- Open Access
Abundance and seasonal activity of Haemaphysalis concinna (Acari: Ixodidae) at the border between China and Russia in Northern Inner Mongolia, China
- Hao Meng†1, 2,
- Shiqi Xu†3,
- Zhijun Yu1,
- Ningxin Li1,
- Rongrong Wang1,
- Xiaohe Gao1,
- Xiaolong Yang1 and
- Jingze Liu1Email author
© Meng et al. 2016
- Received: 3 August 2015
- Accepted: 29 December 2015
- Published: 4 January 2016
Haemaphysalis concinna, a three-host tick vector of several pathogens, poses a high risk to the health of humans and livestock. However, knowledge of the seasonal activities, relative density and other ecological characteristics of this tick is quite limited and fragmentary. This knowledge gap represents a bottleneck in our understanding of the health risks associated with tick-borne pathogens.
We conducted a two-year study from April 2012 to March 2014 in Northern Inner Mongolia situated on the China-Russia border, China, to investigate the seasonal activities and relative density of the three developmental stages of H. concinna. During the study period, feeding ticks were removed weekly from domestic sheep and their attachment sites were recorded. Questing ticks were collected weekly from five habitats (broadleaf forest, coniferous forest, shrubs, grassland and mixed coniferous forest) using the flagging-dragging method of capture. Rodents were captured and examined on two consecutive nights each week from June to September in 2012.
H. concinna ticks were found mainly in shrubs and grasslands habitats. Adults were encountered from February to October with the major peak occurring in June. Larvae, which were observed mainly from late April to late September, reached peak numbers in late July. Nymphs were observed mainly from March to October, and their numbers peaked in early July. H. concinna adults and nymphs were found attached to sheep and their most favored sites of attachment were the face and ears. H. concinna larvae were found on two rodent species, Apodemus peninsulae and Eutamias sibiricus.
The relative density and seasonal activities of H. concinna have been systematically reported for Northern Inner Mongolia, China. The information about the hosts infested by H. concinna and its preferred attachment sites on sheep will help efforts to control this tick and the tick-borne diseases carried by it.
- Haemaphysalis concinna
- Relative density
- Seasonal activity
- China-Russia border
Ticks are arthropods with great medical value and veterinary importance [1, 2]. However, as the vectors of viruses, bacteria and protozoa, they also represent an important hazard to human and animal health world-wide [3, 4]. Tick-borne diseases are ranked highly in terms of their impact on the livelihood of resource-poor farming communities in developing countries . In recent years, tick-borne diseases have occurred in almost all provinces of China and in the Russian Far East [6–8]. Therefore, studying tick ecology is a pivotal step towards obtaining a better understanding of the risk posed to animal and human populations by these arthropods .
Haemaphysalis concinna Koch is a three-host tick of significant importance because it serves as a vector of several pathogens of humans and livestock. It has been reported that H. concinna may carry Lyme borreliosis spirochetes , Far-Eastern subtype of tick-borne encephalitis virus , Coxiella burnetii , Rickettsia sibirica  and Crimean-Congo hemorrhagic fever virus . H. concinna is distributed widely in China , Russia and Poland, as well as some parts of temperate Eurasia [15, 16]. In north China, this species was reported to attack domestic animals and humans, with heavy infestations occurring in summer .
A previous study indicated that H. concinna is abundant from spring to summer, but absent during winter in Cangxi County, Sichuan Province, China . However, knowledge of the seasonal activities, relative density and other ecological characters of this tick species is still limited and fragmentary. The lack of detailed knowledge of tick ecology represents a bottleneck to better understanding of the risk of tick-borne pathogen introduction in this region of China . Hence, the present study aimed to investigate the relative density and seasonal feeding and questing activities of H. concinna along the China-Russia border in Northern Inner Mongolia, China. The work may help predict the seasonality of tick-borne diseases and has potential to support the development of strategies for effective tick control.
Ticks on sheep
Ten randomly selected domestic sheep were tagged and allowed to graze in a natural pasture. Tick collections were carried out weekly from April 2012 to March 2014. Ticks were collected between 8:00 and 10:00 while the sheep were restricted. The ten sheep selected for this investigation were not treated with acaricides during the study period.
