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Rickettsia spp. in bats of Romania: high prevalence of Rickettsia monacensis in two insectivorous bat species
Parasites & Vectors volume 14, Article number: 107 (2021)
Spotted fever group rickettsiae represent one of the most diverse groups of vector-borne bacteria, with several human pathogenic species showing an emerging trend worldwide. Most species are vectored by ticks (Ixodidae), with many zoonotic reservoir species among most terrestrial vertebrate groups. While the reservoir competence of many different vertebrate species is well known (e.g. birds, rodents and dogs), studies on insectivorous bats have been rarely performed despite their high species diversity, ubiquitous urban presence and importance in harboring zoonotic disease agents. Romania has a high diversity and ubiquity of bats. Moreover, seven out of eight SFG rickettsiae species with zoonotic potential were previously reported in Romania. Based on this, the aim of this study was to detect Rickettsia species in tissue samples in bats.
Here we report a large-scale study (322 bats belonging to 20 species) on the presence of Rickettsia spp. in Romanian bat species. Tissue samples from insectivorous bats were tested for the presence of Rickettsia DNA using PCR detection amplifying a 381 bp fragment of the gltA gene. Positive results were sequenced to confirm the results. The obtained results were statistically analyzed by chi-squared independence test.
Positive results were obtained in 14.6% of bat samples. Sequence analysis confirmed the presence of R. monacensis in two bat species (Nyctalus noctula and Pipistrellus pipistrellus) in two locations.
This study provides the first evidence of a possible involvement of these bat species in the epidemiology of Rickettsia spp., highlighting the importance of bats in natural cycles of these vector-borne pathogens.
Among tick-borne diseases, rickettsioses are considered to be the oldest known affecting humanity. Tick-borne rickettsioses are caused by obligate intracellular bacteria belonging to the spotted fever group (SFG) of the genus Rickettsia, one of the most diverse groups among Rickettsiales, comprising a large number of zoonotic agents . The first clinical description of the prototypical tick-borne rickettsiosis (Rocky Mountain spotted fever, RMSF) was made in 1899 by Edward E. Maxey . Its agent, Rickettsia rickettsii, was demonstrated to have vectorial transmission in 1906 by Howard T. Ricketts , which was later confirmed by S. Burt Wolbach .
This complex of diseases is still intensively studied, and newly associated clinical conditions are continuously described. Its importance and recognition have increased considerably over the last 3 decades . More than 24 Rickettsia species and subspecies are associated with human infections, while for many others the public health relevance is still unknown . In Europe, eight tick-borne rickettsiae with known pathogenicity to humans were reported in European patients: R. aeschlimannii, R. conorii subsp. conorii, R. helvetica, R. massiliae, R. monacensis, R. raoultii, R. sibirica subsp. mongolitimonae, and R. slovaca. Additionally, 15 Candidatus Rickettsia species and strains of unknown pathogenicity were also described . Seven of the eight human pathogenic species were previously reported in Romania (Table 1) [5,6,7,8,9,10,11,12,13,14,15]. Despite the common detection of tick-borne rickettsiae in ticks collected from diverse hosts, to the best of our knowledge, they have been reported only in humans and birds in Romania.
Romania has a remarkable biodiversity, having in its territory 21 ecoregions in 5 biogeographical regions . This unique situation is associated with a wide range of habitats and is mirrored by a very rich fauna including 32 species of insectivorous bats , more than 82% of all continental European bat species . Romania is not only diverse in species, but also hosts large bat populations, including two of the largest hibernating colonies of bats from Europe (> 100,000 individuals) .
Bats are well-known reservoir hosts for important zoonotic viruses such as Lyssavirus and Ebola virus, probable reservoirs for Hendra and Nipah henipaviruses, MERS and SARS coronaviruses, probably including SARS-CoV-2, and other emerging viruses [20, 21]. Alongside viruses, in the last few years, bacterial and protozoan pathogens from bats have been intensively studied to clarify their zoonotic potential. As a result, several pathogens have been identified in different samples (blood, tissues, ectoparasites, guano) such as Babesia spp. [22, 23], different strains of Bartonella spp. [24, 25], including species with zoonotic potential , Borrelia spp., some with a possible zoonotic potential [27, 28], and Rickettsia spp. [29, 30].
