The First Molecular Detection of Theileria luwenshuni from Haemaphysalis mageshimaensis on Orchid Island, Taiwan, with No Evidence of SFTSV

TL;DR

Researchers found Theileria luwenshuni in ticks on Orchid Island, Taiwan, marking the first detection there and suggesting potential risks to ruminants.

Contribution

First molecular detection of T. luwenshuni in Haemaphysalis mageshimaensis ticks on Orchid Island, Taiwan.

Findings

T. luwenshuni was detected in H. mageshimaensis ticks via PCR with high sequence identity to known T. luwenshuni.

This is the first report of T. luwenshuni on Orchid Island and in this tick species.

Ruminants on Orchid Island may be at risk of infection, requiring further study.

Abstract

Theileriosis is considered an economically important disease that may decrease productivity and cause a high mortality rate in livestock. Only a few studies have reported Theileria spp., such as T. sergenti and T. buffeli, in recent decades in Taiwan. In the present study, 401 ticks have been collected on Orchid Island in June 2022 and April 2023. Our environmental investigation for SFTSV unintentionally discovered T. luwenshuni in Haemaphysalis mageshimaensis on Orchid Island via PCR. The PCR products were sequenced, and the detected 18S rRNA gene sequences shared a 99.65–99.93% identity with T. luwenshuni sequences from ticks and ruminants in Myanmar and China. Despite the difficulty in clarifying the source of T. luwenshuni within neighboring regions, our findings provide an updated distribution of T. luwenshuni in Asia. This is not only the first time that T. luwenshuni was found in H. mageshimaensis but also the first report of T. luwenshuni on Orchid Island, Taiwan. Our study indicates that ruminants may be at risk of infection. Therefore, further investigations are needed to determine the distribution of T. luwenshuni among ruminants on Orchid Island and in Taiwan.

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1. Introduction

Theileria species infect various types of animals, such as cattle, horses, and sheep [1]. Theileria spp. can be divided into transforming and non-transforming groups based on whether schizonts develop in leukocytes. Non-transforming Theileria species do not develop schizonts in leukocytes and, therefore, do not induce transformation. Consequently, transforming Theileria species can cause fatal lymphoproliferation, while non-transforming Theileria species primarily cause anemia [2,3].

Theileriosis refers to the reproduction of Theileria spp. in the host and is considered an economically important disease [4]. It threatens the livestock economy by decreasing the productivity and increasing the mortality rate of hosts; for instance, T. lesteoquardi, T. luwenshuni, and T. uiolenbergi cause high mortality rates in small ruminants [5]. Moreover, studies have reported a high prevalence of pathogenic Theileria parasites in China and Pakistan, which has been associated with economic damage, particularly in the cattle industry [6,7]. Theileriosis has been reported in hosts of specific species. For instance, T. parva and T. annulata were found in cattle, T. equi in horses, and T. lestoquardi and T. luwenshuni in sheep and goats. Despite some evidence from Ghana indicating that Theileria spp. may be less likely to infect humans, further investigation is required to clarify the human–vector interactions of Theileria spp. [8]. Only a few studies have reported information on Theileria spp. in recent decades in Taiwan. Wang et al. conducted a survey of Theileria spp. infection in cattle and found piroplasms in 4 of 105 blood samples. In addition, they reported the infection of T. sergenti and T. buffeli by allele-specific PCR in 15 of 105 blood samples in 1998 [9]. Another survey executed by Chan et al. in 2010 suggested that equine piroplasmosis was not detected in 489 blood samples from horses [10]. To date, no study has investigated sheep, goats, or ticks in Taiwan.

Ticks and their pathogens may travel across regions and countries with migrating birds [11]. Recently, Yin et al. reported that T. luwenshuni [12] was found in other Eurasian countries, including Korea, Türkiye, northern India, and the Mediterranean region [13,14,15], and that certain tick-borne pathogens (i.e., severe fever with thrombocytopenia syndrome virus, Borrelia burgdorferi, and Babesia divergens) were first discovered or frequently found in cold and/or temperate areas. However, T. luwenshuni has recently been reported in Myanmar [16]. These recent reports imply that T. luwenshuni and its corresponding vectors are of increasing importance in the tropics.

