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First report of Rickettsia felisin China
© Zhang et al.; licensee BioMed Central. 2014
Received: 30 June 2014
Accepted: 3 December 2014
Published: 16 December 2014
Rickettsia felis is a recently described flea-borne spotted fever group Rickettsia that is an emerging human pathogen. Although there is information on the organism from around the world, there is no information on the organism in China.
We used a commercial ELISA to detect antibodies reactive against R. felis in blood samples and developed a PCR to detect the gltA of the organism in blood samples and external parasites.
We found reactive antibodies in people (16%; 28/180), dogs (47%; 128/271) and cats (21%; 19/90) and positive PCRs with DNA from people (0.1%; 1/822), dogs (0.8%; 8/1,059), mice (10%; 1/10), ticks (Rhipicephalus sanguineus; 10%; 15/146), lice (Linognathus setosus; 16%; 6/37), fleas (Ctenocephalides felis felis; 95%; 57/60) and mosquitoes (Anopheles sinensis, Culex pipiens pallens; 6%; 25/428), but not from cats (0/135) or canine fecal swabs (0/43).
This is the first report of R. felis in China where there is serological and/ or PCR evidence of the organism in previously reported [people, dogs, cats, ticks (Rhipicephalus sanguineus), fleas (Ctenocephalides felis felis) and mosquitoes (Anopheles sinensis, Culex pipiens pallens)] and novel species [mice and lice (Linognathus setosus)].
KeywordsRickettsia felis China Serology PCR
Although tick-borne spotted fever group rickettsiae have been described in China , there is no information on the flea-borne emerging human pathogen Rickettsia felis. Described in 2001, R. felis appears to have the cat flea, Ctenocephalides felis felis, as its main vector and reservoir and can infect other arthropods (mosquitoes, ticks and mites) and mammals (rats, opossums, dogs, and cats). It is found worldwide and, in Asia, it has been definitively identified by molecular methods in fleas (Indonesia, Thailand, Afghanistan, South Korea, Laos, Malaysia, Taiwan), ticks (Japan), raccoons (Japan) and people (Taiwan, South Korea) ,. To expand our knowledge on R. felis in Asia, we studied people, animals and arthropods from around China using serology and molecular techniques.
Plasma and buffy coats from people, dogs, cats and wild mice (Figure 1) were stored at −80°C until DNA extraction. Rectal swabs from dogs and organs (spleen, liver and kidney) from the humanely euthanized wild mice were stored at −80°C in 800 μL of RNA/DNA Stabilization Reagent for Blood/Bone Marrow (Roche Molecular Biochemicals, Indianapolis) until DNA extraction. The external parasites collected from dogs and cats, and mosquitoes (Figure 1) were identified using standard morphological criteria and stored as above.
The R. felis EIA IgG Antibody Kit (Fuller Laboratory, USA) was used according to the manufacturer’s instructions with peroxidase-conjugated AffiniPure Goat Anti-Cat, Rabbit Anti-Dog, and Goat Anti-Mouse IgG (H + L) (Jackson ImmunoResearch Laboratories, USA) substituted as secondary antibodies for cat, dog and mouse/shrew assays, respectively. For human plasma, the cut-off level was determined following the manufacturer’s instructions that an index (OD value of test serum divided by the average OD values of the Cutoff Calibrator) above 1.2 should be considered positive. Plasma from cats, mice, shrews and dogs was regarded as positive if they gave an OD value above the mean plus three standard deviations of the respective negative control samples ,.
Samples were thawed at room temperature and DNA was extracted from buffy coats, homogenized organs and arthropods , and canine rectal swabs with the QIAamp® DNA Blood Mini Kit (QIAgen, Valencia, USA), QIAamp® DNA Mini Kit, and QIAamp® DNA Stool Mini Kit, respectively, following the manufacturer’s protocol.
Results and discussion
Details of samples collected in China and the results of ELISA and PCR testing
Source of samples
Sero-positivity (%), pos/total samples
PCR-positivity (%), pos/total samples
Dog Rectal swab
Seropositive dogs were found in each area studied with prevalences from 13-100%, similar to the 51% reported in Spain and Australia, and ≤13% in Brazil ,. There were significantly fewer seropositive cats (5-30%; two-tailed chi square analysis, P < 10−4), similar to the low level reported in the US (< 11%) . All mice (6 Mus musculus) and shrews (4 Suncus murinus) that were trapped were seronegative.
