Development of an immunochromatography strip test based on truncated nucleocapsid antigens of three representative hantaviruses
© Amada et al.; licensee BioMed Central Ltd. 2014
Received: 28 November 2013
Accepted: 23 April 2014
Published: 14 May 2014
Hantaviruses are causative agents of hemorrhagic fever with renal syndrome (HFRS) and nephropathia epidemica (NE) in the Old World and hantavirus pulmonary syndrome (HPS) in the New World. There is a need for time-saving diagnostic methods. In the present study, recombinant N antigens were used as antigens in an immunochromatography strip (ICG) test to detect specific IgG antibodies.
The N-terminal 103 amino acids (aa) of Hantaan virus (HTNV), Puumala virus (PUUV) and Andes virus (ANDV) nucleocapsid (N) protein were expressed in E. coli as representative antigens of three groups (HFRS, NE and HPS-causing viruses) of hantavirus. Five different types of ICG test strips, one antigen line on one strip for each of the three selected hantaviruses (HTNV, PUUV and ANDV), three antigen lines on one strip and a mixed antigen line on one strip, were developed and sensitivities were compared.
A total of 87 convalescent-phase patient sera, including sera from 35 HFRS patients, 36 NE patients and 16 HPS patients, and 25 sera from healthy seronegative people as negative controls were used to evaluate the ICG test. Sensitivities of the three-line strip and mixed-line strip were similar to those of the single antigen strip (97.2 to 100%). On the other hand, all of the ICG test strips showed high specificities to healthy donors.
These results indicated that the ICG test with the three representative antigens is an effective serodiagnostic tool for screening and typing of hantavirus infection in humans.
KeywordsImmunochromatography strip test Hemorrhagic fever with renal syndrome (HFRS) Nephropathia epidemica (NE) Hantavirus pulmonary syndrome (HPS)
Hemorrhagic fever with renal syndrome
Hantavirus pulmonary syndrome
Sin Nombre virus
Laguna Negra virus.
Hantaviruses belong to the genus Hantavirus of the family Bunyaviridae. Hantavirus virions contain three segmented negative-sense RNAs designated S, M, L that encode a nucleocapsid (N) protein, enveloped glycoproteins (Gn and Gc), and an RNA-dependent RNA polymerase (L protein), respectively . Viruses in the genus Hantavirus contain causative agents of two important rodent-borne febrile zoonoses, hemorrhagic fever with renal syndrome (HFRS) in the Old World and hantavirus pulmonary syndrome (HPS) in the New World .
So far, 24 virus species that represent serotypes and genotypes have been registered within the genus Hantavirus by the International Committee on Taxonomy of Viruses . Four of those virus species, Hantaan virus (HTNV), Seoul virus (SEOV), Dobrava-Belgrade virus (DOBV), and Puumala virus (PUUV), are known to cause HFRS. The milder type of HFRS in Northern Europe, caused by PUUV infection, was historically called nephropathia epidemica (NE). Sin Nombre virus (SNV), Andes virus (ANDV), Laguna Negra virus (LANV), and many other related viruses are known as causative agents of HPS . There is a close association between the virus species and their rodent hosts, probably due to the co-evolution of rodent hosts and viruses for many thousands of years . As a consequence, endemic areas of HFRS and HPS depend on the rodent habitat. However, imported cases of HFRS and HPS between different countries and continents have been reported [6–8]. Furthermore, more than one hantavirus species is present in some regions, and the severity of disease differs depending on the virus . In addition, clinical diagnoses of HFRS and HPS patients are not effective in some cases as they represent mixed-syndrome between HFRS and HPS [10, 11]. Therefore, screening and typing of hantavirus infections provides important epidemiologic information.
Hantaviruses can be divided into antigenically distinguished species by neutralization tests, which show the antigenic differences of Gn and/or Gc proteins. While, it has been reported that hantavirus species can be divided into three antigenic groups based on antigenic cross-reactivity mainly at the N terminal end of N protein: group I (HTNV, SEOV, and DOBV, which are derived from Murinae rodents), group II (PUUV, and nonpathogenic vole-borne hantaviruses, Tula virus, Prospect Hill virus, and others, those are derived from Microtinae rodents) and group III (SNV, ANDV and related New World hantaviruses derived from Sigmodontinae and Neotominae rodents) . Therefore, three kinds of antigens from each of the three antigenic groups I, II, and III are necessary for screening of all of the rodent-borne hantavirus infections.
