key: cord-0770392-11whsns9
authors: Trinachartvanit, Wachareeporn; Kaenkan, Warissara; Nooma, Wanwipa; Jeangkhwoa, Pattraporn; Rakthong, Pakavadee; Baimai, Visut; Ahantarig, Arunee
title: Novel phlebovirus-like-AYUT and Stenotrophomonas maltophilia bacterial co-infection in a Rhipicephalus sanguineus s.l. tick
date: 2021-11-02
journal: Vet Res Commun
DOI: 10.1007/s11259-021-09855-7
sha: 94336d286494bbaeb9ee9df1b2a47318886de270
doc_id: 770392
cord_uid: 11whsns9

Tick-borne viruses and bacteria that can cause diseases of animals and humans have high impact and are of concern as significant threats to human health worldwide. In this research, we screened microorganisms related to those pathogens in ticks from dogs, a cat, and a cow. The techniques used were PCR, DNA sequencing and phylogenetic analysis to detect and classify the microorganisms [Flavivirus, severe fever with thrombocytopenia syndrome virus (SFTSV), Phlebovirus, Coronavirus, Canine Parvovirus, eubacteria, Coxiella and Rickettsia]. A novel virus named Phlebovirus-like-AYUT and Stenotrophomonas maltophilia bacteria were found in one individual tick (Rhipicephalus sanguineus s.l.) from a dog. All tick samples were negative for Rickettsia, while 9/21 (42.9 %) were positive for Coxiella bacteria. The novel virus “Phlebovirus-like-AYUT” (the name derives from Phra Nakhon Si Ayutthaya Province in Thailand) was resolved by phylogenetic analysis of the partial L segment by maximum likelihood (ML) method using MEGA X. The phylogenetic tree also indicated that the virus was related to Phlebovirus in brown dog ticks reported in Trinidad and Tobago. In contrast, Phlebovirus-like-AYUT was in a distinct clade from Lihan tick Phlebovirus-Thailand (LTPV), which was previously found in cow ticks, Rhipicephalus microplus, in Nan Province, Thailand. This study reports the Stenotrophomonas maltophilia bacterium with a novel Phlebovirus-like-AYUT in a brown dog tick. The roles of this bacterium in a virus-positive tick or in viral transmission from animal host requires further investigation.

The role of ticks in spreading pathogenic viruses has been recognized for more than 100 years. This includes the discovery of the Flavivirus Louping ill virus, which has been recognized as being responsible for severe encephalitis in sheep and other livestock (Stockman 1918) . Tick-borne viruses (TBVs) that can pass on diseases to animals and humans have caused much concern because of the increasing prevalence of tick-borne viral diseases (TBVDs) and their important influence on human health (Shen et al. 2018) . The Phlebovirus genus belongs to the Phenuiviridae family (Kuhn et al. 2021) , including viruses transmitted mostly by phlebotomine sandflies and by mosquitoes and ticks (Elliott and Brennan 2014) . Two novel tick-borne Phleboviruses (TBPVs) (1) severe fever with thrombocytopenia syndrome virus (SFTSV) and (2) Heartland virus (HRTV), appear to be related to serious human diseases and have resulted in deaths in eastern Asian countries and in the United States (Shen et al. 2018) . Phlebovirus sequences (L-segment) have been repeatedly identified in both questing and feeding ticks, but particularly in Rhipicephalus sanguineus s.l. specimens (Pimentel et al. 2019 ).

In Amblyomma cajennense tick eggs in southeastern Brazil, 16 S rRNA gene sequence examinations discovered 17 different types of bacteria, identified as Serratia marcescens, Stenotrophomonas maltophilia, Pseudomonas fluorescens, Enterobacter spp., Micrococcus luteus, Ochrobactrum anthropi, Bacillus cereus and Staphylococcus spp., separated into 12 phylogroups (Machado-Ferreira et al. 2015) . Stenotrophomonas maltophilia is a gram-negative multidrug resistant organism (MDRO) that is most often related to respiratory infections in humans (Brooke 2012) . In this study, a novel Phlebovirus-like-AYUT (newly named owing to its identification in a sample from Phra Nakhon Si Ayutthaya Province, Thailand) and S. maltophilia bacteria in the same individual dog tick (R. sanguineus s.l.) were detected.