Severe Fever with Thrombocytopenia Syndrome Virus (SFTSV) has emerged as a significant public health threat across East Asia since its identification in China in 2009 [17]. Since then, it has spread across in China and neighboring countries such as Japan, South Korea, and Vietnam [18,19,20,21]. The virus causes Severe Fever with Thrombocytopenia Syndrome (SFTS), a potentially fatal illness characterized by fever, thrombocytopenia, leukocytopenia, and, in severe cases, multi-organ failure [22]. SFTSV was transmitted primarily by the tick Haemaphysalis longicornis but had also been detected in several tick species. Moreover, it has been detected in ruminants, wild animals, and stray animals [23,24]. The presence of SFTSV in both ticks and animals, suggests an increasing transmission risk of SFTSV. In 2019, the first indigenous SFTS case was confirmed in Taiwan [25]. The following investigation was conducted with no findings of SFTSV [26]. In 2022, another SFTS case was confirmed in Orchid Island, Taiwan.

Hence, the purpose of our study was to conduct an environmental investigation due to the confirmation of indigenous SFTS human cases in 2022. Our environmental investigation received a negative result of SFTSV which provides evidence for understanding the prevalence of SFTSV on Orchid Island. The other purpose of our study was to investigate the collected ticks for Hepatozoon, Babesia, and Theileria species with molecular methods.

2. Materials and Methods

An environmental investigation was conducted on Orchid Island in June 2022 and April 2023. During the investigation, 401 wild ticks were collected from local vegetation by flagging, which was conducted between June 2022 and April 2023 with two flags per 50 m^2^ over a period of 4 days. All the collected ticks were kept alive at room temperature until they were transferred to the laboratory on dry ice and stored at −80 °C. All the collected ticks were examined under a dissecting microscope (Leica M205C, Wetzlar, Germany) and identified by morphological characteristics using published keys [27]. After morphological identification, tick species identity was confirmed by PCR and sequencing of the 18S and 12S rRNA genes based on representative ticks (Table S1).

The collected samples were analyzed according to the life stage of ticks. Nymphal and adult ticks from each individual tick sample were homogenized separately via the same method. Larval ticks were separated by collected location and pooled into groups of 2–10 ticks, with an initial pool of 10 ticks. If fewer than 10 ticks remained, they were combined into a smaller pool. Each pool was homogenized in a microcentrifuge tube containing 500 µL of phosphate-buffered saline and stainless-steel beads by using a TissueLyser LT (Qiagen Benelux BV, Venlo, The Netherlands). The supernatants of the homogenized mixtures were collected and stored at −80 °C until subsequent use. To determine whether the collected ticks were infected with SFTSV and tick-borne pathogens recently reported in Asia, molecular tests were performed.

In brief, pathogen RNA was isolated from 140 µL of a homogeneous tick mixture by using the QIAamp viral RNA mini kit (Qiagen GmbH, Hilden, Germany) and then reverse-transcribed (SuperScript IV reverse transcriptase, Invitrogen, Waltham, MA, USA); SFTSV-specific fragments were then detected via PCR (SapphireAmp fast PCR kit, TaKaRa Bio, Kusatsu, Japan) with specific primers (Table S1). In addition, nucleic acids extracted from homogeneous tick mixtures were tested without reverse transcription for piroplasm parasites using a primer set that can simultaneously detect 18S rRNA from Babesia, Theileria, and Hepatozoon species (Table S1). The genomes of tick-borne pathogens (SFTSV and B. microti) and sterile water were included as positive and negative/blank controls, respectively, in each test round. The PCR amplicons used for tick species identification and detection of tick-borne pathogens were further sequenced using an ABI 3730 XL DNA Analyzer (Applied Biosystem, Inc., Foster City, CA, USA). The nucleotide sequences acquired in this study were compared against the NCBI GenBank database by BLAST (https://blast.ncbi.nlm.nih.gov/Blast.cgi) search to identify the species. In addition, the acquired sequences were aligned with sequences already registered in the GenBank database using CLUSTALW. Molecular phylogenetic trees of ticks and tick-borne pathogens were reconstructed by the neighbor-joining method with the Kimura two-parameter model and 1000 bootstrap resampling replicates, as implemented in MEGA software version 11.0.11. Pairwise deletion was used for gaps/missing data.

3. Results

The indigenous SFTS human cases were confirmed on Orchid Island (Figure 1) in 2022. Thus, the environmental investigation on Orchid Island was carried out to identify prevalence of SFTSV in the environment (Figure 1) in June 2022 and April 2023.

