Frequent typing and molecular characterization of influenza A (IAV) strains are crucial for the identification of circulating subtypes and for the selection of the subtypes’ lineages to be included in the annually prepared vaccine cocktail. We investigated IAV sampled from an underrepresented population from Palestine. 200 nasopharyngeal aspirates (NPA) were collected between February and May of 2015 from Palestinians in East Jerusalem and the West Bank suffering from mild to severe symptoms of upper respiratory infections. NPA were screened for the presence of IAV using RT-PCR. Epidemiological data, hemagglutinin (HA) and neuraminidase (NA) gene sequences were analyzed in IAV positive samples. 50 samples tested positive for IAV; 48% of which were identified as A(H1N1)pdm09 and 52% as A(H3N2), respectively. Infection with A(H1N1)pdm09 occurred mainly in April, while A(H3N2) infections were mainly detected in March. Most IAV infections in 6-year-olds and below were attributed to subtype A(H3N2), while A(H1N1)pdm09 was responsible for most infections in adults above 18-year-olds. Analyses of HA and NA amino acid sequences revealed numerous substitutions. Thereafter, and based on the HA analysis, the Palestinian A(H1N1)pdm09 isolates fell into clade 6B, while the A(H3N2) isolates fell into clades 3C.2 and 3C.3, respectively. This study is significant in providing the first insight into the epidemiology and genetic properties of IAV circulating in Palestine. In contrast to international reports for the same season, A(H3N2) was not the dominant subtype as in northern hemisphere, nor was A(H1N1)pdm09 as in WHO reports for the Middle East, however genetic properties of Palestinian A(H3N2) and A(H1N1)pdm09 were in line with global isolates.
Citation: Bakri M, Samuh M, Azzeh M (2019) Molecular epidemiology survey and characterization of human influenza A viruses circulating among Palestinians in East Jerusalem and the West Bank in 2015. PLoS ONE 14(3): e0213290. https://doi.org/10.1371/journal.pone.0213290
Editor: Yongchang Cao, Sun Yat-Sen University, CHINA
Received: October 4, 2018; Accepted: February 18, 2019; Published: March 8, 2019
Copyright: © 2019 Bakri et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All data in this manuscript including figures, tables, and supplemental tables are available publicly.
Funding: Support for this work came, in part, from the internal resources of the Virology Laboratory at the Medical Research Center. No additional external funding was received for this study. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Influenza A virus (IAV) infections cause significant mortality, morbidity, and socio-economic burden throughout the world. One of the diseases described in the ancient history of medicine by Hippocrates in 412 BC is believed to be influenza infection . The first recognized influenza pandemic was in 1510 [2, 3]. Thereafter, another nine epidemics were identified prior to the well-known “Spanish” influenza pandemic of 1918/1919 [2, 3], the causative influenza virus strain of which was only identified and characterized definitely in 1997 [4, 5].
In contrast to many other vaccines, influenza vaccines have to be evaluated and updated annually due to antigenic shift and drift. For example, variability of the circulating A(H3N2) subtype has required four changes in the vaccine component between 2014 and 2018 . Vaccines against influenza are trivalent and contain one A(H1N1), one A(H3N2), and one influenza B strain or quadrivalent and contain one A(H1N1), one A(H3N2), and two influenza B strains. These are predicted as most likely to circulate in the following season. While WHO usually recommended trivalent influenza vaccine, recommendation for 2018/2019 influenza season was to use a quadrivalent vaccine . This decision was made as a consequence of the 2017/2018-influenza season with the majority of circulating influenza B belonging to the B/Yamagata/16/88 lineage; in Europe specifically the majority of influenza infections in 2018 of season 2017/2018 were caused by Influenza B viruses .
