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BMC Infectious Diseases

, 19:796 | Cite as

A case with neurological abnormalities caused by Rickettsia raoultii in northwestern China

  • Zhihui Dong
  • Yicheng Yang
  • Qian Wang
  • Songsong Xie
  • Shanshan Zhao
  • Wenbo Tan
  • Wumei Yuan
  • Yuanzhi WangEmail author
Open Access
Case report
  • 113 Downloads
Part of the following topical collections:
  1. Bacterial and fungal diseases

Abstract

Background

The number of new rickettsial species are rapidly increasing, and increasing numbers of Rickettsia raoultii (R. raoultii) infection cases have been detected in humans. However, neurological abnormalities caused by R. raoultii are rarely reported, especially in northwestern China.

Case presentation

A 36-year-old Kazakh shepherd with an attached tick on part temporalis, presented with right eyelid droop, lethargy, fever, headache, fever (38.0–41.0 °C) and erythematous rash. The examination of cerebrospinal fluid (CSF) showed cerebrospinal pressure of 200 mm H2O, leukocyte count of 300.0 × 106/L, adenosine deaminase of 2.15 U/L, and total protein concentration of 0.93 g/L. The diagnosis of R. raoultii infection was confirmed by six genetic markers, and semi-quantified by enzyme-linked immunosorbent assay for rickettsial antigen. The patient gradually recovered after treatment with doxycycline and ceftriaxone. R. raoultii DNA was found both in a tick detached from this patient and in 0.18% (2/1107) of blood samples collected from local shepherds.

Conclusions

This is the first reported case with neurological abnormalities caused by R. raoultii in northwestern China. It is vital to detect rickettsial agents both in blood and CSF for tick bite patients with neurological abnormalities. Public health workers and physicians should pay attention to neurological abnormalities caused by Rickettsia.

Keywords

Rickettsia raoultii Neurological abnormalities Northwestern China 

Abbreviations

16S rDNA

mitochondrial 16S ribosomal DNA

17-kDa

17 kilodalton antigen

COI

cytochrome c oxidase subunit I

CSF

Cerebrospinal fluid

ELISA

Enzyme-linked immunosorbent assay

gltA

citrate synthase

MEGA7

Molecular Evolutionary Genetics Analysis 7

ompA

outer membrane proteins A

ompB

outer membrane proteins B

PCR

polymerase chain reaction

R. raoultii

Rickettsia raoultii

sca1

cell surface antigen 1

sca4

surface cell antigen 4

SFG

spotted fever group

Background

Rickettsial diseases are prevalent worldwide, although the prevalent organisms differ in different geographical regions [1]. Rickettsia raoultii (R. raoultii) were firstly found in Dermacentor nuttallii (D. nuttallii) ticks in 1999 [2]. Subsequently, it was detected in members of genus Haemaphysalis, Rhipicephalus, Hyalomma and Amblyomma ticks, especially in European and Asian countries [3, 4, 5, 6, 7]. In Xinjiang (northwestern China), R. raoultii was highly prevalent, and 26.35% (263/998) Dermacentor genus ticks were molecularly tested positive [8]. In addition, R. raoultii infections have also been increasingly detected in humans, and mainly distributed in Europe and Far East of Russia [9, 10, 11, 12, 13, 14, 15]. In contrast, only few human infection cases have been reported in China [16, 17, 18]. In 2017, twenty-six tick bite patients infected with R. raoultii were reported. Their clinical syndrome ranged from asymptomatic infection to severe illness. The nonspecific manifestations were common, and included fever (100%), malaise (95%), myalgia (58%), lymphadenopathy (53%) and nausea (42%). Only 5% of them had rash, and 16% had eschar [17].

Here we report a case with neurological abnormalities caused by R. raoultii infection, which was confirmed using two complementary methods, enzyme-linked immunosorbent assay (ELISA) and polymerase chain reaction (PCR), followed by multi-gene sequencing. Epidemiological and rickettsial surveillance were also conducted in Xinjiang.

