Background
The Republic of Congo has one of the highest rates of cervical cancer incidence in Sub-Sahara Africa. According to the World Health Organization (WHO), the reported age-standardized incidence rate and age-standardized mortality rate were 25.6 and 13.0 cases per 100 000 women in 2014 [
1].
Epidemiological and molecular studies are showed that High-risk human papillomaviruses (HPV) types are the etiological agents of cervical cancer [
2,
3]. HPV-16 is the most common high-risk genotype involved in cervical cancer, representing for over 50% of all cases [
4].
However, most HPV infections resolve spontaneously, suggesting that other co-factors are necessary in the persistence and lesion progression to cancer. These cofactors include some variants of high-risk types such as those of HPV16. Several molecular variants were described and classified according to geographical regions for the HPV-16 genotype [
5,
6]. Conventionally, a variant is defined when there is a difference of less than 2% between the complete genomes of the same HPV type. A difference from 1.0% has been used to define the lineage and the sub-lineages variants by a difference from 0.5 to 1.0% between the lineages [
7-
9]. The variants have been classified in six major phylogenetic lineages (European, E; Asian, As; African-1, Af-1; African-2, Af-2; Asian-American, AA and North-American, NA) showing more than 98% nucleotide level similarity in L1 or E6 genes [
10,
11]. However, a new phylogenetic nomenclature was proposed for the HPV-16 in four lineages as follows: A (previously called European-Asian, EAS), B (African 1, Af-1), C (African 2, Af-2), and D (North-American/Asian-American, NA/AA) [
7,
9].
HPV-16 variants studies have shown that certain intratypic-variants would contribute more than others to the persistence of HPV infection and cervical cancer progression [
12,
13]. In particular, non-European variants are more highly oncogenic them European variants [
12,
14,
15]. Indeed, the importance of the E6 and E7 genes lies in their ability to transform and immortalize the host cell. A single nucleotide change in these genes could affect this ability, which would explain the difference in some variants to progress quickly them others to cervical cancer [
16]. E6 and E7 interacts with several cellular proteins in particular, they inactivate the p53 and the pRb respectively, which are two cancer suppressor major proteins [
17].
In this perspective and with the advent of prophylactic vaccines against HPV-16/18 and cervical cancer, it becomes necessary to know the HPV genetic variants present in each population.
In Congo, our previous study showed that the most common genotype in invasive cervical cancer and its precancerous lesions was HPV-16 [
18]. Thus, to better formulate immunization strategies and other preventive measures in Congo, this preliminary study aimed to analyze the nucleotide changes of the HPV-16 E6 and E7 isolates in order to identify the different genetic variants prevalent among infected women with cervical carcinoma in southwest of the Congo.
Discussion
The HPV-16 genotype was recently identified as the most prevalent genotype in cervical cancer cases and high grade precancerous lesions in the southwest of Congo [
18].
To date, there are no molecular epidemiological studies on HPV-16 variants carried out in Congo. In the present study, we characterized the nucleotide changes of the HPV16 mono-infection isolates among infected Congolese women with cervical cancer based on the E6 and E7 viral oncogenes analysis.
Several studies showed that HPV-16 variants may influence viral persistence and progression to cervical cancer, which partly explains the high prevalence of this cancer in some populations compared to other [
12]. Also, their distribution is geographically related and associated with the ethnic group [
19,
20]. The HPV 16 E6 and E7 early genes are essential in cervical cancer pathogenesis [
21]. Any change in their sequences could induce an alteration of the biological function of the proteins encoded by these genes, which would justify the importance of these kinds of studies, especially in the poorly studied populations as ours.
In this study, phylogenetic analysis of HPV16 E6 and E7 genes was performed to analyze the local distribution of HPV16 lineages, according to the Yamada et al. [
5] classification. A total of eighteen point mutations in E6 and four in E7 genomic regions were found. Most nucleotide changes reported in our study have been previously described. At least a nucleotide change was observed in all sequences analyzed. This result is consistent with the literature data indicating that more than 90% of the E6 sequences contains mutations in cervical carcinomas, whereas the E7 gene seems to be more conserved [
5,
6,
22,
23].
