Synchronous Langat Virus Infection of Haemaphysalis longicornis Using Anal Pore Microinjection
The tick-borne encephalitis virus (TBEV) serocomplex of flaviviruses consists of arboviruses that cause important diseases in animals and humans. The transmission of this group of viruses is commonly associated with tick species such as Ixodes spp., Dermacentor spp., and Hyalomma spp. In the case of...
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Published in | Viruses Vol. 9; no. 7; p. 189 |
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Abstract | The tick-borne encephalitis virus (TBEV) serocomplex of flaviviruses consists of arboviruses that cause important diseases in animals and humans. The transmission of this group of viruses is commonly associated with tick species such as Ixodes spp., Dermacentor spp., and Hyalomma spp. In the case of Haemaphysalis longicornis, the detection and isolation of flaviviruses have been previously reported. However, studies showing survival dynamics of any tick-borne flavivirus in H. longicornis are still lacking. In this study, an anal pore microinjection method was used to infect adult H. longicornis with Langat virus (LGTV), a naturally attenuated member of the TBEV serocomplex. LGTV detection in ticks was done by real-time PCR, virus isolation, and indirect immunofluorescent antibody test. The maximum viral titer was recorded at 28 days post-inoculation, and midgut cells were shown to be the primary replication site. The tick can also harbor the virus for at least 120 days and can successfully transmit LGTV to susceptible mice as confirmed by detection of LGTV antibodies. However, no transovarial transmission was observed from the egg and larval samples. Taken together, our results highly suggest that anal pore microinjection can be an effective method in infecting adult H. longicornis, which can greatly assist in our efforts to study tick and virus interactions. |
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AbstractList | The tick-borne encephalitis virus (TBEV) serocomplex of flaviviruses consists of arboviruses that cause important diseases in animals and humans. The transmission of this group of viruses is commonly associated with tick species such as
Ixodes
spp.,
Dermacentor
spp., and
Hyalomma
spp. In the case of
Haemaphysalis longicornis
, the detection and isolation of flaviviruses have been previously reported. However, studies showing survival dynamics of any tick-borne flavivirus in
H. longicornis
are still lacking. In this study, an anal pore microinjection method was used to infect adult
H. longicornis
with Langat virus (LGTV), a naturally attenuated member of the TBEV serocomplex. LGTV detection in ticks was done by real-time PCR, virus isolation, and indirect immunofluorescent antibody test. The maximum viral titer was recorded at 28 days post-inoculation, and midgut cells were shown to be the primary replication site. The tick can also harbor the virus for at least 120 days and can successfully transmit LGTV to susceptible mice as confirmed by detection of LGTV antibodies. However, no transovarial transmission was observed from the egg and larval samples. Taken together, our results highly suggest that anal pore microinjection can be an effective method in infecting adult
H. longicornis
, which can greatly assist in our efforts to study tick and virus interactions. The tick-borne encephalitis virus (TBEV) serocomplex of flaviviruses consists of arboviruses that cause important diseases in animals and humans. The transmission of this group of viruses is commonly associated with tick species such as Ixodes spp., Dermacentor spp., and Hyalomma spp. In the case of Haemaphysalis longicornis, the detection and isolation of flaviviruses have been previously reported. However, studies showing survival dynamics of any tick-borne flavivirus in H. longicornis are still lacking. In this study, an anal pore microinjection method was used to infect adult H. longicornis with Langat virus (LGTV), a naturally