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. 2014 Dec 23:7:607.
doi: 10.1186/s13071-014-0607-2.

Prevalence of Rickettsiales in ticks removed from the skin of outdoor workers in North Carolina

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Prevalence of Rickettsiales in ticks removed from the skin of outdoor workers in North Carolina

Sangmi Lee et al. Parasit Vectors. .

Abstract

Background: Tick-transmitted rickettsial diseases, such as ehrlichiosis and spotted fever rickettsiosis, are significant sources of morbidity and mortality in the southern United States. Because of their exposure in tick-infested woodlands, outdoor workers experience an increased risk of infection with tick-borne pathogens. As part of a double blind randomized-controlled field trial of the effectiveness of permethrin-treated clothing in preventing tick bites, we identified tick species removed from the skin of outdoor workers in North Carolina and tested the ticks for Rickettsiales pathogens.

Methods: Ticks submitted by study participants from April-September 2011 and 2012 were identified to species and life stage, and preliminarily screened for the genus Rickettsia by nested PCR targeting the 17-kDa protein gene. Rickettsia were further identified to species by PCR amplification of 23S-5S intergenic spacer (IGS) fragments combined with reverse line blot hybridization with species-specific probes and through cloning and nucleotide sequence analysis of 23S-5S amplicons. Ticks were examined for Ehrlichia and Anaplasma by nested PCR directed at the gltA, antigen-expressing gene containing a variable number of tandem repeats, 16S rRNA, and groESL genes.

Results: The lone star tick (Amblyomma americanum) accounted for 95.0 and 92.9% of ticks submitted in 2011 (n = 423) and 2012 (n = 451), respectively. Specimens of American dog tick (Dermacentor variabilis), Gulf Coast tick (Amblyomma maculatum) and black-legged tick (Ixodes scapularis) were also identified. In both years of our study, 60.9% of ticks tested positive for 17-kDa. "Candidatus Rickettsia amblyommii", identified in all four tick species, accounted for 90.2% (416/461) of the 23S-5S-positive samples and 52.9% (416/787) of all samples tested. Nucleotide sequence analysis of Rickettsia-specific 23S-5S IGS, ompA and gltA gene fragments indicated that ticks, principally A. americanum, contained novel species of Rickettsia. Other Rickettsiales, including Ehrlichia ewingii, E. chaffeensis, Ehrlichia sp. (Panola Mountain), and Anaplasma phagocytophilum, were infrequently identified, principally in A. americanum.

Conclusions: We conclude that in North Carolina, the most common rickettsial exposure is to R. amblyommii carried by A. americanum. Other Rickettsiales bacteria, including novel species of Rickettsia, were less frequently detected in A. americanum but are relevant to public health nevertheless.

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Figures

Figure 1
Figure 1
Prevalence of tick species collected from subjects in 2011 ( n= 423) and 2012 ( n= 451).
Figure 2
Figure 2
PCR-RLB hybridization results for 23S-5S IGS fragments amplified from genomic DNA extracted from Rickettsia controls and A . americanum ticks. Next to the identification code of tick samples, Rickettsia species identifications as determined by the RLB hybridization patterns are shown in parentheses. Ra = R. amblyommii and Rm = R. montanensis. An example of hybridization patterns for some biotin-labeled A. americanum 23S-5S DNAs are presented in the lower half the figure. All of the ticks exhibited strong hybridization to the Rickettsia genus level (GP-RICK) and SFG (GP-SFG) probes, indicating that they were infected with a spotted fever group Rickettsia species. All but one 23S-5S DNA samples hybridized with probe P-AMB, indicating that these ticks were infected with R. amblyommii. Tick DNA sample 2FT365 hybridized with probe P-MAS/MON, but failed to hybridize to P-MAS/RHIPI, indicating that the tick was infected with R. montanensis.
Figure 3
Figure 3
Neighbor-joining tree showing phylogenetic relationship of partial 23S-5S IGS sequences of known Rickettsia and species identified after cloning of tick genomic DNA samples that were initially classified as unknown and/or were identified as co-infected samples in RLB hybridization assays. Sequence homologies <99% are indicated in parentheses after the sequence identity. The scale bar indicates an estimated change of 5% 23S-5S IGS. Sequences beginning with “FT” or “2FT” were generated in this study. Bootstrap values below 50% are not shown in the tree branch. Accessions numbers for study samples are given in parentheses. *Unpublished GenBank sequences.

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