Bats are hosts for their specific ectoparasites such as bat bugs, flies, fleas, mites and ticks (hard and soft). In Europe, three species of hard ticks (Ixodes ariadnae, I. simplex and I. vespertilionis) and two species of soft tick (Argas vespertilionis and A. transgariepinus) are considered specific to bats . However, other generalist tick species have been occasionally found on bats, including SFG-rickettsiae-vector ticks, such as I. ricinus and Haemaphysalis concinna [1, 17, 29], suggesting the possibility of harboring these pathogens.
Motivated by the high diversity and ubiquity of bats in Romania and their potential to harbor SFG rickettsiae, the aim of this study was to detect Rickettsia species in tissue samples in bats.
The samples were collected from carcasses of bats accidentally killed, mainly by collisions (n = 165), or which died of natural causes (n = 157). The collection of carcasses was performed during all-year periods between 2011-2019. The majority of naturally caused deaths were recorded in the late spring. Bats were identified to the species level using morphological keys . Some of the carcasses are found in the Grigore Antipa National Museum of Natural History in Bucharest. The carcasses were kept individually in plastic bags and deep frozen (– 20 °C) until analysis. A total of 322 bat samples belonging to 20 species (Additional file 1: Table S1) originating from 13 locations in Romania were necropsied. The heart tissue was used for DNA extraction, as this was the only tissue available from all the animals because of carcass damage (smashed, old, partially eaten, etc.). No individual animal was harmed or killed for the purpose of this study.
Genomic DNA was extracted from each tissue sample using commercial kits (ISOLATE II Genomic DNA Kit, Bioline, UK), following the manufacturer’s instructions. To assess cross-contamination between extracts, negative controls consisting only of reaction mixes were used. The DNA quantity and purity were assessed on a Nanodrop ND-1000 spectrophotometer analyzer (NanoDrop Technologies, Inc., Wilmington, DE, USA), using a representative number of randomly selected samples.
Polymerase chain reaction (PCR) and agarose gel electrophoresis
The samples were assessed for the presence of SFG rickettsiae using a group-specific set of primers amplifying a 381 bp fragment of the rickettsial gltA gene (Rsfg877: GGGGGCCTGCTCACGGCGG; Rsfg1258: ATTGCAAAAAGTACAGTGAACA) . The amplification was carried out in 25 µl reaction mixture containing 12.5 µl of Green PCR Master Mix (Rovalab GmBH), 6.5 µl PCR water, 1 µl of each primer (0.01 mM) and a 4 µl aliquot of isolated DNA. The amplification profile consisted of 5 min of initial denaturation at 95 °C, followed by 35 cycles of denaturation at 95 °C for 30 s, annealing at 53 °C for 30 s and extension at 72 °C for 30 s and a final extension at 72 °C for 5 min. In each PCR reaction set, positive and negative controls were included. Positive controls consisted of DNA extracted from Ixodes ricinus collected from a bird infected with R. helvetica, previously confirmed by sequencing (accession no. KR906075). The negative control consisted of reaction mix without DNA. The PCR was carried out using a T100TM Thermal Cycler (Bio-Rad). PCR products were visualized by electrophoresis in a 1.5% agarose gel stained with SYBR® Safe DNA gel stain (Invitrogen).
All positive PCR products were purified using Isolate II PCR and Gel Kit (Bioline). Sequencing analysis was performed (Macrogen Europe, Amsterdam), and the obtained sequences were edited and analyzed using Geneious® (Biomatters LTD) 4.8.7 and compared with those available in the GenBank database by BLASTn analysis (http://blast.ncbi.nlm.nih.gov/Blast.cgi).
The prevalence of Rickettsia spp. infection was calculated using Epi InfoTM 7 (CDC, USA) software with a 95% confidence interval. To evaluate differences in prevalence between localities and bat species, a chi-square test of independence was applied, and a p-value < 0.05 was considered significant.