Case presentation

On June 3, 2017, a 36-year-old previously healthy Kazakh shepherd visited the First Affiliated Hospital of Xinjiang Medical University in Urumqi. He kept a tick detached from left part temporalis, which was identified as a female adult D. marginatus by an entomologist and further confirmed based on two tick-specific genetic markers [mitochondrial 16S ribosomal DNA (16S rDNA) and cytochrome c oxidase subunit I (COI)] according to previous reports [19]. The patient was initially asymptomatic, but 8 days later, his body temperature fluctuated between 38.0–41.0 (Fig. 1), accompanied by headache, malaise and anorexia. The patient gradually developed right eyelid droop, chest tightness, shortness of breath, lethargy and nausea accompanied by a vomiting 1 day before hospitalization. Cerebrospinal fluid (CSF) obtained through lumbar puncture examination showed cerebrospinal pressure of 200 mm H2O (normal range, 80–180 mm H2O), leukocyte count of 300.0 × 106/L (normal range, 0–100 × 106/L), adenosine deaminase of 2.15 U/L (normal range, 4–20 U/L), weakly positive Pandy test [20], and protein concentration of 0.93 g/L (normal range, 0.15–0.45 g/L). Transient leukocytosis developed after the onset and peaked on day 8 at 20.1 × 109/L (normal range, 4–10 × 109/L), with a neutrophilic leukocytosis. Other laboratory findings are shown in Table 1. A blood sample was collected and DNA was extracted using a TIANamp genomic DNA kit (Tiangen Biotechnique Inc., Beijing, China) according to the manufacturer’s instructions. Rickettsial DNA was primarily detected by 17 kilodalton antigen (17-kDa), which was Rickettsia-specific genetic marker [19]. The patient was treated with nasogastric or oral doxycycline 100 mg/day and Intravenous (IV) ceftriaxone 2 g/day for 10 days [12, 17]. Other symptomatic therapies like antipyretics, IV glycerol and fructose injection and IV mannitol were used as required. The patient was admitted to the intensive care unit for 6 days until fever disappeared and clinical manifestations alleviated. Repeated CSF test and routine blood test were normal. The patient has not experienced recurrence of fever or neurological symptoms after 6 months.
Fig. 1

Change in patient’s body temperature

Table 1

Other laboratory findings from the patient

Laboratory findings

Laboratory findings

results

normal range

Hemogram test

A white blood cell count

20.1 × 109/L

4–10 × 109/L

Neutrophil count

18.03 × 109/L

1.4–7 × 109/L

Lymphocyte count

0.82 × 109/L

1.2–3.5 × 109/L

Hemoglobin level

122 g/L

110~ 160 g/L

Platelet count

174 × 109/L

100–300 × 109/L

Blood biochemistry

Albumin

29.26umol/L

35-55umol/L

Total bilirubin

7.35umol/L

2-28umol/L

Glutamic-pyruvic transaminase (ALT)

74.72u/L

0-40u/L

Glutamic-oxaloacetic transaminase (AST)

56.64u/L

0-40u/L

Creatine kinase (CK)

330 IU/L

25-200 IU/L

Potassium ion

3.29 mmol/L

3.5–5.5 mmol/L

Uric aci (UA)

94umol/L

120-440umol/L

Hypersensitive C-reactive protein

63.401 mg/L

0-6 mg/L

Interleukin 6

41.910Pg/mL

<7Pg/mL

Erythrocyte sedimentation Rate (ESR)

54.00 mm/h

0-15 mm/h

ɑ1-acidic glycoprotein

1.56 g/L

0.51–1.17 g/L

Transferrin (TRF)

1.43 g/L

2.02–3.36 g/L

D-dimer

789.0 ng/ml

< 280 ng/ml

Free thyroxine

10.66 pmol/L

12-22 pmol/L

Free triiodothyronine

2.66 pmol/L

3.1–6.8 pmol/L

Routine urine

Urine protein

Positive(+ 2)

negative

Urine acetone bodies

Positive(+ 2)

negative

In order to investigate the presence of tick-borne viruses, RNA was extracted using an UItrapure RNA kit (CWBIO, Jiangsu Province, China) and complementary DNA was synthesized with random hexamers, using the Revert Aid First Strand cDNA synthesis kit (TRANSGEN BIOTECH, Beijing, China) for molecular detection of forest encephalitis virus, severe fever and thrombocytopenia syndrome virus, Crimean-Congo hemorrhagic fever virus and Powassan virus. Meanwhile, the other major tick-borne bacterial pathogens, such as Anaplasma phagocytophilum, Ehrlichia chaffeensis, Babesia spp., Francisella tularensis, Brucella and Borrelia burgorferi sensu lato, was also detected. All these pathogens were tested negative by PCR. To further determine the Rickettsia species, Rickettsia was molecularly detected by other five Rickettsia-specific genetic markers [surface cell antigen 4 (sca4); citrate synthase (gltA); cell surface antigen 1 (sca1); outer membrane proteins A (ompA); outer membrane proteins B (ompB)] as previously described, and R. raoultii was identified by sequencing [19]. Simultaneously, R. raoultii was detected in the feeding tick detached from the patient’s part temporalis using two Rickettsia-specific genetic markers (Sca4 and ompA). BLASTn (http://blast.ncbi.nlm.nih.gov/Blast.cgi) analysis revealed that the six gene fragments of R. raoultii had nucleotide identity of 99.5–100% with the reference R. raoultii strain Khabarovsk genome (accession number: CP010969) (Fig. 2). R. raoultii detected in the feeding D. marginatus tick detached from the patient was identical to those amplified from the patient.
Fig. 2

