Printer Friendly

Novel arenavirus, Zambia.

Arenavirus, a bisegmented ambisense single-stranded RNA virus, is 1 of the viral pathogens responsible for hemorrhagic fever in Africa and South America. Until 2007, Lassa virus was the only known arenavirus to cause hemorrhagic fever in Africa. However, during September-October 2008, 5 hemorrhagic fever cases caused by a novel arenavirus named Lujo virus occurred in South Africa (1). The initial case occurred in Zambia; the patient was transported to South Africa for treatment, where the virus spread to 4 other persons. Four patients died; the source of infection in the index patient was not determined.

The natural reservoir of arenavirus in Africa is rodents of the family Muridae, especially Mastomys natalensis, and nonpathogenic arenaviruses have been found in areas surrounding Zambia (2-5). To further the epizootiologic understanding of arenaviruses, we investigated their prevalence and genetic background among M. natalensis rodents in Zambia during May 22-August 28, 2009.

The Study

We conducted the study with permission from the Zambia Wildlife Authority. Sherman traps (H.B. Sherman, Inc., Tallahassee, FL, USA) were set up on dry, arable lands or scrublands surrounding the cities of Lusaka (15[degrees]26'30.85"S, 28[degrees]26'51.09"E), Namwala (15[degrees]43'01.37"S, 26[degrees]42'33.41"E), and Mfuwe (13[degrees]6'47.92"S, 31[degrees]48'17.24"E). We captured 57, 48, and 158 rodents in each of these cities, respectively. Rodents were euthanized with diethyl ether, and kidney tissues were harvested and stored at -80[degrees]C.

For species identification of the rodents, DNA was extracted by using the DNeasy Blood and Tissue Kit (QIAGEN, Chuo-ku, Tokyo). Mastomys spp. were identified by mitochondrial cytochrome b gene (cytb) (6). Two primers, mCytb-F (5'-ACCCACTGTT TAAAATTATTAACCACTC-3') and mCytb-R (5'-CTC CGATTCAAGTTAGTACTAGTAG-3') were used for PCR amplification of cytb. BLAST (www.ncbi.nlm.nih. gov/blast.cgi) search analysis against the amplified cytb fragments showed that 23 of 57 rodents from Lusaka, 24 of 48 from Namwala, and 143 of 158 from Mfuwe were M. natalensis.

The QIAGEN OneStep RT-PCR Kit (QIAGEN) was used to screen arenaviruses under the following conditions: 30 min at 50[degrees]C, 15 min at 95[degrees]C, 45 cycles of 20 s each at 95[degrees]C, 30 s at 50[degrees]C, 1 min at 72[degrees]C, and 10 at 72[degrees]C. The primer sequences used were 5'-CACATAGTTGGGCCCCACTTGCTGTGATC-3' and 5'-AGGATAAGTGAAAGAGAGAGTAATTC-3', which were designed on the basis of a consensus sequence of the large (L) gene among African arenavirus strains (Old World Arenaviruses [OWAs]), including Lujo virus. The region of the L gene has been reported as well conserved among OWAs (7).

Total RNA samples were extracted from kidney tissues by using TRIzol reagent (Invitrogen, Carlsbad, CA, USA). Reverse transcription (RT) PCR results indicated that 4 (17%) of the 23 rodents captured in Lusaka and 1 (4%) of the 24 captured in Namwala were positive for arenavirus, but none of the 143 rodents captured in Mfuwe were positive. Overall, 5 (3%) of the 190 M. natalensis rodents trapped in Zambia were positive for arenavirus. All amplicons were confirmed by nucleotide sequencing and analyzed by BLAST search.

We used RNA samples extracted from kidney tissues of representative Lusaka and Namwala strains to determine full-genome sequences. After several attempts to amplify the virus genome cDNA of OWAs by using deduced universal primers, we obtained some virus fragments and determined the full-genome sequence by the gap closing and rapid amplification of cDNA ends methods. GenBank accession numbers for the Lusaka strain are AB586644 and AB586645, and for the Namwala strain, AB586646 and AB586647. Sequence analysis indicated that the genome of the Lusaka and Namwala strains have a typical bisegmented structure containing 2 open reading frames in each segment, and the genes in the segments are separated by a stable stem-loop structure (data not shown). The small segments of the Lusaka and Namwala strains are both 3,377 bp, and the large segments are 7,230 and 7,236 bp, respectively. The shortage in the Lusaka strain genome, compared with the Namwala strain genome, was in a noncoding region between the stem-loop and the L gene.