Ticks were collected from four provinces in Thailand (Ranong, Phatthalung, Phra Nakhon Si Ayutthaya and Bangkok) in June 2021 and preserved in liquid nitrogen. The hosts of the collected ticks were dogs, a cat and a cow. The ticks were washed and identified to the species level using standard taxonomic keys (Tanskul and Inlao 1989) and underwent molecular identification with 16 S+1 and 16 S-1 primers (Black and Piesman 1994) .

DNA and RNA were extracted from the same individual tick using AllPrep DNA/RNA Mini Kit from Qiagen, Germany. In this work, Rickettsia and eubacteria (based on DNA) (Table 1) , were investigated. Additionally, the primers PF1/PF2/PF3 (Flavivirus), SFTSV (SFTSV S segment), HRT-GL2759F/HRT-GL3276R (Phlebovirus L segment), CoVproF/CoVproR (Coronavirus) and CPV-2 F/CPV-2R (Canine Parvovirus) were used for RNA detection in the same set of DNA extraction samples (Table 1 ).

The nucleotide sequences obtained from this study were aligned with other reference sequences available at GenBank using ClustalW in MEGA X. Suitable nucleotide substitution models were selected using MEGA X: Hasegawa-Kishino-Yano with gamma distribution (HKY+G) for Phlebovirus (L 

A total of 37 tick samples were identified as follows. There were (i) 11 R. sanguineus s.l. adult females and 9 males from 6 dogs in Ranong, Phatthalung, Phra Nakhon Si Ayutthaya provinces (6 ticks from Ranong and Phatthalung were pooled in 3 samples) (ii) 2 R. microplus adult females from a cow in Phatthalung province were pooled in 1 sample (iii) 11 Rhipicephalus nymphs from 2 dogs in Ranong and Bangkok (iv) 3 Haemaphysalis nymphs and 1 larva from a cat in Ranong [14 nymphal and larval ticks were pooled in 3 samples (within the same genus)] as shown in Phlebovirus-like-AYUT in reference to its sampling location in Phra Nakhon Si Ayutthaya Province, Thailand. All samples were negative for Rickettsia (17 kDa) bacteria, while 9/21 (42.9 %) were positive for the Coxiella 16 S rRNA gene [Coxiella-like endosymbiont of R. sanguineus s.l. KU892220 (100 %)]. Positive results of Coxiella bacteria were found in Rhipicephalus s.l. from the provinces of Ranong and Phra Nakhon Si Ayutthaya.

Several types of eubacteria were found in R. sanguineus s.l. in this study. Interestingly, co-infection of Phleboviruslike-AYUT and S. maltophilia was found in an R. sanguineus s.l. tick from a dog from Phra Nakhon Si Ayutthaya.

A BLASTn search showed that the partial L segment sequence from R. sanguineus s.l. in this study (Phlebovirus-like-AYUT) (accession number MZ356165) was related to brown dog tick Phlebovirus 2 (BDTPV2) (accession number MN025508) (82.6 %). It also shared 72.4 % and 70.3 % identity respectively with BDTPV1 (accession number MN025506) and Bole tick virus 1 (accession number KM817664). These two viruses have both been detected in R. sanguineus s.l. (from Trinidad and Tobago) and Hyalomma asiaticum (from China). The phylogenetic results based on the partial L segment revealed that the Phlebovirus-like virus identified in this study closely clustered with Phlebovirus from brown dog ticks from Trinidad and Tobago (accession number MN025508) (Fig. 1 ). In contrast, Phlebovirus-like-AYUT was in a distinct sister clade from Lihan tick Phlebovirus-Thailand (LTPV-Thailand), which has previously been found in Rhipicephalus microplus-infested cattle in Nan Province, Thailand. Furthermore, pairwise comparison showed that our sequence had 65.9 % similarity to the LTPV-Thailand virus sequence (accession number MN095537).

Phylogenetic results based on the partial sequence of the 16 S rRNA gene revealed that Stenotrophomonas bacteria obtained in this study (accession number MZ348529) grouped with S. maltophilia strain ES-5 (accession number MK537385) (99.5 % identity by BLASTn) with strong support from a high bootstrap value (99 %) and was retrieved in the clade of S. maltophilia, which showed a clear separation from other groups (Fig. 2 ).

