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Genetic diversity of Imjin virus in the Ussuri white-toothed shrew (Crocidura lasiura) in the Republic of Korea, 2004-2010
Virology Journalvolume 8, Article number: 56 (2011)
Recently, Imjin virus (MJNV), a genetically distinct hantavirus, was isolated from lung tissues of the Ussuri white-toothed shrew (Crocidura lasiura) captured near the demilitarized zone in the Republic of Korea. To clarify the genetic diversity of MJNV, partial M- and L-segment sequences were amplified from lung tissues of 12 of 37 (32.4%) anti-MJNV IgG antibody-positive Ussuri white-toothed shrews captured between 2004 and 2010. A 531-nucleotide region of the M segment (coordinates 2,255 to 2,785) revealed that the 12 MJNV strains differed by 0-12.2% and 0-2.3% at the nucleotide and amino acid levels, respectively. A similar degree of nucleotide (0.2-11.9%) and amino acid (0-3.8%) difference was found in a 632-nucleotide length of the L segment (coordinates 962 to 1,593) of nine MJNV strains. Phylogenetic analyses, based on the partial M and L segments of MJNV strains generated by the neighbor-joining and maximum likelihood methods, showed geographic-specific clustering, akin to the phylogeography of rodent-borne hantaviruses.
Genetically distinct hantaviruses have been discovered recently in several species of shrews (Order Soricomorpha, Family Soricidae) across four continents, including the Eurasian common shrew (Sorex araneus) , Chinese mole shrew (Anourosorex squamipes) , Therese's shrew (Crocidura theresae) , masked shrew (Sorex cinereus) , dusky shrew (Sorex monticolus) , northern short-tailed shrew (Blarina brevicauda)  and flat-skulled shrew (Sorex roboratus) . Also, a novel hantavirus, named Imjin virus (MJNV), has been isolated from tissues of the Ussuri white-toothed shrew (Crocidura lasiura) captured in the Republic of Korea . As demonstrated recently, Seewis virus (SWSV) harbored by the Eurasian common shrew throughout its broad geographic range exhibits geographic-specific genetic variation, similar to the phylogeography of rodent-borne hantaviruses [8, 9]. A U.S. Army surveillance program, aimed at monitoring the prevalence of Hantaan virus (HTNV) infection in striped field mouse (Apodemus agrarius) populations near the demilitarized zone (DMZ) in Korea, provided an opportunity to investigate the genetic diversity and phylogeography of MJNV in the crocidurine shrew species reservoir.
A total of 466 Ussuri white-toothed shrews were live caught in multiple sites, located 30 to 370 kilometers from Seoul, during March 2004 to May 2010 (Figure 1): Paju City, Yeoncheon-gun, Pocheon City, Dongducheon City, Yangpyeong-gun, Osan City, Suwon City and Pyeongtaek City in Gyeonggi province; Sincheorwon-gun and Pyeongchang-gun in Gangwon province; Gunsan City in Jeollabuk province; and Haenam-gun in Jeollanam province [10–12]. Sera collected from C. lasiura were initially diluted 1:32 in phosphate buffered saline and examined for IgG antibodies against MJNV, using the indirect immunofluorescent antibody (IFA) test . In the absence of a crocidurine shrew species-specific secondary antibody, an equal mixture of fluorescein isothiocyanate-conjugated goat anti-mouse and rat IgG (ICN Pharmaceuticals, Inc., Aurora, OH) was employed.
Total RNA was extracted from lung tissues of anti-MJNV IgG antibody-positive shrews, using the RNA-Bee™ isolation kit (TEL-TEST, Inc., Friendswood, TX), and reverse transcribed, using M-MLV reverse transcriptase (Promega, Madison, WI) and a universal primer (OSM55: 5'-TAGTAGTAGACTCC-3'). Polymerase chain reaction (PCR) was performed in 50-μL mixtures, containing 200 μM dNTP, 0.5 U of SuperTherm Taq DNA polymerase (JMR Holdings, London, UK), 1 μg of cDNA and 5 pM of each primer. Oligonucleotide primer sequences for nested PCR were MJN-M2235F: 5'-CATGGAAGAGTGCAACATGT-3' and MJN-M2855R: 5'-TATGGTCCCTAGATGTACT-3', MJV-M2235F and MJN-M2805R: 5'-TCTATAATAGGATCAGTCAT-3' for the M segment; MJN-L942F: 5'-TCAGAATATAAACCTATGAC-3' MJN-L1636R: 5'-GATCAACAAACCCATATC-3', then MJN-L942F and MJN-L1612R: 5'-CTTACATGAGCAGTGGCTA-3' for the L segment. Initial denaturation was at 94°C for 5 min, followed by 15 cycles of denaturation at 94°C for 40 sec, annealing at 50°C for 40 sec, elongation at 72°C for 1 min, then 25 cycles of denaturation at 94°C for 40 sec, annealing at 52°C for 40 sec and elongation at 72°C for 1 min, in a Mastercycler ep gradient S (Eppendorf AG, Hamburg, Germany).
PCR products were purified by the QIAquick PCR Purification Kit (QIAGEN Inc., Chatsworth, CA), and DNA sequencing was performed in both directions of each PCR product, using the Big-Dye® Terminator v3.1 cycle sequencing kit (Applied Biosystems, Foster City, CA) on an automated sequencer (Model 3730, Applied Biosystems, Foster City, CA) [1, 13]. For phylogenetic analysis, the neighbor-joining (N-J), maximum likelihood and MrBayes methods were employed . Genetic distances were computed by PAUP (Phylogenetic Analysis Using Parsimony, version 4.0b), and topologies were evaluated by bootstrap analysis of 1,000 iterations .