We used MEGA5 software (8) to calculate values of diversity between the genomic small segment of the Lusaka strain and several OWAs. The lowest value, 0.13, was for Namwala strain; values ranged from 0.365 to 0.640 for the OWAs (Table 1). The divergence among each virus strain, except for the Zambian strains, ranged from 0.279 to 0.670 (Table 1). Analysis of the large segments showed similar results (data not shown). Phylogenetic analysis based on the deduced amino acid sequences of the 4 virus proteins showed clearly distinct sequences between OWAs and South American strains (New World arenavirus) (Figure 1, panels A-D; OWAs indicated in the gray area). The Lusaka and Namwala strains were classified as members of the OWAs; both strains are closely related to the Mobala, Morogoro, and Mopeia viruses. Thus, we concluded that the Zambian strains belong to the same virus species and that the novel arenavirus differs from other known strains. We propose that these Zambian strains be designated Luna virus (Lusaka-Namwala).


The characteristic functional motifs of the Z and glycoprotein precursor (GP-C) were well conserved in Luna virus. The Z protein has a critical role in arenavirus budding, and 2 conserved late-domain motifs, P(T/S) AP and PPPY, in the C-terminal have been reported (9,10). Luna virus also exhibited the [P.sub.83]TAP and [P.sub.93]PPY motifs, which are present in other OWAs, excluding Lujo, Dandenong, and lymphocytic choriomeningitis viruses (Table 2). GP-C was posttranscriptionally processed by S1P (the cellular proprotein convertase site 1 protease) to yield the glycoproteins, and the consensus motif R-(R/K/ H)-L-(A/L/S/T/F) was identified as the S1P recognition site of Luna virus glycoprotein (11,12). Luna virus GP-C contained [R.sub.257]RLM, which is apparently cleaved in a similar fashion; however, its cleavage mechanism has not yet been confirmed. The RRLM sequence is also conserved in the Mobala and Ippy viruses (Table 2). The details of this protein motif suggested that Luna virus is more similar to Mobala virus than to Mopeia and Morogoro viruses.

We attempted to isolate Luna virus from the 5 viral RNA-positive tissue samples. Each kidney homogenate was injected into Vero E6 cells in Dulbecco modified Eagle medium supplemented with 2% fetal bovine serum. The culture medium was changed every 6 days, and the supernatant was harvested after 28 days of cultivation. The harvested culture supernatant was injected into new Vero E6 cells. During the cultivation period, culture supernatant was sampled every 2 days and tested for the presence of Luna virus RNA by 1-step RT-PCR. Finally, the amount of viral RNA in the culture supernatant of 1 Lusaka sample was increased during days 6-12 (Figure 2). During this time, distinct cytopathic effect was not observed (data not shown). To observe the virus particles, the culture supernatant was ultracentrifuged at 100,000 x g, and the precipitates were negatively stained with 2% phosphotungstate. Transmission electron microscopy indicated typical round-shaped, enveloped particles, 75 nm in diameter, with electron-dense dots inside the envelope (data not shown).


We isolated a novel nonpathogenic arenavirus, which we propose be designated Luna virus, from M. natalensis rodents in Zambia. Comparison of the genetic backgrounds of Luna virus and Lujo virus, a novel pathogenic arenavirus also found in Zambia, showed that Luna virus is genetically different from Lujo virus. Luna virus was closely related to nonpathogenic arenaviruses that have been found from central to eastern Africa. To elucidate the epizootiologic aspects of arenaviruses in Zambia, the number of rodent and other species samples must be expanded. Such elucidation can lead to discovery of new arenaviruses, as demonstrated by isolation of a pathogenic New World arenavirus from bats during a study to increase knowledge of the geographic range and genetic diversity of arenaviruses naturally associated with the Mexican woodrat (Neotoma mexicana) in the western United States (13).



We thank the Zambia Wildlife Authority for supporting the arenavirus surveillance program in Zambia.

