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. 2013 Oct 28;6:310. doi: 10.1186/1756-3305-6-310

Microbial communities and symbionts in the hard tick Haemaphysalis longicornis (Acari: Ixodidae) from north China

Li-Meng Liu 1,#, Jian-Nan Liu 1,#, Zhao Liu 1, Zhi-Jun Yu 1, Shi-Qi Xu 1, Xiao-Hong Yang 1, Tuo Li 1, Si-Si Li 1,3, Li-Da Guo 2, Jing-Ze Liu 1,✉
PMCID: PMC3813991  PMID: 24499619

Abstract

Background

Close relationships between ticks and microbial communities are important for tick fitness and pathogen colonization and transmission. Haemaphysalis longicornis, distributed widely in China, can carry and transmit various pathogens and pose serious damages to public health and economics. However, little is known about the broader array of microbial communities and symbionts in H. longicornis under natural conditions. In the present study, we investigated the composition of bacterial communities associated with H. longicornis and evaluated the putative symbionts.

Methods

The eubacterial 16S rRNA gene clone libraries of H. longicornis were constructed and analyzed by restriction fragment length polymorphism (RFLP) and DNA sequencing. In addition, diagnostic PCR was performed to assess the prevalence, vertical transmission and infection sites of the symbionts in H. longicornis.

Results

Vertically-transmitted symbionts, potential pathogens and allochthonous nonpathogenic bacteria were identified from the field-collected H. longicornis. Three types of symbionts (Coxiella-like, Arsenophonus-like and Rickettsia-like symbionts) were identified in a single host simultaneously. A series of analyses revealed the vertical transmission, prevalence, and infection sites of these symbionts. However, only Coxiella-like bacteria were transmitted stably in the laboratory-reared ticks. In addition, we identified a novel Coxiella-like agent with 95.31% sequence similarity to the taxon described previously.

Conclusions

The present study demonstrated that natural H. longicornis harboured a diverse array of microbial communities. Three types of symbionts were identified in a single host simultaneously. Moreover, high prevalence, vertical transmission and the infection sites supported an obligate symbiotic association between Coxiella symbiont and its host. The role of Coxiella symbiont in the host fitness and the interaction among microbial communities remained to be elucidated. Our investigation of microbial communities in the ticks revealed the complexity of ecological interactions between host and microbe and provided insight for the biological control of ticks.

Keywords: Haemaphysalis longicornis, Microbial communities, Coxiella-like symbiont, Arsenophonus-like symbiont, Rickettsia-like symbiont

Background

As obligate blood-feeding arthropods, ticks feed on terrestrial vertebrates and are one of the most important disease vectors worldwide. Ticks are involved in carrying and transmitting a diverse group of pathogenic bacteria, which exert severely negative impacts on human health, livestock production as well as wildlife [1-3]. Hard ticks (Ixodidae) usually have three life stages (larva, nymph, adult) in their lifespan and feed on distinct host species at different developmental stages. Thus, they are prone to acquiring various pathogens and spreading among vertebrate species during the whole life cycle [4].

In addition to pathogens, vertically-transmitted symbionts and foreign nonpathogenic bacteria also colonize the ticks [5-7]. Symbionts are closely associated with the host fitness [8,9] and transmission and virulence of pathogens [10,11]. To date, it is well-known that ticks harbour various symbionts, including Coxiella[12], Francisella[13], Wolbachia[14], Rickettsia[15], Arsenophonus[16], Candidatus Midichloria mitochondrii [17]. Moreover, some of them have crucial effects on the biological characteristics of ticks. For example, the obligate Coxiella-like symbiont manipulates the reproduction of the host Amblyomma americanum[18-20]. Ca. Midichloria mitochondrii, the symbiont of Ixodes ricinus, has the unique ability to enter and destroy mitochondria within ovarian cells of host [21,22], which is coupled with the process of engorgement and molt [23,24]. In addition, colonization of Dermacentor variabilis by R. peacockii can prevent secondary infection with other Rickettsia bacteria, including pathogenic species [25]. Clay [5] found that the infection frequency of Arsenophonus was negatively correlated to Rickettsia in A. americanum, indicating that infection with symbionts may affect the microbial community structure and their interaction.