Host identification of shrews infected with MJNV was confirmed by amplification and sequencing of the cytochrome b gene of mitochondrial DNA (mtDNA) using previously described universal primers [7, 15].
Sera from 37 of 466 (7.9%) Ussuri white-toothed shrews contained IgG antibodies against MJNV by the IFA test (Table 1). Of 242 male and 224 female Ussuri shrews, anti-MJNV IgG antibodies were found in sera of 20 males (8.3%) and 17 females (7.5%). Infection rates in shrews from the northern part of Gyeonggi province (Paju City: 10.7%, 6/56; Yeoncheon-gun: 19.4%, 14/72; Pocheon City: 6.9%, 9/130) were higher than rates in the southern part (Yangpyeong-gun: 0%, 0/1; Osan City: 0%, 0/2; Suwon City: 0%, 0/1; and Pyeongtaek City: 4.5%, 8/179). No seropositive shrews were captured in Sincheorwon-gun (0%, 0/7) and Pyeongchang-gun (0%, 0/1) in Gangwon province; Gunsan City (0%, 0/2) in Jeollabuk province; and Haenam-gun (0%, 0/10) in Jeollanam province.
Of the 37 anti-MJNV IgG antibody-positive Ussuri shrews, MJNV RNA was detected in 12 (nine males and three females) by RT-PCR. This difference in gender-specific prevalence was not statistically significant (Fisher's exact test P = 0.09), possibly because of the small sample size of infected shrews. However, the higher proportion of MJNV RNA-positive male shrews was reminiscent of the over-representation of hantavirus infection in male Norway rats , male deer mice [17, 18], and male marsh rice rats .
All 12 MJNV strains were detected in shrews captured in Gyeonggi province: five in Paju City (04-3, 05-10, 05-11, 09-3, 10-8), three in Yeoncheon-gun (04-39, 04-55, 05-14), three in Pocheon City (05-8, 09-21, 09-136), and one in Pyeongtaek City (08-29) (Figure 1, Table 2). Prevalence of MJNV infection, as determined by IFA and RT-PCR, was highest during the summer and spring, respectively (Figure 2), but only a few shrews were captured during the summer compared to other seasons.
Overall genetic analysis of a 531-nucleotide region (coordinates 2,255 to 2,785) of the Gc glycoprotein-encoding M segment revealed that MJNV strains from Korea differed by 0-12.2%. However, the amino acid sequences were highly conserved (0-2.3%) (Table 3). This degree of genetic diversity was higher than that of HTNV strains among striped field mice in Korea . In a 632-nucleotide region of the L segment (coordinates 962 to 1,593), MJNV strains differed by 0.2-11.9% and 0-3.8% at the nucleotide and amino acid levels, respectively (Table 4). This level of interstrain difference for the MJNV L segment was similar with that of SWSV strains in Eurasian common shrews from Russia . The genetic distance between MJNV strains and other crocidurine and soricine shrew-borne hantaviruses, including Thottapalayam virus (TPMV) and Cao Bang virus (CBNV), based on the M segment was 26.9 to 42.2% and 16.9 to 50.8% at the nucleotide and amino acid levels, respectively, and the nucleotide and amino acid distance based on the L segment was 28.5 to 50.5% and 31.9 to 61.0%, respectively.
Phylogenetic analyses of partial L-segment sequences of MJNV strains, using the N-J, maximum likelihood and Bayesian methods, showed geographic-specific genetic variation (Figure 3). In the N-J tree based on the M segment, MJNV strain 04-39 from Yeoncheon-gun, Gyeonggi province, was the most divergent. This was similar to the phylogeography of rodent-borne hantaviruses, including HTNV in Apodemus agrarius, Soochong virus in Apodemus peninsulae, Puumala virus in Myodes glareolus[21, 22], Muju virus in Myodes regulus and Tula virus in Microtus arvalis. Moreover, as recently shown for SWSV in Sorex araneus[8, 9], the geographic-specific genetic variation of MJNV suggested a long-standing virus-host relationship between MJNV and C. lasiura, with local host-specific adaptation.
Genetic studies of MJNV in Ussuri white-toothed shrews captured beyond Korea, in northern China and far eastern Russia, are warranted to further explore if host sharing exists for MJNV among sympatric and syntopic crocidurine shrews. Also, future research on the genetic diversity of other hantaviruses harbored by shrew species that have broad geographic distributions (such as prototype TPMV carried by the Asian house shrew) might provide additional insights into the phylogeography and evolutionary history of hantaviruses and their soricid hosts.
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This work was supported in part by U.S. Public Health Service grants from the National Institute of Allergy and Infectious Diseases (R01AI075057) and the National Center for Research Resources (P2RR018727 and G12RR003061), National Institutes of Health, and grants from the U.S Department of Defense, Global Emerging Infectious Surveillance and Response System (GEIS), and the Armed Forces Medical Intelligence Center (AFMIC).
The authors declare that they have no competing interests.
SHG performed the RNA extraction, RT-PCR and DNA sequencing. HJK provided the preliminary sequencing data and assisted with the phylogenetic analysis. LJB, HCK and TAK arranged the field expeditions and provided the background data on wild-caught shrews. JYN performed the genetic analysis, RY arranged the collaboration and provided scientific oversight, and JWS conceived the research design, coordinated the implementation of the project, including the design of oligonucleotide primers and phylogenetic analysis. All authors read and approved the final manuscript.