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Surveillance in Jinzhai County, Lu’an City, Anhui Province, China revealed that between May and June 2021, 2 patients developed fever and thrombocytopenia after being bitten by a tick. The local hospitals and CDC could not determine the pathogen, so blood specimens were sent to the National Institute for Communicable Disease Control and Prevention to investigate this event. Nested polymerase chain reactions (PCR) and indirect immunofluorescence assays (IFAs) identified Anaplasma bovis as the pathogen of both cases. Gene sequencing suggested that a tick, Haemaphysalis longicornis, was the source of infection. This is the second report of A. bovis infections in humans worldwide. Clinicians and public health physicians should be more attentive to these diseases and learn how to diagnose them as early as possible.
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In 2021, 2 patients (Patient A and Patient B) developed intermittent fever as an initial clinical symptom after a tick bite. Both of them were characterized by fever, thrombocytopenia, rash, asthenia, anorexia, myalgia, chill, diarrhea, and headache, which were not resolved by common antibiotics. In a local hospital, these patients were clinically diagnosed with endemic typhus.
On May 10, 2021, a 67-year-old man (Patient A) developed a fever with chills, asthenia, anorexia, and myalgia after being bitten by a tick in a mountainous area. Even with routine anti-infection treatments, his body was covered with a rash 3 days later. He was brought to the Department of Infectious Disease of Jinzhai County People’s Hospital (JCPH; Lu’an City, Anhui Province, China) on May 17, 2021, with persistent intermittent fever and rashes. Based on his medical history and epidemiological and clinical manifestations, he was admitted to JCPH with clinically diagnosed typhus. Blood tests revealed eosinophilic granulocytes of 0.00 × 109/L, thrombocytes of 87 × 109/L, alanine aminotransferase of 117.07 U/L, and aspartate transaminase of 104.13 U/L. After treatment with azithromycin for 7 days, his clinical symptoms disappeared.
On June 5, 2021, a 57-year-old man (Patient B) developed a fever reaching 39 °C accompanied by headache, asthenia, anorexia, myalgia, and occasional diarrhea after working in a field. He was brought to the Department of Infectious Disease of JCPH on June 8, 2021, with progressive exacerbation of his symptoms. He was admitted to JCPH with “fever of undetermined origin,” and his general status upon hospital admission was poor. Blood tests revealed leukocytes of 3.94 × 109/L and thrombocytes of 95 × 109/L. After treatment with azithromycin for 7 days, his clinical symptoms disappeared, and his general status improved greatly.
The blood specimens collected from these two patients were sent to determine the pathogen through nested PCR and IFA. DNA was extracted with the QIAamp DNeasy Blood & Tissue Kit (Qiagen, Hilden, Germany), and several human pathogens were tested using nested PCR targeting the 16S ribosomal RNA (rrs) gene. Specific immunoglobulin IgG and IgM antibodies against spotted fever group and related rickettsia (Rickettsia typhi, Orientia tsutsugamushi, A. phagocytophilum, Ehrlichia chaffeensis, and A. bovis in sera) were detected by IFA (Fuller Laboratories, Fullerton, CA, USA). The A. bovis substrate slides were developed by our department. According to the manufacturer’s instructions, an IgG titer of ≥1∶64 and IgM titer of ≥1∶20 denoted a positive result.
To investigate the presence of infections in relevant ticks, we collected parasitic and free-living ticks from the regions where the two patients lived and worked. All ticks were identified morphologically by an entomologist based on differences in their bodies and basis capituli. All tick DNA was extracted individually. We tested for the presence of Rickettsiales bacteria using a nested or semi-nested PCR targeting the rrs, citrate synthase (gltA), and 60-kDa heat shock protein (groEL) genes as described previously (Supplementary Table S1)(1). Phylogenetic trees of the data were created using the Maximum Likelihood (ML) method by employing the GTR+Γ+I model of substitution, as implemented in PhyML (version 3.0) http://www.atgc-montpellier.fr/phyml/ (2).
