dermacentor andersoni ticks were identified as competent vectors for B. bacilliformis in an experimental infection of nonhuman primates (37), and a B. bacilliformis-like agent was recently isolated from an I. ricinus tick in Wal/cz, Poland (31). According to a recent seroepidemiological study of dogs from North Carolina and Virginia, heavy tick infestation was a more important factor associated with B. vinsonii subsp. berkhoffii infection than heavy flea infestation (38). Breitschwerdt et al. further found that dogs infected with tick-transmitted Ehrlichiaspecies are frequently coinfected with B. vinsonii subsp.berkhoffii (8). These findings suggest that ticks could play a role in the transmission of Bartonellaorganisms.
I. pacificus is very common in California, as it has been identified in 50 of the 58 counties (19). These ticks are three-host Ixodid ticks. During their larval and nymphal stages, they feed mainly on small mammals and reptiles (19). As rodents are the likely reservoir for B. washoensis (9), a Bartonella species isolated from a patient with myocarditis (R. L. Regnery et al., unpublished data), these small mammals could serve as an important source of infection to Ixodes larvae and nymphs. If transstadial transmission was successful after molting, questingI. pacificus nymphal or adult ticks could then transmitB. washoensis to large animals and possibly humans through tick bites.
The likelihood of ticks acquiring B. henselae and B. vinsonii subsp. berkhoffii from rodents should be low, as these Bartonella organisms have not yet been identified in any rodent reservoir (4, 5, 17, 18, 20-22, 28). Nevertheless, as B. vinsonii subsp. vinsonii andB. vinsonii subsp. arupensis have been identified in rodents (2, 22, 45), the existence of a rodent reservoir for B. vinsonii subsp. berkhoffii still needs to be further investigated. Regarding other sources of infection, there is evidence that cats are the main reservoir for B. henselae, and B. vinsonii subsp. berkhoffiihas been isolated from domestic dogs and a large number of California wild coyotes (Canis latrans) (7, 8, 10, 13, 15, 27). Although these large mammals are not the preferred hosts for I. pacificus nymphs, their role as accidental hosts for the nymphs cannot be excluded (19). However, the percentage (3% [5 of 151]) of Bartonella PCR-positive ticks that were found to be infected with a B. henselae-like strain could not be explained simply by this hypothesis and would suggest the possibility of other reservoirs. In the present study, several ticks were demonstrated to be infected with B. henselae-like strains, supporting previous studies involving ticks as a possible source of human infection (34, 46). Similarly, the identification of B. vinsonii subsp.berkhoffii in one questing I. pacificus adult tick supports the potential role of tick transmission, as previously suggested for domestic dogs (38). Furthermore, the major foci of B. vinsonii subsp. berkhoffii infection in coyotes were distributed mainly in California's coastal and central counties, which coincides with the known distribution of several arthropods, including I. pacificus ticks (13, 15).
The identification of the B. quintana-like strain inI. pacificus ticks is quite surprising and raises questions about the role of this arthropod in human infection. At present, humans are considered to be the only reservoir for B. quintana. The likelihood that ticks acquire B. quintana directly from humans must be considered very low, as humans are not the preferred host for I. pacificus nymphs. Moreover, it would be necessary for a nymphal tick to feed on a B. quintana-bacteremic human long enough to acquire the infection. Our results could suggest the presence of other reservoirs for B. quintana, which could serve as an alternative blood source of infection to I. pacificus nymphs. Western fence lizards (Sceloporus occidentalis) have been found to be one of the preferred hosts for immature Ixodes ticks in California (19), but no investigation has been conducted to isolateBartonella spp. in these vertebrates. Therefore, attempts to isolate various Bartonella species from lizards will be of major importance.
In California, high Bartonella bacteremia prevalences have been reported for beef cattle (89%) and mule deer (90%), and ticks have been suspected to be a potential source of infection for these ruminants based on epidemiological evidence (13). Similarly, 98% of 58 roe deer (Capreolus capreolus) from France were Bartonella bacteremic (Heller et al., Abstr. Int. Conf. Emerg. Infect. Dis., p. 21.18) and 60% of 121 tick samples collected on roe deer in The Netherlands reacted with aBartonella genus-specific probe (43). However, such a high percentage of positive ticks must be interpreted with caution, as most ticks could have fed on bacteremic animals. On the contrary, we detected Bartonella infection in questing adult ticks, suggesting infection at an earlier stage. We also identified infection of these ticks with a Bartonella strain similar toBartonella isolated from domestic and wild ruminants and toB. weissii, initially isolated from domestic cats (13). Therefore, it will be necessary to evaluate the possible role of ticks in transmission between cattle and domestic cats.
It will also be important to determine the possibility of transovarial and transstadial transmission of these Bartonella organisms in female I. pacificus ticks. In the case of Rocky Mountain spotted fever, after the last meal of D. andersoni adult females on large mammals, Rickettsia rickettsii can invade the ovaries of adult female ticks and infect the oocytes, producing infected larvae (11). Despite the absence ofBartonella bacteremia in the preferred hosts for immatureI. pacificus ticks, transovarial and transstadial transmissions of Bartonella could represent another route of infection for the questing adult ticks to acquire theseBartonella infections.
Based on the PCR-RFLP analysis of the gltA gene with three different endonucleases, two tick samples showed a mixed profile of different Bartonella strains, one with B. henselae and Bartonella strain cattle-1 and the other with B. henselae and B. vinsonii subsp.berkhoffii. The mixed profile could result from a coinfection in ticks that fed on different hosts infected with variousBartonella species and subspecies. Nevertheless, the partial sequences of the gltA gene identified only one specificBartonella strain in these two samples.
To confirm the role of Ixodes ticks in Bartonellatransmission, epidemiological and experimental transmission studies will be necessary. We could not demonstrate if theBartonella strains identified in the tick samples were still alive and transmissible to the next host. However, such a high prevalence of Bartonella infection in I. pacificus ticks from natural environments warrants further investigation all over California to elucidate the potential role of this tick species as a vector for Bartonella organisms, especially for human Bartonella pathogens. Finally, and most importantly, clinicians need to be aware of possibleBartonella infections in human patients after tick bites.


We thank Robert S. Lane (Department of Environmental Science, Policy and Management, College of Natural Resources, University of California, Berkeley) and Ian A. Gardner (Department of Medicine and Epidemiology, School of Veterinary Medicine, University of California, Davis) for their valuable comments on the manuscript.
C. C. Chang was supported by a graduate student scholarship from the Center for Companion Animal Health (George and Phyllis Miller Fund), University of California, Davis.


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Published In

cover image Journal of Clinical Microbiology
Journal of Clinical Microbiology
Volume 39Number 41 April 2001
Pages: 1221 - 1226
PubMed: 11283031


Received: 18 September 2000
Returned for modification: 29 November 2000
Accepted: 20 January 2001
Published online: 1 April 2001


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C. C. Chang
Department of Population Health and Reproduction, School of Veterinary Medicine, University of California, Davis,1 and
B. B. Chomel
Department of Population Health and Reproduction, School of Veterinary Medicine, University of California, Davis,1 and
R. W. Kasten
Department of Population Health and Reproduction, School of Veterinary Medicine, University of California, Davis,1 and
V. Romano
Santa Clara County Department of Health Services, Wildlife, Unit, Vector Control Section, San Jose,2 California
N. Tietze
Santa Clara County Department of Health Services, Wildlife, Unit, Vector Control Section, San Jose,2 California

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