SFG rickettsiae DNA was detected in 14.6% (n = 47/322, 95%CI: 11.02–19.04) of samples. Positive samples were detected in Nyctalus noctula (22 out of 188 tested), Pipistrellus pipistrellus (13 out of 55 tested), Myotis alcathoe (5 out of 12 tested), P. nathusii (4 out of 25 tested), Plecotus auritus (1 out of 6 tested), Vespertilio murinus (1 out of 4 tested) and P. pygmaeus (1 out of 2 tested) from five different locations (Table 2). The prevalence of Rickettsia spp. was 23.64% (95%CI: 13.23-37.02) in P. pipistrellus and 11.7% (95%CI: 7.48-17.18) in N. noctula. For the remaining species, Rickettsia spp. prevalence was not considered because of the small number of individuals tested.
Among the 47 positive samples, only 17 were suitable for sequencing (> 30 ng/μl DNA concentration). The sequences analysis showed 99.7% to 100% identity with R. monacensis found in I. ricinus from different geographical origins such as: Romania, Italy or Serbia (accession no. JX003686; GQ925822; KY203388). Four obtained sequences of gltA fragments (MT741493–MT741496) were deposited in the GenBank database. The short length of the sequences allowed the confirmation of the Rickettsia species, but they were inappropriate for further testing of strain genetic variability.
Following sequence analysis, R. monacensis presence was confirmed in all 17 sequences of bat samples, in 5 P. pipistrellus (accession no. MT741493-MT741494) and in 12 N. noctula (accession no. MT741495-MT741496).
All the confirmed positive samples originated from two distinct locations (Table 2). Since in these two locations these two species represented almost half of the collected samples (104 out of 188 N. noctula in Cheile Bicazului and 53 out of 55 P. pipistrellus from “Huda lui Papara” Cave, Additional file 1: Table S1), the differences in prevalence obtained for different locations or species were not significant.
To the best of our knowledge, this study is the first report of SFG rickettsiae in bat tissue samples in Europe and the first report of R. monacensis in tissues of P. pipistrellus and N. noctula (insectivorous bats) worldwide. Although SFG rickettsiae were not previously detected in bat tissue samples in Europe, SFG rickettsiae and related Rickettsia species were detected in bat specialist ectoparasites in Europe as well in other parts of the world (Table 3) [33,34,35,36,37,38,39,40,41,42,43,44,45]. This may suggest bat’s and/or their ectoparasites potential involvement in the transmission of these pathogens. This hypothesis is also sustained by the detection of SFG rickettsiae in bat tissue samples on other continents. For instance, in serological studies, antibodies against several Rickettsia spp. (R. amblyommii, R. conorii, R. parkeri, R. rickettsia and R. rhipicephali) were identified in bat samples collected from North and South America and from Asia [46,47,48]. Moreover, SFG Rickettsia spp. DNA was identified in blood or tissue samples from bats in Africa, America and Asia [49,50,51]. Different bat species (Miniopterus natalensis, Nycteris thebaica, Epomophorus wahlbergi, Scotophilus dinganii and Glauconycteris variegata) from South Africa were found positive for the presence of Rickettsia DNA, belonging to the SFG group, closely related to R. conorii . In Saint Kitts, rickettsial DNA (99% similar to R. africae 17 kD protein gene) was detected in blood samples of Artibeus jamaicensis and Ardops nichollsi . In China, R. parkeri, R. lusitaniae, R. slovaca and R. raoultii were detected in tissue samples collected from P. pisterellus . In addition, R. raoultii and R. rickettsii were also detected in their ectoparasites (A. vespertilionis). Among these, four ticks positive for R. raoultii were removed from a R. raoultii-positive bat , suggesting the possible involvement of A. vespertilionis in the transmission of SFG rickettsiae among bats.
