Literature DB >> 19624931

Rickettsia slovaca and R. raoultii in tick-borne Rickettsioses.

Philippe Parola1, Clarisse Rovery, Jean Marc Rolain, Philippe Brouqui, Bernard Davoust, Didier Raoult.   

Abstract

Tick-borne lymphadenopathy (TIBOLA), also called Dermacentor-borne necrosis erythema and lymphadenopathy (DEBONEL), is defined as the association of a tick bite, an inoculation eschar on the scalp, and cervical adenopathies. We identified the etiologic agent for 65% of 86 patients with TIBOLA/DEBONEL as either Rickettsia slovaca (49/86, 57%) or R. raoultii (7/86, 8%).

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Year:  2009        PMID: 19624931      PMCID: PMC2744242          DOI: 10.3201/eid1507.081449

Source DB:  PubMed          Journal:  Emerg Infect Dis        ISSN: 1080-6040            Impact factor:   6.883


In 1968, Rickettsia slovaca, a spotted fever group (SFG) rickettsia, was isolated from Dermacentor marginatus ticks in the former Czechoslovakia before being detected in D. marginatus or D. reticulatus ticks throughout Europe (Figure 1) (). In 1997, R. slovaca was described as a human pathogen and an agent of tick-borne lymphadenopathy (TIBOLA) (). This syndrome, also called Dermacentor-borne necrosis erythema and lymphadenopathy (DEBONEL), is defined as the association of a tick bite, an inoculation eschar on the scalp, and cervical lymphadenopathies ().
Figure 1

Dermacentor reticulatus, the ornate dog tick (A) (female, left; male, right), and D. marginatus, the ornate sheep tick (B) (engorged female, left; unfed female, center; male, right; scale bar = 1 cm), and their distribution. D. marginatus is most frequently found in Mediterranean areas of Europe with dense bush and tree cover and is common under oak and pine vegetation. It also has a restricted distribution in North Africa, in the cooler and more humid areas associated with the Atlas Mountains. Adults infest large mammals such as sheep, cattle, goats, and wild boars. Larvae and nymphs feed mostly on small mammals and medium sized carnivores. D. reticulatus is most frequently found in colder northern areas of western Europe and the former Soviet Union, with high humidity and mild winters. D. reticulatus is primarily a tick of dogs and carnivores, but it can be found on ungulates such as sheep, cattle, and horses (). D. marginatus and D. reticulatus have been suggested as reservoirs of R. slovaca and R. raoultii, which are maintained in ticks through transstadial and transovarial transmission. Therefore, the geographic distribution of these rickettsiae likely parallels that of Dermacentor ticks (C).

Dermacentor reticulatus, the ornate dog tick (A) (female, left; male, right), and D. marginatus, the ornate sheep tick (B) (engorged female, left; unfed female, center; male, right; scale bar = 1 cm), and their distribution. D. marginatus is most frequently found in Mediterranean areas of Europe with dense bush and tree cover and is common under oak and pine vegetation. It also has a restricted distribution in North Africa, in the cooler and more humid areas associated with the Atlas Mountains. Adults infest large mammals such as sheep, cattle, goats, and wild boars. Larvae and nymphs feed mostly on small mammals and medium sized carnivores. D. reticulatus is most frequently found in colder northern areas of western Europe and the former Soviet Union, with high humidity and mild winters. D. reticulatus is primarily a tick of dogs and carnivores, but it can be found on ungulates such as sheep, cattle, and horses (). D. marginatus and D. reticulatus have been suggested as reservoirs of R. slovaca and R. raoultii, which are maintained in ticks through transstadial and transovarial transmission. Therefore, the geographic distribution of these rickettsiae likely parallels that of Dermacentor ticks (C). Since 1999, several rickettsial genotypes, called DnS14, DnS28, and RpA4, have been detected in Dermacentor spp. ticks throughout Europe (Figure 1). Isolates have been obtained and shown to belong to a unique new SFG rickettisia species named R. raoultii (). In 2002, R. raoultii DNA was detected in a D. marginatus tick taken from the scalp of a patient in whom TIBOLA/DEBONEL developed in France (). Moreover, DNA of what is now known to be R. raoultii has been found in the blood of 1 patient with TIBOLA/DEBONEL (). The goal of this study was to identify the rickettsial agents in patients with TIBOLA/DEBONEL symptoms and in those who had an isolated tick bite on the scalp.