To determine the preferred attachment sites of the ticks, the body surface of each sheep was divided into seven areas: face, ears, neck, horn bases, back, belly and legs. All attached ticks were removed with a pair of forceps. The ticks collected were identified for species using a stereoscopic microscope  and counted after being brought back to the laboratory.
Ticks on rodents
To investigate the presence of ticks on small mammals, rodents were captured for two consecutive nights each week under natural conditions from June to September in 2012. Two hundred live traps with the measure of 30 × 15 × 10 cm (Sichuan Shujile Trading Co., Chengdu, Sichuan, China) were placed along five lines covering an area of about 10000 m2. The traps, set up at around 18:00 h, were checked the following morning at around 07:00 h, as described previously . Trapped rodents were anaesthetized by injection with 2 % pelltobarbitalum natricum (Tianjin Yongda Chemical Reagent Co., Tianjin, China) at a dose of 0.2 ml/100 g per bodyweight and identified for species according to a previous report . The rodents were checked carefully and all the attached ticks were removed with forceps. Ticks at all three developmental stages were collected and identified . The rodents were released back to the wild in their field of capture after tick removal. The prevalence of infestation was defined as the number of infested rodents divided by the total number of the host species examined, and the mean intensity represents the total number of ticks collected from each rodent species divided by the total number of infested hosts .
From March to October in 2012 and 2013, the seasonal activities of the questing stages of H. concinna were monitored. Five 1000 m2 plots were chosen from five different habitat types representing broadleaf forest (120°04′08″E, 51°35′06″N), coniferous forest (120°03′12″E, 51°37′38″N), shrubs (120°03′20″E, 51°37′01″N), grassland (120°03′09″E, 51°35′06″N) and mixed coniferous forest (120°04′02″E, 51°36′07″N), receptively. We used a 1.2 m × 1 m flannel cloth to observe the ticks, which was pulled weekly over the vegetation in the plots [2, 22]. Relative density was defined as the number of ticks collected in a 1000 m2 plot. Sampling was performed between 09:00 and 11:00 h at each site, and the flannel cloth was checked every 20 m. All the ticks attached to the flannel cloth were removed using tweezers and kept in vials for subsequent counting and identification.
Statistical analyses were performed using STATISTICA Version 6.0 (StatSoft, Tulsa, OK, USA). Analysis of variance (ANOVA) and the correlation coefficient (r) were adopted to compare the collections in different biotopes and the relative density between the feeding and the questing ticks during the research period. The prevalence and mean intensity of infestation of different rodents by H. concinna larvae were analyzed using chi-squared analysis with the Bonferroni adjustment and the Kruskal–Wallis ANOVA test. Origin 7.0 (Microcal, Northampton, MA, USA) and Microsoft Excel were used to draw the figures and manage the data, respectively.
Seasonality and relative density of H. concinna on sheep
Attachment sites on sheep
The face and ears were found to be the preferred attachment sites for H. concinna. 59 % (1843 ticks) of the total number of ticks were found on the face and 33 % (1031 ticks) of ticks were found on the ears. Only 8 % (250 ticks) of the ticks were found on the other body parts of the sheep.
Seasonality of rodent infestation by larvae
Prevalence and mean intensity of infestation of rodents by H. concinna larvae
No. of total
No. of infested
Seasonal changes in relative density of questing ticks
The border region between China and the Far-Eastern region of Russia has a cold temperate continental climate with an annual mean temperature of −3 °C (ranged from −46 to 34 °C), an annual mean rainfall of 400 mm (ranged from 414 to 528 mm), and five different habitat types including broadleaf forest, coniferous forest, shrubs, grassland and mixed coniferous. Because of the long cold weather in winter and the relatively short hot weather in summer, there was much overlap between the activities of three different questing stages of H. concinna in the hottest months (Fig. 4). The seasonal activities of H. concinna in temperate Europe overlap with the three different questing stages during the months of June, July and August . Similar activity patterns of different developmental stages were also reported in H. longicornis  and H. punctata .