This study was supported in part by grants; the Program of Founding Research Centers for Emerging and Reemerging Infectious Disease; the Global COE program "Establishment of International Collaboration Centers for Zoonosis Control" from the Ministry of Education, Culture, Sports, Science and Technology; and the Ministry of Health, Labor and Welfare, Japan.

Dr Ishii is an assistant professor at the Research Center for Zoonosis Control, Hokkaido University, Japan. His research interests include virology and immunology, in particular, innate immune host defense.


(1.) Paweska JT, Sewlall NH, Ksiazek TG, Blumberg LH, Hale MJ, Lipkin WI, et al. Nosocomial outbreak of novel arenavirus infection, southern Africa. Emerg Infect Dis. 2009;15:1598-602.

(2.) Bowen MD, Rollin PE, Ksiazek TG, Hustad HL, Bausch DG, Demby AH, et al. Genetic diversity among Lassa virus strains. J Virol. 2000;74:6992-7004. doi:10.1128/JVI.74.15.6992-7004.2000

(3.) Wulff H, McIntosh BM, Hamner DB, Johnson KM. Isolation of an arenavirus closely related to Lassa virus from Mastomys natalensis in south-east Africa. Bull World Health Organ. 1977;55:441-4.

(4.) Gunther S, Hoofd G, Charrel R, Roser C, Becker-Ziaja B, Lloyd G, et al. Mopeia virus-related arenavirus in natal multimammate mice, Morogoro, Tanzania. Emerg Infect Dis. 2009;15:2008-12. doi:10.3201/eid1512.090864

(5.) Palacios G, Savji N, Hui J, Travassos da Rosa A, Popov V, Briese T, et al. Genomic and phylogenetic characterization of Merino Walk virus, a novel arenavirus isolated in South Africa. J Gen Virol. 2010;91:1315-24. doi:10.1099/vir.0.017798-0

(6.) Lecompte E, Brouat C, Duplantier J-M, Galan M, Granjon L, Loiseau A, et al. Molecular identification of four cryptic species of Mastomys (Rodentia, Murinae). Biochem Syst Ecol. 2005;33:681-9. doi:10.1016/j.bse.2004.12.015

(7.) Vieth S, Drosten C, Lenz O, Vincent M, Omilabu S, Hass M, et al. RT-PCR assay for detection of Lassa virus and related Old World arenaviruses targeting the L gene. Trans R Soc Trop Med Hyg. 2007;101:1253-64. doi:10.1016/j.trstmh.2005.03.018

(8.) Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S. MEGA5: Molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol. 2011; [Epub ahead of print].

(9.) Perez M, Craven RC, de la Torre JC. The small RING finger protein Z drives arenavirus budding: implications for antiviral strategies. Proc Natl Acad Sci U S A. 2003;100:12978-83. doi:10.1073/ pnas.2133782100

(10.) Strecker T, Eichler R, Meulen J, Weissenhorn W, Dieter Klenk H, Garten W, et al. Lassa virus Z protein is a matrix protein and sufficient for the release ofvirus-like particles. J Virol. 2003;77:10700-5. Erratum in: J Virol. 2003;77:12927. doi:10.1128/JVI.77.19.10700 10705.2003

(11.) Rojek JM, Lee AM, Nguyen N, Spiropoulou CF, Kunz S. Site 1 protease is required for proteolytic processing of the glycoproteins of the South American hemorrhagic fever viruses Junin, Machupo, and Guanarito. J Virol. 2008;82:6045-51. doi:10.1128/JVI.02392-07

(12.) Beyer WR, Popplau D, Garten W, von Laer D, Lenz O. Endoproteolytic processing of the lymphocytic choriomeningitis virus glycoprotein by the subtilase SKI-1/S1P. J Virol. 2003;77:2866-72. doi:10.1128/JVI.77.5.2866-2872.2003

(13.) Downs WG, Anderson CR, Spence L, Aitken THG, Greenhall AH. Tacaribe virus, a new agent isolated from Artibeus bats and mosquitoes in Trinidad, West Indies. Am J Trop Med Hyg. 1963;12:640-6.

