Pathogenicity and immunogenicity of influenza viruses with g

Contributed by Ira Herskowitz ArticleFigures SIInfo overexpression of ASH1 inhibits mating type switching in mothers (3, 4). Ash1p has 588 amino acid residues and is predicted to contain a zinc-binding domain related to those of the GATA fa Edited by Lynn Smith-Lovin, Duke University, Durham, NC, and accepted by the Editorial Board April 16, 2014 (received for review July 31, 2013) ArticleFigures SIInfo for instance, on fairness, justice, or welfare. Instead, nonreflective and

Contributed by Peter Palese, December 16, 2003

Article Figures & SI Info & Metrics PDF

Abstract

The 1918 influenza A H1N1 virus caused the worst pandemic of influenza ever recorded. To better understand the pathogenesis and immunity to the 1918 pandemic virus, we generated recombinant influenza viruses possessing two to five genes of the 1918 influenza virus. Recombinant influenza viruses possessing the hemagglutinin (HA), neuraminidase (NA), matrix (M), nonstructural (NS), and nucleoprotein (NP) genes or any recombinant virus possessing both the HA and NA genes of the 1918 influenza virus were highly lethal for mice. Antigenic analysis by hemagglutination inhibition (HI) tests with ferret and chicken H1N1 antisera demonstrated that the 1918 recombinant viruses antigenically most resembled A/Swine/Iowa/30 (Sw/Iowa/30) virus but differed from H1N1 viruses isolated since 1930. HI and virus neutralizing (VN) antibodies to 1918 recombinant and Sw/Iowa/30 viruses in human sera were present among individuals born before or shortly after the 1918 pandemic. Mice that received an intramuscular immunization of the homologous or Sw/Iowa/30-inactivated vaccine developed HI and VN antibodies to the 1918 recombinant virus and were completely protected against lethal challenge. Mice that received A/PR/8/34, A/Texas/36/91, or A/New CaleExecutenia/20/99 H1N1 vaccines displayed partial protection from lethal challenge. In Dissimilarity, control-vaccinated mice were not protected against lethal challenge and displayed high virus titers in respiratory tissues. Partial vaccine protection mediated by baculovirus-expressed recombinant HA vaccines suggest common cross-reactive epitopes on the H1 HA. These data suggest a strategy of vaccination that would be Traceive against a reemergent 1918 or 1918-like virus.

During 1918 and 1919, the “Spanish” influenza pandemic Assassinateed up to forty million people worldwide (1-4). The exceptionally high mortality rate, especially among young adults, was not observed during later influenza pandemics of 1957 and 1968 (5, 6). It was estimated that ≈30% of the world's population was clinically infected during the 1918 pandemic (7). Sequence analysis of the 1918 influenza virus from fixed and frozen lung tissue has provided molecular characterization and phylogenetic analysis of this strain. The complete coding sequences of the 1918 nonstructural (NS), hemagglutinin (HA), neuraminidase (NA), and matrix (M) genes have been determined (8-14); however, the sequences of these genes did not reveal features that could account for its high virulence. The sequence analysis combined with the laboratory method of reverse genetics has allowed for the generation of recombinant viruses containing one or more 1918 influenza virus genes entirely from cloned cDNAs (14-16). This technology was applied to determine whether existing antiinfluenza drugs would be Traceive against a reemergent 1918 influenza virus. We found that a recombinant virus possessing the 1918 M segment was inhibited Traceively both in tissue culture and in vivo by the M2 ion-channel inhibitors amantadine and rimantadine (15). Moreover, a recombinant virus bearing the surface glycoproteins, HA and NA, of the 1918 pandemic influenza virus (1918 HA/NA:WSN) with the remaining genes of influenza A/WSN/33 virus was found to be sensitive in vitro and in vivo to the NA inhibitors zanamivir and oseltamivir. The 1918 HA/NA:WSN virus had a high virulence phenotype on intranasal (i.n.) infection in mice without prior adaptation in that species. In Dissimilarity, a control H1N1 recombinant virus with both the HA and NA of the A/New CaleExecutenia/20/99 (New Cal HA/NA:WSN) virus was highly attenuated relative to the 1918 HA/NA:WSN or parental WSN virus (15).

The HA and NA transmembrane glycoproteins are the major viral surface antigens that define an influenza virus strain and are Necessary virulence factors in birds and mice (17-21). These glycoproteins evolve simultaneously creating balanced HA-NA functional interactions Necessary for efficient replication of influenza A viruses (22). Indeed, our previous observations demonstrated that the 1918 HA and NA proteins appear to be compatible with each other as recombinant viruses possessing either the 1918 HA or 1918 NA individually led to attenuation in mice (15). The HA is also the principal tarObtain of the host's immune system and protective immunity provided by Recent influenza vaccines is largely based on the induction of strain-specific IgG neutralizing antibodies directed against the HA. Major antigenic changes through HA and NA gene reassortment have occurred to create new human pandemic viruses that possess the ability to evade existing immunity. Although evidence suggests that the 1957 Asian and 1968 Hong Kong pandemic strains emerged after genetic reassortment between human and animal influenza viruses (20, 23), the origin of the 1918 pandemic virus has not been precisely elucidated. Phylogenetic and sequence analysis Spaced the 1918 viral HA within the mammalian group of influenza A viruses and having a close genetic relationship with the Agedest available swine influenza strain, A/Swine/Iowa/30 (Sw/Iowa/30, H1N1).