Rickettsia monacensis has a wide distribution, and has been detected all over Europe in its main vector, I. ricinus [reviewed by 1,52,53]. The prevalence of R. monacensis in ticks varied between 0.5% in Germany and 57% in Italy [reviewed by 1,53]. Currently R. monacensis is considered a zoonotic species, causing MSF-like illness in humans [54, 55]. Its presence in bat tissues observed in this study may suggest bats' involvement in Rickettsia spp. epidemiology also in Europe. Soft ticks collected from P. pipistrellus have already yielded five different Rickettsia spp. DNA (Rickettsia sp. AvBat , R. sibirica and R. conorii—, R. lusitaniae and Rickettsia africae-like—), while fleas and feces collected from N. noctula tested positive for Rickettsia spp. in Hungary [30, 42]. In addition, R. helvetica was previously detected in its vector (I. ricinus) tick collected from bats (Rhinolophus hipposideros and M. myotis) from Poland . Thus, either these two bat species regularly harbor Rickettsia spp. infections or their associated ectoparasites (especially the soft tick, A. vespertilionis) may play a vectorial role in these bacteria. Argas vespertilionis commonly infests these bats and also is known to bite humans . In addition, P. pipistrellus and N. noctula species are the most common bats in urbanized areas, with important populations roosting in anthropogenic roosts , altogether making them of interest in the study of vector-borne pathogen cycles and highlighting their importance as possible candidates for Rickettsia spp. reservoirs in urbanized habitats.
The detection of R. monacensis in the present study reconfirms the presence and circulation of this SFG rickettsiae in insectivorous bats. To the best of our knowledge, this study represents the first detection of R. monacensis in bat tissue samples in Europe and its first detection in P. pipistrellus and N. noctula bat species. Considering the zoonotic potential of R. monacensis, the detection of putative and also known vectors in bats and its detection in bat tissue samples, it is important to establish the importance of bats in the epidemiology of Rickettsia spp. in general, and R. monacensis in particular, by further research.
Availability of data and materials
All data generated or analyzed during this study are included in this published article [and its supplementary information files].
- Acc. no.:
GeneBank accession number
Mediterranean spotted fever
Middle East respiratory syndrome
Polymerase chain reaction
Rickettsia felis group
Rocky Mountain Spotted Fever
Severe Acute Respiratory Syndrome
Spotted Fever Group
Parola P, Paddock CD, Socolovschi C, Labruna MB, Mediannikov O, Kernif T, et al. Update on tick-borne rickettsioses around the world: a geographic approach. Clin Microbiol Rev. 2013;26:657–702.
Maxey EE. Some observations of the so-called spotted fever of Idaho. Med Sentinel. 1899;10:433–8.
Ricketts HT. The transmission of Rocky Mountain Spotted Fever by the bite of the wood-tick (Dermacentor occidentalis). JAMA. 1906;47:358.
Wolbach SB. Studies on Rocky Mountain spotted fever. The J Med Res. 1919;41:1.
Andersson MO, Tolf C, Tamba P, Stefanache M, Radbea G, Frangoulidis D, et al. Molecular survey of neglected bacterial pathogens reveals an abundant diversity of species and genotypes in ticks collected from animal hosts across Romania. Parasit Vectors. 2018;11:144.
Pitigoi D, Olaru ID, Badescu D, Rafila A, Arama V, Hristea A. Mediterranean spotted fever in southeastern Romania. Bio Med Res Int. 2013. https://doi.org/10.1155/2013/395806.
Serban R, Pistol A, Neguţ M, Cucuiu R. Rickettsia conorii infection in Romania, 2000–2008, Bacteriologia, virusologia, parazitologia, epidemiologia (Bucharest, Romania: 1990). 2009;54:177–83
Ionita M, Silaghi C, Mitrea IL, Edouard S, Parola P, Pfister K. Molecular detection of Rickettsia conorii and other zoonotic spotted fever group rickettsiae in ticks Romania. Ticks Tick Borne Dis. 2016;7:150–3.
Raileanu C, Moutailler S, Porea D, Oslobanu L, Anita D, Anita A, et al. Molecular evidence of Rickettsia spp., Anaplasma phagocytophilum, and “Candidatus Neoehrlichia mikurensis” in ticks from natural and urban habitats in Eastern Romania. Vector Borne Zoonotic Dis. 2018;18:343–9.
Ionita M, Mitrea IL, Pfister K, Hamel D, Silaghi C. Molecular evidence for bacterial and protozoan pathogens in hard ticks from Romania. Vet Parasitol. 2013;196:71–6.
