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Print version ISSN 0036-4665
Rev. Inst. Med. trop. S. Paulo vol.54 no.3 São Paulo May/June 2012
Rickettsia parkeri: patógeno rickettsial transmitido por garrapatas en áreas endémicas de rickettsiosis por fiebre manchada en el sur de Uruguay
José M. VenzalI; Agustín Estrada-PeñaII; Aránzazu PortilloIII; Atilio J. MangoldIV; Oscar CastroV; Carlos G. De SouzaV; María L. FélixI; Laura Pérez-MartínezIII; Sonia SantibánezIII; José A. OteoIII
IDepartamento de Parasitología Veterinaria, Facultad de Veterinaria, Universidad de la República, Regional Norte, Salto, Uruguay
IIFacultad de Veterinaria, Universidad de Zaragoza, Zaragoza, Spain
IIIÁrea de Enfermedades Infecciosas, Hospital San Pedro - Centro de Investigación Biomédica de La Rioja, Logroño, La Rioja, Spain
IVEstación Experimental Agropecuaria Rafaela. Instituto Nacional de Tecnología Agropecuaria (INTA), Rafaela, Santa Fe, Argentina
VDepartamento de Parasitología Veterinaria, Facultad de Veterinaria, Universidad de la República, 11600 Montevideo, Uruguay
At first Rickettsia conorii was implicated as the causative agent of spotted fever in Uruguay diagnosed by serological assays. Later Rickettsia parkeri was detected in human-biting Amblyomma triste ticks using molecular tests. The natural vector of R. conorii, Rhipicephalus sanguineus, has not been studied for the presence of rickettsial organisms in Uruguay. To address this question, 180 R. sanguineus from dogs and 245 A. triste from vegetation (flagging) collected in three endemic localities were screened for spotted fever group (SFG) rickettsiosis in southern Uruguay. Tick extracted DNA pools were subjected to PCR using primers which amplify a fragment of the rickettsial gltA gene. Positive tick DNA pools with these primers were subjected to a second PCR round with primers targeting a fragment of the ompA gene, which is only present in SFG rickettsiae. No rickettsial DNA was detected in R. sanguineus. However, DNA pools of A. triste were found to be positive for a rickettsial organism in two of the three localities, with prevalences of 11.8% to 37.5% positive pools. DNA sequences generated from these PCR-positive ticks corresponded to R. parkeri. These findings, joint with the aggressiveness shown by A. triste towards humans, support previous data on the involvement of A. triste as vector of human infections caused by R. parkeri in Uruguay.
Keywords: Rhipicephalus sanguineus; Amblyomma triste; Rickettsia parkeri; Spotted fever group (SFG); Uruguay.
Inicialmente, Rickettsia conorii fue señalada como el agente causal de la fiebre manchada en Uruguay, diagnosticada mediante pruebas serológicas. Posteriormente, Rickettsia parkeri fue detectada mediante técnicas moleculares en garrapatas Amblyomma triste colectadas sobre humanos. El vector natural de R. conorii, Rhipicephalus sanguineus, no ha sido estudiado en cuanto a rickettsias en Uruguay. Para abordar este tema, 180 R. sanguineus fueron colectados sobre perros y 245 A. triste sobre vegetación en tres localidades consideradas endémicas para fiebres manchadas en el sur de Uruguay. El ADN de las garrapatas fue extraído en pools y sometido a una primera PCR utilizando cebadores que amplifican un fragmento del gen gltA, presente en prácticamente todas las especies de Rickettsia. Las muestras positivas fueron sometidas a una segunda PCR con cebadores que amplifican un fragmento del gen ompA, presente sólo en rickettsias del grupo de las fiebres manchadas (GFM). No se detectó ADN rickettsial en R. sanguineus. Sin embargo, muestras de A. triste fueron positivas a rickettsiales en dos de las tres localidades estudiadas, con prevalencias de pools positivos del 11.8 y 37.5% respectivamente. La secuenciación del ADN evidenció la presencia de R. parkeri. Basados en estos resultados junto a los anteriores y la agresividad de A. triste hacia los humanos, se concluye que esta garrapata es vector de rickettsiosis humana por R. parkeri en Uruguay.
In the beginning of the 21st century, Rickettsia rickettsii, the agent of the Rocky Mountain spotted fever (RMSF) was the only Rickettsia known in ticks collected in South America11. This organism has been detected in Argentina, Brazil, Canada, Colombia, Costa Rica, the USA, México and Panama, and causes fatal cases in the majority of these countries11. Based on development of new molecular biology tools, other rickettsiae have been described in ticks from South America during the last few years11,26. The history of spotted fever group (SFG) rickettsiosis in Uruguay is rather complex. The first three autochthonous cases of human rickettsiosis were diagnosed by Indirect Fluorescent Antibody Test (IFAT)5. Rickettsia conorii, the agent of Mediterranean spotted fever (MSF) was implicated as the causative agent, and the tick Amblyomma maculatum was found attached to at least one of the patients5. The natural vector and potential reservoir of R. conorii in the Old World is the R. sanguineus group, implicated in the transmission of other Rickettsia species affecting humans23,34. In Argentina, Rickettsia massiliae was detected in R. sanguineus collected in the city of Buenos Aires, and recently a human case of R. massiliae infection has been confirmed in the same country3,9.