The Study

We included all patients with TIBOLA/DEBONEL symptoms (Figure 2) and those who had an isolated tick bite on the scalp without any symptoms from whom samples (serum, skin biopsy, or ticks harvested from the scalp) were received at our laboratory from January 2002 through December 2007. Epidemiologic and clinical data were collected retrospectively. The study was approved by the ethics committee of the Medicine School of Marseille under reference 08-008.
Figure 2

Typical signs of TIBOLA (tick-borne lymphadenopathy)/DEBONEL (Dermacentor-borne necrosis erythema and lymphadenophy). Here, infections were caused by Rickettsia slovaca , resulting in cervical lymphadenopathy (left panel, arrow), inoculation on the scalp (middle panel), and residual alopecia 4 weeks later (right panel).

Typical signs of TIBOLA (tick-borne lymphadenopathy)/DEBONEL (Dermacentor-borne necrosis erythema and lymphadenophy). Here, infections were caused by Rickettsia slovaca , resulting in cervical lymphadenopathy (left panel, arrow), inoculation on the scalp (middle panel), and residual alopecia 4 weeks later (right panel). Immunoglobulin (Ig) G and IgM titers against rickettsial antigens were estimated by microimmunofluorescent assay; results were verified by Western blot and cross-absorption studies (). Ticks found on persons and skin biopsy specimens were cultured on human embryonic lung cells (). These samples were also used to amplify and identify outer membrane protein A–encoding gene fragments of rickettsiae by PCR (). Also, the so-called suicide PCR-assay was used with acute-phase serum samples (). Among 98 study patients, 86 were classified as TIBOLA/DEBONEL patients. Twelve (12.2%) patients made up the second group with an isolated tick bite. All but 1 patient, who was bitten in Belgium, were bitten in France. Tick bites more frequently occurred from February through May (50/86, 58.1%). Because of results of serologic techniques, we could conclude that 66 (84.6%) of 78 TIBOLA/DEBONEL patients with obtained serum specimens had a recent rickettsial disease. Western blot and cross-adsorption analyses enabled detection of antibodies specifically directed against R. slovaca and R. raoultii in 34 and 4 patients, respectively (Appendix Table). Two patients who were infected with R. slovaca were found to be co-infected with Coxiella burnetii in an acute form of Q fever. Serologic testing was performed in 12 patients with isolated tick bites, and results were negative in all cases. A total of 19 skin biopsy specimens were obtained. Four R. slovaca infections were diagnosed by regular PCR, and 3 isolates of this rickettsia were obtained. The suicide PCR on acute-phase serum samples identified 1 additional case of R. slovaca infection. Because of molecular tools and culture, 6 patients received the diagnosis of an R. slovaca infection, including 5 who did not receive a diagnosis by serologic assays (Appendix Table). Ticks removed from 28 TIBOLA/DEBONEL patients consisted of 23 D. marginatus (88.4%), 2 Dermacentor spp., 1 Haemaphysalis punctata, and 2 that were not identified. Overall, the tick studies enabled us to suggest the diagnosis of R. slovaca and R. raoultii infections in 10 and 3 patients, respectively, whose conditions were not diagnosed with previous tests (Appendix Table). All DNA sequences obtained showed 100% identity with R. raoultii or R. slovaca, excluding the coexistence of several rickettsiae in the corresponding samples. According to our investigations, 49 (57%) of 86 patients with TIBOLA/DEBONEL had probable or certain R. slovaca infections, and 7 (8%) of 86 had probable R. raoultii infections. The characteristics of these patients are shown in the Table.
Table

Characteristics of TIBOLA/DEBONEL patients with certain or probable Rickettsia slovaca infection compared with patients with certain or probable R. raoultii infection*

