Emerging threat of ranavirus: prevalence, genetic diversity, and climatic drivers of Ranavirus (Iridoviridae) in ectothermic vertebrates of Asia

Ranavirus disease, caused by viruses within the genus ( ), is considered a globally emerging infectious disease linked to mass mortality events in both wild and cultured ectothermic vertebrates. Surveillance work is, however, limited in Asia hence prevalence and the dynamics of the disease remain po...

Full description

Saved in:
Bibliographic Details
Published inFrontiers in veterinary science Vol. 10; p. 1291872
Main Authors Herath, Jayampathi, Sun, Dan, Ellepola, Gajaba, Subramaniam, Kuttichantran, Meegaskumbura, Madhava
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 2023
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Ranavirus disease, caused by viruses within the genus ( ), is considered a globally emerging infectious disease linked to mass mortality events in both wild and cultured ectothermic vertebrates. Surveillance work is, however, limited in Asia hence prevalence and the dynamics of the disease remain poorly understood. To understand disease burden and the potential biotic and abiotic drivers in southern China region, we conducted a systematic surveillance of the ranavirus across Guangxi Zhuang Autonomous region (GAR). For this, we used a multifaceted approach involving screening of amphibians and other potential hosts, diagnostic tests, phylogenetic analyses, prevalence estimation, co-infection assessments, and climatic niche analyses. Over one thousand individuals were sampled across 25 sampling sites. We found ninety-two individuals from 18 species of ectothermic vertebrates to be infected with ranavirus. Two lineages were responsible - Rana nigromaculata ranavirus and tiger frog virus were identified using phylogenetic analysis based on the major capsid protein (MCP) gene fragment. Out of these two lineages, the presence of tiger frog virus is rare as we came across only one case. We also found evidence of a co-infection with ranavirus and that can be highly detrimental to host populations; possibly the first such documentation in Asia. Our niche modelling analysis suggests that precipitation seasonality plays an important role in ranavirus prevalence in GAR - southwestern, southeastern, central and northeastern regions of GAR can be considered to be optimum habitats for ranaviruses. Infection rates in wild frog species have reached 100% in some areas, even in nature reserves. Our research also indicates that culture facilities and pet markets are frequently infected, serving as likely vectors for the regional and global spread of ranaviruses. The knowledge generated suggests the need for systematic surveillance, stringent biosecurity measures, and control of international animal trade to prevent further transmission and protection of biodiversity and aquaculture industries across Asia.
AbstractList Ranavirus disease, caused by viruses within the genus Ranavirus (Iridoviridae), is considered a globally emerging infectious disease linked to mass mortality events in both wild and cultured ectothermic vertebrates. Surveillance work is, however, limited in Asia hence prevalence and the dynamics of the disease remain poorly understood. To understand disease burden and the potential biotic and abiotic drivers in southern China region, we conducted a systematic surveillance of the ranavirus across Guangxi Zhuang Autonomous region (GAR).IntroductionRanavirus disease, caused by viruses within the genus Ranavirus (Iridoviridae), is considered a globally emerging infectious disease linked to mass mortality events in both wild and cultured ectothermic vertebrates. Surveillance work is, however, limited in Asia hence prevalence and the dynamics of the disease remain poorly understood. To understand disease burden and the potential biotic and abiotic drivers in southern China region, we conducted a systematic surveillance of the ranavirus across Guangxi Zhuang Autonomous region (GAR).For this, we used a multifaceted approach involving screening of amphibians and other potential hosts, diagnostic tests, phylogenetic analyses, prevalence estimation, co-infection assessments, and climatic niche analyses. Over one thousand individuals were sampled across 25 sampling sites.MethodsFor this, we used a multifaceted approach involving screening of amphibians and other potential hosts, diagnostic tests, phylogenetic analyses, prevalence estimation, co-infection assessments, and climatic niche analyses. Over one thousand individuals were sampled across 25 sampling sites.We found ninety-two individuals from 18 species of ectothermic vertebrates to be infected with ranavirus. Two lineages were responsible - Rana nigromaculata ranavirus and tiger frog virus were identified using phylogenetic analysis based on the major capsid protein (MCP) gene fragment. Out of these two lineages, the presence of tiger frog virus is rare as we came across only one case. We also found evidence of a co-infection with ranavirus and Batrachochytrium dendrobatidis that can be highly detrimental to host populations; possibly the first such documentation in Asia. Our niche modelling analysis suggests that precipitation seasonality plays an important role in ranavirus prevalence in GAR - southwestern, southeastern, central and northeastern regions of GAR can be considered to be optimum habitats for ranaviruses. Infection rates in wild frog species have reached 100% in some areas, even in nature reserves.ResultsWe found ninety-two individuals from 18 species of ectothermic vertebrates to be infected with ranavirus. Two lineages were responsible - Rana nigromaculata ranavirus and tiger frog virus were identified using phylogenetic analysis based on the major capsid protein (MCP) gene fragment. Out of these two lineages, the presence of tiger frog virus is rare as we came across only one case. We also found evidence of a co-infection with ranavirus and Batrachochytrium dendrobatidis that can be highly detrimental to host populations; possibly the first such documentation in Asia. Our niche modelling analysis suggests that precipitation seasonality plays an important role in ranavirus prevalence in GAR - southwestern, southeastern, central and northeastern regions of GAR can be considered to be optimum habitats for ranaviruses. Infection rates in wild frog species have reached 100% in some areas, even in nature reserves.Our research also indicates that culture facilities and pet markets are frequently infected, serving as likely vectors for the regional and global spread of ranaviruses. The knowledge generated suggests the need for systematic surveillance, stringent biosecurity measures, and control of international animal trade to prevent further transmission and protection of biodiversity and aquaculture industries across Asia.DiscussionOur research also indicates that culture facilities and pet markets are frequently infected, serving as likely vectors for the regional and global spread of ranaviruses. The knowledge generated suggests the need for systematic surveillance, stringent biosecurity measures, and control of international animal trade to prevent further transmission and protection of biodiversity and aquaculture industries across Asia.