Andersson MO, Marga G, Banu T, Dobler G, Chitimia-Dobler L. Tick-borne pathogens in tick species infesting humans in Sibiu County, central Romania. Parasitol Res. 2018;117:1591–7.
Matei IA, Kalmár Z, Lupşe M, D’Amico G, Ionică AM, Dumitrache MO, et al. The risk of exposure to rickettsial infections and human granulocytic anaplasmosis associated with Ixodes ricinus tick bites in humans in Romania: a multiannual study. Ticks Tick Borne Dis. 2017;8:375–8.
Mărcuţan ID, Kalmár Z, Ionică AM, D’Amico G, Mihalca AD, Vasile C, et al. Spotted fever group rickettsiae in ticks of migratory birds in Romania. Parasit Vectors. 2016;9:294.
Zaharia M, Popescu CP, Florescu SA, Ceausu E, Raoult D, Parola P, et al. Rickettsia massiliae infection and SENLAT syndrome in Romania. Ticks Tick Borne Dis. 2016;7:759–62.
Sándor AD, Kalmár Z, Matei I, Ionică AM, Mărcuţan ID, et al. Urban breeding corvids as disseminators of ticks and emerging tick-borne pathogens. Vector-Borne Zoonotic Dis. 2017;17:152–4.
National Environment Protection Agency, Annual report 2018. http://www.anpm.ro/raport-de-mediu. Accessed in 13 May 2020.
Sándor AD, Corduneanu A, Péter Á, Mihalca AD, Barti L, Csősz I, et al. Bats and ticks: host selection and seasonality of bat-specialist ticks in eastern Europe. Parasit Vectors. 2019;12:1.
Russo D, Billington G, Bontadina F, Dekker J, Dietz M, Gazaryan S, et al. Identifying key research objectives to make European forests greener for bats. Front Ecol Evol. 2016;4:87.
Coroiu I. Bat fauna in caves of Romania. In: Ponta GML, Onac BP, editors. Cave and karst systems of Romania. Cham: Springer; 2019. p. 493–9.
Brook CE, Dobson AP. Bats as ‘special’ reservoirs for emerging zoonotic pathogens. Trends Microbiol. 2015;23:172–80.
Zhou P, Yang XL, Wang XG, Hu B, Zhang L, Zhang W, et al. A pneumonia outbreak associated with a new coronavirus of probable bat origin. Nature. 2020;579:270–3.
Hornok S, Szőke K, Kováts D, Estók P, Görföl T, Boldogh SA, et al. DNA of piroplasms of ruminants and dogs in ixodid bat ticks. PLoS ONE. 2016;11:e0167735.
Corduneanu A, Hrazdilová K, Sándor AD, Matei IA, Ionică AM, Barti L, et al. Fuehrer, Babesia vesperuginis, a neglected piroplasmid: new host and geographical records, and phylogenetic relations. Parasit Vectors. 2017;11:598.
Corduneanu A, Sándor AD, Ionică AM, Hornok S, Leitner N, Bagó Z, et al. Bartonella DNA in heart tissues of bats in central and eastern Europe and a review of phylogenetic relations of bat-associated bartonellae. Parasit Vector. 2018;11:598.
Urushadze L, Bai Y, Osikowicz L, McKee C, Sidamonidze K, Putkaradze D, et al. Prevalence, diversity, and host associations of Bartonella strains in bats from Georgia (Caucasus). PLoS Negl Trop Dis. 2017;11:e0005428.
Veikkolainen V, Vesterinen EJ, Lilley TM, Pulliainen AT. Bats as reservoir hosts of human bacterial pathogen, Bartonella mayotimonensis. Emerg Infect Dis. 2014;20:960.
Socolovschi C, Kernif T, Raoult D, Parola P. Borrelia, Rickettsia, and Ehrlichia species in bat ticks, France, 2010. Emerg Infect Dis. 2012;18:1966.
Qiu Y, Nakao R, Hang’ombe BM, Sato K, Kajihara M, Kanchela S, et al. Human borreliosis caused by a new world relapsing fever borrelia–like organism in the old world. Clin Infect Dis. 2019;69:107–12.