CharacteristicTIBOLA/DEBONEL patients, n = 86
No. R. slovaca infections (%), n = 49†‡No. R. raoultii infections (%), n = 7†p value
Female sex33/49 (67)7/7 (100)0.04
Mean age, y32320.90
Age <12 y20/49 (41)3/7 (43)0.46
Hiking or recreational activities such as a walk in the forest21/28 (75)4/5 (80)0.44
Fever§21/39 (54)4/5 (80)0.27
Painful eschar14/22 (64)3/3 (100)0.30
Painful adenopathies18/26 (69)5/5 (100)0.20
Face edema6/31 (19)2/5 (40)0.30
Rash7/30 (23)1/5 (20)0.68
Headache16/30 (53)4/4 (100)0.10
Alopecia16/27 (59)0/40.09
Asthenia23/33 (70)5/5 (100)0.20
Prolonged asthenia¶10/29 (35)2/4 (50)0.46
Chronic asthenia#4/28 (14)1/4 (25)0.51

*Certain cases were those with positive culture, PCR, or suicide PCR results in blood or skin biopsy samples or with lymph node aspirates. Probable cases were those with identification by PCR and sequencing of the corresponding Rickettsia spp. in ticks, Western blot results demonstrating R. slovaca– or R. raoultii–specific antibodies, or a cross-absorption assay demonstrating specific antibodies against R. slovaca or R. raoultii. TIBOLA, tick-borne lymphadenopathy; DEBONEL, Dermacentor-borne necrosis erythema and lymphadenopathy.
†Denominators indicate the number of patients for whom the criterion was available.
‡Includes 14 patients previously reported ().
§Temperature >37°5C.
¶Self-reported, persistent asthenia of 1 to 6 months.
#Self-reported persistent or relapsing asthenia of >6 consecutive months.

*Certain cases were those with positive culture, PCR, or suicide PCR results in blood or skin biopsy samples or with lymph node aspirates. Probable cases were those with identification by PCR and sequencing of the corresponding Rickettsia spp. in ticks, Western blot results demonstrating R. slovaca– or R. raoultii–specific antibodies, or a cross-absorption assay demonstrating specific antibodies against R. slovaca or R. raoultii. TIBOLA, tick-borne lymphadenopathy; DEBONEL, Dermacentor-borne necrosis erythema and lymphadenopathy.
†Denominators indicate the number of patients for whom the criterion was available.
‡Includes 14 patients previously reported ().
§Temperature >37°5C.
¶Self-reported, persistent asthenia of 1 to 6 months.
#Self-reported persistent or relapsing asthenia of >6 consecutive months.

Conclusions

We report 86 patients with TIBOLA/DEBONEL; this group includes 14 patients whose conditions had been preliminarily reported (). We also describe several cases caused by the emerging pathogen R. raoultii (), including patients with indirect molecular evidence of infection because the pathogen was detected in the ticks that had bitten them. Original findings also include facial edema as a new clinical feature in TIBOLA/DEBONEL, and the report of the second patient co-infected with R. slovaca and C. burnetii (). Because acute Q fever, a worldwide zoonosis, may be asymptomatic, we recommend that patients infected with tick-borne pathogens also undergo testing for concurrent infections with C. burnetii. No TIBOLA/DEBONEL cases were recorded during the warmest summer months; peak incidence occurred during March–May and during September–November, linked with the activity of Dermacentor ticks in Europe (Figure 1) (). However, to date, we have no explanation for the finding that children and women are at higher risk for TIBOLA/DEBONEL or why D. marginatus and D. reticulatus ticks prefer to bite persons on the scalp. A possible explanation could be that Dermacentor ticks usually bite hairy domestic and wild animals and the longer hair of women and children may attract them. One of the most remarkable findings of this work is the proportional importance of R. slovaca in TIBOLA/DEBONEL patients, compared with R. raoultii. In 2006, Ibarra et al. reported on 14 persons in Spain who had a D. marginatus tick attached to the scalp (). All ticks were found to be infected by rickettsiae: 8 (58%) were infected by R. slovaca, and 6 (42%) by R. raoultii. In 10 of the patients, TIBOLA/DEBONEL symptoms developed, including in all 8 of the patients who had been bitten by a tick infected by R. slovaca and in 2 of the 6 patients who had been bitten by a tick infected by R. raoultii. R. slovaca was more significantly associated with TIBOLA/DEBONEL patients than was R. raoultii (p<0.05) (). Here, focusing on the studies of ticks removed from TIBOLA/DEBONEL patients, we found that 12 of 19 ticks harbored R. slovaca, whereas only 3 of 19 harbored R. raoultii (p = 0.047). In the patients with asymptomatic tick bites, from whom 9 ticks were obtained, all ticks positive by PCR harbored R. raoultii. Moreover, R. raoultii seems to be more highly prevalent in D. marginatus and D. reticulatus ticks in nature than is R. slovaca. Although comparing field surveys of ticks is difficult because of the sampling methods, the sizes of the samples, and the potential PCR inhibitors, R. raoultii has been more frequently detected in D. marginatus ticks than has R. slovaca. In southeastern Spain, 73% of 101 D. marginatus ticks were infected by R. raoultii and 27% by R. slovaca (). Similar differences have been shown in Germany, Portugal, the Netherlands, and Spain (–). Although interpreting these data definitively is difficult, the recurrence of similar published results by different teams suggests that exposure to R. raoultii through the bite of a Dermacentor spp. tick is likely more frequent than exposure to R. slovaca. However, more cases of R. slovaca infection have been recorded, which suggests that R. raoultii is less pathogenic. TIBOLA/DEBONEL is a newly recognized disease, and its incidence is likely underestimated. In our laboratory, TIBOLA/DEBONEL is the most frequently reported rickettsial disease, except during the dry summer period. Doxycycline remains the treatment of choice, with new macrolides as alternative treatments (). Although we report 6 more cases of R. raoultii infection in addition to the 2 recently reported (,), this Dermacentor-borne rickettsia seems to be less pathogenic than R. slovaca.