Although it has been suggested there might be high specificity of R. felis in serological tests  there is at least some serological cross reactivity between R. felis and other Rickettsia spp. present in China . We therefore used PCR to definitively identify R. felis in our study populations and provide further prevalence data. The GenBank BLAST program showed primers and probes of our FRET-PCR and nested PCR recognized all Rickettsia spp., but none in the other genera of the Rickettsiaceae. The detection limit of our combination PCR system was one gene copy per 20 μl reaction system.
Our PCRs showed one person had DNA of R. felis (0.1%; 1/822), a twenty-seven year old man with a normal CBC who was seronegative. This might have been an acute infection or an asymptomatic infection with no serological response as reported previously . Dogs from 2 of the 10 areas studied were also PCR positive (0.8%; 8/1,059), similar to Australia where up to 9% of dogs are PCR positive . Previously, R. felis was found in feces from great apes in Africa  but all our canine rectal swabs were negative by PCR. These dogs, however, had negative serology and blood PCRs and were probably then not infected.
As found previously , all the cats we studied were negative by PCR, despite many being seropositive and many harboring PCR positive Ctenocephalides felis, cat fleas. Fleas were the only ectoparasites found on cats and almost all were PCR positive (95%; 57/60), consistent with the very high levels of infection found worldwide and the generally accepted hypothesis that cat fleas are the primary arthropod vectors and reservoirs . Our finding that dogs have a higher seroprevalence and are positive by PCRs supports the hypothesis that they, rather than cats, might be the main mammalian reservoir of R. felis .
The spleen of one M. musculus was PCR positive for R. felis which is the first definitive report of the organism in mice. A PCR positive Rattus norvegicus has also been reported  and investigation into the role of rodents in the epidemiology of R. felis appears warranted.
Details of the sequences we obtained in our study and submitted to GenBank
Dog - Canis lupus familiaris
Dog - Canis lupus familiaris
Louse - Linognathus setosus
Louse - Linognathus setosus
Mosquito - Anopheles sinensis
Mosquito - Culex pipiens pallens
Tick - Rhipicephalus sanguineus
Louse - Linognathus setosus
Mosquito - Anopheles sinensis
Ten percent of the ticks (146 Rhipicephalus sanguineus) we collected from dogs were PCR positive. The sequences were all identical to R. felis (CP000053) except one (KJ440521) which was 99% identical to R. felis (CP000053) and R. typhi (U59714). Sixteen percent (6/37) of the dog lice (all Linognathus setosus) were positive; four had amplicons identical to R. felis (CP000053) while two amplicons from dog lice (KJ440522) were similar to R. endosymbiont (EU760765) (97%), R. bellii (U59716) (96%) and R. felis (CP000053) (86%). While R. felis has been reported in R. sanguineus in South America , ours is the first report of the organism in lice. All the dogs with PCR positive lice or ticks were sero- and PCR negative for R. felis suggesting these arthropods might not be competent vectors.
Six percent (25/428) of the mosquitoes (32 Anopheles sinensis, 396 Culex pipiens pallens) were PCR positive with 23 (2 An. sinensis, 21 C. p. pallens) having sequences identical to R. felis (CP000053) and 2 (C. p. pallens) having 99% and 96% similarity. The latter was 99% identical to a novel Rickettsia sp. (JN620082) found in An. gambiae in Africa which may be a new human pathogen . Ours is the first report of R. felis and the new Rickettsia sp. in mosquitoes outside of Africa and the first of the organisms in An. sinensis and C. p. pallens. Further studies are indicated to determine the role of mosquitoes in the epidemiology of these rickettsias and the influence of the Rickettsia spp. might have on the biology of mosquitoes.
Our study indicates that R. felis occurs widely in China and infects a variety of previously reported (people, dogs, cats, ticks, fleas and mosquitoes) and novel species (mice and lice). Further studies are indicated to investigate the epidemiology and transmission mechanisms of R. felis, particularly in mosquitoes, lice and mice.
This project was supported by grant from the National Natural Science Foundation of China (NO: 31472225) and the Priority Academic Program Development of Jiangsu Higher Education Institutions, Yangzhou, Jiangsu, P. R. China.
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