The rrs gene was amplified from Patient A using a PCR assay, while it was not detected from Patient B. Using BLASTN with a nucleotide collection, genetic analysis of the recovered rrs sequence revealed that it was most closely related to that of the A. bovis isolate Zhouzhi-cattle-10 (GenBank: MH255937.1, 99.75%), and we named it “A. bovis strain JZPA.” The IgM titer against A. bovis of these 2 patients was 1∶80, whereas the IgG titer of Patient A was 1∶256, and that of Patient B was 1∶1,024 (Figure 1). Therefore, PCR and IFA indicated that both patients had been infected with A. bovis.
Figure 1.Photomicrographs of an IFA test with Anaplasma bovis infected patients’ sera. (A) IFA of patient sera; (B) The IFA assays tested with negative control.
Note: Green fluorescence shows the positive cells for A. bovis bacteria, and red fluorescence shows the host cells. Abbreviation: IFA=immunofluorescence assay.To investigate the source of this pathogen, we carried out an investigation into the vectors present in the areas where the two patients lived and worked. We collected 270 tick samples, which were tested for the A. bovis strain JZPA. The rrs, gltA, and groEL genes were detected in 63 samples, and the positive rate in ticks was 23.3%. Each of the 63 samples contained all the three genes. In the rrs tree (Figure 2), sequences from Patient A’s sample (A. bovis strain JZPA) and sequences of the tick (A. bovis strain JZT018) clustered together and formed a distinct lineage. There was 100% similarity of the rrs gene sequences for the patient and the tick (H. longicornis). In the gltA and groEL trees (Supplementary Figure S1), the amplified tick sequences also clustered with A. bovis, and they were closely related to sequences from other A. bovis strains. These results suggested that A. bovis was prevalent in ticks within certain areas of Lu’an City and that these pathogens may infect humans to cause fevers and other symptoms (Table 1).
Figure 2.Phylogenetic relationship of Anaplasma species based on rrs sequences.
Note: All trees were mid-point rooted for clarity only. Bootstrap values (>70%) were shown for appropriate nodes. Scale bar represents number of nucleotide substitutions per site. The sequence obtained from Patient A is marked in red, and the sequence obtained from ticks is marked in blue.Item Patient A Patient B Clinical characterization Fever + + Rash + − Asthenia + + Anorexia + + Myalgia + + Chill + − Headache − + Dizziness − − Nausea − − Lymphadenopathy − − Vomiting − − Diarrhea − + Eschar − − Cough − − Arthralgia − − Laboratory findings* White blood cell count 6.41×109/L 3.94×109/L Platelet count 87×109/L 95×109/L CRP 62.75 mg/L 4.93 mg/L ALT 117.07 U/L 14 U/L AST 104.13 U/L 24 U/L *Normal ranges: white–cell count: 4.0–10.0 × 109 /L, platelet count: 100–300 × 109 /L, CRP 0–8 mg/L, ALT: 0–40 U/L, AST: 5–40 U/L.
Abbreviations: CRP=C-reaction protein; ALT=alanine aminotrans
ferase; AST=glutamic oxaloacetic acid transferase.Table 1. Clinical manifestations and laboratory findings of two patients infected with Anaplasma bovis in Jinzhai County, Anhui Province, China, 2021.
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No conflicts of interest declared.
Gene Name Primers (5'–3') Fragment size rrs fd1 AGAGTTTGATCCTGGCTCAG 1,500 bp rp2 ACGGCTACCTTGTRACGACTT groEL bovis-groF1 GTATGCARTTTGATCGYGGAT 1,330 bp bovis-groF2 GAAGTTGGAAGRGAYGGDGT bovis-groR GCCTTWACAGCDGCAACTTG 1,300 bp gltA bovis-gltA-F1 TACATCWACWGTAAGAATGG 1,100 bp bovis-gltA-F2 ACWGTAAGAATGGTKGGCTC bovis-gltA-R CCRGCAGTDCGTCCCAGTGC 1,057 bp COI Ron GGAGCYCCWGATATAGCTTTCCC 488 bp Nancy CCTGGTAAAATTAAAATATAAACTTC Abbreviations: PCR=polymerase chain reaction; rrs=16S ribosomal RNA; groEL=60-kDa heat shock protein; gltA=citrate synthase; COI=cytochrome-cytochrome oxidase. Table S1. The PCR primers used in this study.
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