We previously developed an Escherichia coli (E. coli) and baculovirus-expressed recombinant N protein for screening and serotyping patient samples in an enzyme-linked immunoassay (ELISA) for HFRS and HPS viruses [12, 13]. Herein, we describe a pilot study to assess a new rapid immunochromatography (ICG) test with recombinant antigens using E. coli-expressed common antigenic sites located in the N terminal end of N protein for detection of specific IgG antibodies in acute and convalescent samples of patients with clinical infection caused by various hantavirus species. In addition, the ICG test was evaluated for the ability to discriminate among the three main hantavirus groups.
ICG test lines of different ICG strips
Comparison of the results of ICG tests with patient sera
Comparison of reactivities of HFRS, NE and HPS patient sera in ICG tests and ELISA
Type of disease
Mixed-line strip (+)
HTNV or SEOV
SNV, ANDV or LANV
Seronegative healthy donar
The HTNV, PUUV and ANDV strips showed high sensitivities to homologous sera with 100%, 92.3% and 100% in acute-phase, respectively. The three-line strip showed almost the same sensitivities: 100%, 88.5% and 100% in acute-phase sera, respectively. The mixed-line strip showed sensitivities of 95%, 92.3% and 100% in acute-phase sera, respectively.The PUUV strip was able to detect antibodies in 14/28 (50%) of the HPS patient sera (acute and convalescent) but in only 2/56 (3.6%) of the HFRS patient sera (acute and convalescent). Similarly, the ANDV strip was able to detect antibodies in 19/62 (30.6%) of the NE patient sera (acute and convalescent) but in none of the HFRS patient sera. The HTNV strip, on the other hand, showed no cross-reactivity to NE and HPS patient sera. The three-line strip showed the same cross-reactive patterns as those of the HTNV, PUUV and ANDV strips. In the three-line strip, all of the cross-reactive sera showed a weak band to the heterologous antigen compared to that with the homologous antigen, as shown in Figure 2.
Comparison of sensitivities of the 5 different ICG strips with ELISA
Representative sera from SEOV, ANDV or PUUV-infected patients in convalescent phase were examined for antibody titers with the 5 different ICG strips and ELISA. The single antigen strips, including the HTNV strip, ANDV strip and PUUV strip, and the three-line strip showed the same titers as that of ELISA with homologous combinations. The mixed-line strip also showed the same titer as that of ELISA (data not shown). Therefore, detection limit of IgG antibody was almost the same as that of conventional ELISA.
In this study, N-terminal 103 aa of N protein of HTNV, PUUV and ANDV expressed in E. coli were successfully applied as antigens for an ICG test to detect hantavirus IgG antibody in patient sera.
It has been reported that hantavirus N protein contains immunodominant and cross-reactive epitopes, a characteristic that is common to HFRS-causing viruses such as HTNV, SEOV and DOBV (group I), NE-causing viruses such as PUUV (group II) and HPS-causing viruses such as SNV, ANDV, and LANV (group III), at about the N-terminal 100 aa region.
In this study, we demonstrated that N-terminal 103 aa of N protein of one virus from each group were useful antigens in the ICG test for a rapid and simple serological test to screen for hantavirus IgG antibodies in human sera. Five different types of ICG test strips were evaluated. Sensitivities were almost the same for all of the ICG strips and ELISA test. The three-line strip was considered to be the most effective as it covered all of the hantavirus infections as well as distinguishing its antigenic groups. Unrecognized cases of hantavirus infection might exist even in countries where HFRS or HPS prevalence has not been reported. To know the actual situation of hantavirus prevalence, serological surveillance against all of the serotypes of hantavirus is required. Particularly in Europe and Far Eastern Asian regions, both HFRS and NE-causing viruses are co-circulating [14, 15]. For this purpose, the multiplex three-line strip ICG test is considered to be the most useful for a rapid and safe serological test as it covers all antigenic groups of human pathogenic hantaviruses. Furthermore, the ICG test was applicable to diluted whole blood instead of serum specimens . This allows the use of the ICG test in field surveillance or in resource-limited settings where adequate laboratory equipment is not available. An ICG test to detect IgM antibody has been reported for diagnosis of NE [17, 18]. Our ICG tests were developed for IgG antibody detection for the purpose of retrospective seroepidemiological study. Although the rates of detection of anti-hantavirus IgG antibody evaluated with convalescent phase patient sera were more than 97.2%. One convalescent-phase NE patient serum showed negative results in both single PUUV strip and mixed-line strip. This specimen showed low ELISA OD values and made the sensitivities of ICG tests for NE low (97.2%) comparing to HPS and HFRS (100%). Totally, three-line strip showed relatively better sensitivity than those of single-antigen and mixed-line strips by evaluation with convalescent.