In Uruguay, R. sanguineus is the second most frequently identified tick involved in bites of humans31. However, the infection by R. conorii has been neither reported in autochthonous form in the New World nor associated to ticks of the genus Amblyomma19,23. In Uruguay new human cases have been confirmed suggesting that Amblyomma triste tick is the vector (not Amblyomma maculatum, a tick species absent in Uruguay) and making the disease considered as "endemic and emergent" in this country4.
Rickettsia parkeri has been reported as a pathogen of humans in the United States, where it is transmitted by A. maculatum17. A. triste has been found infected with R. parkeri in Uruguay16,32. In addition to the USA and Uruguay, R. parkeri has been also detected in A. triste from Brazil, Argentina and in Amblyomma tigrinum from Bolivia14,25,30. Recently in Argentina, nine cases of SFG rickettsiosis associated to R. parkeri infection have been reported. Two of them were confirmed by PCR21. In Uruguay, new cases of human rickettsiosis confirmed by serological antibody-absorption tests with purified antigens of R. parkeri associated with immunofluorescence assays indicated that the patients were infected by R. parkeri6.
A. triste is the tick species most frequently implicated in human bites in Uruguay and it is particularly aggressive31.
The main aim of this study was to evaluate the prevalence of Rickettsia spp. in ticks collected in a region considered as endemic for human SFG rickettsiosis in Uruguay4.
MATERIALS AND METHODS
Studied area and collection of ticks. A total of 245 A. triste ticks (155 females and 90 males) were collected from August to October (adult activity season) 2004, by flagging on vegetation in three suburban areas in southern Uruguay, two of them in Canelones county (Toledo Chico, at 34º44´S, 56º06´W, and Escuela Militar de Aeronáutica - EMA, at 34º44´S, 55º58´W), and the other one in Montevideo county (Villa García, at 34º46´S, 56º02´W) (Fig. 1). Details of captures of questing ticks are included in Table 1. Furthermore, 180 R. sanguineus ticks (88 females, 64 males, 24 nymphs and four larvae) were collected on dogs in urban and suburban areas from November 2000 to February 2005 in Montevideo and Canelones counties. These samples were obtained after the examination of dogs in rural areas and in private veterinary clinics, as well as from arthropods submitted to the Department of Parasitology, Veterinary Faculty, Montevideo (Uruguay) for diagnosis.
Ticks were immediately fixed and stored in tubes containing ethanol 70º to preserve DNA, and identified using standard taxonomic keys1,7.
DNA extraction and polymerase chain reaction (PCR) assays. Ticks were rinsed with distilled water for 10 minutes and dried on sterile filter paper in a laminar-flow hood. Specimens were longitudinally cut, and the DNA of five "half-tick" pools was extracted using the JETQUICK Tissue DNA Spin Kit (GENOMED). The other half of each tick was stored for other studies on pathogen and symbiont.
Specimens were processed by PCR assays using primers CS-78 (forward) (5'-GCAAGTATCGGTGAGGATGTAAT-3') and CS-323 (reverse) (5'-GCTTCCTTAAAATTCAATAAATCAGGAT-3'), which amplify a 401 bp fragment of the citrate synthase gene (gltA), previously reported as adequate for detection of Rickettsia spp.12. PCR cycling conditions were as follows: an initial three min. denaturation cycle at 95 °C followed by 40 cycles of denaturation (95 °C for 15 s), annealing (48 °C for 30 s), and extension (72 °C for 30 s) with a final seven min extension at 72 °C. Distilled water and DNA from Rickettsia slovaca (a rickettsial species not present in Uruguay to minimize contamination risks) were used as negative and positive controls, respectively. Ten microliters of the PCR product were separated by electrophoresis in a 1% agarose gel, stained with ethidium bromide, and examined by UV transillumination.
Tick DNA pools found to be positive with primers CS-78 and CS-323 (gltA) were subjected to a second PCR round with primers Rr190.70p (forward) (5'-ATGGCGAATATTTCTCCAAAA-3') and Rr190.701n (reverse) (5'-GTTCCGTTAATGGCAGCATCT-3'), which amplify a 631 bp fragment of the ompA gene22. Conditions for these procedures were an initial three min denaturation cycle at 95 °C, followed by 40 cycles of denaturation (95 °C for 20 s), annealing (46 °C for 30 s), and extension (63 °C for 60 s) with a final seven min extension at 72 °C. Controls were as previously described.
