Literature DB >> 27198009

Complete Genome Sequences of Eight Human Papillomavirus Type 16 Asian American and European Variant Isolates from Cervical Biopsies and Lesions in Indian Women.

Paramita Mandal1, Bornali Bhattacharjee2, Shrinka Sen1, Amrapali Bhattacharya1, Rahul Roy Chowdhury3, Nidhu Ranjan Mondal3, Sharmila Sengupta2.   

Abstract

Human papillomavirus type 16 (HPV16), a member of the Papillomaviridae family, is the primary etiological agent of cervical cancer. Here, we report the complete genome sequences of four HPV16 Asian American variants and four European variants, isolated from cervical biopsies and scrapings in India.
Copyright © 2016 Mandal et al.

Entities:  

Year:  2016        PMID: 27198009      PMCID: PMC4878291          DOI: 10.1128/genomeA.00243-16

Source DB:  PubMed          Journal:  Genome Announc


GENOME ANNOUNCEMENT

Human papillomavirus type 16 (HPV16), a member of the Papillomaviridae family, is phylogenetically clustered within the Alphapapillomavirus 9 species group and is predominantly associated with cervical cancer (CaCx) (1, 2). Corresponding to geographical regions, HPV16 is classified into five variant lineages (3–5), namely, European (E), Asian (A), Asian American (AA), African-1 (Af1), and African-2 (Af2). In India, HPV16 has been found to be the most prevalent high-risk type associated with CaCx cases (6), and, in an earlier report from our laboratory, the presence of AA variants was confirmed for the first time along with E variants using Sanger sequencing (7–9). Here, we report the complete genome sequences of four viral isolates belonging to the AA variant lineage and four viral isolates belonging to the E variant lineage, isolated from cervical biopsies and scrapings in India. DNA was isolated from cervical specimens using the Qiagen DNA minikit (Qiagen, Germany) according to the manufacturer’s instructions. HPV screening was carried out using broad range GP5+/GP6+ primer pairs, and the presence of HPV16 was confirmed by quantitative E6 PCR (10). Viral genomes were enriched using a 100-ng DNA template, two long-range overlapping primer sets, and an Expand Long Template PCR enzyme mix (Roche, Switzerland). The amplicons were purified, quantitated, and mixed in equimolar proportions to generate 1 µg of starting material. The pooled amplicons were subsequently sheared to low molecular weight fragments. Adapter ligation was carried out using an Ion Plus fragment library kit (Thermo Fisher Scientific, USA) and each library was labeled using Ion Xpress bar code adapters (Thermo Fisher Scientific, USA). The ligated libraries were size-selected using E‐Gel SizeSelect 2% agarose gels (Thermo Fisher Scientific, USA) and assessed on an Agilent 2100 Bioanalyzer (Agilent Technologies, Germany). The libraries were quantified using the Ion Library TaqMan quantitation kit (Thermo Fisher Scientific, USA) and the bar-coded library pools were amplified onto Ion Sphere particles by emulsion PCR. High-throughput sequencing was performed on an Ion PGM sequencer platform (Thermo Fisher Scientific, USA), and the Torrent Suite version 3.0 data processing pipeline was used to generate sequence reads. Per genome, approximately 2,300 paired-end reads with an average insert length of 200 bp were generated (~46,000 bases/genome). De novo assembly was carried out to form consensus sequences using the Geneious version 7.0.3 assembler (11). Whole-genome Sanger sequences, generated independently using short range primers sets (8) from each specimen, were aligned to respective consensus sequences for confirmation. Each consensus sequence was manually checked to identify variant lineages on the basis of differences in the L1 region and whole genome BLAST search. The curated genome sequences were annotated with genome annotation transfer utility software (12) using HPV16 E or AA reference sequences (NC_001526.2 and AB818689) as templates. The annotated genome sequences thus generated were further validated manually.

Nucleotide sequence accession numbers.