On the other hand, antibody-positive rates in acute-phase sera (88.5 - 100%) were slightly lower than those in convalescent-phase sera. This might be due to the lower IgG antibody titer in acute-phase sera. Furthermore, 3 of the ICG-negative sera from NE acute patients (Table 1) were collected 4 and 5 days after onset of the disease. These results indicated the limitation of these ICG strips. All of the patient sera used in this study were derived from patient with confirmed hantavirus infection. Therefore, even if sera were negative in ELISA, they were considered as true positive. Although several sera from acute-phase patients were IgG-negative in ELISA, the results of sensitivities from acute-phase patients must be informative for the use of these ICG strips.
Protein A binds with high affinity to human IgG antibody molecule as well as to human IgM antibody molecule with moderate affinity. Therefore, our ICG test which utilized Protein A-labeled colloidal gold, able to detect both hantavirus IgG antibody and lesser extent IgM antibody. However, since the ICG test was judged by the detection of visualized accumulated colloidal gold particles, it is difficult to distinguish IgG and IgM detection. Therefore, the ICG test for specific to IgM antibody detection is necessary for detecting antibody from acute-phase patient sera and for differential diagnoses between acute infection and past infection in endemic countries.
The three-line strip developed in this study enables a homologous reaction and a hererologous cross-reaction to be easily distinguished by the intensity of lines. On the other hand, the mixed-line strip enables detection of hantavirus antibody in all of the three antigenic groups with high sensitivity.
This applicability indicates that a multiplex ICG strip or the mixed-line strip or single antigen-strips were useful for serological survey of hantavirus infections among human. Depending on the situation, these strips were effective for survey. To test imported cases found in non-endemic countries, one strip have to screen for various antigens including similar infectious diseases, such as leptospirosis, severe fever with thrombocytopenia syndrome (SFTS) and other viral hemorrhagic fever. On the other hand, in endemic area and its neighbor, use of single antigen strip might be enough for screening. These ICG strips reported in this paper would be a useful tool for serological surveillance of hantavirus infection.
A total of 56 serum specimens from 21 HFRS patients (12 pairs, 4 triads and 5 quartets, including acute-phase serum) were kindly provided by H. Wang of the Institute of Virology, Chinese Academy of Preventive Medicine, Beijing, China. These sera were confirmed to be positive for hantavirus infection by neutralization test as previously reported . Because of the lack of precise records, the sera collected the first time were regarded as acute-phase sera and rest of them were regarded as convalescent-phase sera.
Nine NE patient sera, including 4 acute-phase sera and 5 convalescent-phase sera, were kindly provided by Dr. Rainer Ulrich, Friedrich-Loeffler Institut, Federal Research Institute for Animal Health, Institute for Novel and Emerging Infectious Diseases, Germany. These sera were confirmed to be antibody-positive to PUUV by a neutralization test [22, 23]. A total of 17 sera, including 4 acute-phase and 13 convalescent-phase sera, were kindly provided by Dr. Ake Lundkvist, Swedish Institute for Infectious Disease Control, Sweden and were confirmed to be antibody-positive to PUUV as previously described . In addition, a total of 18 paired (acute and convalescence-phase) sera obtained from hospitalized NE patients in northern Sweden were included. They were confirmed to be infected with PUUV by an indirect immunofluorescence assay (IFA).
Eleven serum specimens from HPS patients infected with SNV in the United States were kindly supplied by Brian Hjelle of the University of New Mexico Health Sciences Center. Eleven serum specimens from HPS patients infected with ANDV and six serum specimens from HPS patients infected with LANV, which is the most antigenically related to ANDV and is co-circulating in the area where ANDV is prevalent, were obtained from Dr. Delia Enria, Instituto Nacional de Enfermedades Vigrales Humanas and Dr. Julio I. Maiztegui, Pergamino, Argentina. Twenty-five sera from healthy donors that were confirmed to be hantavirus antibody-negative were used as a negative control group . This study was approved by the ethics committee of Hokkaido University Graduate School of Medicine.
Preparation of recombinant antigens
Hantavirus N protein possesses an immunodominant antigenic region within the N-terminus of about 100 aa [25–27]. In this study, N-terminal 103 aa of N protein of HTNV (HS103), PUUV (PUU103) and ANDV (AND103) were selected as representative antigens of the three antigenic groups. HS103 and PUU103 were expressed as an NUS and 6 X histidine -tagged recombinant protein using the pET43.1 plasmid vector (Novagen, Madison, WI, USA) and E. coli host strain BL21 (Novagen pET System Manual 10th ed.) as described previously [16, 23]. The coding region of AND103 was amplified using primers ANDVSATG-speI (5′-aaaactagtatgagcaacctccaagaa-3′) and ANDVS103stop-xho1 (5′ - aatctcgagttaatccaggacatttccata -3′) by a previously described procedure . A TAA stop codon, indicated by an underline, was added to terminate recombinant protein translation. Additional target sequences for the restriction enzymes SpeI and XhoI are indicated by italics. Fragments were cloned into the SpeI/XhoI restriction site of the pET43.1 vector in-frame with the NUS and histidine (his)-tag, and the resultant plasmids were introduced into E. coli host BL21 (DE3). HTN103, PUU103 and AND103 were purified using HisTrap HP columns (Amersham, Piscataway, NJ, USA) according to the manufacturer’s instructions. Purified antigens were evaluated by SDS- PAGE analysis followed by protein staining with Simply blue (Invitrogen, Carlsbad, CA, USA, data not shown).