Piksa K, Stańczak J, Biernat B, Górz A, Nowak-Chmura M, Siuda K. Detection of Borrelia burgdorferi sensu lato and spotted fever group rickettsiae in hard ticks (Acari, Ixodidae) parasitizing bats in Poland. Parasitol Res. 2016;115:1727–31.
Hornok S, Szőke K, Estók P, Krawczyk A, Haarsma AJ, Kováts D, et al. Assessing bat droppings and predatory bird pellets for vector-borne bacteria: molecular evidence of bat-associated Neorickettsiasp. in Europe. Anton Leeuw. 2018;111:1707–17.
Dietz C, Von Helversen O, Nill D. Bats of Britain, Europe and northwest Africa. London: A&C Black; 2009.
Regnery RL, Spruill CL, Plikaytis BD. Genotypic identification of rickettsiae and estimation of intraspecies sequence divergence for portions of two rickettsial genes. J Bacteriol. 1991;173:1576–89.
Do Amaral RB, Lourenco EC, Famadas KM, Garcia AB, Machado RZ, Andre MR. Molecular detection of Bartonella spp. and Rickettsia spp. in bat ectoparasites in Brazil. PLoS ONE. 2018;13:e0198629.
Moreira-Soto RD, Moreira-Soto A, Corrales-Aguilar E, Calderón-Arguedas Ó, Troyo A. ‘Candidatus Rickettsia nicoyana’: a novel Rickettsia species isolated from Ornithodoros knoxjonesi in Costa Rica. Ticks Tick Borne Dis. 2017;8:532–6.
Tahir D, Socolovschi C, Marié JL, Ganay G, Berenger JM, Bompar JM, et al. New Rickettsia species in soft ticks Ornithodoros hasei collected from bats in French Guiana. Ticks Tick Borne Dis. 2016;7:1089–96.
Colombo VC, Montani ME, Pavé R, Antoniazzi LR, Gamboa MD, Fasano AA, et al. First detection of “Candidatus Rickettsia wissemanii” in Ornithodoros hasei (Schulze, 1935) (Acari: Argasidae) from Argentina. Ticks Tick Borne Dis. 2020;14:101442.
Luz HR, Muñoz-Leal S, de Carvalho WD, Castro IJ, Xavier BS, Toledo JJ, et al. Detection of “Candidatus Rickettsia wissemanii” in ticks parasitizing bats (Mammalia: Chiroptera) in the northern Brazilian Amazon. Parasitol Res. 2019;118:3185–9.
Hornok S, Szőke K, Meli ML, Sándor AD, Görföl T, Estók P, et al. Molecular detection of vector-borne bacteria in bat ticks (Acari: Ixodidae, Argasidae) from eight countries of the Old and New Worlds. Parasit Vectors. 2019;12:1–7.
Hornok S, Kovács R, Meli ML, Gönczi E, Hofmann-Lehmann R, Kontschan J, et al. First detection of bartonellae in a broad range of bat ectoparasites. Vet Microbiol. 2012;3:541–3.
Sánchez-Montes S, Guzmán-Cornejo C, Martínez-Nájera Y, Becker I, Venzal JM, Labruna MB. Rickettsia lusitaniae associated with Ornithodoros yumatensis (Acari: Argasidae) from two caves in Yucatan, Mexico. Ticks Tick Borne Dis. 2016;7:1097–101.
Ullah H, Kontschán J, Takács N, Wijnveld M, Schötta AM, Boldogh SA. A new Rickettsia honei-related genotype, two novel soft tick haplotypes and first records of three mite species associated with bats in Pakistan. Syst Appl Acarol. 2019;24:2106–18.
Szubert-Kruszyńska A, Stańczak J, Cieniuch S, Podsiadły E, Postawa T, Michalik J. Correction to: Bartonella and Rickettsia infections in haematophagous Spinturnix myoti Mites (Acari: Mesostigmata) and their bat host, Myotis myotis (Yangochiroptera: Vespertilionidae), from Poland. Microb Ecol. 2019;77:769.
Loftis AD, Gill JS, Schriefer ME, Levin ML, Eremeeva ME, Gilchrist MR, et al. Detection of Rickettsia, Borrelia, and Bartonella in Carios kelleyi (Acari: Argasidae). J Med Entomol. 2005;42:473–80.