IntroductionRanavirus disease, caused by viruses within the genus Ranavirus (Iridoviridae), is considered a globally emerging infectious disease linked to mass mortality events in both wild and cultured ectothermic vertebrates. Surveillance work is, however, limited in Asia hence prevalence and the dynamics of the disease remain poorly understood. To understand disease burden and the potential biotic and abiotic drivers in southern China region, we conducted a systematic surveillance of the ranavirus across Guangxi Zhuang Autonomous region (GAR).MethodsFor this, we used a multifaceted approach involving screening of amphibians and other potential hosts, diagnostic tests, phylogenetic analyses, prevalence estimation, co-infection assessments, and climatic niche analyses. Over one thousand individuals were sampled across 25 sampling sites.ResultsWe found ninety-two individuals from 18 species of ectothermic vertebrates to be infected with ranavirus. Two lineages were responsible – Rana nigromaculata ranavirus and tiger frog virus were identified using phylogenetic analysis based on the major capsid protein (MCP) gene fragment. Out of these two lineages, the presence of tiger frog virus is rare as we came across only one case. We also found evidence of a co-infection with ranavirus and Batrachochytrium dendrobatidis that can be highly detrimental to host populations; possibly the first such documentation in Asia. Our niche modelling analysis suggests that precipitation seasonality plays an important role in ranavirus prevalence in GAR – southwestern, southeastern, central and northeastern regions of GAR can be considered to be optimum habitats for ranaviruses. Infection rates in wild frog species have reached 100% in some areas, even in nature reserves.DiscussionOur research also indicates that culture facilities and pet markets are frequently infected, serving as likely vectors for the regional and global spread of ranaviruses. The knowledge generated suggests the need for systematic surveillance, stringent biosecurity measures, and control of international animal trade to prevent further transmission and protection of biodiversity and aquaculture industries across Asia.
Ranavirus disease, caused by viruses within the genus ( ), is considered a globally emerging infectious disease linked to mass mortality events in both wild and cultured ectothermic vertebrates. Surveillance work is, however, limited in Asia hence prevalence and the dynamics of the disease remain poorly understood. To understand disease burden and the potential biotic and abiotic drivers in southern China region, we conducted a systematic surveillance of the ranavirus across Guangxi Zhuang Autonomous region (GAR). For this, we used a multifaceted approach involving screening of amphibians and other potential hosts, diagnostic tests, phylogenetic analyses, prevalence estimation, co-infection assessments, and climatic niche analyses. Over one thousand individuals were sampled across 25 sampling sites. We found ninety-two individuals from 18 species of ectothermic vertebrates to be infected with ranavirus. Two lineages were responsible - Rana nigromaculata ranavirus and tiger frog virus were identified using phylogenetic analysis based on the major capsid protein (MCP) gene fragment. Out of these two lineages, the presence of tiger frog virus is rare as we came across only one case. We also found evidence of a co-infection with ranavirus and that can be highly detrimental to host populations; possibly the first such documentation in Asia. Our niche modelling analysis suggests that precipitation seasonality plays an important role in ranavirus prevalence in GAR - southwestern, southeastern, central and northeastern regions of GAR can be considered to be optimum habitats for ranaviruses. Infection rates in wild frog species have reached 100% in some areas, even in nature reserves. Our research also indicates that culture facilities and pet markets are frequently infected, serving as likely vectors for the regional and global spread of ranaviruses. The knowledge generated suggests the need for systematic surveillance, stringent biosecurity measures, and control of international animal trade to prevent further transmission and protection of biodiversity and aquaculture industries across Asia.