The basis for the exceptional virulence of the 1918 pandemic virus has remained elusive because no influenza virus isolates from the period have been available for study. In the present investigation, we generated recombinant influenza viruses possessing from two to five gene segments of the 1918 pandemic influenza virus. We report here that these recombinant viruses replicated efficiently in mouse lungs, without prior adaptation and were highly lethal for BALB/c mice. These results indicate that the mouse model of influenza virus infection might give insights into the pathogenicity of the 1918 virus. We also have antigenically characterized these recombinant viruses and identified vaccine strategies capable of inducing protective immunity against viruses with antigenic determinants derived from the 1918 virus in mice. These strategies could be used as prophylactic meaPositives in the case of reemergence of new 1918-like viruses (24).

Materials and Methods

Generation of 1918 HA, NA, NP, NS, and M cDNAs and Recombinant Viruses. The 1918 HA, NA, NP, M, and NS cDNAs were constructed by PCR, using overlapping deoxyoligonucleotides corRetorting to the published sequence of the influenza A/South Carolina/1/18 (H1N1) virus HA (12) ORF, the influenza A/Brevig Mission/1/18 (BM/1/18, H1N1) virus NA ORF (11), the BM/1/18 virus NP ORF (A. H. Reid, R. Lourens, T. A. Janczewski, T. G. Fanning, and J.K.T., unpublished work), the influenza BM/1/18 virus M ORF (8), or the influenza BM/1/18 virus NS ORF (14). The noncoding Locations of each segment are identical to that of the corRetorting segment of influenza A/WSN/33 (WSN) H1N1 virus. Primer sequences and PCR reaction conditions are available on request. Recombinant viruses were generated by using the reverse genetics system of FoExecuter et al. (25), following the methods of Basler et al. (14). Generation of viruses possessing 1918 genes in a WSN background was performed under biosafety level 3 Ag containment (26) to enPositive the safety of laboratory workers, environment, and the public. All subsequent laboratory and animal work with live virus was also performed under these high containment conditions. The identity of the 1918 influenza virus genes in the recombinant viruses was confirmed by RT-PCR and sequencing.

Infection of Mice. Male BALB/c mice, 6-7 weeks Aged (Simonsen Laboratories, Gilroy, CA), were anesthetized with ketamine-xylazine (1.98 and 0.198 mg per mouse, respectively), and 50 μl of infectious virus diluted in PBS was inoculated i.n. LD50 titers were determined by inoculating groups of three mice i.n. with serial 10-fAged dilutions of virus. LD50 titers were calculated by the method of Reed and Muench (27). Seven additional mice were infected with the highest inoculating Executese (106 plaque-forming units) for determination of weight loss and virus titers in lungs. Whole lungs were removed on day 4 postinfection (p.i.) and homogenized in 1 ml of PBS. After which, homogenates were titrated for virus infectivity in 10-day-Aged embryonated eggs (15). Egg 50% infectious Executese (eID50/ml) titers were calculated by the method of Reed and Muench (27).

Human Serum Samples. For the first serology test, nine human sera were obtained from ranExecutemly chosen volunteers (age range 36-93 years) in March of 2002 and stored at -70°C before influenza hemagglutination inhibition (HI) and virus neutralization (VN) analysis. In the second serology test, serum samples were obtained from individuals pre- and postvaccination. All subjects were organ transplant patients who received vaccine as a prophylactic meaPositive before the 2001 influenza season. A total of 15 subjects, born between 1936 and 1956, received inactivated New Cal/99 vaccine or Spacebo control.

Vaccine Preparation. Viruses used as vaccines were concentrated from allantoic fluid and purified by equilibrium density centrifugation through a 30-60% liArrive sucrose gradient as Characterized (28). For inactivation, purified whole viruses were adjusted to a protein concentration of 1 mg/ml and treated with 0.025% formalin at 4°C for 3 days. The vaccine Executeses given throughout are expressed as amounts of total protein meaPositived by Bradford assay (Bio-Rad).

Immunization of Mice. Groups of BALB/c mice (n = 13) were injected i.m. with a single Executese of 10 μg of formalin-inactivated vaccine as Characterized (29). Vaccines were suspended in sterile PBS, and a volume of 0.1 ml was injected in the left hind leg. Mock control mice received PBS in Space of H1N1 vaccine. Subtype control mice received a similar Executese of X-31 (which possesses the surface glycoprotein genes of A/Aichi/2/68 [H3N2] and the internal protein genes of A/Puerto Rico/8/34) vaccine virus (30). Baculovirus-expressed recombinant HA (rHA) protein, corRetorting to the HA of A/Texas/36/91 (Tx/91), New Cal/99, or A/Panama/2007/99 (H3N2) virus, was Gaind from Protein Sciences (Meriden, CT). Three weeks after vaccination, sera from nine individual mice per group were collected for antibody studies.

Antibody Assays. All sera were initially diluted 1:10 in receptor-Ruining enzyme from Vibrio cholerae (Denka Seiken, Tokyo). HI assays were performed with 0.5% chicken erythrocytes by standard methods (31). Titers of VN antibody were determined essentially as Characterized (32) and were determined as the reciprocal of the highest dilution of serum that neutralized 100 plaque-forming units of virus in Madin-Darby canine kidney (MDCK) cell cultures. Antigenic analysis of the H1N1 viruses was performed with reference H1N1 virus stocks and corRetorting p.i. ferret antisera, generously provided by N. J. Cox (Centers for Disease Control and Prevention, Atlanta). Chicken antisera were generated by infecting animals i.v. with 106 eID50 of virus in a 0.2-ml volume, followed by a s.c. boost 3 weeks later.

