Molecular Detection of Novel Borrelia Species, Candidatus Borrelia javanense, in Amblyomma javanense Ticks from Pangolins

Abstract

A novel Borrelia species, Candidatus Borrelia javanense, was found in ectoparasite ticks, Amblyomma javanense, from Manis javanica pangolins seized in anti-smuggling operations in southern China. Overall, 12 tick samples in 227 (overall prevalence 5.3%) were positive for Candidatus B. javanense, 9 (5.1%) in 176 males, and 3 (5.9%) in 51 females. The phylogenetic analysis, based on the 16S rRNA gene and the flagellin gene sequences of the Borrelia sp., exhibited strong evidence that Candidatus B. javanense did not belong to the Lyme disease Borrelia group and the relapsing fever Borrelia group but another lineage of Borrelia. The discovery of the novel Borrelia species suggests that A. javanense may be the transmit vector, and the M. javanica pangolins should be considered a possible origin reservoir in the natural circulation of these new pathogens. To our knowledge, this is the first identification of a novel Borrelia species agent in A. javanense from pangolins. Whether the novel agent is pathogenic to humans is unknown and needs further research.

1. Introduction

Borrelia, a bacteria genus of the spirochete phylum, are the causative agents of major vector-borne diseases, including Lyme disease (LD) and relapsing fevers (RFs), which are transmitted by ticks and lice worldwide [1]. The LD and RF Borrelia species from two separate sister groups are considered two sister genera [2,3,4,5]. However, recent surveys have uncovered new Borrelia species and strains that do not belong to the LD or RF group. They form the third group, encompassing only two designated species, B. turcica and “Candidatus Borrelia tachyglossi”, and a few strains not taxonomically described [6,7,8,9,10,11,12,13,14,15,16,17]. The third Borrelia group has been detected in Amblyomma, Hyalomma, Bothriocroton, and Ixodes genera hard ticks, mainly associated with reptiles and echidna. However, only two genomes sequenced confirmed that these Borrelia are substantially different from the LD and RF Borrelia groups [15].

Here, we report a novel Borrelia species in Amblyomma javanense ticks collected from 25 M. javanica pangolins from uncertain countries in Southeast Asia, seized in anti-smuggling operations by Guangxi Customs officers in Fang Cheng Gang and Nan Ning cities, southern China, during the period October 2016–January 2018. We obtained the complete 16S rRNA gene (rrs) and the partial flagellin gene (flaB) by PCR and sequencing. All positive samples have 100% similar nucleotide sequences to each other. Both the rrs and the flaB gene sequences did not fall into either the Lyme disease Borrelia group or the relapsing fever Borrelia group but into another Borrelia group lineage in phylogenetic analysis.

2. Results

2.1. Identification of Borrelia sp. in Ticks

During the study period, we screened a total of 227 adult ticks captured from 25 M. javanica pangolins seized in anti-smuggling operations in southern China (Figure 1). The animals were brought to the wildlife medical-aid center during the veterinary examination, and the ticks were removed and preserved. All ticks were not engorged or not fully engorged and identified as A. javanense by morphologic features to the species level and the developmental stage by two entomologists (Y. Sun and R.-M. Xu). Twelve tick samples (overall prevalence 5.3%) were screened positive for Borrelia, 9 (5.1%) in 176 males and 3 (5.9%) in 51 females, with no significant gender difference. All nucleotide sequences of the 353-bp amplicons were sequenced and identical to one another. The nucleotide sequences of nearly entire rrs (1532 bp) were obtained by nested PCR for segmented amplification, sequencing, and splice according to the overlap area from 5 tick samples; all of them were identical to one another (GenBank accession no. MW889882) and similar to Borrelia crocidurae (GenBank accession no. CP004267), with 25 base-pair differences (1507/1532, homologous 98%). We also amplified and sequenced the partial flagellin gene (flaB) (GenBank accession no. MW916611) by nested PCR from 3 tick samples; these sequences were 100% homologous to one another and shown to be 92% (424/460) homologous with the corresponding sequence of the Borrelia johnsonii strain from bat tick Carios kelleyi from the US [18]. Both the rrs and flaB showed relatively large differences with the Borrelia sp. in GenBank and cannot be clustered into their Borrelia group. Therefore, they should be considered a separate branch or another Borrelia group.