Author Subramaniam, Kuttichantran
Herath, Jayampathi
Sun, Dan
Ellepola, Gajaba
Meegaskumbura, Madhava
Author_xml – sequence: 1
  givenname: Jayampathi
  surname: Herath
  fullname: Herath, Jayampathi
– sequence: 2
  givenname: Dan
  surname: Sun
  fullname: Sun, Dan
– sequence: 3
  givenname: Gajaba
  surname: Ellepola
  fullname: Ellepola, Gajaba
– sequence: 4
  givenname: Kuttichantran
  surname: Subramaniam
  fullname: Subramaniam, Kuttichantran
– sequence: 5
  givenname: Madhava
  surname: Meegaskumbura
  fullname: Meegaskumbura, Madhava
BackLink https://www.ncbi.nlm.nih.gov/pubmed/38076556$$D View this record in MEDLINE/PubMed
BookMark eNp9kc9qGzEQxkVJadI0L9BD0TGF2NW_Xe32FkLaGgKF0p6FVho5CruSK8mGvEUeufLaCaWHXmaG0e_7xPC9RSchBkDoPSVLzrv-k9tByUtGGF9S1tNOslfojLFeLqhs-5O_5lN0kfMDIYQ2QvKOvEGntcq2adoz9HQ7QVr7sMblPoEuODqcdNA7n7b5M94k2OkRgoErvIYAxRts_Q5S9uXxCutgsRn9pOd9mh_2Dj-eHfDlKnkb6-ytho_YBwymxHIPaaqSyhcYki4wy66z1-_Qa6fHDBfHfo5-fbn9efNtcff96-rm-m5hBOVlIRvWdqzrhWF26GVnGdeC0IEzp6XUmptWuN4yMVSCDYNhwnHLCHXccck4P0erg6-N-kFtUj0iPaqovZoXMa2VTvWsERTtnLZOcNFUt9bxgQvTUSGtaaEdrK1elwevTYq_t5CLmnw2MI46QNxmxXrCetEQLiv64Yhuhwnsy8fPiVSAHQCTYs4J3AtCidonr-bk1T55dUy-irp_RMaXGkoMJWk__k_6B20Itig
CitedBy_id crossref_primary_10_1002_jobm_202400289
crossref_primary_10_1007_s10393_025_01703_3
crossref_primary_10_1186_s13567_024_01347_1
crossref_primary_10_1371_journal_ppat_1012736
Cites_doi 10.1080/08997659.2014.886637
10.1007/978-3-319-13755-1_4
10.1007/s00705-012-1316-9
10.1093/bioinformatics/btp348
10.1007/978-3-319-13755-1_8
10.3354/dao02436
10.1006/viro.1996.8435
10.1186/1471-2164-10-224
10.1017/s0030605314000842
10.3390/rs15051291
10.1111/j.1469-1795.2010.00373.x
10.1093/molbev/msab120
10.1371/journal.pone.0092476
10.7589/0090-3558-40.3.420
10.1038/s41467-021-22792-y
10.1111/j.1365-294x.2009.04384.x
10.1038/35002501
10.1007/978-3-319-13755-1_7
10.2193/2008-264
10.1101/2023.01.23.525302
10.3354/dao02096
10.3354/dao048027
10.1007/s10393-014-0950-y
10.1016/j.cub.2021.08.056
10.3390/jof9090911
10.1007/978-3-319-13755-1
10.3354/dao02670
10.1371/journal.ppat.1003850
10.3390/v3112351
10.3354/dao02036
10.1098/rsbl.2009.0793
10.1016/j.micpath.2018.06.047
10.3354/dao03214
10.1672/7-20
10.1038/nmeth.4285
10.22392/actaquatr.577595
10.1002/ece3.8243
10.1186/s13071-021-04796-1
10.1099/vir.0.052837-0
10.1016/j.cub.2014.09.028
10.1371/journal.pone.0090750
10.2994/057.006.0203
10.3201/eid1507.081636
10.1038/sdata.2017.122
10.1016/j.virol.2017.08.001
10.1111/2041-210x.12261
10.1111/j.1558-5646.1964.tb01622.x
10.1371/journal.pone.0145864
10.1111/tbed.13534
10.1016/j.aquaculture.2012.12.018
10.1111/j.2041-210x.2009.00001.x
10.1186/1297-9716-44-101
10.1002/aah.10090
10.4269/ajtmh.16-0427
10.1139/facets-2020-0043
ContentType Journal Article
Copyright Copyright © 2023 Herath, Sun, Ellepola, Subramaniam and Meegaskumbura.
Copyright_xml – notice: Copyright © 2023 Herath, Sun, Ellepola, Subramaniam and Meegaskumbura.