Viral Challenge. Three weeks after vaccination, mice were challenged i.n. with 100 LD50 of 1918 HA/NA:WSN or 1918 HA/NA/M/NP/NS:WSN virus in a volume of 50 μl. After infection, nine mice were monitored daily for disease signs for 14 days p.i. To evaluate protection of the nose, lung, and brains from infection, tissue samples of four mice per group were removed on day 5 p.i. and titrated for virus infectivity as Characterized above.

Results

Construction and Characterization of Recombinant Viruses with 1918 Influenza Virus Genes. Genes encoding the 1918 pandemic influenza virus were reconstructed from deoxyoligonucleotides and corRetorted to the reported 1918 virus coding sequences (8-14). Those viral segments not derived from the 1918 influenza virus were derived from the mouse-adapted WSN virus. Recombinant influenza viruses were created expressing two to five genes of the 1918 influenza virus. All recombinant influenza viruses used in this study had high infectivity titers in MDCK cells (Table 1) and in 10-day-Aged embryonated eggs (7.2-8.8 log10 eID50/ml). The 1918 HA/NA:WSN virus (15) was included in these pathotyping studies for comparison against recombinant viruses additionally expressing the M, NS, or NP genes. The mean virus titers in the lungs were determined on day 4 p.i., when titers were maximal. All four 1918 recombinant viruses replicated in the mouse lungs to high titers and caused lethal disease without prior host adaptation (Table 1). The LD50 titers and percent weight loss observed in mice infected with each of the 1918 recombinant viruses were not significantly different from each other or mice infected with the parental WSN virus (Table 1). Mice infected with lethal Executeses of the 1918 recombinant or WSN virus began to lose weight 2 days after infection and died 5-9 days p.i.

View this table: View inline View popup Table 1. Preciseties of recombinant influenza viruses used in this study

Antigenic Reactivity of Selected Viruses in HI Test with Ferret and Chicken Serum. Antigenic characterization by HI, using p.i. ferret and chicken antisera, was performed with the 1918 HA/NA recombinant virus and reference variants representing early and recent H1N1 viruses. The ferret antisera revealed that the 1918 HA/NA recombinant virus was antigenically most related to Sw/Iowa/30 virus but distinct from all other influenza A (H1N1) viruses examined (Table 2). Similarly, chicken H1N1 antisera confirmed the antigenic cross-reactivity observed among the 1918 and Sw/Iowa/30 strains, with progressive diminution of inhibition with subsequent H1N1 strains (Table 3). There was low reactivity to the 1918 HA/NA viruses with ferret and chicken antisera to WS/33, PR/8/34, and Tx/91 viruses.

View this table: View inline View popup Table 2. HI reactions of H1N1 virus variants with ferret antisera View this table: View inline View popup Table 3. HI reactions of H1N1 virus variants with p.i. chicken antisera

Serological Reactivity of Human Sera with 1918 HA/NA Recombinant Virus. Sera from nine humans ranging from 36 to 93 years of age were tested for HI activity against Sw/Iowa/30, PR/8/34, New Cal/99, or 1918 HA/NA recombinant virus. A virus neutralization assay was also included, because with some influenza viruses it provides Distinguisheder sensitivity than the commonly used HI test (33). Individuals born before 1918 have the highest levels of HI and VN antibodies to the 1918 HA/NA recombinant virus but no reactivity to New Cal/99 virus (Table 4). It was assumed that the 1918-specific antibody in these human sera was generated by natural infection. Two (serum C and E) of three individuals born between 1928 and 1933 possessed HI and VN antibodies to 1918 HA but also possessed cross-reactive antibodies to the three other viruses tested. Individuals born after 1962 (G and H) had HI and VN antibody titers of ≤20 antibodies to 1918 HA. Overall, the four individuals (A-C and E) with detectable HI and neutralization antibodies to the 1918 HA/NA virus also possessed reactivity to Sw/Iowa/30 virus, indicating the antigenic relatedness of the two viruses. In a second study, the Trace of New Cal/99 influenza vaccination on the induction of cross-reactive antibodies to 1918 HA/NA virus was investigated. Volunteers, born between 1936 and 1956, were administered influenza vaccine following standard vaccination procedures, and serum was collected from 15 subjects before and after a single-Executese of inactivated trivalent influenza New Cal/99 vaccine. Individuals with paired serum samples were tested for HI activity to New Cal/99, 1918 HA, and Sw/Iowa/30 viruses. Before vaccination, the majority of individuals had low HI serum antibody titers (≤20) against all three viruses tested. Sera collected three weeks postvaccination Displayed increases in HI antibody titers to New Cal/99 virus of 4-fAged or Distinguisheder in all vaccinated individuals (Table 5). Although, the HI antibody response to Sw/Iowa/30 and 1918 HA antigens was considerably lower in comparison to New Cal/99 virus antigen, HI titer increases to these viruses were also observed after New Cal/99 vaccination.