Whole-genome sequences of all eight viral isolates have been deposited in GenBank using NCBI’s BankIt tool, and the accession numbers are listed in Table 1.
TABLE 1 

List of HPV16 isolate genomes released to NCBI

Isolate IDAccession numberSourceGenome size (bp)Variant type
IND-T119KU641509Cervical biopsy7,908Asian American
IND-T121KU684314Cervical biopsy7,908Asian American
IND-T488KU684311Cervical biopsy7,916Asian American
IND-CMCP14KU684315Cervical scrape7.909Asian American
IND-T395KU684313Cervical biopsy7,909European
IND-T315KU684316Cervical biopsy7,906European
IND-T338KU684317Cervical biopsy7,906European
IND-JNM434KU684312Cervical scrape7,906European
List of HPV16 isolate genomes released to NCBI
  11 in total

1.  Association of viral load with HPV16 positive cervical cancer pathogenesis: causal relevance in isolates harboring intact viral E2 gene.

Authors:  Damayanti Das; Bornali Bhattacharjee; Shrinka Sen; Indranil Mukhopadhyay; Sharmila Sengupta
Journal:  Virology       Date:  2010-04-14       Impact factor: 3.616

2.  HPV16 E2 gene disruption and polymorphisms of E2 and LCR: some significant associations with cervical cancer in Indian women.

Authors:  Bornali Bhattacharjee; Sharmila Sengupta
Journal:  Gynecol Oncol       Date:  2005-10-24       Impact factor: 5.482

3.  Characterization of sequence variations within HPV16 isolates among Indian women: prediction of causal role of rare non-synonymous variations within intact isolates in cervical cancer pathogenesis.

Authors:  Bornali Bhattacharjee; Nidhu Ranjan Mandal; Sudipta Roy; Sharmila Sengupta
Journal:  Virology       Date:  2008-05-20       Impact factor: 3.616

4.  Human papillomavirus type 16 genetic variants: phylogeny and classification based on E6 and LCR.

Authors:  Iris Cornet; Tarik Gheit; Silvia Franceschi; Jerome Vignat; Robert D Burk; Bakary S Sylla; Massimo Tommasino; Gary M Clifford
Journal:  J Virol       Date:  2012-04-04       Impact factor: 5.103

5.  The genetic drift of human papillomavirus type 16 is a means of reconstructing prehistoric viral spread and the movement of ancient human populations.

Authors:  L Ho; S Y Chan; R D Burk; B C Das; K Fujinaga; J P Icenogle; T Kahn; N Kiviat; W Lancaster; P Mavromara-Nazos
Journal:  J Virol       Date:  1993-11       Impact factor: 5.103

6.  HPV16 genetic variation and the development of cervical cancer worldwide.

Authors:  I Cornet; T Gheit; M R Iannacone; J Vignat; B S Sylla; A Del Mistro; S Franceschi; M Tommasino; G M Clifford
Journal:  Br J Cancer       Date:  2012-11-20       Impact factor: 7.640

7.  Geneious Basic: an integrated and extendable desktop software platform for the organization and analysis of sequence data.

Authors:  Matthew Kearse; Richard Moir; Amy Wilson; Steven Stones-Havas; Matthew Cheung; Shane Sturrock; Simon Buxton; Alex Cooper; Sidney Markowitz; Chris Duran; Tobias Thierer; Bruce Ashton; Peter Meintjes; Alexei Drummond
Journal:  Bioinformatics       Date:  2012-04-27       Impact factor: 6.937

8.  Prevalence and distribution of high-risk human papilloma virus (HPV) types in invasive squamous cell carcinoma of the cervix and in normal women in Andhra Pradesh, India.

Authors:  A Pavani Sowjanya; Meenkashi Jain; Usha Rani Poli; S Padma; Manik Das; Keerti V Shah; B N Rao; Radha Rama Devi; Patti E Gravitt; Gayatri Ramakrishna
Journal:  BMC Infect Dis       Date:  2005-12-22       Impact factor: 3.090

9.  Genome Annotation Transfer Utility (GATU): rapid annotation of viral genomes using a closely related reference genome.

Authors:  Vasily Tcherepanov; Angelika Ehlers; Chris Upton
Journal:  BMC Genomics       Date:  2006-06-13       Impact factor: 3.969

10.  Higher prevalence of human papillomavirus infection in adolescent and young adult girls belonging to different Indian tribes with varied socio-sexual lifestyle.

Authors:  Kirti Sharma; Atul Kathait; Asha Jain; Karmila Kujur; Shirish Raghuwanshi; Alok Chandra Bharti; Asha Chandola Saklani; Bhudev Chandra Das
Journal:  PLoS One       Date:  2015-05-08       Impact factor: 3.240

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