At the E6 genomic region, five characteristic mutations, C143G, G145T, T286A, A289G, and C335T defining the African lineage were found in our study as well as it’s was previously described [
8,
11,
24]. However, some of the observed mutations are significant in the literature; in particular the two non-synonymous changes African lineage located in E6 N-terminus coding region at codon 10 and 14, which lead to amino acid changes R10T and Q14D respectively. These amino acid changes may lead to a difference in affinity with p53 and significantly altered its degradation rate by this oncogene [
25,
26]. Crook et al. [
27] showed that the amino acid mutations in these positions increased by 180% the affinity of E6 with p53. It is also reported that the amino acid change R10I in addition to other mutations described between nucleotide position 106 and 113 could lead to a low affinity for binding of E6 and degrade p53 [
25], although these findings remain controversial and poorly documented.
In contrast to E6, the E7 gene variability has been less studied. Our studies on E7 showed a highly conserved region of the HPV genome with some mutations (mainly point mutations) described and few lead to amino acid changes [
23,
28]. Out of four mutations identified in our study, two were the common silent variations found in all sequences. The two others were non-synonymous mutations, of which a common described N29S was found in three isolates (23%). This mutation often described in Asia, was located in the cervical carcinoma in Africa [
23,
29,
30]. The importance of this amino acid change was suggested by Zehbe et al. [
22] because of its location in an immunoreactive region. However, E7 protein with the N29S mutation present an identical power transforming has the prototype strain, after measuring the cooperation E7/activated
ras gene in rat embryo fibroblast cells [
31]. In addition, N29S is involved in binding to pRB and could alter the affinity of the E7 protein for pRB, or modification of the oncogenic potential. But it was also proved that the variant A647G only binds with similar affinity to that of the prototype [
32,
33]. The D21N mutation (G622A) described in this study seems to be for the first time. Only one case showed this variation; future studies by sequencing after cloning in a vector are needed to confirm its description in our population.
All HPV-16 isolates examined in this study belonged to the African lineage, of which 53.8% belonged to Af-1 lineage and 46.1% to Af-2 lineage. Our results are in agreement with the literature. Indeed, the pioneering studies of Yamada and Wheeler showed that the African lineage was dominated in the continent. More than 90.7% of the variants in Africa region are African lineage, of which 61% belongs to the Af-1 lineage and 29.7% to the Af-2 lineage [
6,
11].
Tu et al. [
34] in South Africa, Qmichou et al. [
35] in Morocco and Buonaguro et al. [
30] in Uganda reported have identified in their respective studies 41%, 64.5% and 100% of variants belonging to the African lineage. These results substantially similar show the importance of taking into account the African variants in the global effort to fight against cervical cancer. The findings obtained by Qmichou et al. [
30] which reported 35.5% of variants belonged to the Af-1 lineage and 29% to the Af-2 lineage such as Yamada (61% Af-1 and 29.7% Af-2) are consistent with ours by showing that the Af-1 lineage is predominant on the continent [
11]. However, non-African lineages were also reported in the continent, especially in North Africa and South Africa regions. The introduction of these lineages could be explained by the diversity of their population with European populations. In our study, the absence of non-African lineages could be explained by the small size of our sample, but also by the fact that their frequency is very low in a homogeneous African black population. However, further investigation seems to be necessary to confirm this hypothesis.
Knowing that HPV variants data are important in developing HPV diagnostics, vaccines, and other therapeutic approaches to monitoring virus-induced diseases [
28], the major limitation of this study was the small size of DNA-sample analyzed. However, this is the first study that provides information on HPV-16 E6 and E7 genetic diversity in Congolese women. A larger sample size of HPV 16 including E6 and E7, but also L1 and LCR genes will be necessary to better identify all the genomic changes and appreciate their impact on the various grades of cervical lesions.
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Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
LMAB was responsible for design and the experiment of the study. SZA and JVM participated in drafting the manuscript. DM and LMAB have conducted the recruitment process of the sample. LH and MME were responsible for project implementation and participated in the critical reading of the manuscript. All authors read and approved the final manuscript.