attenuated member of the TBEV serocomplex. LGTV detection in ticks was done by real-time PCR, virus isolation, and indirect immunofluorescent antibody test. The maximum viral titer was recorded at 28 days post-inoculation, and midgut cells were shown to be the primary replication site. The tick can also harbor the virus for at least 120 days and can successfully transmit LGTV to susceptible mice as confirmed by detection of LGTV antibodies. However, no transovarial transmission was observed from the egg and larval samples. Taken together, our results highly suggest that anal pore microinjection can be an effective method in infecting adult H. longicornis, which can greatly assist in our efforts to study tick and virus interactions. The tick-borne encephalitis virus (TBEV) serocomplex of flaviviruses consists of arboviruses that cause important diseases in animals and humans. The transmission of this group of viruses is commonly associated with tick species such as Ixodes spp., Dermacentor spp., and Hyalomma spp. In the case of Haemaphysalis longicornis, the detection and isolation of flaviviruses have been previously reported. However, studies showing survival dynamics of any tick-borne flavivirus in H. longicornis are still lacking. In this study, an anal pore microinjection method was used to infect adult H. longicornis with Langat virus (LGTV), a naturally attenuated member of the TBEV serocomplex. LGTV detection in ticks was done by real-time PCR, virus isolation, and indirect immunofluorescent antibody test. The maximum viral titer was recorded at 28 days post-inoculation, and midgut cells were shown to be the primary replication site. The tick can also harbor the virus for at least 120 days and can successfully transmit LGTV to susceptible mice as confirmed by detection of LGTV antibodies. However, no transovarial transmission was observed from the egg and larval samples. Taken together, our results highly suggest that anal pore microinjection can be an effective method in infecting adult H. longicornis, which can greatly assist in our efforts to study tick and virus interactions.The tick-borne encephalitis virus (TBEV) serocomplex of flaviviruses consists of arboviruses that cause important diseases in animals and humans. The transmission of this group of viruses is commonly associated with tick species such as Ixodes spp., Dermacentor spp., and Hyalomma spp. In the case of Haemaphysalis longicornis, the detection and isolation of flaviviruses have been previously reported. However, studies showing survival dynamics of any tick-borne flavivirus in H. longicornis are still lacking. In this study, an anal pore microinjection method was used to infect adult H. longicornis with Langat virus (LGTV), a naturally attenuated member of the TBEV serocomplex. LGTV detection in ticks was done by real-time PCR, virus isolation, and indirect immunofluorescent antibody test. The maximum viral titer was recorded at 28 days post-inoculation, and midgut cells were shown to be the primary replication site. The tick can also harbor the virus for at least 120 days and can successfully transmit LGTV to susceptible mice as confirmed by detection of LGTV antibodies. However, no transovarial transmission was observed from the egg and larval samples. Taken together, our results highly suggest that anal pore microinjection can be an effective method in infecting adult H. longicornis, which can greatly assist in our efforts to study tick and virus interactions. |
Author | Yoshii, Kentaro Fujisaki, Kozo Kusakisako, Kodai Tanaka, Tetsuya Mochizuki, Masami Talactac, Melbourne Galay, Remil Hernandez, Emmanuel |