This report describes influenza A viruses circulating in Palestine in 2015, a country with very limited surveys in the epidemiology and genetic properties of infectious agents. Influenza season 2014/2015 was a season featured with low vaccine efficacy against the A(H3N2) vaccine component (A/Texas/50/2012), which consequently led to its replacement by A/Switzerland/9715293/2013 [8, 9]. Molecular characterization of circulating influenza viruses is indispensible for the annual vaccine recommendation. To the best of our knowledge, this is the first report tackling molecular epidemiology and characterization of human influenza A viruses circulating in Palestine.
Materials and methods
The Al-Quds University ethical committee approved this study (8/REC/16 in 2014 and 4/REC/19 in 2015). Al-Makassed Islamic Charitable Hospital (MICH), the referral hospital for Palestine, two kindergartens, and a private clinic approved sampling in their entity. Every single participant signed a consent form before sampling, with parents or legal guardians signing for children. Consent form contained the following participants’ data: sex, age, residency, symptoms, hospitalized days, vaccination status, and administration of antibiotics.
Study population and collection of nasopharyngeal aspirate
The study population included Palestinian children and adults from East Jerusalem and the West Bank that suffered mild to severe upper respiratory infection symptoms. Participants were either hospitalized, outpatients, kindergarten children, family members and acquaintance (referred to as private in the manuscript), or visiting a private clinic. Nasopharyngeal aspirate (NPA) were collected using FLOQSwabsTM (#502CS01, Copan Diagnostics Inc., USA).
Influenza A RNA extraction and RT-PCR
Influenza A RNA was extracted from the nasopharyngeal aspirate using the QIAamp Viral RNA Mini kit (Qiagen, Hilden, Germany). Amplification of the hemagglutinin (HA) and neuraminidase (NA) genes occurred in a one step RT-PCR reaction using One-Step RT-PCR Kit (Qiagen, Hilden, Germany). Complete HA and NA ORFs were basically amplified using primer sets recommended by WHO . Hereby, two primer pairs were used to amplify each segment. The primer pair H3N2R1104 and N2F257 for A(H3N2) amplification were modified during this research based on initial sequencing results to enhance the yield of the RT-PCR product as following H3N2R1104 (ATCCACACGTCATTTCCATCATCA) and N2F257 (AAACCAGCAGAATACAGAAATTGGTC). Screening for A(H1N1)pdm09 and A(H3N2) was performed using the N1F401/NARUc and H3A1F3/HARUc primer pairs respectively .
Sequence analysis and typing
Sequences were aligned with NCBI- and GISAID-archived  HA and NA sequences (S1 Table), using MegAlign program (Lasergene, version 14, DNASTARInc., WI, USA). The Lasergene MegAlign software marks nucleotide differences between the aligned sequences. Subsequently, chromatograms of our sequences were inspected visually for these nucleotides to check if the chromatogram peak and deduced bases match. This procedure is essential to verify whether a detected nucleotide substitution was due to real mutation or to a technical problem in the automatic chromatogram base calling. The annotated Palestinian sequences were submitted to GenBank and assigned the accession numbers KY075819-KY075852.
Substitution events in the Palestinian HA and NA genes were identified by comparing sequences to the A(H1N1)pdm09 and A(H3N2) vaccine strains of the isolation season 2014/2015, A/California/07/2009(H1N1) and A/Texas/50/2012(H3N2). Occurrence of these substitutions in archived sequences (S1 Table) and recent vaccine strains (A/Michigan/45/2015(H1N1), A/Switzerland/9715293/2013(H3N2), and A/Hong Kong/4801/2014(H3N2)) was also recorded. Substitution analysis was performed using MegAlign program. Additionally, amino acid substitution/mutation report provided by FluServer  was used to assess circulation of the substitution. To delineate substitutions, PubMed and FluServer  databases were queried. Information regarding location of substitution within antigenic sites of A(H3N2) isolates was identified based on epitope mapping reports [13–15]. Substitution residues in the antigenic sites of A(H1N1)pdm09 isolates were identified based on recent studies, which used A/California/07/2009 for mapping epitopes [16–18].