The distribution patterns of ticks in one location can vary because of fluctuations in the relative density of host animals or human interventions . Correlations between tick population density and host density have been reported in numerous investigations conducted globally [25, 26]. In the present study, significantly high numbers of ticks were found in grassland and shrubs, unlike the three other habitat types. Different host density is likely to be the major factor contributing to the inter-site differences we observed. Sheep graze mainly in grassland and shrubs and rarely enter other areas. Grassland and shrubs may act as shelter for rodents. These areas probably provide plenty of hosts for ticks, thereby improving their survival rates. If newly molted ticks were put on a host immediately, H. concinna can complete one generation per year in the field . This finding is similar to previous results illustrating that host activity plays an important role in where ticks are distributed in the environment [28–30].
Previous studies indicate that H. concinna adult-stage ticks feed mainly on large-size animals, and occasionally attack humans. The most important hosts for immature stages of H. concinna are small- to medium-sized mammals . Some surveys have been carried out to investigate the occurrence of ticks infesting dogs [31, 32], and one survey reported that the infestation intensity ranged from 1 to 78 ticks per dog . In the present study, sheep and rodents were chosen as the hosts for ticks and the intensity of infestation is shown in Figs. 2 and 3. Wild ruminants usually carry ticks of all life stages in the field. Roe deer and goats were found to be the important hosts for the larvae and nymphs of H. concinna in South Hungary . However, data on such hosts of H. concinna are limited in China because of the difficulty in capturing them. Nevertheless, only a few (n < 10) nymphs were collected from the rodents captured in our study area, although many more nymphs were collected from sheep. Additionally, larvae were only detected on rodents, and adults only captured from sheep. Our statistical analysis showed that the infestation prevalence in A. peninsulae did not differ significantly from that of E. sibiricus (P > 0.05), but the mean intensity of infestation did differ significantly between the two host species (P < 0.05). Larvae were not found on large-sized mammals such as sheep, but they were present on small-sized rodents. This study further revealed the host selection of H. concinna under natural conditions at the border between China and Russia in Northern Inner Mongolia, China.
A large number of studies on tick infestation have been conducted, in which, the whole host body was divided into a small number of areas [34, 35]. In our study, we divided the sheep body into the face, ears, neck, horn bases, and other body parts. The results showed that 59 and 33 % of the total number of H. concinna ticks were distributed on the face and ears, respectively. In contrast, only 8 % of the total ticks collected were found on the other body parts of the sheep. Our result is similar to previous findings for other tick species, including H. bispinosa, H. intermedia , H. longicornis , Ixodes ricinus and Dermacentor reticulatus . The face and ears of sheep are at the front while walking through the vegetation and more importantly, the skin of these areas is thin. The finding of major attachment sites of ticks on sheep would allow the targeted application of pesticides to control ticks on sheep.
The adult and nymphal populations of H. concinna could be controlled by acaricide application on sheep from late April to June. The information provided by our study concerning the preferred attachment sites of ticks could help to improve the effectiveness of acaricides by targeting both the face and ears of sheep susceptible to tick infestation.
Our study has provided data on the relative density and seasonal activities of H. concinna on the China-Russia border in Northern Inner Mongolia, China. The relative density and seasonal activities of H. concinna were studied in questing ticks and ticks infesting sheep and rodents. The face and ears of sheep were found to be the preferred attachment sites for H. concinna. These results should help raise awareness in people living in this region of China about the health risks associated with tick bites, and that ticks are more likely to be encountered in the natural environment from late April to June.
Experiments involving animals were approved by the Animal Ethics Committee of Hebei Normal University (Protocol number: IACUC-127001).
This work was supported by National Natural Science Foundation of China (31272372), Key Basic Research Foundation of Hebei Province, China (15966502D), Natural Science Foundation of Hebei (C2015205124), and Natural Science Research Programs of Educational Department of Hebei Province (Q2012072).