AuthorAffiliation | 5 Department of Clinical and Population Health, College of Veterinary Medicine and Biomedical Sciences, Cavite State University, Cavite 4122, Philippines 2 Department of Pathological and Preventive Veterinary Science, The United Graduate School of Veterinary Science, Yamaguchi University, Yoshida, Yamaguchi 753-8515, Japan 6 National Agriculture and Food Research Organization, 3-1-5 Kannondai, Tsukuba, Ibaraki 305-0856, Japan; acarikf@nifty.com 3 Laboratory of Public Health, Faculty of Veterinary Medicine, Hokkaido University, Kita-ku Kita-18 Nishi-9, Sapporo, Hokkaido 060-0818, Japan; kyoshii@vetmed.hokudai.ac.jp 1 Laboratory of Infectious Diseases, Joint Faculty of Veterinary Medicine, Kagoshima University, 1-21-24 Korimoto, Kagoshima 890-0065, Japan; talactacdvm@cvsu.edu.ph (M.R.T.); jhunemman@yahoo.com (E.P.H.); seigi26jp@yahoo.co.jp (K.K.); masamimochizuki@gmail.com (M.M.) 4 Department of Veterinary Paraclinical Sciences, College of Veterinary Medicine, University of the Philippines Lo |
AuthorAffiliation_xml | – name: 6 National Agriculture and Food Research Organization, 3-1-5 Kannondai, Tsukuba, Ibaraki 305-0856, Japan; acarikf@nifty.com – name: 2 Department of Pathological and Preventive Veterinary Science, The United Graduate School of Veterinary Science, Yamaguchi University, Yoshida, Yamaguchi 753-8515, Japan – name: 3 Laboratory of Public Health, Faculty of Veterinary Medicine, Hokkaido University, Kita-ku Kita-18 Nishi-9, Sapporo, Hokkaido 060-0818, Japan; kyoshii@vetmed.hokudai.ac.jp – name: 5 Department of Clinical and Population Health, College of Veterinary Medicine and Biomedical Sciences, Cavite State University, Cavite 4122, Philippines – name: 4 Department of Veterinary Paraclinical Sciences, College of Veterinary Medicine, University of the Philippines Los Baños, Los Baños, Laguna 4031, Philippines; rlgalay.dvm@gmail.com – name: 1 Laboratory of Infectious Diseases, Joint Faculty of Veterinary Medicine, Kagoshima University, 1-21-24 Korimoto, Kagoshima 890-0065, Japan; talactacdvm@cvsu.edu.ph (M.R.T.); jhunemman@yahoo.com (E.P.H.); seigi26jp@yahoo.co.jp (K.K.); masamimochizuki@gmail.com (M.M.) |
Author_xml | – sequence: 1 givenname: Melbourne surname: Talactac fullname: Talactac, Melbourne – sequence: 2 givenname: Kentaro surname: Yoshii fullname: Yoshii, Kentaro – sequence: 3 givenname: Emmanuel surname: Hernandez fullname: Hernandez, Emmanuel – sequence: 4 givenname: Kodai surname: Kusakisako fullname: Kusakisako, Kodai – sequence: 5 givenname: Remil surname: Galay fullname: Galay, Remil – sequence: 6 givenname: Kozo surname: Fujisaki fullname: Fujisaki, Kozo – sequence: 7 givenname: Masami surname: Mochizuki fullname: Mochizuki, Masami – sequence: 8 givenname: Tetsuya surname: Tanaka fullname: Tanaka, Tetsuya |
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Cites_doi | 10.1007/s00436-010-2053-1 10.1016/j.ttbdis.2013.07.009 10.1139/m69-090 10.3201/eid2110.150126 10.1016/j.molbiopara.2011.12.002 10.1017/S0031182004005220 10.1093/jmedent/31.1.148 10.2307/3276992 10.1016/S0014-4894(03)00113-9 10.1016/j.ttbdis.2011.07.004 10.1099/0022-1317-70-5-1093 10.1016/j.dci.2015.12.015 10.1086/426397 10.1016/j.jviromet.2006.03.009 10.1016/0168-1702(89)90071-3 10.1016/j.virol.2007.03.057 10.1016/j.ibmb.2007.05.006 10.1146/annurev.en.26.010181.000451 10.1016/j.ttbdis.2015.08.002 10.1111/j.1365-2915.2008.00755.x |
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Keywords | anal pore microinjection Langat virus Haemaphysalis longicornis virus transmission |
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Snippet | The tick-borne encephalitis virus (TBEV) serocomplex of flaviviruses consists of arboviruses that cause important diseases in animals and humans. The... |
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SubjectTerms | Anal Canal - virology anal pore microinjection Animals Arachnid Vectors - virology Encephalitis Viruses, Tick-Borne - genetics Encephalitis Viruses, Tick-Borne - physiology Encephalitis, Tick-Borne - transmission Encephalitis, Tick-Borne - virology Haemaphysalis longicornis Ixodes - virology Langat virus Mice Microinjections Real-Time Polymerase Chain Reaction virus transmission |
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Title | Synchronous Langat Virus Infection of Haemaphysalis longicornis Using Anal Pore Microinjection |
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