DBID AAYXX
CITATION
NPM
7X8
DOA
DOI 10.3389/fvets.2023.1291872
DatabaseName CrossRef
PubMed
MEDLINE - Academic
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
PubMed
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic

PubMed
Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Veterinary Medicine
EISSN 2297-1769
ExternalDocumentID oai_doaj_org_article_18fadf43454b46f3b34c8147dc6e6bdd
38076556
10_3389_fvets_2023_1291872
Genre Journal Article
GroupedDBID 53G
5VS
9T4
AAFWJ
AAYXX
ACGFS
ACXDI
ADBBV
ADRAZ
AFPKN
ALMA_UNASSIGNED_HOLDINGS
AOIJS
BCNDV
CITATION
ECGQY
GROUPED_DOAJ
HYE
KQ8
M48
M~E
OK1
PGMZT
RPM
EYRJQ
IAG
IAO
IEA
IPNFZ
NPM
RIG
7X8
ID FETCH-LOGICAL-c413t-752682894c2db978d23a401b32fa77aa3c64f9d24b4c22bbc24f3d201f3f37233
IEDL.DBID M48
ISSN 2297-1769
IngestDate Wed Aug 27 01:31:29 EDT 2025
Fri Jul 11 01:14:52 EDT 2025
Thu Jan 02 22:40:53 EST 2025
Thu Apr 24 23:04:01 EDT 2025
Tue Jul 01 04:03:21 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Keywords climatic niche
phylogenetic relationships
co-infection
ranavirus
introduced species
Language English
License Copyright © 2023 Herath, Sun, Ellepola, Subramaniam and Meegaskumbura.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c413t-752682894c2db978d23a401b32fa77aa3c64f9d24b4c22bbc24f3d201f3f37233
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
OpenAccessLink https://doaj.org/article/18fadf43454b46f3b34c8147dc6e6bdd
PMID 38076556
PQID 2902945037
PQPubID 23479
ParticipantIDs doaj_primary_oai_doaj_org_article_18fadf43454b46f3b34c8147dc6e6bdd
proquest_miscellaneous_2902945037
pubmed_primary_38076556
crossref_primary_10_3389_fvets_2023_1291872
crossref_citationtrail_10_3389_fvets_2023_1291872
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2023-00-00
PublicationDateYYYYMMDD 2023-01-01
PublicationDate_xml – year: 2023
  text: 2023-00-00
PublicationDecade 2020
PublicationPlace Switzerland
PublicationPlace_xml – name: Switzerland
PublicationTitle Frontiers in veterinary science
PublicationTitleAlternate Front Vet Sci
PublicationYear 2023
Publisher Frontiers Media S.A
Publisher_xml – name: Frontiers Media S.A
References Lessler (ref36) 2017; 96
Mu (ref40) 2018; 123
Teacher (ref59) 2010; 13
Mao (ref19) 1997; 229
Gray (ref23) 2015
Huang (ref42) 2009; 10
Rowley (ref8) 2010; 6
Chinchar (ref6) 2017
Mazzoni (ref47) 2009; 86
Steidl (ref30) 2008; 72
(ref56) 2019
Kolby (ref10) 2014; 9
Price (ref58) 2014; 24
Laurent (ref29) 1964; 18
Tamura (ref20) 2021; 38
Zhang (ref45) 2001; 48
Herczeg (ref55) 2021; 14
Kalyaanamoorthy (ref22) 2017; 14
Lei (ref43) 2012; 157
Sriwanayos (ref48) 2020; 5
Sun (ref35) 2023
Pessier (ref14) 2017
Bardua (ref28) 2021; 12
Petranka (ref60) 2003; 23
Miller (ref5) 2011; 3
Sun (ref34) 2023; 9
Earl (ref57) 2014; 11
Karger (ref27) 2017; 4
Annis (ref24) 2004; 40
Gold (ref16) 2013; 107
Chen (ref39) 2013; 44
Gray (ref13) 2012; 99
Cunningham (ref50) 2015; 50
Stilwell (ref18) 2018; 128
Goka (ref25) 2009; 18
Hao (ref12) 2023; 15
Zhou (ref51) 2013
Herath (ref3) 2021; 11
Xiao (ref17) 2019; 31
Une (ref44) 2009; 15
Both (ref46) 2011; 6
Gray (ref1) 2015
Myers (ref37) 2000; 403
Yu (ref41) 2020
Bryan (ref15) 2009; 84
Capella-Gutierrez (ref21) 2009; 25
Brenes (ref52) 2014; 26
Abrams (ref49) 2013; 94
Chinchar (ref2) 2014; 10
Chen (ref38) 2007; 92
Brunner (ref4) 2015
Erişmiş (ref53) 2019; 15
Price (ref7) 2017; 511
Burnham (ref26) 2002
Brenes (ref11) 2014; 9
Warne (ref54) 2016; 11
Hughes (ref9) 2021; 31
Miller (ref33) 2015
Muscarella (ref32) 2014; 5
Zuur (ref31) 2010; 1
References_xml – volume: 26
  start-page: 118
  year: 2014
  ident: ref52
  article-title: Susceptibility of fish and turtles to three ranaviruses isolated from different ectothermic vertebrate classes
  publication-title: J Aquat Anim Health
  doi: 10.1080/08997659.2014.886637
– start-page: 71
  year: 2015
  ident: ref4
  article-title: Ranavirus ecology and evolution: from epidemiology to extinction
  publication-title: Ranaviruses
  doi: 10.1007/978-3-319-13755-1_4
– volume: 157
  start-page: 1559
  year: 2012
  ident: ref43
  article-title: Sequencing and analysis of the complete genome of Rana grylio virus (RGV)
  publication-title: Arch Virol
  doi: 10.1007/s00705-012-1316-9
– volume: 92
  start-page: 480
  year: 2007
  ident: ref38
  article-title: Biogeography and hotspots of amphibian species of China: implications to reserve selection and conservation