Appendix Table

Results of microbiologic investigations regarding rickettsial diseases of patients with TIBOLA/DEBONEL or tick-bite*
  14 in total

1.  Rickettsia slovaca infection: DEBONEL/TIBOLA.

Authors:  V Ibarra; J A Oteo; A Portillo; S Santibáñez; J R Blanco; L Metola; J M Eiros; L Pérez-Martínez; M Sanz
Journal:  Ann N Y Acad Sci       Date:  2006-10       Impact factor: 5.691

2.  Prevalence data of Rickettsia slovaca and other SFG Rickettsiae species in Dermacentor marginatus in the southeastern Iberian peninsula.

Authors:  F J Márquez; A Rojas; V Ibarra; A Cantero; J Rojas; J A Oteo; M A Muniain
Journal:  Ann N Y Acad Sci       Date:  2006-10       Impact factor: 5.691

3.  DEBONEL/TIBOLA: is Rickettsia slovaca the only etiological agent?

Authors:  V Ibarra; A Portillo; S Santibáñez; J R Blanco; L Pérez-Martínez; J Márquez; J A Oteo
Journal:  Ann N Y Acad Sci       Date:  2005-12       Impact factor: 5.691

4.  A new tick-transmitted disease due to Rickettsia slovaca.

Authors:  D Raoult; P Berbis; V Roux; W Xu; M Maurin
Journal:  Lancet       Date:  1997-07-12       Impact factor: 79.321

5.  Spotless rickettsiosis caused by Rickettsia slovaca and associated with Dermacentor ticks.

Authors:  Didier Raoult; Andras Lakos; Florence Fenollar; Jean Beytout; Philippe Brouqui; Pierre-Edouard Fournier
Journal:  Clin Infect Dis       Date:  2002-04-19       Impact factor: 9.079

6.  Tick-borne rickettiosis in Guadeloupe, the French West Indies: isolation of Rickettsia africae from Amblyomma variegatum ticks and serosurvey in humans, cattle, and goats.

Authors:  P Parola; G Vestris; D Martinez; B Brochier; V Roux; D Raoult
Journal:  Am J Trop Med Hyg       Date:  1999-06       Impact factor: 2.345

Review 7.  Tick-borne rickettsioses around the world: emerging diseases challenging old concepts.

Authors:  Philippe Parola; Christopher D Paddock; Didier Raoult
Journal:  Clin Microbiol Rev       Date:  2005-10       Impact factor: 26.132

8.  Spotted fever group Rickettsia in ticks from southeastern Spain natural parks.

Authors:  Francisco J Márquez
Journal:  Exp Appl Acarol       Date:  2008-08-02       Impact factor: 2.132

9.  Rickettsia sp. strain RpA4 detected in Portuguese Dermacentor marginatus ticks.

Authors:  Liliana Vitorino; Rita De Sousa; Fatima Bacellar; Líbia Zé-Zé
Journal:  Vector Borne Zoonotic Dis       Date:  2007       Impact factor: 2.133

10.  Evidence for an increased geographical distribution of Dermacentor reticulatus in Germany and detection of Rickettsia sp. RpA4.