In 2015, LTPV was first found in R. microplus ticks from China and has since been found in other countries (Li et al. 2015; López et al. 2020) . This virus is a Phlebovirus-like. Lihan tick Phlebovirus-Thailand was found in R. microplus from Thailand and was tentatively named LPTV-Thailand; Fig. 1 Phylogenetic relationship based on the partial sequence (687 bp) of Phlebovirus (L segment). The analysis was performed by the maximum likelihood method with the HKY+G model using 1,000 bootstrap replicates. Bootstrap values greater than 50 are shown above the nodes. Bold and circular sequences were obtained in this study. Gouleako virus was used as the outgroup it has 97 to 100 % amino acid identity with Rhipicephalusassociated Phlebovirus 1, a new strain of LTPV identified in R. microplus ticks from China (Temmam et al. 2019) . In this work, an L RNA segment of virus in a brown dog tick sample from Phra Nakhon Si Ayutthaya Province was related to Phlebovirus in brown dog ticks from Trinidad and Tobago (82.6 % similarity) (Sameroff et al. 2019) and was clustered in the same clade with Bole tick virus and LTPV. This group shared a common ancestor with Uukuniemi virus. We named this virus Phlebovirus-like-AYUT and it is novel as indicated by percent DNA sequence similarity as compared with previously described forms.

In addition, S. maltophilia bacteria, which may cause serious infections in humans and have been isolated in several environments, was discovered here for the first time in an R. sanguineus s.l. tick from a domestic dog in Thailand. Rhipicephalus sanguineus s.l. usually infests dogs or domestic animals that are close to humans. This indicates the possibility that R. sanguineus s.l. may act as a vector to transmit disease from animals to humans. Such ticks that accidentally come into close contact with humans are very troubling because they may cause bacterial infection in humans. In Thailand, there have been no previous reports about this bacterium in R. sanguineus s.l. However, there are reports of the presence of Stenotrophomonas sp. in Rhipicephalus eggs and R. microplus-infested cattle from Colombia (Machado-Ferreira et al. 2015; Segura et al. 2020) . Stenotrophomonas maltophilia has also been extracted from the eggs of A. cajennese tick (Machado-Ferreira et al. 2015) . However, our study is the first report of S. maltophilia in R. sanguineus s.l. ticks from Thailand.

Diverse bacterial pathogens and soil organisms have previously been identified in ticks, e.g., Pseudomonas, Acinetobacter, uncultured gamma proteobacterium, Stenotrophomonas and Enterobacter spp. (Moreno et al. 2006 ). In the current study, several types of eubacteria (Moraxella osloensis, Coxiella-like endosymbiont, Hymenobacter gummosus, S. maltophilia and uncultured bacterium) were discovered in R. sanguineus s.l., in which M. osloensis and S. maltophilia are causative organisms of infections in humans. Hymenobacter gummosus is an environmental bacterium that has been isolated from water samples (Chen et al. 2017) . Moraxella osloensis is a causative agent that can be found in several environments. A previous study reported that I. scapularis could be infected with Moraxella species (Moreno et al. 2006) , while S. maltophilia bacteria are pathogenic in humans. Additionally, Coxiella-like endosymbionts have been detected in a wide variety of ticks, including R. sanguineus s.l. (Oskam et al. 2017) .

Co-infection with Phlebovirus-like-AYUT and S. maltophilia was found in an R. sanguineus s.l. tick from a domestic dog in Phra Nakhon Si Ayutthaya Province for the first time. The co-infection of Phlebovirus-like-AYUT (RNA) and S. maltophilia bacteria (DNA) is an important issue because both are pathogenic to humans. The dog infected with these two pathogens exhibited weakness prior to mortality; however, the exact reasons for its death are not fully understood. The roles of this bacterium in a virus-positive tick or in viral transmission from animal hosts also requires further investigation.

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The authors thank Ronnayuth Sudsangiem for technical assistance.

Authors' contributions WT, PR, VB and AA conceived, designed and performed the experiments. PR and PJ carried out the field collection of samples. WT, WK, WN, PJ and AA wrote the manuscript with