Ticks could also obtain allochthonous nonpathogenic bacteria by sucking host blood and contact with the natural environment [26-28]. Although allochthonous bacteria are not directly related to the pathogenicity of hosts, they can reflect the habitats of hosts and even have the potential to impact on the density and transmission of host-borne agents [29]. Overall, diverse microbial communities can exert great impact on the fitness of ticks and the colonization and transmission of tick-borne pathogens.

Haemaphysalis longicornis (Acari: Ixodidae), a three-host tick, extensively distributed in China [30], Korea, Japan, New Zealand, and Australia [31,32], has inflicted serious damage on public health and economics. It is reported that this tick species transmitted a variety of pathogens [33,34], including Babesia microti[35], Ehrlichia chaffeensis[36], Anaplasma bovis[37], A. phagocytophilum[38], C. burnetii[39], Spotted fever group rickettsiae [40], and Borrelia burgdorferi[41]. With regard to the human health and economic significance, pathogens carried by H. longicornis have been well investigated in China [42-47]. However, little is known about the broader array of the microbial community in H. longicornis under natural conditions.

In the present study, we investigated the composition of bacterial communities associated with H. longicornis using PCR-RFLP and DNA sequencing approaches, and evaluated the putative symbionts.

Methods

Sample collection and storage

H. longicornis samples were collected in Xiaowutai National Natural Reserve Area in China by flag dragging. A total of 500 ticks were collected and stored at -80°C. We also collected 1,000 ticks, which were reared on rabbits as described by Liu et al. [48]. Colonies of these ticks were reared on the ears of rabbits. Rabbits were maintained in a room with 50-55% relative humidity (RH) at 25–27°C and exposed to daylight. After detachment, ticks were collected and incubated in cotton-plugged glass tubes filled with folded filter paper in an incubator with 75 ± 5% RH and 6/18 h of L/D cycle at 26 ± 1°C. The protocol of all animal experiments was approved by the Institutional Animal Care and Use Committee of Hebei Normal University.

DNA extraction

The genomic DNA for constructing eubacterial 16S rRNA gene libraries were extracted from a group of adults (10 females and 10 males). To assess the prevalence, vertical transmission and infection sites, DNA was isolated from individual field-collected adults, and pooled ticks at different developmental stages (500 eggs, 200 larvae and 50 nymphs) and different tissues (ovaries, salivary glands, Malpighian tubules and midguts), respectively. Before DNA extraction, the whole tick samples were sterilized as described previously [5], and dissected tissues were washed in sterile phosphate-buffered saline (PBS) (137 mM NaCl, 2.7 mM KCl, 4.3 mM Na2HPO4 · 7H2O, 1.4 mM KH2PO4, pH 7.4) for three times. Subsequently, all samples were snap-frozen in liquid nitrogen and purified using the DNeasy Tissue Kit (Qiagen, Germany) according to the manufacturer’s instructions.

Eubacterial 16S rRNA gene library construction, RFLP analysis and sequencing

The eubacterial 16S rRNA gene clone library was constructed by amplifying about 1500 bp fragment of 16S rRNA gene using eubacterial universal primers 27 F/1492R [49]. Purified PCR products were cloned into pEASY-T1 vector (TransGen, China) and transformed into Escherichia coli TOP10 competent Cell (TransGen, China). The positive clones were subjected to restriction fragment length polymorphism (RFLP) analyses using both HaeIII and RsaI restriction endonucleases. Sequencing of the positive clones with different restriction fragment patterns were performed by Sangon Biotech Company (China).