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- Jongejan F, Uilenberg G. The global importance of ticks. Parasitology. 2004;129:S3–14.View ArticlePubMedGoogle Scholar
- Dantas-Torres F, Otranto D. Species diversity and abundance of ticks in three habitats in southern Italy. Ticks Tick Borne Dis. 2013;4:251–5.View ArticlePubMedGoogle Scholar
- Barandika JF, Berriatua E, Barral M, Juste RA, Anda P, García-Pérez AL. Risk factors associated with ixodid tick species distributions in the Basque region in Spain. Med Vet Entomol. 2006;20:177–88.View ArticlePubMedGoogle Scholar
- Yu ZJ, Wang H, Wang TH, Sun WY, Yang XL, Liu JZ. Tick-borne pathogens and the vector potential of ticks in China. Parasit Vectors. 2015;8:24.PubMed CentralView ArticlePubMedGoogle Scholar
- Uspensky I. Tick pests and vectors (Aari: Ixodoidea) in European towns: introduction, persistence and management. Ticks Tick Borne Dis. 2014;5:41–7.View ArticlePubMedGoogle Scholar
- Zhao JW, Wang HY, Wang Y. Regional distribution profiles of tick-borne pathogens in China. Chin J Bio Contr. 2012;5:445–7 (in Chinese).Google Scholar
- Mediannikov O, Sidelnikov Y, Ivanov L, Fournier PE, Tarasevich I, Raoult D. Far eastern tick-borne rickettsiosis identification of Two New cases and tick vector. Ann N Y Acad Sci. 2006;1078:80–8.View ArticlePubMedGoogle Scholar
- Shpynov S, Fournier PE, Rudakov N, Tarasevich I, Raoult D. Detection of members of the genera rickettsia, anaplasma, and ehrlichia in ticks collected in the Asiatic part of Russia. Ann N Y Acad Sci. 2006;1078:378–83.View ArticlePubMedGoogle Scholar
- Dantas-Torres F, Figueredo LA, Otranto D. Seasonal variation in the effect of climate on the biology of Rhipicephalus sanguineus in southern Europe. Parasitology. 2011;138:527–36.View ArticlePubMedGoogle Scholar
- Li Z, Liu Z, Fei J, Xu R, Guo H, Zhang F, et al. Investigation of Lyme disease natural epidemic focus in Shaanxi Province. Chin J Hyg Insect Equip. 2010;16:356–9 (in Chinese).Google Scholar
- Ju J, Gong Z. Relationship between small mammals and natural focus diseases in China. Chin J Vector Biol Contr. 2010;21:293–6 (in Chinese).Google Scholar
- Špitalská E, Kocianová E. Detection of Coxiella burnetii in ticks collected in Slovakia and Hungary. Eur J Epidemiol. 2003;18:263–6.View ArticlePubMedGoogle Scholar
- Tekin S, Bursali A, Mutluay N, Keskin A, Dundar E. Crimean-Congo hemorrhagic fever virus in various ixodid tick species from a highly endemic area. Vet Parasitol. 2012;186:546–52.View ArticlePubMedGoogle Scholar
- Teng KF, Jiang ZJ. Economic Insect Fauna of China, Fasc 39, Acari: Ixodidae. Beijing: Science Press; 1991. p. 359. in Chinese.Google Scholar
- Nosek J. The ecology, bionomics and behaviour of Haemaphysalis (Haemaphysalis) concinna tick. Z Parasitenkd. 1971;36:233–41.PubMedGoogle Scholar
- Fuehrer HP, Biro N, Harl J, Worliczek HL, Beiglböck C, Farkas R, et al. Molecular detection of Theileria sp. ZS TO4 in red deer (Cervus elaphus) and questing Haemaphysalis concinna ticks in Eastern Austria. Vet Parasitol. 2013;197:653–7.View ArticlePubMedGoogle Scholar
- Jiang JF, Jiang BG, Yu JH, Zhang WY, Gao HW, Zhan L, et al. Anaplasma phagocytophilum infection in ticks, China-Russia border. Emerg Infect Dis. 2011;17:932–4.PubMed CentralView ArticlePubMedGoogle Scholar
- Sun JG, Li KJ, Wei H, He ZW. Studies of Haemaphysalis concinna outbreaks in Cangxi Country of Sichuan Province. Chin Vet Sci. 2006;9:719–23 (in Chinese).Google Scholar