  publication-title: Curr Sci
– volume: 25
  start-page: 1972
  year: 2009
  ident: ref21
  article-title: trimAl: a tool for automated alignment trimming in large-scale phylogenetic analyses
  publication-title: Bioinformatics
  doi: 10.1093/bioinformatics/btp348
– start-page: 209
  year: 2015
  ident: ref23
  article-title: Design and analysis of Ranavirus studies: surveillance and assessing risk
  publication-title: Ranaviruses
  doi: 10.1007/978-3-319-13755-1_8
– volume: 99
  start-page: 1
  year: 2012
  ident: ref13
  article-title: Reliability of non-lethal surveillance methods for detecting ranavirus infection
  publication-title: Dis Aquat Org
  doi: 10.3354/dao02436
– volume: 229
  start-page: 212
  year: 1997
  ident: ref19
  article-title: Molecular characterization, sequence analysis, and taxonomic position of newly isolated fish Iridoviruses
  publication-title: Virology
  doi: 10.1006/viro.1996.8435
– volume: 10
  start-page: 224
  year: 2009
  ident: ref42
  article-title: Complete sequence determination of a novel reptile iridovirus isolated from soft-shelled turtle and evolutionary analysis of Iridoviridae
  publication-title: BMC Genomics
  doi: 10.1186/1471-2164-10-224
– volume: 50
  start-page: 265
  year: 2015
  ident: ref50
  article-title: Development of the Chinese giant salamander Andrias davidianus farming industry in Shaanxi Province, China: conservation threats and opportunities
  publication-title: Oryx
  doi: 10.1017/s0030605314000842
– volume: 15
  start-page: 1291
  year: 2023
  ident: ref12
  article-title: Evaluation of global land use–land cover data products in Guangxi, China
  publication-title: Remote Sens
  doi: 10.3390/rs15051291
– volume: 13
  start-page: 514
  year: 2010
  ident: ref59
  article-title: Assessing the long-term impact of Ranavirus infection in wild common frog populations
  publication-title: Anim Conserv
  doi: 10.1111/j.1469-1795.2010.00373.x
– volume: 38
  start-page: 3022
  year: 2021
  ident: ref20
  article-title: MEGA11: molecular evolutionary genetics analysis version 11
  publication-title: Mol Biol Evol
  doi: 10.1093/molbev/msab120
– volume: 9
  start-page: e92476
  year: 2014
  ident: ref11
  article-title: Transmission of ranavirus between ectothermic vertebrate hosts
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0092476
– start-page: 589
  volume-title: Manual of diagnostic tests for aquatic animals
  year: 2019
  ident: ref56
– volume: 40
  start-page: 420
  year: 2004
  ident: ref24
  article-title: A DNA-bases assay identifies Batrachochytrium dendrobatidis in amphibians
  publication-title: J Wildl Dis
  doi: 10.7589/0090-3558-40.3.420
– volume: 12
  start-page: 2503
  year: 2021
  ident: ref28
  article-title: Size, microhabitat, and loss of larval feeding drive cranial diversification in frogs
  publication-title: Nat Commun
  doi: 10.1038/s41467-021-22792-y
– volume: 18
  start-page: 4757
  year: 2009
  ident: ref25
  article-title: Amphibian chytridiomycosis in Japan: distribution, haplotypes and possible route of entry into Japan
  publication-title: Mol Ecol
  doi: 10.1111/j.1365-294x.2009.04384.x
– volume: 403
  start-page: 853
  year: 2000
  ident: ref37
  article-title: Biodiversity hotspots for conservation priorities
  publication-title: Nature
  doi: 10.1038/35002501
– start-page: 171
  year: 2015
  ident: ref33
  article-title: Comparative pathology of ranaviruses and diagnostic techniques
  publication-title: Ranaviruses
  doi: 10.1007/978-3-319-13755-1_7
– volume: 72
  start-page: 1658
  year: 2008
  ident: ref30
  article-title: Model based inference in the life sciences: a primer on evidence. David R. Anderson
  publication-title: J Wildl Manag
  doi: 10.2193/2008-264
– year: 2023
  ident: ref35
  article-title: New climatically specialized lineages of Batrachochytrium dendrobatidis and their sub-lethal effects on amphibians establish the Asiatic origins of the pathogen
  publication-title: bioRxiv
  doi: 10.1101/2023.01.23.525302
– volume: 86
  start-page: 181
  year: 2009
  ident: ref47
  article-title: Mass mortality associated with a frog virus 3- like Ranavirus infection in farmed tadpoles Rana catesbeiana from Brazil
  publication-title: Dis Aquat Org
  doi: 10.3354/dao02096
– volume: 48
  start-page: 27
  year: 2001