Wilkinson DA, Duron O, Cordonin C, Gomard Y, Ramasindrazana B, Mavingui P, et al. The bacteriome of bat flies (Nycteribiidae) from the Malagasy region: a community shaped by host ecology, bacterial transmission mode, and host-vector specificity. Appl Environ Microbiol. 2016;82:1778–88.
Lv J, de Marco MD, Goharriz H, Phipps LP, McElhinney LM, Hernández-Triana LM, et al. Detection of tick-borne bacteria and Babesia with zoonotic potential in Argas (Carios) vespertilionis (Latreille, 1802) ticks from British bats. Sci Rep. 2018;8:1–9.
Choi CS, Lee YT. Seroepidemiological survey of Rickettsia in rodents and bats. J Korean Soc Microbiol. 1996;31:367–72.
Reeves WK, Streicker DG, Loftis AD, Dasch GA. Serologic survey of Eptesicus fuscus from Georgia, USA for Rickettsia and Borrelia and laboratory transmission of a Rickettsia by bat ticks. J Vector Ecol. 2006;31:386–9.
D’Auria SR, Camargo MC, Pacheco RC, Savani ES, Dias MA, da Rosa AR, et al. Serologic survey for rickettsiosis in bats from São Paulo city, Brazil. Vector Borne Zoonotic Dis. 2010;10(5):459–63.
Dietrich M, Tjale MA, Weyer J, Kearney T, Seamark EC, Nel LH, et al. Diversity of Bartonella and Rickettsia spp. in bats and their blood-feeding ectoparasites from South Africa and Swaziland. PLoS ONE. 2016;11:e0152077.
Reeves WK, Beck J, Orlova MV, Daly JL, Pippin K, Revan F, et al. Ecology of bats, their ectoparasites, and associated pathogens on Saint Kitts Island. J Med Entomol. 2016;53:1218–25.
Zhao S, Yang M, Liu G, Hornok S, Zhao S, Sang C, et al. Rickettsiae in the common pipistrelle Pipistrellus pipistrellus (Chiroptera: Vespertilionidae) and the bat soft tick Argas vespertilionis (Ixodida: Argasidae). Parasit Vectors. 2020;13:1–6.
Oteo JA, Portillo A. Tick-borne rickettsioses in Europe. Ticks Tick Borne Dis. 2012;3:271–8.
Simser JA, Palmer AT, Fingerle V, Wilske B, Kurtti TJ, Munderloh UG. Rickettsia monacensis sp. nov, a spotted fever group Rickettsia, from ticks (Ixodes ricinus) collected in a European city park. Appl Environ Microbiol. 2002;68:4559–66.
Jado I, Oteo JA, Aldámiz M, Gil H, Escudero R, Ibarra V, et al. Rickettsia monacensis and human disease, Spain. Emerg Infect Dis. 2007;13:1405.
Madeddu G, Mancini F, Caddeo A, Ciervo A, Babudieri S, Maida I, et al. Rickettsia monacensis as cause of Mediterranean spotted fever–like illness, Italy. Emerg Infect Dis. 2012;18:702.
Estrada-Peña A, Jongejan F. Ticks feeding on humans: a review of records on human-biting Ixodoidea with special reference to pathogen transmission. Exp Appl Acarol. 1999;23:685–715.
We acknowledge the help provided by L. Barti and I. Coroiu in the fieldwork.
This work was supported by the CNCS-UEFISCDI Grant Agency Romania, grant numbers PD34/2018, PD39/2020 and PCCDI 57/2018, and ADS was supported by the János Bolyai Research Scholarship of the Hungarian Academy of Science and the ÚNKP 19-4-ÁTE-10 New National Excellence Program of the MIT and NKFIH 132794.
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Matei, I.A., Corduneanu, A., Sándor, A.D. et al. Rickettsia spp. in bats of Romania: high prevalence of Rickettsia monacensis in two insectivorous bat species. Parasites Vectors 14, 107 (2021). https://doi.org/10.1186/s13071-021-04592-x
- Insectivorous bats
- SFG rickettsiae
- Vector-borne diseases
- Zoonotic reservoir