Phylogenetic analyses

The 16S rRNA gene sequences of the most closely related species were retrieved from GenBank and then aligned. The similarity analyses were performed using the CLUSTAL_W program [50]. The phylogenetic tree was constructed using neighbour-joining method implemented in MEGA4.0 [51]. The stability of the tree clustering was evaluated by means of a bootstrap analysis of 1000 datasets [52].

Diagnostic PCR

To assess their prevalence, vertical transmission and infection site of symbionts, diagnostic PCR assay was performed with four sets of specific primers (Table 1). The PCR reaction contained 20 mM Tris–HCl (pH 8.4), 50 mM KCl, 1.5 mM MgCl2, 200 μM each dNTP, 2.5 U Platinum Taq DNA Polymerase (Invitrogen, America), and 0.5 mM each primer. PCR cycling conditions were as follows: 1 cycle of 94°C for 2 min; 30 cycles of 94°C for 30 s, 55°C for 30 s, and 72°C for 15 s, and 72°C for 10 min.

Table 1.

Oligonucleotide primers used for PCR amplification and sequencing

Primer name Genera or Species Target gene Nucleotide sequence (5′-3′) Annealing temperature (°C) Approx product size (bp) Reference
CLS F
 Coxiella
 16S rRNA
 CACGTAGGAATCTACCTTGTAG
 55
 90
 55
CLS R
  
  
 CGTTTTGTTCCGAAGAAATTAT
  
  
  
ALS 82 F
 Arsenophonu
 16S rRNA
 AGGGAGCTTGCTTCCTGGCCGG
 59
 130
 55
ALS 198R
  
  
 CGAAGGTGTGAGGCCTAATGG
  
  
  
Rickettsia 354 F
 Rickettsia
 16S rRNA
 CAGCAATACCGAGTGAGTGATGAAG
 56
 350
 69
Rickettsia 647R
  
  
 AGCGTCAGTTGTAGCCCAGATG
  
  
  
NCLS F
 NCLS
 16S rRNA
 TCCCTGGCGGCGAGTGG
 55
 110
 This study
NCLS R
  
  
 CGTATTAGAGATTAGAGAAACC
  
  
  
Rr190.70p
 Rickettsia
 rompA
 ATGGCGAATATTTCTCCAAAA
 48
 540
 57
Rr190.602n     GTTCCGTTAATGGCAGCATCT      
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Results

Diversity of bacterial communities from field-collected H. longicornis

Our results revealed diverse microbial communities associated with field-collected H. longicornis (Table 2). In the 16S rRNA gene clone libraries, the most abundant sequences (belonged to Coxiella and designated as CLS-Hl) in both males and females share 99.5% similarity to the symbiont of H. longicornis (GenBank: AB001519) [53]. In females, the second abundant sequence (designated as NCLS-Hl) belonged to Coxiella, sharing 95.3% similarity to Coxiella-like symbionts of Rhipicephalus sanguine (GenBank: D84559). Following NCLS-Hl, sequences belonged to Rickettsia (designated as RLS-Hl) and E. coli. Rickettsia bacteria shared the highest sequence similarity (99.8%) with symbiotic Rickettsia of D. varibilis (GenBank: U55820) [54]. In males, the second abundant microbes (designated as ALS-Hl) belonged to Arsenophonus, sharing over 99.5% and 97.9% similarity to symbionts of D. silvarum (GenBank: JN866582) [55] and D. variabilis (GenBank: AY265342) [56], respectively. Following ALS-Hl, there were RLS-Hl and NCLS-Hl. Interestingly, the top four abundant bacteria in females were consistent with those in males.

Table 2.