Author affiliations: Hokkaido University, Sapporo, Japan (A. Ishii, Y. Thomas, I. Nakamura, A. Ohnuma, A. Takada, H. Sawa); and University of Zambia, Lusaka, Zambia (A. Ishii, Y. Thomas, L. Moonga, I. Nakamura, B. Hang'ombe, A. Takada, A. Mweene, H. Sawa)


Address for correspondence: Akihiro Ishii, Research Center for Zoonosis Control, Hokkaido University, N20, W10, Sapporo, Hokkaido, 001-0020, Japan; email:
Table 1. Nucleotide sequence comparison among Old World
arenaviruses *

Strain     Lusaka    Namwala      MOBV       MORV

Lusaka       0
Namwala    0.130        0
MOBV       0.365      0.367        0
MORV       0.372      0.365      0.392        0
MOPV       0.375      0.385      0.388      0.279
LASV       0.406      0.406      0.413      0.434
LUJV       0.640      0.646      0.667      0.670

Strain      MOPV       LASV       LUJV

MOPV         0
LASV       0.417        0
LUJV       0.654      0.666        0

* MOBV, Mobala virus (GenBank accession no. NC_007903); MORV,
Morogoro virus (NC_013057); MOPV, Mopeia virus (NC_006575); LASV,
Lassa virus (NC 004296); LUJV, Lujo virus (FJ952384). The number of
nucleotide substitutions per site is shown. The small segment
nucleotide sequences from 7 arenavirus strains were analyzed. All
positions containing gaps and missing data were eliminated. The
final dataset comprised 3,130 positions.

Table 2. Functional motifs in the Z and glycoprotein precursor
proteins of Old World arenaviruses *

Strain                  Late domains               Strain

LUNV (Lusaka)        PTAP#KESASNPPPY#SP        LUNV (Lusaka)
LUNV (Namwala)       PTAP#KEPARNPPPY#SP        LUNV (Namwala)
MOBV                 PTAP#PPEATNPPPY#SP             MOBV
MOPV                PTAP#PEIPPSQNPPPY#SP           IPPYV
MORV                PTAP#PEAMPSQQPPPY#QP            LUJV
LASV                PTAP#PTGAADSIRPPPY#SP           MOPV
IPPYV                 PSAP#PSPSPPPY#SP              MORV
LCMV             STAP#SSPPPY#EE ([section])         LASV
DANV                   STAP#SSPPPY#EE               LCMV
LUJV                       PSAP#PL                  DANV

Strain             S1P cleavage
                 ([double dagger])

LUNV (Lusaka)       RRLM-GTFTW
LUNV (Namwala)      RRLM-GTFTW
MOBV                RRLM-GTFTW
MOPV                RRLM-STFTW
MORV                RKLM-KLFQW
LASV                RRLL-GLFTW
IPPYV               RRLL-GLFTW
LCMV                RRLL-GTFTW
DANV                RRLA-GTFTW
LUJV                RRLA-GTFTW

* S1P, cellular proprotein convertase site 1 protease; LUNV, Luna
virus; -, S1P cleavage site; MOBV, Mobala virus; MOPV, Mopeia virus;
MORV, Morogoro virus; LASV, Lassa virus; IPPYV, Ippy virus; LCMV,
lymphocytic choriomeningitis virus; DANV, Dandenong virus; LUJV,
Lujo virus.

([dagger]) Conserved P(T/S)AP and PPPY motifs in the Z protein are
in boldface.

([double dagger]) R(R/K)LM is considered a putative, although
unconfirmed, S1P cleavage site.

([section]) STAP is considered a putative, although unconfirmed,
PTAP motif.

Note: Conserved P(T/S)AP and PPPY motifs in the Z protein are
in boldface indicated with #.
COPYRIGHT 2011 U.S. National Center for Infectious Diseases
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2011 Gale, Cengage Learning. All rights reserved.

Article Details
Printer friendly Cite/link Email Feedback
Title Annotation:DISPATCHES
Author:Ishii, Akihiro; Thomas, Yuka; Moonga, Ladslav; Nakamura, Ichiro; Ohnuma, Aiko; Hang'ombe, Bernard; T
Publication:Emerging Infectious Diseases
Article Type:Report
Geographic Code:6ZAMB
Date:Oct 1, 2011
Previous Article:Antimicrobial ointments and methicillin-resistant Staphylococcus aureus USA 300.
Next Article:Pandemic (H1N1) 2009 encephalitis in woman, Taiwan.

Terms of use | Privacy policy | Copyright © 2021 Farlex, Inc. | Feedback | For webmasters |