We noticed that the HA substitutions’ numbering in the literature was not consistent, as some authors used the amino acid (aa) position on the HA protein while others used aa positions on the HA1 and HA2 subunits. Therefore, we decided to indicate both position numberings in our tables to avoid confusion; however, we used the HA1 and HA2 substitution numbering throughout the manuscript and underlined the HA2 substitutions to distinguish them from HA1 ones.
In MegAlign program aligned Palestinian and reference sequences (S1 Table) were used to create phylogenetic trees. Phylogenetic trees were generated in Mega 7 program (https://www.megasoftware.net) using Maximum likelihood test, HKY+G model, and with 1,000 bootstrap replicates; only bootstrap values over 50 were shown.
Study sample data and demographics
200 NPA samples were collected between February and May of 2015 distributed as 9.5% in February, 48% in March, 33.5% in April, and 9% in May. Most of the NPA samples were collected from kindergarten (48%), with an almost equal number of samples collected from hospitalized patients/outpatients (17.5%), private clinic patients (17%), and private (17.5%). The study sample was divided into four age groups: infants (≤1 year), children before school age (1–6 years), school age (7–18 years), and adults (>18 years). Their distribution percentages were 11.5%, 63%, 5% and 20.5% respectively. As for sex of the study sample, 58.5% were males and 41.5% were females. The majority of study sample was from East Jerusalem (75.5%), while 24.5% was from the West Bank.
Runny nose was the most common symptom among the participants (76.5%), followed by cough (42.2%) and fever (21.4%). Single cases presented with sore throat, diarrhea, vomit, ear infection, bronchitis, chest pain, shortness of breath, and sputum discharge.
Influenza A positive samples
50 samples (25%) of the collected 200 NPA tested positive for IAV, from which 24 represented A(H1N1)pdm09, and 26 represented A(H3N2) subtype, respectively. IAV infection distributed almost equally between males (54%) and females (46%), while subtype H3N2 was responsible for most IAV infections among males (65.4%), H1N1 caused more infections in females (58.3%); this was not statistically significant.
Antibiotics were administrated in 23 cases, 6 of which tested positive for IAV (3 H1N1 and 3 H3N2). In six cases, patients received antibiotics and Tamiflu or Tamiflu alone, none of them tested positive for IAV. As only 15 of the study sample consented to have received the flu shot, four of which tested positive for IAV (2 H1N1 and 2 H3N2), we were unable to make a statement about significance in that regard.
While the monthly distribution of IAV positive samples relative to collected samples each month did not significantly vary between the months (26.3% on February, 21.8% on March, 29.9% on April and 22.2% on May), the monthly distribution of the subtypes changed. In fact, the majority of the A(H1N1)pdm09 cases were detected in April, while the majority of the A(H3N2) cases were detected in March (Fig 1). Fisher’s Exact Test for count data was performed to test whether being infected by A(H1N1)pdm09 and A(H3N2) is associated with the month of sampling. The test was significant for both subtypes (p-value = 0.00019 for A(H1N1)pdm09 and 0.0011 for A(H3N2)).
The percentages reflect the numbers of each subtype in each month in relevance to the 50 total positive IAV cases.
The percentages of cases infected with IAV throughout the four age groups relative to the number of total samples presented in each group were 30.4%, 23.8%, 20%, and 26.8% for age group ≤1 year, 1–6 years, 7–18 years, and >18 years, respectively. However, the distribution of IAV subtypes throughout the different age groups varied. Most of the IAV infections in the eldest age group (>18 years) were due to A(H1N1)pdm09 (Fig 2). Infections with A(H1N1)pdm09 and A(H3N2) were equal in the age group 7–18 years, while most of the IAV infections in the youngest age groups; 1–6 years and ≤1 year, were caused by A(H3N2) subtype (Fig 2). Although this finding was not statistically significant based on Fisher’s exact test (p-value = 0.078 for H1N1 and 0.094 for H3N2), the test revealed that the odds of being infected with A(H1N1)pdm09 among adults were higher than the odds of being infected with A(H1N1)pdm09 in those ≤6 years, while the odds of being infected with A(H3N2) in subjects ≤6 years were higher than in adults.