Phylogenetic tree of 17-kDa-gltA-sca1-sca4-ompA-ompB concatenated sequences of R. raoultii in blood from patient, tick detached from patient and shepherds (▲). The target nucleotide sequences were compared to sequences that were available in public databases using BLAST (http://blast.ncbi.nlm.nih.gov/Blast.cgi). The tree was constructed on the basis of maximum-likelihood (ML; 1000 bootstrap replicates) of concatenated sequence data of six genes (17-kDa-gltA-sca1-sca4-ompA-ompB) using Molecular Evolutionary Genetics Analysis (MEGA, version 7.0; http://www.megasoftware.net/). The sequences of R. bellii were used as the outgroup

To determine rickettsial antigen content at different stages of treatment in the patient’s blood, heparinized blood samples obtained from the patient 1 and 7 days after admission were tested using human rickettsia ELISA kits according to the manufacturer’s instructions (Shanghai enzyme-linked immunization, Shanghai, China). Rickettsial antigen content gradually decreased after treatment (the results were 33.98 pg/ml after first day of hospitalization and 17.78 pg/ml after seventh day of antibiotic therapy, respectively).

To further investigate the prevalence of rickettsial infection in shepherds, 1107 blood samples were collected from the local human population in Manasi County, Xinjiang. DNA was extracted from anti-coagulated blood samples as described above. PCR was performed to amplify rickettsial Sca1 or ompA fragments, followed by sequencing [19]. Two R. raoultii and one R. slovaca DNAs were detected (Fig. 2). Fifteen nucleotide sequences have been deposited in GenBank [17 kDa: MG190332; gltA: MG190324; sca1: MG811838, MK562056, MK535095, MG190331; sca4: MG190326, MK721054; ompA: MG190325, MK721055-MK721057; ompB: MH036479; 16srDNA: TMK813858; COI: TMK813859].

Discussion and conclusions

It is well known that Q fever, spotted fever group (SFG) and typhus group rickettsial infection may cause central nervous system infection [21]. Among SFG Rickettsia, R. rickettsii, R. conorii, R. helvetica, Candidatus R. tarasevichiae and R. japonica have documented association with meningitis [21, 22, 23, 24]. In China and Europe, 2 Patients infected with R. raoultii were reported to show meningeal syndrome, respectively [17, 25]. In this study, the patient showed right eyelid droop, lethargy, fever, headache, high cerebrospinal pressure and leukocytosis in CSF after bitten by D. marginatus tick. Our study has a limitation related to detection of Rickettsia DNA in blood but not in CSF sample. As for biochemical parameters in blood and CSF is unspecific to patients with R. raoultii infection, it is vital to detect rickettsial agents both in blood and CSF for tick bite patients with neurological abnormalities.

The previous recommended therapeutic regimen for rickettsiosis is administration of doxycycline or chloramphenicol [26]. In this study, the patient recovered after treatment with doxycycline & ceftriaxone. This finding indicates that doxycycline combined with ceftriaxone should be recommended when the tick bite patient shows neurological abnormalities caused by rickettsial infection.

In this study, two R. raoultii (0.18%, 2/1107) and one R. slovaca (0.09%, 1/1107) were molecularly detected in local shepherds. In addition, the prevalence of SFG Rickettsia in ticks was high in Xinjiang [8]. Therefore, public health workers and physicians need to be aware of the wide distribution and clinical complexity of rickettsial infection, especially higher risk for tick exposure.

Notes

Acknowledgments

Not applicable.

Authors’ contributions

YZW conceived and designed the study. SSZ and QW critically revised the manuscript. ZHD and YCY completed the experiment, analyzed the data and drafted the manuscript. SSX treated the patient, and carried out the clinical diagnosis, WBT and WMY conducted molecular analyses. All authors read and approved the final manuscript.

Funding

This research was supported in part by the National Key Research and Development Program of China (2018ZX10101002–002-007) and National Natural Science Foundation of China (81560338). The funding source had no influence in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.

Ethics approval and consent to participate

The research was approved by the First Affiliated Hospital of Shihezi Medical University. (Letter Number: 2017–112-03). Written informed consent was obtained for all research participants.

Consent for publication

Written informed consent was obtained from the patient for publication of this Case Report and any accompanying images. A copy of the written consent is available for review by the Editor of this journal.

Competing interests

The authors declare that they have no competing interests.

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© The Author(s). 2019

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors and Affiliations

  • Zhihui Dong
    • 1
  • Yicheng Yang
    • 1
  • Qian Wang
    • 2
  • Songsong Xie
    • 3
  • Shanshan Zhao
    • 1
  • Wenbo Tan
    • 1
  • Wumei Yuan
    • 1
  • Yuanzhi Wang
    • 1
    Email author
  1. 1.School of MedicineShihezi UniversityShiheziChina
  2. 2.Kaifeng Central HospitalHenanChina
  3. 3.The First Affiliated Hospital of Shihezi University Medical CollegeShiheziChina

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