Volume 18, Number 10—October 2012
Bartonella spp. Infection Rate and B. grahamii in Ticks
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|EID||Janecek E, Mietze A, Goethe R, Schnieder T, Strube C. Bartonella spp. Infection Rate and B. grahamii in Ticks. Emerg Infect Dis. 2012;18(10):1689-1690. https://dx.doi.org/10.3201/eid1810.120390|
|AMA||Janecek E, Mietze A, Goethe R, et al. Bartonella spp. Infection Rate and B. grahamii in Ticks. Emerging Infectious Diseases. 2012;18(10):1689-1690. doi:10.3201/eid1810.120390.|
|APA||Janecek, E., Mietze, A., Goethe, R., Schnieder, T., & Strube, C. (2012). Bartonella spp. Infection Rate and B. grahamii in Ticks. Emerging Infectious Diseases, 18(10), 1689-1690. https://dx.doi.org/10.3201/eid1810.120390.|
To the Editor: Bacteria of the genus Bartonella are transmitted by arthropods and are often implicated in human disease. Even though ticks are known to transmit a variety of pathogens, vector competences for transmission of Bartonella spp. by ticks were speculative (1) until recently, when in vivo transmission of B. birtlesii by Ixodes ricinus ticks was demonstrated in mice (2). This finding suggests that this tick species, which is common in Europe, may also transmit zoonotic Bartonella spp. Evidence of possible tick transmission of bartonellae to humans under natural conditions was provided by Eskow et al. (3) and Angelakis et al. (4), who identified Bartonella spp. in tissue samples of patients who were recently bitten by ticks. We determined the prevalence of Bartonella spp. in questing I. ricinus ticks in the city of Hanover, Germany, which is nicknamed The Green Metropolis and was selected the German Capital of Biodiversity in 2011.
During April–October 2010, we collected 2,100 questing ticks, consisting of 372 adults (177 female and 195 male), 1,698 nymphs, and 30 larvae, from 10 recreation areas in Hanover. Tick DNA was extracted by using the NucleoSpin 8 Blood kit (Macherey-Nagel, Düren, Germany). Plasmid DNA constructed from B. henselae reference strain ATCC49793 containing the 249-bp target sequence of the gltA gene was used as positive control. Bartonella spp. in ticks was detected by quantitative PCR (qPCR) by using the Mx3005 Multiplex Quantitative PCR System (Stratagene, Heidelberg, Germany) according to the protocol described by Mietze et al. (5), with minor modifications. Samples positive by qPCR were verified by gel electrophoresis. Bartonella species were differentiated by sequencing (Eurofins MWG Operon, Ebersberg, Germany), and obtained sequences underwent BLAST (http://blast.ncbi.nlm.nih.gov/Blast.cgi) comparison to published sequences.
On the basis of the amplicon-specific melting temperature and DNA bands representing the specific size of 249-bp after gel electrophoresis, results of qPCR showed 100 (4.76%) infected I. ricinus ticks (Table). Positive results did not vary by developmental tick stages; 4.84% (18/372) adult ticks (5.08% [9/177] female and 4.62% [9/195] male), 4.71% (80/1,698) nymphs, and 6.67% (2/30) larvae were infected (Table). Because Bartonella spp. do not seem to be transmitted transovarially (6), it is likely that larvae had interrupted blood meals and thus did not take up enough blood to develop into the nymphal stage.
Seasonal changes in Bartonella spp. infection rates resulted in a higher peak in May (38/300 [12.67%]) than in the other months (Table). For sampling locations, infection rates for grassy sampling location 6 (4/210 [1.90%] infected ticks) differed significantly (Bonferroni-Holm adjusted p<0.001; *<0.0011) from that of densely wooded sampling location 9 (22/210 [10.48%] infected ticks).
Sequencing of the gltA fragment resulted in Bartonella species identification for 56/100 positive samples; 52 of these samples (from 38 nymphs, 13 adults, and 1 larva) were identified as infected with B. henselae. In 51 samples (92.86%), maximum identity with the BLAST top hit sequence was 99% because of nucleotide substitutions in position 198 (T→C) and in position 136 (A→G) of the 249-bp fragment. The remaining sample showed 100% identity with B. henselae strains Brazil-1 and 45-00249 (GenBank accession nos. HQ012580 and GQ225709).
Four of the 56 successfully sequenced samples (7.14%; all samples from nymphs) showed the sequence pattern of B. grahamii. One sample revealed 100% identity with B. grahamii (GenBank accession no. EU014266); the remaining 3 samples showed an identity of 98% with the B. grahamii strain Hokkaido-1 (GenBank accession no. AB426652) and 99% (T→C in position 93) with a sequence described as B. grahamii–like (GenBank accession no. AY435122). Sequences obtained in this study (deposited in GenBank under accession nos. JQ770304 and JK758018) support the genetic variability of Bartonella spp., as demonstrated by others (5,7,8).
It remains unclear whether ticks are involved in transmission of pathogenic Bartonella spp. to humans under natural conditions. However, the total prevalence rate of 4.76% (100/2,100) questing I. ricinus ticks infected with B. henselae and B. grahamii highlights the need for public awareness and draws attention to the possibility of an infection with zoonotic Bartonella spp. after a tick bite (3,4). B. henselae, the predominantly identified species, has been associated with cat scratch disease, peliosis hepatis, and bacillary angiomatosis in humans. Eskow et al. (3) also connected chronic symptoms of Lyme disease to co-infections with Borrelia burgdorferi and B. henselae. B. grahamii has been associated with neuroretinitis and ocular artery thrombosis in humans (9,10). The potential risk for zoonotic Bartonella spp. infection in urban recreation areas should not be underestimated.
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- Eskow E, Rao RV, Mordechai E. Concurrent infection of the central nervous system by Borrelia burgdorferi and Bartonella henselae: evidence for a novel tick-borne disease complex. Arch Neurol. 2001;58:1357–63.
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- Kerkhoff FT, Bergmans AM, van Der Zee A, Rothova A. Demonstration of Bartonella grahamii DNA in ocular fluids of a patient with neuroretinitis. J Clin Microbiol. 1999;37:4034–8.
- Table. Seasonal distribution of Ixodes ricinus ticks infected with Bartonella spp., Hanover, Germany, 2010
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Christina Strube, Institute for Parasitology, University of Veterinary Medicine Hannover, Buenteweg 17, 30559 Hanover, Germany
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