Eubacterial 16S rRNA gene clone libraries from females and males of Haemaphysalis longicornis

Classification Closest taxon (GenBank No.) Identity % Sequences # (F/M)* Accession No. (GenBank)
Proteobacteria
  
  
  
  
α-proteobacteria
 Rhizobium spp. (EF363715)
 99%
 4/0
 JN866565
Rickettsia spp. (CP003319)§
 99%
 9/12
 JN866571
Devosia psychrophila (GU441678)
 98%
 0/1
 JN866597
Asticcacaulis excentricus (CP002395)
 99%
 2/0
 JN866569
β-proteobacteria
 Janthinobacterium lividum (EU275366)
 99%
 0/5
 JN866578
γ-proteobacteria
 Escherichia coli (CP001673)
 100%
 8/7
 JN866566
Moraxella osloensis (AB643592)
 99%
 4/0
 KF421818
Pseudomonas spp. (AB334768)
 99%
 0/7
 JN866577
Coxiella-like symbionts of H. longicornis (AB001519)§
 99%
 36/19
 JN866564
Coxiella-like symbionts of R. sanguine (D84559)§
 95%
 21/11
 JN866567
Arsenophonus-like symbionts of Dermacentor silvarum (JN866582)§
 99%
 5/16
 JN866572
Bacteroidetes
  
  
  
  
Sphingobacteria
 Mucilaginibacter sp. (GU139695)
 98%
 1/0
 JN866568
Sphingomonas asaccharolytica (AY509241)
 98%
 0/1
 JN866579
Actinobacteria
  
  
  
  
Actinobacteria Williamsia maris (NR024671)
 99%
 0/2
 JN866598
Conexibacter woesei (CP001854) 98% 0/1 JN866581
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*Source of the sequences from female ticks (F) or male ticks (M).

#Sequences indicate the number of 16S rRNA gene sequences obtained for each 16S rRNA gene clone libraries.

§Sequences are related phylogenetically to previously reported tick-associated bacteria.

Symbionts

OmpA gene sequence analyses revealed that RLS-Hl belonged to Ca. Rickettsia hebeiii, with 99.1% sequence similarity [57]. To confirm vertical transmission of symbionts, eggs and the first generation of laboratory-reared ticks (larvae, nymphs and adults) was tested by diagnostic PCR assay. The putative symbionts were found in all samples detected, with the exception of NCLS-Hl. These results indicated that CLS-Hl, ALS-Hl and RLS-Hl were inherited from progeny to the next generation, while NCLS-Hl was not (Figure 1). To determine the stability of vertical transmission, we investigated the presence of each bacterium in the 7th generation of laboratory-reared ticks (F7). The results showed only CLS-Hl was detected in F7 ticks, while ALS-Hl and RLS-Hl were not, suggesting that CLS-Hl can be maintained stably in laboratory-reared ticks.

Figure 1.

Figure 1

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Detection of vertical transmission of CLS-Hl (a), RLS-Hl (b) and ALS-Hl (c) by diagnostic PCR amplification. Lanes 1 to 8: M, DNA ladder; E, eggs from field-collected females; L, larvae; N, nymphs; AF: adult females; AM: adult males; E1: eggs from lab-reared females; N, negative control (distilled water).

In natural field populations, CLS-Hl showed 100% infection rate; ALS-Hl occurred in 33.3% (14/36) females and 83.3% (10/12) males; the prevalence of RLS-Hl was 88.9% (32/36) and 100% (12/12) in females and males, respectively. In the laboratory population, the prevalence of CLS-Hl was 100%.

Analysis of the infection site showed that three types of symbionts infected all tissues detected (accessory glands, testes, salivary glands, midguts) and there is no significant difference among all tissues in males. In females, CLS-Hl colonized specifically in the ovaries and Malpighian tubules, while ALS-Hl and RLS-Hl infected all tissues tested (ovaries, salivary glands, Malpighian tubules and midguts) (Figure 2).

Figure 2.

Figure 2

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Detection of infection sites of CLS-Hl (a), RLS-Hl (b) and ALS-Hl (c) by diagnostic PCR amplification. Lanes 1 to 6: M, DNA ladder; O, ovaries; Mt, Malpighian tubules; Gs, salivary glands; Mg, midguts; N, negative control (distilled water).