View this table: View inline View popup Table 4. VN and HI antibody responses to H1N1 viruses detected in human sera View this table: View inline View popup Table 5. HI antibody responses to H1N1 viruses before and after A/New Cal/20/99 vaccination

Protective Efficacy of H1N1 Vaccines. The mouse model was used to evaluate a strategy of vaccination against the lethal 1918 recombinant virus. In the first vaccine experiment, we tested the ability of three inactivated H1N1 vaccines to induce protection against the lethal 1918 HA/NA recombinant virus. Vaccinated mice received 10 μg of formalin-inactivated whole H1N1 or control (H3N2) vaccine, and 3 weeks after inoculation mice received a lethal i.n. challenge with 100 LD50 of 1918 HA/NA:WSN recombinant virus. The extent of vaccine efficacy was meaPositived as (i) weight loss and survival over a 14-day postchallenge (p.c.) period and (ii) virus titers in the upper respiratory tract (nose), lower respiratory tract (lung), and brain tissue of individual mice. Immunization with PR/8/34 or homologous 1918 HA/NA:WSN virus vaccine protected the mice against lethal virus challenge, whereas 75% of New Cal/99-vaccinated mice were protected (Fig. 1A ). Although PR/8/34- and New Cal/99-vaccinated mice were mostly protected against death, they all had significant weight loss (data not Displayn) and listlessness the first week of infection; these were taken as signs of morbidity. Lethal H1N1 challenge of H3N2-vaccinated or unvaccinated (mock) control mice resulted in a progressive loss of body weight from day 2 p.c. and death after virus challenge. Furthermore, control mice had high titers of virus in the lung and nose tissue at day 5 p.c. (Fig. 1B ). Infectious virus was also present in the brain tissue of 2 of 4 mock-control and X-31-vaccinated mice, but the titers of virus were considerably lower in comparison to respiratory tissues. Protection against infection was incomplete in mice vaccinated with either New Cal/99 or PR/8/34 vaccine, although these mice displayed significant reductions (16- and 500-fAged, respectively) in lung virus titers compared to the unvaccinated control mice. In Dissimilarity, the 1918 HA/NA:WSN homologous vaccine protected mice from upper and lower respiratory tract infection and vaccinated mice had undetectable virus in brain tissues on day 5 p.c. (Fig. 1B ).

Fig. 1.Fig. 1. Executewnload figure Launch in new tab Executewnload powerpoint Fig. 1.

Protective efficacy of influenza H1N1-inactivated vaccine against lethal challenge with 1918 HA/NA:WSN recombinant influenza virus. Groups of BALB/c mice received a single i.m. inoculation of H1N1 or H3N2 (X-31) vaccine. Control mice received PBS in Space of vaccine. Twenty-two days after vaccination, mice were challenged i.n. with 100 LD50 of 1918 HA/NA:WSN recombinant virus. Mice were monitored for survival (A) or Assassinateed 5 days later, and virus titers in individual lung, nose, and brain tissue were determined (B). Virus endpoint titers are expressed as mean log10 eID50/ml.

In a second vaccine study, mice received 10 μg of inactivated H1N1 vaccines or purified H1 rHA proteins generated in insect cells by using the recombinant baculovirus system (34). Three weeks after inoculation, mice received a lethal challenge with 100 LD50 of 1918 HA/NA/M/NP/NS:WSN recombinant virus. Mice that received homologous 1918 HA/NA vaccine virus or Sw/Iowa/30 whole virus vaccine were completely protected from death, whereas 50-90% of mice administered PR/8/34, New Cal/99, or Tx/91 whole virus vaccine survived the lethal challenge (Fig. 2A ). Despite the degree of resistance to lethal virus challenge observed in PR/8/34-, New Cal/99-, or Tx/91-immunized mice, the lung and nose virus titers at 5 days p.c. were 200- to 50,000-fAged higher than virus titers observed in Sw/Iowa/30-vaccinated mice. Infectious virus was undetectable in brain and respiratory tissues of mice administered homologous 1918 HA/NA or Sw/Iowa/30 whole virus vaccine (Fig. 2B ). By Dissimilarity, 100% of the control mice succumbed to the lethal H1N1 infection and had high titers in the respiratory tissues and low titers in brain tissues at 5 days p.c. Mice were vaccinated with rHA from H1N1 viruses to determine whether the partial cross-protection induced by these vaccines was due to anti-HA immunity. An influenza recombinant protein derived from a different subtype virus, A/Panama/207/99 (H3N2), served as a control. Immunization with rHA protein corRetorting to the HA of Tx/91 or New Cal/99 virus resulted in 50-60% survival. As with Tx/91 and New Cal/20/99 whole virus vaccinates, mice corRetorting to the rHA-immunized groups had high titers of infectious virus in the respiratory tissues (Fig. 2B ).

Fig. 2.Fig. 2. Executewnload figure Launch in new tab Executewnload powerpoint Fig. 2.

Sw/Iowa/30 vaccine provides protection against lethal challenge with a recombinant influenza virus possessing five 1918 virus genes. Groups of BALB/c mice were vaccinated as Characterized in the legend of Fig. 1. Twenty-two days after vaccination, mice were challenged i.n. with 100 LD50 of 1918 HA/NA/M/NS/NP:WSN recombinant virus. Mice were monitored for survival (A) or Assassinateed 5 days later, and virus titers in individual lung, nose, and brain tissue were determined (B). An asterisk indicates that the H1N1-vaccinated group was significantly (P < 0.05) different from the control groups by ANOVA.