  ident: ref45
  article-title: Characterization of an iridovirus from the cultured pig frog Rana grylio with lethal syndrome
  publication-title: Dis Aquat Organ
  doi: 10.3354/dao048027
– volume: 11
  start-page: 581
  year: 2014
  ident: ref57
  article-title: Introduction of ranavirus to isolated wood frog populations could cause local extinction
  publication-title: EcoHealth
  doi: 10.1007/s10393-014-0950-y
– volume: 31
  start-page: R1218
  year: 2021
  ident: ref9
  article-title: Wildlife trade
  publication-title: Curr Biol
  doi: 10.1016/j.cub.2021.08.056
– volume-title: DR a. model selection and multimodel inference: a practical information-theoretic approach
  year: 2002
  ident: ref26
– volume: 9
  start-page: 911
  year: 2023
  ident: ref34
  article-title: Ecological barriers for an amphibian pathogen: a narrow ecological niche for Batrachochytrium salamandrivorans in an Asian Chytrid hotspot
  publication-title: J Fungi
  doi: 10.3390/jof9090911
– volume-title: Ranaviruses
  year: 2015
  ident: ref1
  doi: 10.1007/978-3-319-13755-1
– volume: 107
  start-page: 77
  year: 2013
  ident: ref16
  article-title: Efficacy of common disinfectants and terbinafine in inactivating the growth of Batrachochytrium dendrobatidis in culture
  publication-title: Dis Aquat Org
  doi: 10.3354/dao02670
– volume: 10
  start-page: e1003850
  year: 2014
  ident: ref2
  article-title: Ranaviruses: not just for frogs
  publication-title: PLoS Pathog
  doi: 10.1371/journal.ppat.1003850
– volume: 3
  start-page: 2351
  year: 2011
  ident: ref5
  article-title: Ecopathology of ranaviruses infecting amphibians
  publication-title: Viruses
  doi: 10.3390/v3112351
– volume: 84
  start-page: 89
  year: 2009
  ident: ref15
  article-title: Efficacy of select disinfectants at inactivating Ranavirus
  publication-title: Dis Aquat Org
  doi: 10.3354/dao02036
– volume: 6
  start-page: 336
  year: 2010
  ident: ref8
  article-title: Impending conservation crisis for southeast Asian amphibians
  publication-title: Biol Lett
  doi: 10.1098/rsbl.2009.0793
– volume: 123
  start-page: 111
  year: 2018
  ident: ref40
  article-title: FV3-like ranavirus infection outbreak in black-spotted pond frogs (Rana nigromaculata) in China
  publication-title: Microb Pathog
  doi: 10.1016/j.micpath.2018.06.047
– volume: 128
  start-page: 105
  year: 2018
  ident: ref18
  article-title: Partial validation of a TaqMan real-time quantitative PCR for the detection of ranaviruses
  publication-title: Dis Aquat Org
  doi: 10.3354/dao03214
– volume: 23
  start-page: 278
  year: 2003
  ident: ref60
  article-title: Responses of amphibians to restoration of a southern Appalachian wetland: perturbations confound post-restoration assessment
  publication-title: Wetlands
  doi: 10.1672/7-20
– volume: 14
  start-page: 587
  year: 2017
  ident: ref22
  article-title: ModelFinder: fast model selection for accurate phylogenetic estimates
  publication-title: Nat Methods
  doi: 10.1038/nmeth.4285
– volume: 15
  start-page: 239
  year: 2019
  ident: ref53
  article-title: Investigation of prevalence of co-infection by Batrachochytrium dendrobatidis and ranavirus in endemic Beyşehir frog (Pelophylax caralitanus)
  publication-title: Acta Aquat Turc
  doi: 10.22392/actaquatr.577595
– volume: 11
  start-page: 15498
  year: 2021
  ident: ref3
  article-title: Patterns of infection, origins, and transmission of ranaviruses among the ectothermic vertebrates of Asia
  publication-title: Ecol Evol
  doi: 10.1002/ece3.8243
– volume: 14
  start-page: 296
  year: 2021
  ident: ref55
  article-title: Host–multiparasite interactions in amphibians: a review
  publication-title: Parasit Vectors
  doi: 10.1186/s13071-021-04796-1
– volume: 94
  start-page: 2082
  year: 2013
  ident: ref49
  article-title: Recent host-shifts in ranaviruses: signatures of positive selection in the viral genome
  publication-title: J Gen Virol
  doi: 10.1099/vir.0.052837-0
– volume: 24
  start-page: 2586
  year: 2014
  ident: ref58
  article-title: Collapse of amphibian communities due to an introduced ranavirus
  publication-title: Curr Biol
  doi: 10.1016/j.cub.2014.09.028
– volume: 9
  start-page: e90750
  year: 2014
  ident: ref10
  article-title: First evidence of amphibian Chytrid fungus (Batrachochytrium dendrobatidis) and Ranavirus in Hong Kong amphibian trade