A total of 401 H. mageshimaensis samples were captured by flagging them from vegetation, and subsequently identified with characteristics—for instance, the flat anterior surface of the basis capitulum perpendicular to the longitudinal axis of the hypostome. The samples included 377 larvae, 23 nymphs, and 1 adult; and 40 pooled larvae samples, 23 nymphs, and 1 adult were analyzed (Table S2). Taxonomic identification was based on 18S and 12S rRNA gene sequences, and the accession numbers for the representative ticks are shown in Figure S1. Among 64 samples, we received a negative result for SFTSV in all samples and found a positive result for the 18S rRNA gene in a nymph sample. The PCR product was subjected to DNA sequencing analysis. The positive nymphal H. mageshimaensis sample was collected in April 2023 from a grassland inhabited by wild goats. The 18S rRNA gene sequence was identified as a Theileria parasite and phylogenetically grouped within a cluster of T. luwenshuni, which is distinct from other Theileria spp. clusters (Figure 2).

The 18S rRNA gene sequence of T. luwenshuni that we detected on Orchid Island (OR857397) showed a high nucleotide sequence identity with T. luwenshuni sequences from ticks, ruminants, and wild animals in Myanmar and China. These included sequences with GenBank accession numbers LC326009 and LC602484 from Myanmar and OQ540587, OQ134882, JX469518, KC429038, MH208630, OR104985, and OR104986 from China (Table S3).

4. Discussion

Severe Fever with Thrombocytopenia Syndrome Virus is a tick-borne virus that leads to a 30% morality rate. It was first identified in China in 2009. In Taiwan, it was first reported in humans in 2019 [25]. Studies have shown the SFTSV RNA was detected in 29.9% of ruminants and 23% of dogs and cats in Taiwan [23]. However, no SFTSV RNA has been reported from animals or ticks on Orchid Island. In 2022, indigenous SFTS human cases were confirmed on Orchid Island. Thus, an environmental investigation has been conducted to clarify the potential infective source. Despite the prevalence of SFTSV in Taiwan being around 23–29.9% in animals, no SFTSV has been detected in our 401 ticks collected from Orchid Island. The samples we collected from Orchid Island were further examined by the nested-PCR to examine if it was infected with Theileria spp., Babesia spp., and Hepatozoon spp. We discovered that a nymphal H. mageshimaensis carried the DNA of Theileria luwenshuni, which has not been reported before on Orchid Island. The sequence of our finding shares a high similarity with LC326009 and LC602484 from Myanmar and OQ540587, OQ134882, and JX469518 from China. Furthermore, a phylogenetic analysis revealed that our Theileria sequences were grouped within the T. luwenshuni clade, with a high sequence similarity (>99%) to previously reported isolates from Myanmar and China.

Bovine theileriosis has existed in Tibet and China for more than 100 years [28]. Orchid Island is geographically close to many provinces or regions in which Theileria parasites have been detected, such as Korea, Türkiye, northern India, and the Mediterranean region [13,14,15]. These records indicate that the presence of Theileria parasites on the islet may result from bovine theileriosis on the Asian continent and on neighboring islands. Although reports of T. luwenshuni-infected birds are still limited, the distribution of T. luwenshuni may be influenced by the movement of East Asian migratory birds across countries [29]. However, reports on the economic importance of T. luwenshuni are limited. A study by Philip et al. revealed that T. luwenshuni was associated with disease and mortality during an outbreak in sheep in approximately 2005 in Great Britain [30]. In contrast, an outbreak of T. luwenshuni-induced theileriosis in sheep in India did not result in any reported illness [4]. Together, these studies indicate that T. luwenshuni may lead to illness and mortality.

Initially, T. luwenshuni was reported to cause theileriosis in small ruminants, such as cattle, sheep, and goats [31]. A recent study highlighted the ability of T. luwenshuni to infect mice, revealing the complexity of its transmission cycle [32]. Furthermore, we identified T. luwenshuni in a new putative vector, H. mageshimaensis, which has been found on Artiodactyla animals, including goats, cattle, buffaloes, and pigs, on Orchid Island [33]. However, further investigations are needed to clarify the transmission cycle and the impact of T. luwenshuni on ruminants.

In conclusion, this is not only the first time that T. luwenshuni has been found in H. mageshimaensis but also the first report of T. luwenshuni on Orchid Island, Taiwan. Our study indicates that ruminants may be at risk of infection. However, further epidemiological studies are necessary in order to reveal the infection status of T. luwenshuni in domestic goats and other livestock on Orchid Island and in Taiwan. More importantly, our results provide an insight into the distribution of tick-borne parasites in Asia. The limitation of this study is that the primers that we used to screen for Theileria spp. may also detect Babesia spp. and Hepatozoon spp. Thus, we are not able to exclude the possibility of co-infection. Nevertheless, the limitation does not compromise the finding of T. luwenshuni.