Sequencing and phylogenetic analysis. Nucleotide sequences of PCR products for gltA and ompA were compared with those available in GenBank using Basic Local Alignment Search Tool (BLAST) (http://www.ncbi.nlm.nih.gov/blast). Phylogenetic analyses were conducted using MEGA version 4.029. A Neighbor-Joining24 tree was generated using Tajima-Nei method28 and gaps were excluded in the pairwise comparison. Support for the NJ topology was tested by bootstrapping over 1,000 replications8.
A total of 49 pools of A. triste (31 pools of females and 18 of males) were analyzed. Eight out of 49 pools showed positive PCR results for gltA and ompA genes. The prevalence of Rickettsia in ticks using PCR primers CS-78 / CS-323 and Rr190.70p / Rr190.701n is shown in Table 1, and expressed as percentage and minimum infection rate (MIR) or the minimum percentage of ticks in a pool with detectable Rickettsia. This calculation is based on the assumption that a PCR-positive pool contains only one positive tick2,13. It is interesting to note the high variability in infection rates of questing ticks between localities, with a maximum of 7.5% MIR and 37.5% infected pools in Toledo Chico. The ompA nucleotide sequence (462 bp) was deposited in Genbank (accession number JN664898), and it was named R. parkeri Canelones. The alignment of our sequence with 19 partial ompA sequences from SFG rickettsiae available in GenBank resulted in a total of 450 sites including gaps. Our sequence grouped with sequences of R. parkeri obtained in several countries and R. parkeri (strain Cooperi) and Rickettsia sp. for Amblyomma nodosum in the phylogenetic tree based on these partial ompA sequences, but it is separated from other species of Rickettsia detected in ticks in South America, as well as R. conorii (Fig. 2).
Rickettsial DNA was not found in any of the 36 pools prepared with the 180 R. sanguineus ticks, using CS-78 and CS-323 primers for gltA gene.
R. parkeri has been the only pathogen detected in A. triste ticks collected in a region considered endemic for human SFG rickettsiosis in Uruguay. In our study, all R. sanguineus tested showed negative PCR results, and neither R. conorii nor any other Rickettsia species was detected. Nevertheless, our data do not rule out that the population of R. sanguineus of Uruguay harbors Rickettsia spp. These findings further support that R. parkeri is the most frequently found SFG rickettsia circulating in this region, A. triste being the main vector. It seems that R. parkeri has been a neglected pathogen in wide areas of the American continent. It was unequivocally associated to a case of human disease in Virginia (USA) and proved to be transmitted by A. maculatum17. Since the first association with human disease, more cases have been confirmed in humans in Virginia, Mississippi and probably other states of the USA18,35. A recent survey on the range of R. parkeri in the USA shows that it is within the known range of the vector A. maculatum with prevalence varying according to the different states, averaging 11% of collected ticks in Florida, Georgia, Kentucky, Mississippi and Oklahoma27. Additional work carried out in Uruguay, Brazil and Argentina demonstrated variable rates of infection by R. parkeri (2.5-9.7%) in A. triste, also suggesting that R. parkeri may be relatively common in populations of A. triste14,25,32. By comparison, prevalence of infection of tick vectors with R. rickettsii is typically much lower, from 0.05% to 1.3%, as determined by surveys in the USA and Brazil20,27.
The reasons for differences in tick infection rates among the three studied localities in this work are unknown. All three regions are socially and ecologically similar and are in an endemic area for rickettsiosis.
The first reports implicating R. conorii as the etiological agent of human rickettsiosis in the area of study are unsupported by our results. Previous studies on human cases in Uruguay seem to be biased due to crossed reactions using a commercial IFAT kit5. To date, autochthonous cases of R. conorii infection have not been confirmed in the Americas19,23.
Previous efforts to detect Ehrlichia spp. and Anaplasma spp. DNA by PCR in both R. sanguineus and A. triste in the same area were unsuccessful33.
Recent research has pointed out the presence of different strains of R. parkeri in some domestic and wild animals in Brazil, in areas where A. triste is absent10,15,26. These studies indicate that other tick species that replace A. triste in areas of Brazil (such as Amblyomma dubitatum, A. nodosum and A. ovale) might be involved in the transmission of this pathogen. Of these three ticks species only A. dubitatum is recorded for Uruguay. Further assessment is required to understand the role of other tick species in the spread and maintenance of R. parkeri in the Neotropics.
This work was supported by the Programa Iberoamericano de Ciencias y Tecnologia para el Desarrollo (CYTED) to Red Iberoamericana para la Investigación y Control de las Enfermedades Rickettsiales (RIICER). We thank Dr. Marcelo B. Labruna (USP) for critical comments on the paper.
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Prof. Dr. José M. Venzal,
Departamento de Parasitología Veterinaria
Facultad de Veterinaria
Universidad de la República
Salto, Rivera 1350
50000 Salto, Uruguay
Received: 12 September 2011
Accepted: 20 March 2012