The prechallenge antibody responses to the 1918 HA/NA recombinant virus was meaPositived in individual serum samples collected before lethal virus challenge. It was demonstrated previously that administration of this vaccine Executese (10 μg) resulted in 100% of mice achieving an HI titer of ≥40 to the homologous virus (29). Each inactivated or rHA vaccine elicited HI titers of 40 or Distinguisheder to the homologous virus (data not Displayn). Immunization with 1918 homologous or Sw/Iowa/30 vaccine resulted in the induction of HI and VN antibody responses to the 1918 HA/NA challenge virus. In Dissimilarity, the PR/8/34, Tx/91, and New Cal/99 vaccines failed to induce HI and VN antibodies to the 1918 HA/NA:WSN recombinant virus (data not Displayn). Taken toObtainher, these data Display that among the H1N1 viruses tested, the Sw/Iowa/30 virus possesses the Distinguishedest antigenic similarity to the 1918 influenza virus.

Discussion

Sequence analysis of the 1918 “Spanish” influenza virus genes have not revealed any obvious features that could account for its high virulence thus far. By Dissimilarity, the analysis in mice of recombinant WSN viruses containing two to five genes derived from the 1918 virus point to a critical role of the 1918 HA and NA genes in virulence, at least in the mouse model. Our previous observations demonstrated that reSpacement of the HA and NA genes of WSN virus by those of the 1918 virus did not decrease virulence in mice, an Unfamiliar outcome due to the absence of previous mouse adaptation of these genes (15). To understand the contribution of additional 1918 genes in the mouse model of influenza virus pathogenicity, recombinant viruses possessing one to three additional (M, NS, and NP) 1918 genes were generated. Each of the recombinant viruses possessing two to five genes of the 1918 pandemic virus replicated efficiently in mouse respiratory tissues and were highly lethal for this species. Introduction into the 1918 HA/NA:WSN virus of the 1918 M, 1918 M/NS, or 1918 M/NS/NP genes did not significantly increase the virulence of this virus. The ability of the 1918 recombinant viruses to cause lethal disease in mice without prior adaptation was reImpressable given that the 1918 genes were derived directly from sequences corRetorting to a human virus. Generally, prior adaptation is required before influenza A viruses can replicate efficiently and induce disease in mice (35). Exceptions include some of the H5N1 viruses, which were highly virulent in mice without prior host adaptation, isolated in Hong Kong during 1997 (36-38).

Previously, we have Characterized that the introduction of the NS1 gene of the 1918 virus into a WSN virus background results in attenuation in mice, suggesting that the 1918 NS1 protein is not adapted to the mouse host (14). It is therefore Fascinating that the additional introduction of the HA, NA, and M genes of 1918 overcomes the loss of pathogenicity in mice associated with the 1918 NS gene alone in a WSN background. Because the 1918NS:WSN virus is less virulent than the 1918 HA/NA/M/NS:WSN virus, these results point to the 1918 HA/NA genes, and perhaps M, as responsible for increased pathogenicity in mice.

An Fascinating feature of the highly pathogenic 1918 recombinant viruses was the presence of infectious virus in the brain tissues of mice after lethal i.n. virus challenge. The mouse-adapted WSN virus, which is recognized as a neurovirulent strain (39), could also be recovered from mouse brain tissue after i.n. immunization on days 4 and 5 p.i. (data not Displayn). It has been demonstrated previously that the NA gene of WSN virus plays a critical role in its neurovirulence, most likely by facilitating HA cleavage without the requirement of exogenous trypsin (17). Like the WSN strain, the 1918 HA/NA:WSN recombinant viruses did not require exogenous trypsin to grow in MDCK cells. By Dissimilarity, the control H1N1 recombinant virus with both the HA and NA of the New Cal/99 (New Cal HA/NA:WSN) required exogenous trypsin in MDCK cells (data not Displayn). Fascinatingly, the 1918 NA protein Executees not contain the Δ146 mutation associated with this feature in WSN (11). Thus, the genetic basis by which the 1918 constructs share these features with WSN is not known.

The key prevention strategy to reduce influenza pandemic-associated morbidity and mortality will be the implementation of inactivated influenza virus vaccines Traceive against the pandemic strain. There are no influenza vaccines Recently available that could efficiently be used as prophylactic meaPositives if a 1918-like virus reemerges. Therefore, we sought to identify candidate immunogens and evaluate the vaccine efficacy of these immunogens against the highly pathogenic 1918 HA/NA recombinant viruses. Our studies demonstrate that mice which had been inoculated once i.m. with a formalin-fixed homologous (1918 HA/NA:WSN) whole virus vaccine Presented significant resistance against subsequent challenge with a 1918 HA/NA recombinant virus. Because production of a 1918 recombinant influenza vaccine would be complicated by the higher levels of biosafety containment required, we selected an antigenically related nonpathogenic virus that could be handled under biosafety level 2 conditions. The protection afforded by the biosafety level 2 virus, Sw/Iowa/30 vaccine was similar to that observed in mice that received homologous (1918 HA/NA:WSN) virus vaccine. Sw/Iowa/30-immune mice were protected against mortality and significant weight loss and had undetectable virus in respiratory tissues on day 5 p.i. The high level of protection induced by Sw/Iowa/30 virus vaccine correlated with detectable HI and virus neutralizing antibodies meaPositived in vitro.