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0090750
– volume: 6
  start-page: 127
  year: 2011
  ident: ref46
  article-title: Widespread occurrence of the American bullfrog, Lithobates catesbeianus (Shaw 1802) (Anura: Ranidae), in Brazil
  publication-title: S Am J Herpetol
  doi: 10.2994/057.006.0203
– volume: 15
  start-page: 1146
  year: 2009
  ident: ref44
  article-title: Ranavirus outbreak in north American bullfrogs (Rana catesbeiana), Japan, 2008
  publication-title: Emerg Infect Dis
  doi: 10.3201/eid1507.081636
– volume: 4
  start-page: 170122
  year: 2017
  ident: ref27
  article-title: Climatologies at high resolution for the earth’s land surface areas
  publication-title: Sci Data
  doi: 10.1038/sdata.2017.122
– volume: 511
  start-page: 272
  year: 2017
  ident: ref7
  article-title: From fish to frogs and beyond: impact and host range of emergent ranaviruses
  publication-title: Virology
  doi: 10.1016/j.virol.2017.08.001
– volume: 5
  start-page: 1198
  year: 2014
  ident: ref32
  article-title: ENMeval: an R package for conducting spatially independent evaluations and estimating optimal model complexity for Maxent ecological niche models
  publication-title: Methods Ecol Evol
  doi: 10.1111/2041-210x.12261
– volume: 18
  start-page: 458
  year: 1964
  ident: ref29
  article-title: Adaptive modifications in frogs of an isolated highland fauna in Central Africa
  publication-title: Evolution
  doi: 10.1111/j.1558-5646.1964.tb01622.x
– volume-title: Virus taxonomy the ICTV report on virus classification and taxon nomenclature Iridoviridae chapter Iridoviridae citation
  year: 2017
  ident: ref6
– volume: 11
  start-page: e0145864
  year: 2016
  ident: ref54
  article-title: Co-infection by Chytrid fungus and Ranaviruses in wild and harvested frogs in the tropical Andes
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0145864
– start-page: 1954
  year: 2020
  ident: ref41
  article-title: Characterization and genomic analysis of a ranavirus associated with cultured black-spotted pond frogs (Rana nigromaculata) tadpoles mortalities in China
  publication-title: Transbound Emerg Dis
  doi: 10.1111/tbed.13534
– start-page: 66
  year: 2013
  ident: ref51
  article-title: Characterization of a ranavirus isolated from the Chinese giant salamander (Andrias davidianus, Blanchard, 1871) in China
  publication-title: Aquaculture
  doi: 10.1016/j.aquaculture.2012.12.018
– volume: 1
  start-page: 3
  year: 2010
  ident: ref31
  article-title: A protocol for data exploration to avoid common statistical problems
  publication-title: Methods Ecol Evol
  doi: 10.1111/j.2041-210x.2009.00001.x
– volume-title: A manual for control of infectious diseases in amphibian survival assurance colonies and reintroduction programs
  year: 2017
  ident: ref14
– volume: 44
  start-page: 101
  year: 2013
  ident: ref39
  article-title: Genome architecture changes and major gene variations of Andrias davidianus ranavirus (ADRV)
  publication-title: Vet Res
  doi: 10.1186/1297-9716-44-101
– volume: 31
  start-page: 364
  year: 2019
  ident: ref17
  article-title: Isolation and characterization of a ranavirus associated with disease outbreaks in cultured hybrid grouper (♀ Tiger grouper Epinephelus fuscoguttatus × ♂ Giant Grouper E. lanceolatus) in Guangxi, China
  publication-title: J Aquat Anim Health
  doi: 10.1002/aah.10090
– volume: 96
  start-page: 1270
  year: 2017
  ident: ref36
  article-title: What is a hotspot anyway?
  publication-title: Am J Trop Med Hyg
  doi: 10.4269/ajtmh.16-0427
– volume: 5
  start-page: 963
  year: 2020
  ident: ref48
  article-title: Phylogenomic characterization of ranaviruses isolated from cultured fish and amphibians in Thailand
  publication-title: Facets
  doi: 10.1139/facets-2020-0043
SSID ssj0001547380
Score 2.2413108
Snippet Ranavirus disease, caused by viruses within the genus ( ), is considered a globally emerging infectious disease linked to mass mortality events in both wild...
Ranavirus disease, caused by viruses within the genus Ranavirus (Iridoviridae), is considered a globally emerging infectious disease linked to mass mortality...
IntroductionRanavirus disease, caused by viruses within the genus Ranavirus (Iridoviridae), is considered a globally emerging infectious disease linked to mass...