Sequencing results of HA and NA genes
HA and NA segments of all 50 positive IAV samples were subjected to gene amplification and sequencing. Complete or partial HA and/or NA sequencing were obtained in 10 H1N1 (three samples with full length HA and NA genes’ sequences, seven with ~70% partial NA sequences only) and 12 H3N2 (six samples with full length HA and NA sequences, one with full length HA and partial NA, three with full length HA only, and two with partial HA gene sequence only).
Substitutions in the HA and NA of Palestinian A(H1N1)pdm09 isolates
Twenty non-synonymous substitutions were detected in the three HA genes of the Palestinian A(H1N1)pdm09 isolates; three occurred in the signal peptide, ten in the HA1 domain, and seven in the HA2 domain (Table 1). With the exception of A3D substitution in the signal peptide, all other substitutions occurred in NCBI- and/or GISAID-archived  sequences. Seven out of the ten substitutions in the HA1 domain of the Palestinian A(H1N1)pdm09 isolates; P83S, S84N, K163Q, S185T, S203T, K283E, and I295V were located within antigenic epitopes. 27 synonymous substitutions were also detected in HA of the Palestinian A(H1N1)pdm09 isolates (S2 Table). The NA gene of the A(H1N1)pdm09 isolates exhibited 20 non-synonymous (Table 2) and 21 synonymous (S3 Table) substitutions.
Substitutions in the HA and NA of Palestinian A(H3N2) isolates
23 non-synonymous substitutions were identified in the HA genes of the Palestinian influenza A virus subtype A(H3N2) (Table 3). 18 of the 23 substitutions occurred in the HA1 domain and five in the HA2 domain, respectively. HA1 substitutions D53N, E62K, N121K, N121A, N122D, N128A, N128T, R142G, N144S, N144R, N145S, L157S, F159Y, K160T, P198S, N225D, and Q311H were located within antigenic epitopes of the HA gene. 26 synonymous substitutions were also detected in the Palestinian HA genes of the A(H3N2) isolates (S4 Table). Eight non-synonymous (Table 4) and 21 synonymous substitutions (S5 Table) occurred in the NA genes of Palestinian A(H3N2) isolates.
Phylogenetic analysis of Palestinian A(H1N1)pdm09 isolates
Both HA and NA sequences of Palestinian A(H1N1)pdm09 isolates showed percent identity around 97–98% with A/California/7/2009, the H1N1 vaccine component between 2011 and 2016, which includes our sampling season. Percent identity was however ~99% for HA and >99% for NA with A/Michigan/45/2015(H1N1)pdm09, the H1N1 vaccine component since season 2016/2017. All three Palestinian isolates with full length HA gene carried substitutions D97N, K163Q, S185T, S203T, A256T, K283E in the HA1 domain and E47K, S124K, E172K in the HA2 domain and consequently fell into clade 6B (Table 1 and Fig 3), respectively. Phylogenetic analysis showed that Palestinian A(H1N1)pdm09 isolates did not necessarily cluster with regional isolates (Fig 3). Palestinian KY075819 was almost identical with an isolate from California of the same year (KT836680), Palestinian KY075820 clustered with an isolate from Hawaii (KT836860), and Palestinian KY075821 clustered with an isolate from India (KT241020) and Jordan (EPI589572) on the same branch with A/Michigan/45/2015(H1N1).
Palestinian HA sequences (in red) were compared with those from regional and international isolates, as well as vaccine strain of the season 2014/2015 and the current vaccine strain (in dark blue). NCBI and GISAID accession numbers are indicated for all archived sequences. HA1 aa substitutions are in green and HA2 aa substitutions are in green and underlined.