2.2. Genetic Characteristics of Borrelia sp.

The rrs and flaB phylogenetic trees were constructed using the neighbor-joining method based on the trimmed rrs and flaB sequences generated in this study, together with 36 rrs sequences and 31 flaB sequences from other Borrelia spp. retrieved from GenBank. The phylogenetic trees based on nearly complete rrs (1401 bp; Figure 2) and partial flaB (466 bp; Figure 3) demonstrated that the Borrelia sp. identified from the A. javanense ticks in this study were clustered in a separate clade that was distinct from both LD Borrelia and RF Borrelia groups.

3. Discussion

Ticks (Acari: Ixodidae), which are obligate blood-feeding arthropods, are distributed worldwide from tropic to subarctic regions, capable of transmitting the broadest spectrum of pathogens, including bacteria, protozoa, fungi, nematodes, and viruses, to humans, livestock, and wildlife. Here, we report a non-described Borrelia species in A. javanense ticks attached below the scales of M. javanica pangolins distributed in south Asia, southeast Asia, and southern China. This novel Borrelia species is prevalent in this tick species, abundantly attached to the Malayan pangolins. The novel Borrelia species is divergent not only from the LD species and the RF species but also from a third Borrelia group, B. turcica and B. tachyglossi, the reptile- and echidna-associated Borrelia group that was recently described [19]. Sequence analysis showed that this novel Borrelia sp. perhaps has a unique genome and indicates that this novel Borrelia is an intermediate taxon between the LD and RF species. The designation “Candidatus Borrelia javanense” is proposed for this species.

We reported for the first time the identification of novel Borrelia agents in A. javanense from pangolins. A. javanense is an important ectoparasite of M. javanica pangolin. A. javanense has been found in almost all the pangolin species and could be the coendangered tick species on pangolins in Asia [20]. It is reported that the tick also infests various wild animals such as wild boar, lizards, python, skink, hill turtle, bat, hyena, bear, and sambar deer [21,22]. A previous study also reported that A. javanense could infect humans [23]. The geographical distribution of the tick is also very extensive. Voltzit and Keirans have reported A. javanense from Pakistan, India, Sri Lanka, Myanmar, Thailand, Vietnam, Malaysia, Singapore, Indonesia, Philippines, and China [24,25]. Among the 227 ticks tested in this study, 12 (overall prevalence 5.3%) were infected with the new agents, indicating that A. javanense may be acting as the tick vector of the newly identified Borrelia sp. There is a low probability of transmission to people, but whether it is pathogenic to humans is unknown and needs further exploration.

In conclusion, we have identified a novel Borrelia species, Candidatus Borrelia javanense, in ectoparasite ticks, Amblyomma javanense, from M. javanica pangolin. This is the first report of Borrelia agents in A. javanense from pangolins. Further studies should be conducted to isolate this bacterium and investigate its epidemiologic, genetic, and pathogenic features.

4. Materials and Methods

4.1. Ethics Statement

The Malayan pangolins studied here were rescued and treated by the Guangxi Zhuang Autonomous Region Terrestrial Wildlife Medical-Aid and Monitoring Epidemic Diseases Research Center under ethics approval (Wild Animal Treatment Regulation No. [2011] 85). The tick samples were collected following the procedure guideline (Pangolins Rescue Procedure, November 2016).

4.2. Tick Sample Collection and Identification

Ticks were collected from under the scales of the M. javanica pangolins seized by Guangxi Customs officers in anti-smuggling operations in Fang Cheng Gang city (108.35342° S, 21.76913° E) and Nan Ning city (108.33639° S, 22.87786° E). All the pangolins were from southeast Asian countries. Briefly, smugglers in the Sino-Vietnamese border collected the pangolins from Vietnam, Myanmar, Laos, Cambodia, Philippines, Malaysia, Indonesia, and Thailand and illegally introduced them into China. In the process of smuggling, the pangolins were intercepted and seized. During the rescue of the pangolins, all ticks, including engorged and not-engorged adults and nymphs, were removed from the body surface, preserved in a moist breathable bottle at 4 degrees, and sent to the Beijing Institute of Microbiology and Epidemiology for species identification and molecular analyses. All ticks were identified by entomologists Yi Sun and Rong-Man Xu. All identified ticks corresponded to Amblyomma javanense. For this study, a total of 227 adult ticks, including 176 males and 51 females, were collected, and 156 ticks that were not fully engorged were used for DNA isolation and molecular detection. Nymphs were not processed.