Enzyme-linked immunosorbent assay (ELISA)
(i) IgG ELISA
Ninety-six-well plates were first coated with 1 μg/ml of HS103, PUU103 or AND103 in PBS for 1 h at 37°C as a capture antigen. After being washed three times with PBS containing 0.05% Tween 20 (PBS-T), the wells were blocked with PBS containing 3% bovine serum albumin (BSA) for 1 h at 37°C. After blocking, human sera at 1:200 dilution with ELISA buffer (PBS containing 0.5% BSA and 0.05% Tween 20) were added to the wells. After incubation for 1 h at 37°C, the wells were washed three times with PBS-T. Bound antibody was detected with horseradish peroxidase (HRP)-labeled goat anti-human IgG antibody (Invitrogen™) for 1 h at 37°C. After being washed as above, color reactions were performed with o-phenylenediamine dihydrochloride (OPD) (Sigma-Aldrich, St. Louis, MO) and allowed to develop for 10 min. Absorbance was measured at 450 nm by using a SpectraMax 340 microplate spectrophotometer (Molecular Device, Sunnyvale, CA). The optical density (OD) of each test sample was subtracted from the OD value of the control antigen, which was a purified NUS-tag protein alone, run on the same plate. Samples with OD values of less than 0.2 were considered negative for IgG antibody.
(ii) IgM ELISA
IgM ELISA was carried out as previously described . Briefly, ninety-six-well plates were coated overnight at 4°C with goat anti-human-μ-chain antibody (Cappel, Aurora, OH). After washing and blocking as described above, patient sera at 1:200 dilution were added to capture IgM antibodies in sera. Then a recombinant N protein of HTNV, PUUV or ANDV, prepared by using a baculovirus vector as described previously [12, 13], was added. To detect bound antigens, biotinylated MAb clone E5/G6 against N protein of HTNV [29, 30] was added. After reaction with streptavidin-HRP conjugate (Prozyme), the color was developed with TMB (3,3′,5, 5′-tetramethylbenzidine) for 15 min, and development was stopped with 0.5 M sulfuric acid. Absorbance was measured at 450 nm by using a SpectraMax 340 microplate spectrophotometer (Molecular Device). Samples with OD values of less than 0.2 were considered negative for IgM antibody. Reagena Poc Puumala® was used for detection of IgM antibody against PUUV in NE patient sera at the Department of Clinical Virology, Umeå University Hospital [17, 18].
Preparation of an ICG strip
(i) Preparation of a conjugate pad
A glass-fiber conjugate pad (5 mm × 300 mm, GFCP103000, MILLIPORE) was soaked in 0.5% casein in 20 mM PBS (pH 7.0) for 20 min. The pad was washed with 3.0% sucrose PBS and dried in air overnight. Protein A-conjugated colloidal gold (Protein A-Colloidal Gold conjugate, EY Laboratories, CA., USA) was put onto the pad at 500 μl for both ICG strips “Single-antigen strip” and “Mixed-line strip”, and at 1000 μl for the “three-line strip” described as below. The pad was dried in air overnight and kept at room temperature.
(ii) Preparation of a nitrocellulose membrane
(iii) Procedure for the ICG test
Serum dilution was prepared by mixing 2 μl of serum with 150 μl of PBS in a microplate well, and an ICG strip was directly put into the well (Figure 3B). After standing still for 15 min, the ICG line was examined by the naked eye. A serum sample that showed both test and control lines was regarded as positive, and a serum sample that showed only the control line was regarded as negative.
This study was supported in part by the Program of Founding Research Centers for Emerging and Reemerging Infectious Diseases, MEXT, Japan. This work was also supported in part by a grant from the Global COE Program (Establishment of International Collaboration Center for Zoonosis Control) and also supported in part by Grants-in-Aid for Research on Emerging and Re-emerging Infectious Diseases from the Ministry of Health, Labour and Welfare including H22-emerging-ippan-006. We also would like to thank Dr. Akira Takakura and Dr. Nina M T Lagerqvist for useful suggestions and technical support. All authors read and approved the final manuscript.
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