Phylogenetic analysis of Palestinian A(H3N2) isolates
Percent identities between 11 of the 12 HA sequences of Palestinian A(H3N2) and A/Texas/50/2012(H3N2), vaccine component of our isolation season 2014/2015, ranged from 97.4–98.4%. However, it was >99% with A/Hong Kong/4801/2014(H3N2), the vaccine component of seasons 2016/2017 and 2017/2018. Ten of these 11 Palestinian sequences exhibited substitutions L3I, N144S, N145S, F159Y, K160T, N225D, Q311H in the HA1 domain, and D160N in the HA2 (Table 3) designating them to subclade 3C.2a. One (KY075834) of these 11 Palestinian sequences possessed all above substitutions but N144S and therefore fell into clade 3C.2. The twelfth Palestinian HA sequence (KY075845) contained N128A, R142G, N145S substitutions, and therefore fell into clade 3C.3. Ten (with full length HA gene) of the 12 HA sequences of Palestinian H3N2 isolates subjected to phylogenetic analysis (Fig 4) clustered together or/and with isolates from Bangkok (KP877361), Hawaii (KT842604), and Jordan (EPI589747 and EPI589759). Palestinian KY075845 clustered with an isolate from Washington (KT843007).
Palestinian HA sequences (in red) were compared with those from regional and international isolates, as well as vaccine strain of seasons 2014/2015-2017/2018 (in dark blue). NCBI and GISAID accession numbers are indicated for all archived sequences. HA1 aa substitutions are in green and HA2 are in green and underlined.
In regards to NA sequences of Palestinian H3N2 isolates, all, including the NA of the isolate to which KY075845 belongs, showed percent identity >99% with A/Switzerland/9715293/2013(H3N2), vaccine strain of 2015/2016.
Human influenza A viruses continue to show significant impacts on public health and global economy by causing annual outbreaks and occasional pandemics. Though from 2015, hitherto, this is the first molecular epidemiology study on influenza A circulating in Palestine and is actually one of the few reports in that regard from and on the Middle East [19, 20].
Our study demonstrated that the rate of infection with IAV among the different Palestinian age groups did not differ significantly and ranged from 20%-30%. The highest infection rate was detected in the ≤1-year-olds group, which in this study, were subjects that were either hospitalized, or visited a private clinic. Indeed, infants are considered to be at a high risk for influenza infection and associated with hospitalization (reviewed in ). Nevertheless, Fell et al.  argue, that there is a lack of studies in this regard and the majority of the data was from the USA. On the other hand, a comprehensive Flu Watch Group cohort study , concluded that influenza A infected 24% or 22% of unvaccinated people in the season preceding pandemic or during pandemic season, and that infection rates were highest in children, which generally agrees with our findings.
Our study elucidated that both A(H1N1)pdm09 and A(H3N2) were co-circulating in Palestine between February and May 2015 without an overall predominance of one subtype or the other. This finding was in accordance or was partially in accordance with regional studies from Lebanon, Iran, and Tunisia [19, 23, 24], which were performed during the same influenza season of our sampling. However, our findings did not agree with WHO weekly influenza surveillance reports of 2015 for season 2014/2014, which revealed a predominance of A(H1N1)pdm09 subtype in the Middle East . Hence, we reviewed the Flumart Outputs of the WHO FluNet database  for the Middle Eastern and North African countries for the exact period of our sampling. Reasonable data (IAV subtyped cases ≥ 50 over 8 weeks of our sampling time) were available from Algeria, Egypt, Iran, Israel, Jordan, Oman, Qatar, Tunisia and Turkey. While no one single A(H3N2) case was indicated from Qatar, the A(H1N1)pdm09 reported cases by far outnumbered A(H3N2) cases from Algeria, Egypt, Jordan, Oman, Tunisia and Turkey. The percentages of subtyped A(H3N2) and A(H1N1)pdm09 cases from Iran were similar to our results and to those of Moasser et al.  showing no predominance of one subtype. Interestingly, A(H3N2) was predominant in Israel according to the WHO Flumart Outputs  and a recent Israeli study , which was in line with surveillance reports from the northern hemisphere for season 2014/2015, including the USA, Canada and Europe, [8, 25, 28–30]. The discrepancies between our findings and regional reports, including the WHO influenza surveillance report in regard to subtype dominance cannot be attributed to our study setting in regard to targeted study sample, as both subtypes were present in all groups of our study sample; hospitalized patients, outpatients, kindergarten children, private clinic patients, and private individuals. From another aspect, our study revealed that the odds of being infected with A(H1N1)pdm09 among adults was higher than in infants and children ≤ 6-year-old, while the odds of being infected with A(H3N2) was higher in infants and children ≤ 6-year-old. Nevertheless, The relationship between age and infection with a specific influenza A subtype is a matter of inconsistencies between different reports, which may vary with season, epidemic timing, lack of pre-existing immunity against novel A(H3N2), and study settings [31, 32]. In our case, this result could be attributed to the limitation of our study in regard to the number of samples collected in these different groups and the months of collection.