4.3. DNA Extraction, Borrelia-Specific PCR, and Sequencing

Ticks were surface-sterilized with 10% sodium hypochlorite and washed with sterile and DNA-free water and 70% ethanol. The ticks were grounded individually in 200 μL phosphate-buffered saline buffer, and total DNA was extracted with the DNeasy Tissue Kit (QIAGEN, Germantown, MD, USA). The ticks were subjected to two Borrelia genus-specific PCR assays (ABI9700, ). The Borrelia-specific nested-PCR assays were conducted by targeting the 16S rRNA gene (rrs) and the flagellin gene (flaB) (

Table 1. Primers used for Borrelia-specific 16S rRNA and flaB gene amplification in this study, including primer sequences, annealing temperature, and expected product size.

Gene	Primer	Sequence (5′-3′)	Annealing Temperature	Expected Product Size	Reference
16S rRNA	External
	Bor-0F	AAAATAACGAAGAGTTTGATCCTGG			This study
	Bor-1533R	GTGATCCAGCCACACTTTCCAGTA	55 °C	1533 bp	This study
	Internal
	Brm1	CGCTGTAAACGATGCACACTTGGTGTTAATC			[26]
	Brm2	CGGCAGTCTCGTCTGAGTCCCCATCT	60 °C	353 bp	[26]
	Brm1-R	GATTAACACCAAGTGTGCATCGTTTACAGCG	55 °C	790 bp/Bor-0F	This study
flaB	External
	FLA120F	AGAATTAATMGHGCWTCTGATGATG			[26]
	Flab764R	GCATCTTCGATCTTTGAAAGTGACATATT	55 °C	645 bp	This study
	Internal
	Flab625R	CTGGAGCTGCTTGAGCACCTTCT	55 °C	506 bp/FLA120F	This study

). Each 25 μL PCR reaction contained 1× PerfectTaq buffer, 2.5 mM MgCl2, 1 mM dNTPs, 400 nM of each primer, 1.25 U PerfectTaq polymerase, and 2 μL undiluted DNA. Both the primary and nested Borrelia 16S PCR assays were performed with the following thermal conditions: initial denaturation at 95 °C for 5 min, 35 cycles of denaturation at 95 °C for 30 s, annealing at 55 °C for 30 s, and extension at 72 °C for 1.5 min, and a final extension at 72 °C for 7 min. The flaB PCR assays were performed with an initial denaturation at 95 °C for 5 min, 35 cycles of denaturation at 95 °C for 30 s, annealing at 55 °C (primary and nested) for 30 s, and extension at 72 °C for 30 s, and a final extension at 72 °C for 7 min. Amplified PCR products were electrophoresed through 1.5% agarose gels, stained with ethidium bromide, and visualized under UV light. To avoid the risk of contamination, the DNA extraction, PCR reagent setup, amplification, and agarose gel electrophoresis were performed in separate rooms, and a negative control (distilled water) was concurrently included in each amplification. All the PCR products were purified with the QIAmp Gel Extraction Kit (QIAGEN, Germantown, MD, USA) and then directly sequenced on an automated DNA sequencer (3730 DNA Sequencer; Applied Biosystems, Carlsbad, CA, USA). We compared the sequences obtained with previously published sequences deposited in GenBank by using BLAST (http://blast.ncbi.nim.nih.gov/Blast.cgi, accessed on 15 June 2020).

4.4. Sequence Analysis

Phylogenetic analysis based on the 16S rRNA gene (rrs) and the flagellin gene (flaB) was conducted using MEGA7 software. The phylogenetic tree was constructed using the neighbor-joining method based on the trimmed sequences generated in this study, together with sequences from other Borrelia spp. retrieved from GenBank. The stability of the tree was evaluated by bootstrap analysis with 1000 replications. The 16S rRNA and flagellin nucleotide sequences determined in this study have been submitted to Genbank under accession numbers MW889882 and MW916611.