- Dantas-Torres F. The brown dog tick, Rhipicephalus sanguineus (Latreille,1806) (Acari: Ixodidae): from taxonomy to control. Vet Parasitol. 2008;152:173–85.View ArticlePubMedGoogle Scholar
- Yu Z, Zheng H, Yang X, Chen Z, Wang D, Hao M, et al. Seasonal abundance and activity of the tick Dermacentor silvarum in Northern China. Med Vet Entomol. 2011;25:25–31.View ArticlePubMedGoogle Scholar
- Chen W, Gao F. Fauna Sinica, Mammalia, Rodentia, vol. 6. Beijing: Science Press; 2000.Google Scholar
- Zheng H, Yu Z, Zhou L, Yang X, Liu J. Seasonal abundance and activity of the hard tick Haemaphysalis longicornis (Acari: Ixodidae) in North China. Exp Appl Acarol. 2012;56:133–41.View ArticlePubMedGoogle Scholar
- Nosek J. The ecology, bionomics, and behaviour of haemaphysalis (aboimisalis) punctata tick in central Europe. Z Parasitenk. 1971;37:198–210.View ArticlePubMedGoogle Scholar
- Schulz M, Mahling M, Pfister K. Abundance and seasonal activity of questing Ixodes ricinus ticks in their natural habitats in southern Germany in 2011. J Vet Ecol. 2014;39:56–65.View ArticleGoogle Scholar
- Wilson ML, Adler GH, Spielman A. Correlation between deer abundance and that of the tick Ixodes dammini (Acari: Ixodidae). Ann Entomol Soc Am. 1985;78:172–6.View ArticleGoogle Scholar
- Gray J, Kahl O, Janetzki C, Stein J. Studies on the ecology of Lyme disease in a deer forest in Country Galway, Ireland. J Med Entomol. 1992;29:915–20.View ArticlePubMedGoogle Scholar
- Meng H, Xu SQ, Yu ZJ, Liu Z, Liu JN, Yang XL, et al. The life cycle and occurrence of Haemaphysalis concinna (Acari: Ixodidae) under field conditions. Ticks Tick Borne Dis. 2014;5:887–91.View ArticlePubMedGoogle Scholar
- Perret JL, Guigoz E, Rais O, Gern L. Influence of saturation deficit and temperature on Ixodes ricinus tick questing activity in a Lyme borreliosis-endemic area (Switzerland). Parasitol Res. 2000;86:554–7.View ArticlePubMedGoogle Scholar
- Oorebeek M, Kleinorfer S. Climate or host availability: what determines the seasonal abundance of ticks? Parasitol Res. 2008;103:871–5.View ArticlePubMedGoogle Scholar
- Andrew DMD, Jennifer LT, Sarah ER. Tick (Ixodes ricinus) abundance and seasonality at recreational sites in the UK: Hazards in relation to fine-scale habitat types revealed by complementary sampling methods. Ticks Tick Borne Dis. 2011;2:67–74.View ArticleGoogle Scholar
- Földvari G, Farkas R. Ixodid tick species attaching to dogs in Hungary. Vet Parasitol. 2005;129:125–31.View ArticlePubMedGoogle Scholar
- Papazahariadou MG, Saridomichelakis MN, Koutinas AF, Papadopoulos EG, Leontides L. Tick infestation of dogs in Thessaloniki, northern Greece. Med Vet Entomol. 2003;17:110–3.View ArticlePubMedGoogle Scholar
- Hornok S, Horvath G, Jongejan F, Farkas R. Ixodid ticks on ruminants, with on-host initiated moulting (apolysis) of Ixodes, Haemaphysalis and Dermacentor larvae. Vet Parasitol. 2012;187:350–3.View ArticlePubMedGoogle Scholar
- Matthee S, Meltzer DGA, Horak IG. Sites of attachment and density assessment of ixodid ticks (Acari: Ixodidae) on impala (Aepyceros melampus). Exp Appl Acarol. 1997;21:179–92.View ArticlePubMedGoogle Scholar
- Duscher GG, Feiler A, Leschnik M, Joachim A. Seasonal and spatial distribution of ixodid tick species feeding on naturally infested dogs from Eastern Austria and the influence of acaricides/repellents on these parameters. Parasit Vectors. 2013;6:76.PubMed CentralView ArticlePubMedGoogle Scholar
- Latha BR, Aiyasami SS, Pattabiraman G, Sivaraman T, Rajavelu G. Seasonal activity of ticks on small ruminants in Tamil Nadu State, India. Trop Anim Health Prod. 2004;36:123–33.View ArticlePubMedGoogle Scholar