Seventeen non-synonymous substitution events were recorded in the HA1 and HA2 aa sequences of the Palestinian A(H1N1)pdm09. The Palestinian A(H1N1)pdm09 isolates fell into clade 6B. A(H1N1)pdm09 with clade 6B were predominant for season 2014/2015 as indicated by the WHO , regional , and International reports [33–35]. Most of the 6B clade-defining substitutions evolved during the last years and were reported earlier in some studies before being attributed to the new clades. S185T was previously reported in isolates from Tunisians with severe influenza A infection . S203T contributes to antigenic drift  and is a common variant marker within an outbreak . Substitution S84N, found in HA gene of one Palestinian isolate is one of the substitutions defining the novel genetic subclade 6B.1 [33, 34, 38]. Substitution I321V is also a common variant marker within outbreaks  and was found in all Palestinian isolates. E47K, S124K, and E172K substitutions located in the HA2 do not only define clade 6B; they were reported, along with other substitutions, to increase HA stability through generation of favorable inter- and intramonomer interactions . A variant with E47K was also shown to induce infection in ferrets .
We detected 20 non-synonymous substitutions in the NA sequences from 10 Palestinian A(H1N1)pdm09 isolates. All of these substitutions were circulating in NCBI- and GISAID-archived sequences. Some of these substitutions were detected in oseltamivir-resistant strains, but do not confer resistance per se, such as N44S, N200S, V241I, and N369K . Substitutions S79L and K331N, occurred independently in three and in one Palestinian NA sequences, were studied thoroughly by Ilyushina et al. , who demonstrated that S79L reduced the activity of the NA enzyme, while the K331N was associated with evidently increased resistance to IFN-λ1. Substitutions V241I, N369K, N386K and K432E, detected in all Palestinian A(H1N1)pdm09 NA sequences, may alter the binding affinity between oseltamivir and NA, and consequently affect susceptibility of A(H1N1)pdm09 strains to oseltamivir . Substitution I365T, which occurred in one Palestinian sequence, was related to virulence and antigenic drift/escape mutant . Substitution N44S detected in four Palestinian samples created a new potential N-glycosylation site at position 42, while N386K, detected in all Palestinian isolates, removes a potential N-glycosylation site at position 386, both cases may affect antigenic properties of the strain .