Discussion

In this study, we showed that the natural H. longicornis harboured a diverse group of bacterial species. Previous studies have shown that some tick species were colonized with complex microbial communities, including A. americanum, I. ricinus, I. scapularis and Rh. microplus[5-7,26-28,58,59]. Investigation of microbiota in the ticks revealed the complexity of ecological interactions between host and microbe and provided insight for the biological control of ticks.

Symbionts

Interestingly, some sequences were phylogenetically related to previously reported tick-associated bacteria, including (1) two types of Coxiella-like bacteria, CLS-Hl and NCLS-Hl, (2) Arsenophonus-like symbiont, ALS-Hl, (3) Rickettsia-like symbiont, RLS-Hl. It is now widely accepted that the co-infection with multiple symbionts occurs in many arthropod hosts [60]. However, co-infection with symbionts has been demonstrated only in a few tick species, such as A. americanum[5], Ornithodoros moubata[61], D. silvarum[55] and Rh. sanguineus[62]. We reported here for the first time that Coxiella-like, Arsenophonus-like and Rickettsia-like symbionts were detected simultaneously in wild H. longicornis. Interestingly, we identified two different types of Coxiella. CLS-Hl, with 95.1% similarity to the C. burnetii, shared 99.5% sequence identify with the symbionts of H. longicornis previously reported [39,53]. However, NCLS-Hl, with 95.1% and 95.3% similarity to the C. burnetii and symbionts of Rh. sanguine, respectively, was regarded as a novel Coxiella-like agent and has never been described before. Phylogenetic analyses revealed (Figure 3) that CLS-Hl and NCLS-Hl form an individual clade, although both of them belong to the cluster of hard tick species (Ixodidae). CLS-Hl was clustered with symbionts of Haemphysalis (H. longicornis and H. shimoga), while NCLS-Hl was grouped together with the symbionts of Rhipicephalus (Rh. sanguineus and Rh. turanicus). However, the determination of vertical transmission does not support that NCLS-Hl was a symbiont. Further studies are needed to confirm the pathogenicity of this novel Coxiella agent to vertebrate hosts.

Figure 3.

Figure 3

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Phylogenetic tree of two types of Coxiella-like bacteria based on 16S rRNA gene sequence similarity. The tree was rooted with Bacillus subtilis (GenBank: X60646) and constructed using neighbour-joining method and clustering nodes were also recovered in maximum likelihood method. Numbers at nodes represent the levels of bootstrap support (%) based on neighbour-joining analysis of 1000 replicated data sets. GenBank accession numbers are given in parentheses. Bar represents 2% sequence divergence.

In ticks, Coxiella bacteria are the most common agent, exhibiting diverse genotypes in different tick species [5,12,63-68]. By comparing the phylogeny between the tick mitochondrial 16S rRNA gene and the Coxiella agents carried by ticks, Almeida [12] showed that ticks were phylogenetically associated with their Coxiella agents, suggesting that Coxiella symbionts and ticks shared a long co-evolution process. In H. longicornis, Coxiella symbionts from different areas, such as Japan [53] and Korea [39], shared identical genotypes. This wide geographical distribution indicates that Coxiella symbionts form ancient symbiotic associations with their host before spreading.

Previous studies suggested that Coxiella symbionts in A. americanum, with 100% infection, vertical transmission, reduced-genome, regulation of the reproduction of the host, was closely related to the fitness of the ticks. Besides, in O. rostratus[12], D. silvarum[55] and Rh. sanguineus[62], Coxiella-like symbionts exhibited nearly perfect prevalence and were presumed as obligate symbionts. In this study, 100% infection rate, perfect vertical transmission, colonization in specialized tissues, CLS-Hl was regarded as obligate and contributed to the fitness of ticks.