SourceID doaj
proquest
pubmed
crossref
SourceType Open Website
Aggregation Database
Index Database
Enrichment Source
StartPage 1291872
SubjectTerms climatic niche
co-infection
introduced species
phylogenetic relationships
ranavirus
SummonAdditionalLinks – databaseName: DOAJ Directory of Open Access Journals
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lb9QwELZQT1wQlEeXUmQkDqA2dONx7IRbQVQL0nKoaNVb5KeItM2ustn-Dn5yZ5zsqhyAC5coSvyKZ5yZsWe-YeytDOArZ0zmXVCZzPFiYm4zAKhciVwSEuLN_LuaXcpv18X1vVRf5BM2wAMPE3eal9H4KEEW0koVwYJ0ZS61dyoo6z39fVHm3TOmhvhgqaGcDlEyaIVVp_E29ATPLeADiri81OI3SZQA-_-sZSZpc_6YPRrVRH42DO8JexDafbZ_Rb4rKYCWz8cz8afsF-0rUaoh3v8kDZAvI0cBZG6bbrP-yFcdAXrT-j3hyCwUs8j91hnjhJvWc7doEnAr9116QS1cbFvg7752jV_ifeNNeM-bltNGP-mNN1iF0jnT2TNqrFTtbN2YZ-zy_MuPz7NszLOQORRhfaYJ8gUNL-mEt2hVegEGzS4LIhqtjQGnZKy8QAI4Iax1QkbwqDlEiKAFwHO21y7bcMC4qooi2ujIt1lqLEv4eFYUoUJNDS2jCcu3c167EYSccmEsajRGiE51olNNdKpHOk3Y8a7OaoDg-GvpT0TKXUmCz04PkKnqkanqfzHVhL3ZMkKNy43OUEwblhvsqpqKShZT0BP2YuCQXVeE3a-KQr38H0M4ZA_ps4bdnldsr-824Qj1n96-Tqx-BzMwBUI
  priority: 102
  providerName: Directory of Open Access Journals
Title Emerging threat of ranavirus: prevalence, genetic diversity, and climatic drivers of Ranavirus (Iridoviridae) in ectothermic vertebrates of Asia
URI https://www.ncbi.nlm.nih.gov/pubmed/38076556
https://www.proquest.com/docview/2902945037
https://doaj.org/article/18fadf43454b46f3b34c8147dc6e6bdd
Volume 10
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1Zi9RAEG6W9cUX0fUaj6UFHxQ366ar0z0RRFZxWYXxQRzZt9CnBsZkzWQW_Rf-ZKs6yYDgCr6EHN2do6pSX_XxFWOPZQBfOmMy74LKZI4bE3ObAUDp5qglITHeLD6o06V8f1ac7bAp3dH4Add_De0on9SyWx3--P7zFRr8S4o40d8-jxehJ-ZtAYfovfK5xl_yFfRMmgx1McL9YdWw1JCSqQlRJm7EclhHc0kzf_iqROl_OQ5N_ujkOrs2Akl-PEj-BtsJzR7b-0yzW9ISW74YR81vsl_U80TJiHj_lTAibyNHF2Uu6m6zfsHPO6L8Jgs_4KhOtKqR-2m6xgE3jeduVSdqV-67dIFa-Di1wJ-862rf4n7tTXjK64bTUAAhy29YhRI-0-g0YlqqdryuzS22PHn76c1pNmZiyBw6uT7TRAqDoZl0wluMO70Ag4GZBRGN1saAUzKWXkiLJYS1TsgIHrFFhAhaANxmu03bhLuMq7Iooo2OZj9LjWWJQc-KIpSI5TB2mrF8-uaVG2nKKVvGqsJwheRUJTlVJKdqlNOMPdvWOR9IOv5Z-jWJcluSCLbTibb7Uo32WuXzaHyUIAt8JxXBgnTzXGrvVFDW-xl7NClChQZJoyymCe0Gb1UeiVIWR6Bn7M6gIdtbEbu_Kgp1778e-D67SodDx88Dttt3m_AQoVBv91MXwn7S8t9k5gdz
linkProvider Scholars Portal
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Emerging+threat+of+ranavirus%3A+prevalence%2C+genetic+diversity%2C+and+climatic+drivers+of+Ranavirus+%28Iridoviridae%29+in+ectothermic+vertebrates+of+Asia&rft.jtitle=Frontiers+in+veterinary+science&rft.au=Herath%2C+Jayampathi&rft.au=Sun%2C+Dan&rft.au=Ellepola%2C+Gajaba&rft.au=Subramaniam%2C+Kuttichantran&rft.date=2023&rft.issn=2297-1769&rft.eissn=2297-1769&rft.volume=10&rft_id=info:doi/10.3389%2Ffvets.2023.1291872&rft.externalDBID=n%2Fa&rft.externalDocID=10_3389_fvets_2023_1291872
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2297-1769&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2297-1769&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2297-1769&client=summon