Ten Palestinian 2015 A(H3N2) isolates fell into subclade 3C.2a, one into clade 3C.2, and one into clade 3C.3, respectively. This result was in accordance with the WHO, regional and international reports of the same season [9, 24, 28, 35, 43–45]. Interestingly, the neuraminidase gene sequences of all Palestinian A(H3N2) were closely related to A/Switzerland/9715293/2013(H3N2), subclade 3C.3a, which was a distinctive finding observed for the A(H3N2) isolates from 2015 [35, 45]. Each of non-synonymous substitutions N144S, N144R and N122D remove a potential N-glycosylation site, while K160T and N128T create a new potential N-glycosylation, with the consequences of affecting antigenic properties . Some of the substitutions (N121K, P198S, L157S), which were detected only in the single Palestinian 3C.3 HA sequence (KY075845) are of significant interest. N121K became dominant in 2017 and was detectd in isolates from severe influenza cases in Hong Kong in 2017  and was attributed to lower vaccine effectiveness in clades 3C.2a and 3C.2a1 . Substitutions P198S and L157S had been related to virulence and antigenic drift/escape mutant .
Of the eight non-synonymous substitutions recorded in the NA sequences of the Palestinian A(H3N2), H150R, E221N and E221D, and N329 are positions where substitutions had been related to antigenic drift/escape mutants . N329K removes a potential N-glycosylation site at position 329, which may affect antigenic properties of this strain .
Finally, we detected one single synonymous substitution in the HA signal peptide region of each subtype; T30C: Y10Y in one A(H1N1)pdm09 isolate and T18C: A6A in one A(H3N2) isolate (S2 and S4 Tables). Although none of these synonymous substitutions were addressed in the literature, in vitro experiments in a recent study revealed that synonymous mutations at the beginning of the HA gene may affect viral fitness .
The emergence of IAV substitutions/mutations should be carefully monitored for public health concerns, as detailed above, many amino acid substitutions evolved during outbreaks and were only detected in few cases before becoming dominant few years later. Therefore, we believe that our study contributes to the international efforts by providing epidemiological and molecular biological insights into influenza A viruses circulating in Palestine and advocate for comprehensive annual typing and mutation analyses of Influenza A in Palestine and the region.
S1 Table. Accession numbers of archived sequences used for substitution analysis.
S2 Table. Synonymous substitutions in the H1 gene of Palestinian H1N1 isolates (N = 3).
The aa substitutions are presented by the position on HA gene as well as HA1 and HA2 subunits. 2015+ = 2015 isolates including A/Michigan/45/2015(H1N1), the H1N1 vaccine component for the years 2017/2018 and 2018/2019.
S3 Table. Synonymous substitutions in the NA gene of the Palestinian H1N1 isolates (n = 10).
2015+ = 2015 isolates including A/Michigan/45/2015(H1N1), the H1N1 vaccine component for the years 2017/2018 and 2018/2019.
S4 Table. Synonymous substitutions in the HA gene of the Palestinian H3N2 sequences (n = 12).
The aa substitutions are presented by their position on the HA gene and by HA1 and HA2 subunits. + = Substitution occurs also in A/Switzerland/9715293/2013(H3N2), vaccine strain 2015/2016, ^ = Substitution occurs also in A/Hong Kong/4801/2014(H3N2), vaccine strain 2016/2017 and 2017/2018.
S5 Table. Synonymous substitutions in the NA gene of the Palestinian H3N2 sequences (n = 7).
+ = Substitution occurs also in A/Switzerland/9715293/2013(H3N2), vaccine strain 2015/2016, ^ = Substitution occurs also in A/Hong Kong/4801/2014(H3N2), vaccine strain 2016/2017 and 2017/2018.
This work comprises, in part, Maysoon Bakri’s master thesis, which was performed at the Virology Research Laboratory-Medical Research Center, Al-Quds University, Palestine. We would like to thank Dr. Amin Thalji, for his kind cooperation allowing us to sample at his private clinic in Ramallah, Palestine. We would also like to thank MICH, specifically Dr. Hatem Khamash, Head of the Neonatal Department at MICH, for their kind cooperation. We would like to thank Al-Sanafer and Al-Iman Kindergartens for approving the sampling at their facilities and reaching out to the parents. We are thankful for friends, acquaintance, and family members for allowing us to take their samples. Finally, we would like to thank Prof. Donald Seto (School of Systems Biology, George Mason University, USA) for critical review of this manuscript.
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