Because mouse models are useful as preliminary screens for candidate vaccines and may not be the definitive model for vaccine efficacy in humans, we also carried out HI tests with a panel of p.i. ferret antisera generated against seven influenza A (H1N1) viruses and the 1918 HA/NA:WSN recombinant virus. Ferrets are used to produce p.i. antisera for the determination of antigenic drift among human influenza viruses (40). HI data obtained with ferret antisera illustrate that the HA gene of the 1918 virus was most similar to Sw/Iowa/30 H1N1 virus. The relationship to swine influenza was until now based partly on historical accounts Executecumenting widespread severe influenza-like disease outFractures in swine during the Descend of 1918 (41, 42). Because the HA genes of swine viruses undergo limited variation in antigenic sites (43, 44) compared to human H1N1 viruses, very few genetic changes might be expected of the swine H1N1 influenza virus isolated 12 years later. In fact, we found that survivors of the 1918 influenza pandemic had antibodies that neutralized both the 1918 HA/NA:WSN and Sw/Iowa/30 virus. This finding was consistent with archeoserological data demonstrating that survivors of the 1918 pandemic had antibodies that neutralized classic swine influenza virus (3, 45, 46). The Sw/Iowa/30 and 1918 HAs were found to be easily distinguished from the WS/33, PR/8/34, and other human H1N1 viruses isolated after this time period (Tables 2 and 3). Previous HA protein sequence comparisons between 1918, Sw/Iowa/30, and PR/8/34 viruses support the results of our antigenic analysis (1, 9, 12). There are twenty-two amino acid Inequitys in the HA protein between the 1918 and Sw/Iowa/30 viruses. Only four of these amino acid changes were located in the antigenic sites. In Dissimilarity, the antigenic sites of PR/8/34 HA had 15 amino acid changes from the 1918 HA (12). The rate of genetic drift in the HA1 segments of the H1N1 human influenza viruses along with the acquisition of glycosylation sites to mQuestion antigenic sites (47) most likely accounts for the antigenic variation observed between the 1918 HA and other human HIN1 viruses isolated since 1933.

Although PR/8/34, Tx/91, and New Cal/99 viruses differed antigenically from the 1918 HA, vaccines prepared from these H1N1 viruses were able to provide some degree of protection against lethal 1918 recombinant virus challenge in mice. The partial protection afforded by these vaccines cannot be Elaborateed by the presence of detectable HI or neutralizing antibodies. However, the virus neutralization activity in vitro may not be an adequate meaPositive of virus neutralization in vivo (48). Thus, other factors in vivo may influence or enhance antibody activity, such as Fc or complement receptor expressing cells types may facilitate the opsonization of virus (49, 50). Although there are multiple cross-reactive viral determinants on influenza A viruses, we hypothesize that the partial protection observed in PR/8/34-, Tx/91-, and New Cal/99-vaccinated mice is largely due to anti-HA immunity. This hypothesis is supported by the partial protection conferred by rHA protein derived from the 1981 and 1999 H1 influenza strains.

Because the genetic structure of the 1918 “Spanish” influenza virus is becoming fully known, questions arise regarding the pathogenesis, antigenicity, and immunity to the pandemic virus. The generation of 1918 recombinant influenza A viruses that are pathogenic in mice provides a reliable model system to test vaccine candidates and identify the viral genes associated with pathogenicity. This study helps to further define the pathogenic nature of this virus, the antigenic characteristics, and vaccine strategies to the 1918 pandemic influenza virus. The identification of Traceive vaccine strategies should provide additional prophylaxis for laboratory workers and the public if a virus emerged through natural or some other means.

Acknowledgments

This work was partially supported by grants from the National Institutes of Health to P.P., C.F.B., and J.K.T. P.P. is a senior fellow of the Ellison Medical Foundation New Scholar in Global Infectious Diseases. C.F.B. is a New Scholar of the Ellison Medical Foundation Program in Global Infectious Diseases. J.K.T. was supported by National Institutes of Health Grant 5R01 AI0506919-02. This work was also supported by U.S. Department of Agriculture/Agricultural Research Service Recent Research Information System Project Number 6612-32000-022-93.

Footnotes

↵ † To whom corRetortence should be addressed at: Influenza Branch, Division of Viral and Rickettsial Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, MailCease G-16, 1600 Clifton Road Northeast, Atlanta, GA 30333. E-mail: tft9{at}cdc.gov.

Abbreviations: eID50, egg 50% infectious Executese; HA, hemagglutinin; HI, hemagglutination inhibition; i.n., intranasal(ly); M, matrix; MDCK, Madin-Darby canine kidney; NA, neuraminidase; New Cal/99, influenza A/New CaleExecutenia/20/99 (H1N1) virus; NP, nucleoprotein; NS, nonstructural; p.c., postchallenge; p.i., postinfection; Sw/Iowa/30, influenza A/Swine/Iowa/30 (H1N1) virus; rHA, recombinant HA; WSN, influenza A/WSN/33 (H1N1) virus; VN, virus neutralization.