Arsenophonus is one of the four major inherited symbionts of arthropods with an infection rate of 5% [60]. Arsenophonus has been reported to infect A. americanum[5], D. variablilis[16], D. andersoni[16] and D. silvarum[55]. Interestingly, the sequence of ALS-Hl was identical to that of D. silvarum collected from the same place as the H. longicornis, possibly suggesting horizontal transmission of Arsenphonus-like symbionts between different genera of ticks. Previous studies also provided evidence of horizontal transmission of symbionts between D. variabilis and D. andersoni[16]. Therefore, Arsenophonus possessed not only intragenus, but also intergenus horizontal transmission.

Rickettsia, with both symbiotic and pathogenic lifestyle, inhabits multiple tick species. Pathogenic rickettsiae have been extensively investigated, while only few studies on symbiotic rickettsiae have been reported. To date, Rickettsia-like symbionts have been identified in D. variabilis[54], D. andersoni[69], D. silvarum[55]I. scapularis[15] and A. americanum[5]. In this study, we showed molecular evidence for the vertical transmission of the Rickettsia-like symbiont (Ca. Rickettsia hebeiii) in H. longicornis. Moreover, high prevalence in the natural environment suggested interaction between RLS-Hl and their hosts.

However, RLS-Hl and ALS-Hl were not detected in F7 laboratory-reared ticks, suggesting that they cannot be maintained stably from one generation to the progeny in the laboratory. This phenomenon was also observed in I. ricinus, whose symbionts IricES1 were lost from female adults to progeny in the laboratory [70]. The transmission efficiency of symbionts decreased significantly in the laboratory, which was partially due to the competition among symbionts and bottlenecks during vertical transmission [71]. Alternatively, transmission reduction may be due to temperature differences between natural and laboratory environments [72].

Conclusions

A diverse array of microbial communities were identified from field-collected H. longicornis. Three types of symbionts were detected in a single host simultaneously. Moreover, analysis on the prevalence, vertical transmission and infection sites supported obligate symbiotic association between Coxiella symbionts and its host. The role of Coxiella symbionts in the host fitness and the interaction among microbial communities remains to be elucidated. Our investigation of microbial communities in the ticks revealed the complexity of ecological interactions between host and microbe and provided insight for the biological control of ticks.

Abbreviations

F7: The 7th generation of laboratory-reared ticks; CLS-Hl: Coxiella-like symbiont of H. longicornis; NCLS-Hl: Novel Coxiella-like symbiont of H. longicornis; RLS-Hl: Rickettsia-like symbiont of H. longicornis; ALS-Hl: Arsenophonus-like symbiont of H. longicornis.

Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

Liu L-M and Liu J-Z conceived and designed the study, constructed 16S rRNA gene libraries and performed RFLP analyses, drafted the manuscript, and critically revised the manuscript. Liu J-N carried out RFLP analyses and diagnostic PCR. Liu Z, Yu Z-J, Xv S-Q and Yang X-H, participated in sample collection, study implementation and data collection and helped to revise the manuscript. Li T, Li S-S and Guo L-D participated in sample collection and tick feeding. All authors read and approved the final manuscript.

Contributor Information

Li-Meng Liu, Email: liulimeng81@126.com.

Jian-Nan Liu, Email: ljn_19881029@163.com.

Zhao Liu, Email: youqing139@gmail.com.

Zhi-Jun Yu, Email: yzj116@163.com.

Shi-Qi Xu, Email: xsqcdmu@163.com.

Xiao-Hong Yang, Email: yangxiaohong02@163.com.

Tuo Li, Email: 409704881@qq.com.

Si-Si Li, Email: li_sisi_2010@126.com.

Li-Da Guo, Email: lidaguo815@foxmail.com.

Jing-Ze Liu, Email: jzliu21@heinfo.net.

Acknowledgements

This work was supported by grants from the National Natural Science Foundation of China (Grant No. 31272372) and the Specialized Research Fund for the Doctoral Program of Higher Education of China (Grant No. 20131303130001).

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