Authors:  Hans Dautel; Cornelia Dippel; Rainer Oehme; Kathrin Hartelt; Elvira Schettler
Journal:  Int J Med Microbiol       Date:  2006-03-09       Impact factor: 3.473

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  80 in total

Review 1.  Host, pathogen and treatment-related prognostic factors in rickettsioses.

Authors:  E Botelho-Nevers; D Raoult
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2011-04-26       Impact factor: 3.267

2.  Habitat and occurrence of ixodid ticks in the Liguria region, northwest Italy.

Authors:  Leonardo A Ceballos; Maria D Pintore; Laura Tomassone; Alessandra Pautasso; Donal Bisanzio; Walter Mignone; Cristina Casalone; Alessandro Mannelli
Journal:  Exp Appl Acarol       Date:  2014-03-30       Impact factor: 2.132

3.  Scalp eschar and neck lymphadenopathy after tick bite: an emerging syndrome with multiple causes.

Authors:  G Dubourg; C Socolovschi; P Del Giudice; P E Fournier; D Raoult
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2014-03-29       Impact factor: 3.267

Review 4.  Update on tick-borne rickettsioses around the world: a geographic approach.

Authors:  Philippe Parola; Christopher D Paddock; Cristina Socolovschi; Marcelo B Labruna; Oleg Mediannikov; Tahar Kernif; Mohammad Yazid Abdad; John Stenos; Idir Bitam; Pierre-Edouard Fournier; Didier Raoult
Journal:  Clin Microbiol Rev       Date:  2013-10       Impact factor: 26.132

5.  Ticks and bacterial tick-borne pathogens in Piemonte region, Northwest Italy.

Authors:  Dario Pistone; Massimo Pajoro; Eva Novakova; Nadia Vicari; Cesare Gaiardelli; Roberto Viganò; Camilla Luzzago; Matteo Montagna; Paolo Lanfranchi
Journal:  Exp Appl Acarol       Date:  2017-11-30       Impact factor: 2.132

6.  Contact with horses is a risk factor for tick-borne lymphadenopathy (TIBOLA): a case control study.

Authors:  András Lakos; Adám Kőrösi; Gábor Földvári
Journal:  Wien Klin Wochenschr       Date:  2012-08-10       Impact factor: 1.704

7.  Spotted fever group Rickettsiae in ticks in Cyprus.

Authors:  Dimosthenis Chochlakis; Ioannis Ioannou; Vassilios Sandalakis; Theodoros Dimitriou; Nikolaos Kassinis; Byron Papadopoulos; Yannis Tselentis; Anna Psaroulaki
Journal:  Microb Ecol       Date:  2011-08-11       Impact factor: 4.552

8.  Approaches for Reverse Line Blot-Based Detection of Microbial Pathogens in Ixodes ricinus Ticks Collected in Austria and Impact of the Chosen Method.

Authors:  Anna-Margarita Schötta; Michiel Wijnveld; Hannes Stockinger; Gerold Stanek
Journal:  Appl Environ Microbiol       Date:  2017-06-16       Impact factor: 4.792

9.  First molecular detection of the human pathogen Rickettsia raoultii and other spotted fever group rickettsiae in Ixodid ticks from wild and domestic mammals.

Authors:  Valentina Chisu; Cipriano Foxi; Giovanna Masala
Journal:  Parasitol Res       Date:  2018-08-04       Impact factor: 2.289

10.  Matrix-assisted laser desorption ionization-time of flight mass spectrometry for rapid identification of tick vectors.

Authors:  Amina Yssouf; Christophe Flaudrops; Rezak Drali; Tahar Kernif; Cristina Socolovschi; Jean-Michel Berenger; Didier Raoult; Philippe Parola
Journal:  J Clin Microbiol       Date:  2012-12-05       Impact factor: 5.948

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