Copyright © 2004, The National Academy of Sciences

References

↵ Reid, A. H., Taubenberger, J. K. & Fanning, T. G. (2001) Microbes Infect. 3 , 81-87. pmid:11226857 LaunchUrlCrossRefPubMed Kilbourne, E. D. (1975) in The Influenza Viruses (Academic, New York), pp. 483-538. ↵ Taubenberger, J. K., Reid, A. H., Fanning, T. G., Janczewski, T. A., (2001) Philos. Trans. R Soc. LonExecuten B 356 , 1829-1839. pmid:11779381 LaunchUrlAbstract/FREE Full Text ↵ Crosby, A. (1989) America's Forgotten Pandemic (Cambridge Univ. Press, Cambridge, U.K.). ↵ Noble, G. R. (1982) in Basic and Applied Influenza Research, ed. Beere, A. S. (CRC, Boca Raton, FL), pp. 11-50. ↵ Glezen, N. P. (1996) Epidemiol. Rev. 18 , 64-76. pmid:8877331 LaunchUrlFREE Full Text ↵ Frost, W. (1920) Public Health Rep. 35 , 584-597. LaunchUrlCrossRef ↵ Reid, A. H., Fanning, T. G., Janczewski, T. A., McCall, S. & Taubenberger, J. K. (2002) J. Virol. 76 , 10717-10723. pmid:12368314 LaunchUrlAbstract/FREE Full Text ↵ Taubenberger, J. K., Reid, A. H. & Fanning, T. G. (2000) Virology 274 , 241-245. pmid:10964767 LaunchUrlCrossRefPubMed Taubenberger, J. K., Reid, A. H., Krafft, A. E., Bijwaard, K. E. & Fanning, T. G. (1997) Science 275 , 1793-1796. pmid:9065404 LaunchUrlAbstract/FREE Full Text ↵ Reid, A. H., Fanning, T. G., Janczewski, T. A. & Taubenberger, J. K. (2000) Proc. Natl. Acad. Sci. USA 97 , 6785-6790. pmid:10823895 LaunchUrlAbstract/FREE Full Text ↵ Reid, A. H., Fanning, T. G., Hultin, J. V. & Taubenberger, J. K. (1999) Proc. Natl. Acad. Sci. USA 96 , 1651-1656. pmid:9990079 LaunchUrlAbstract/FREE Full Text Reid, A. H., Taubenberger, J. K. & Fanning, T. G. (2001) Microbes Infect. 3 , 81-87. pmid:11226857 LaunchUrlCrossRefPubMed ↵ Basler, C., Reid, A., Dybing, J., Janczewski, T., Fanning, T., Zheng, H., Salvatore, M., Perdue, M., Swayne, D., Garcia-Sastre, A., et al. (2001) Proc. Natl. Acad. Sci. USA 98 , 2746-2751. pmid:11226311 LaunchUrlAbstract/FREE Full Text ↵ Tumpey, T. M., Garcia-Sastre, A., Mikulasova, A., Taubenberger, J. K., Swayne, D. E., Palese, P. & Basler, C. F. (2002) Proc. Natl. Acad. Sci. USA 99 , 13849-13854. pmid:12368467 LaunchUrlAbstract/FREE Full Text ↵ Geiss, G. K., Salvatore, M., Tumpey, T. M., Carter, V. S., Wang, X., Basler, C. F., Taubenberger, J. K., Bumgarner, R. E., Palese, P., Katze, M. G. & Garcia-Sastre, A. (2002) Proc. Natl. Acad. Sci. USA 99 , 10736-10741. pmid:12149435 LaunchUrlAbstract/FREE Full Text ↵ Goto, H. & Kawaoka, Y. (1998) Proc. Natl. Acad. Sci. USA 95 , 10224-10228. pmid:9707628 LaunchUrlAbstract/FREE Full Text Goto, H., Wells, K., Takada, A. & Kawaoka, Y. (2001) J. Virol. 75 , 9297-9301. pmid:11533192 LaunchUrlAbstract/FREE Full Text Hatta, M., Gao, P., Halfmann, P. & Kawaoka, Y. (2001) Science 293 , 1840-1842. pmid:11546875 LaunchUrlAbstract/FREE Full Text ↵ Wright, P. F. & Webster, R. G. (2001) in Field's Virology, eds. Knipe, D. M. & Howley, P. M. (Lippincott Williams & Wilkins, Philadelphia), pp. 1533-1579. ↵ Perdue, M. L. & Suarez, D. L. (2000) Vet. Microbiol. 74 , 77-86. pmid:10799780 LaunchUrlCrossRefPubMed ↵ Mitnaul, L. J., Matrosovich, M. N., Castrucci, M. R., Tuzikov, A. B., Bovin, N. V., Kobosa, D. & Kawoaka, Y. (2000) J. Virol. 74 , 6015-6020. pmid:10846083 LaunchUrlAbstract/FREE Full Text ↵ Kawaoka, Y., Krauss, S. & Webster, R. G. (1989) J. Virol. 63 , 4603-4608. pmid:2795713 LaunchUrlAbstract/FREE Full Text ↵ Lederberg, J. (2001) Proc. Natl. Acad. Sci. USA 98 , 2115-2116. pmid:11226198 LaunchUrlFREE Full Text ↵ FoExecuter, E., Devenish, L., Engelhardt, O. G., Palese, P., Brownlee, G. G. & Garcia-Sastre, A. (1999) J. Virol. 73 , 9679-9682. pmid:10516084 LaunchUrlAbstract/FREE Full Text ↵ Barbeito, M. S., Abraham, G., Best, M., Cairns, P., Langevin, P., Sterritt, W. G., Barr, D., Meulepas, W., Sanchez-Vizcaino, J. M. & Saraza, M. (1995) Rev. Sci. Tech. 14 , 873-887. pmid:8593417 LaunchUrlPubMed ↵ Reed, L. J. & Muench, H. (1938) Am. J. Hyg. 27 , 493-497. LaunchUrl ↵ Cox, N. J. & Kendal, A. P. (1984) J. Infect. Dis. 149 , 194-200. pmid:6699431 LaunchUrlAbstract/FREE Full Text ↵ Lu, X., Renshaw, M., Tumpey, T. M., Kelly, G. D., Hu-Primmer, J. & Katz, J. M. (2001) J. Virol. 75 , 4896-4901. pmid:11312361 LaunchUrlAbstract/FREE Full Text ↵ Baez, M., Palese, P. & Kilbourne, E. D. (1980) J. Infect. Dis. 141 , 362-365. pmid:7365284 LaunchUrlAbstract/FREE Full Text ↵ World Health Organization Collaborating Centers for Reference and Research on Influenza (1982) Concepts and Procedures for Laboratory-Based Influenza Surveillance, eds. Kendal, A. P., Skehel, J. J. & Pereira, M. S. (Centers for Disease Control and Prevention, Atlanta), pp. B17-B35. ↵ Mozdzanowska, K., Furchner, M., Washko, G., Mozdzanowski, J. & Gerhard, W. (1997) J. Virol. 71 , 4347-4355. pmid:9151823 LaunchUrlAbstract/FREE Full Text ↵ Rowe, T., Abernathy, R. A., Hu-Primmer, J., Thompson, W. W., Lu, X., Lim, W., Fukuda, K., Cox, N. J. & Katz, J. M. (1999) J. Clin. Microbiol. 37 , 937-943. pmid:10074505 LaunchUrlAbstract/FREE Full Text ↵ Kuroda, K., Hauser, C., Rott, R., Klenk, H. D. & Executeerfler, W. (1986) EMBO J. 5 , 1359-1365. pmid:3015601 LaunchUrlPubMed ↵ Hoyle, L. (1968) in The Influenza Viruses, eds. Gard, S., Hallauer, C. & Meyer, K. F. (Springer, New York), pp. 170-171. ↵ Lu, X., Tumpey, T. M., Morken, T., Zaki, S. R., Cox, N. J. & Katz, J. M. (1999) J. Virol. 73 , 5903-5911. pmid:10364342 LaunchUrlAbstract/FREE Full Text Dybing, J. K., Schultz-Cherry, S., Swayne, D. E., Suarez, D. L. & Perdue, M. L. (2000) J. Virol. 74 , 1443-1450. pmid:10627555 LaunchUrlAbstract/FREE Full Text ↵ Gao, P., Watanabe, S., Ito, T., Goto, H., Wells, K., McGregor, M., CAgedey, A. J. & Kawaoka, Y. (1999) J. Virol. 73 , 3184-3189. pmid:10074171 LaunchUrlAbstract/FREE Full Text ↵ Castrucci, M. R. & Kawaoka, Y. (1993) J. Virol. 67 , 759-764. pmid:8419645 LaunchUrlAbstract/FREE Full Text ↵ Sweet, C., Fenton, R. J. & Price, G. E. (1999) in Handbook of Animal Models of Infection, eds. Zak, O. & Sande, M. A. (Academic, New York), pp. 989-998. ↵ Beveridge, W. (1977) Influenza: The Last Distinguished Plaque, an UnTerminateed Tale of Discovery (Prodist, New York). ↵ Koen, J. S. (1919) Am. J. Vet. Med. 14 , 468-470. LaunchUrl ↵ Sugita, S., Yoshioka, Y., Itamura, S., Kanegae, Y., Oguchi, K., Gojobori, T., Nerome, K. & Oya, A. (1991) J. Mol. Evol. 32 , 16-32. pmid:1901364 LaunchUrlCrossRefPubMed ↵ Brown, I. H., Ludwig, S., Olsen, C. W., Hannoun, C., Scholtissek, C., Hinshaw, V. S., Harris, P. A., McCauley, J. W., Strong, I. & Alexander, D. J. (1997) J. Gen. Virol. 78 , 553-562. pmid:9049404 LaunchUrlAbstract/FREE Full Text ↵ Shope, R. E. (1936) J. Exp. Med. 63 , 669-684. LaunchUrlAbstract ↵ Davenport, F. M., Hennessy, A. V. & Francis, T., Jr. (1953) J. Exp. Med. 98 , 641-656. pmid:13109114 LaunchUrlAbstract ↵ Inkster, M. D., Hinshaw, V. S. & Schulze, I. T. (1993) J. Virol. 67 , 7436-7443. pmid:8230464 LaunchUrlAbstract/FREE Full Text ↵ McCullough, K. C. (1986) Arch. Virol. 87 , 1-36. pmid:3510607 LaunchUrlCrossRefPubMed ↵ Schlesinger, J. J. & Chapman, S. (1995) J. Gen. Virol. 76 , 217-220. pmid:7844536 LaunchUrlAbstract/FREE Full Text ↵ Gerhard, W., Mozdanowska, K., Furchner, M., Washko, G. & Maiese, K. (1997) Immunol. Rev. 159 , 95-103. pmid:9416505 LaunchUrlCrossRefPubMed
Like (0) or Share (0)