Abstract
Lactotransferrin, also known as lactoferrin, is an iron binding glycoprotein that displays antiviral activity against many different infectious agents, including human immunodeficiency virus (HIV)-1. Lactotransferrin is present in the breast milk and in the female genitourinary mucosa and it has been hypothesised as a possible candidate to prevent mother-to-child HIV-1 transmission. To verify if two functional polymorphisms, Thr29Ala and Arg47Lys, in the lactotransferrin encoding gene (LTF) could affect HIV-1 infection and vertical transmission, a preliminary association study was performed in 238 HIV-1 positive and 99 HIV-1 negative children from Brazil, Italy, Africa and India. No statistically significant association for the Thr29Ala and Arg47Lys LTF polymorphisms and HIV-1 susceptibility in the studied populations was found. Additionally LTF polymorphisms frequencies were compared between the four different ethnic groups.
Keywords: AIDS, HIV-1, innate immunity, lactoferrin, SNPs, vertical transmission
In 2013, about 240,000 children acquired human immunodeficiency virus (HIV)-1 infection worldwide (WHO 2013). The main route of HIV-1 infection for a child is through the HIV-1 positive mother, during delivery or breastfeeding. Without antiretroviral intervention, caesarean delivery (Legardy-Williams et al. 2010) or safer alternatives to breastfeeding, the transmission rate of HIV-1 from an infected mother to her infant varies from 30-45% (Datta et al. 1994).
In this context, innate immunity effector molecules have an important role in fighting against HIV-1 infection. Among them, lactotransferrin (also known as lactoferrin) seemed to be a possible candidate to prevent mother-to-child transmission (MTCT) of the virus. Lactotransferrin, in fact, has been reported as possessing antiviral activity against HIV-1: through the binding to dendritic cell-specific intercellular adhesion molecule-3-grabbing non-integrin, the protein blocks the attachment to the viral gp120, so the virus transmission from dendritic cells to T cells is inhibited (Groot et al. 2005).
Lactotransferrin is found in breast milk and at the mucosal level in the female genitourinary tract (Kazmi et al. 2006): a reduction in maternal serum lactotransferrin has been correlated with increased risk of HIV-1 MTCT (Defer et al. 1995, Semba et al. 1998). Reduced lactotransferrin serum level have been detected in HIV-1 infected individuals compared to healthy controls (Dapsanse et al. 2001) and in acquired immune deficiency syndrome (AIDS) patients compared to asymptomatic and symptomatic HIV-1 positive individuals or controls (van der Strate et al. 2001).
The LTF gene (chromosomal localisation: 3p21.3) encodes lactotransferrin; more than 60 single nucleotide polymorphisms (SNPs) have been identified within the promoter region, exons or introns. Two nonsynonymous polymorphisms, Thr29Ala and Arg47Lys (rs1126477 and rs1126478, respectively) in the first exon of the LTF gene, resulting in amino acid changes in the mature peptide and located within the strongly basic N-terminal region of the protein, that mediates its antibacterial properties (Shanbacher et al. 1992) have been described as associated with different pathologies, such as periodontitis (Velliyagounder et al. 2003, Jordan et al. 2005, Wu et al. 2009), dental caries (Azevedo et al. 2010, Fine et al. 2013), ovarian cancer (Cao et al. 2011), nasopharyngeal carcinoma (Zhou et al. 2012), dyslipidaemia (Moreno-Navarrete et al. 2008) and coronary artery stenosis (Videm et al. 2012).
The Thr29Ala amino acid change results from an A-G substitution at nucleotide 88 and the Arg47Lys change results from an A-G transition at nucleotide 140 (Teng & Gladwell 2006).
This preliminary study aims at investigating the role of these two nonsynonymous SNPs in HIV-1 positive newborns infected by vertical transmission and children not infected but born from HIV-1 positive mothers, in four different populations from Brazil, Italy, Africa and India. Frequency differences within the four ethnic groups will be also described.
SUBJECTS, MATERIALS AND METHODS
Patients - Genomic DNAs from 238 HIV-1 positive children (all within 6 and 14 years of age; 126 females - 53% and 112 males - 47%) were obtained. The sample consisted of 78 Brazilian children (40 females and 38 males) from the state of Pernambuco, Northeast Region of Brazil, collected at the Prof Fernando Figueira Integral Medicine Institute, Recife, 89 Italians (49 females and 40 males), collected at the Children Hospital Regina Margherita, Turin, 26 Zimbabwe Africans (14 females and 12 males) and 45 Kerala Indians (23 females and 22 males). The last two samples both came from a historical cohort kindly provided by Prof Trabattoni (Sacco Hospital, Milan, Italy).
The children were infected during delivery [exposed infected (EI)]. Ninety-nine exposed uninfected (EU) HIV-1 negative children (all within 6 and 14 years of age; 53 females - 54% and 46 males - 46%; 35 Brazilian, 20 females and 15 males; 18 Italian, 9 females and 9 males; 15 Zimbabwe African, 9 females and 6 males; 31 Kerala Indians, 15 females and 16 males), born from HIV-1 positive mothers, were already available at the Laboratory of Immunogenetics of Scientific Institute For Research, Hospitalization and Care (IRCCS) Burlo Garofolo and were used for this study. Biological material from the mothers was not available and the sole information available to us was that none of the infected mothers underwent antiretroviral therapy before delivery or caesarean section to prevent HIV-1 infection of the newborns.
DNA extraction and SNPs genotyping - DNA extraction from whole blood was performed using the DNeasy Blood and Tissue Kit (Qiagen, Germany), in accordance with the manufacturers’ manual.
The two LTF (National Center for Biotechnology Information Reference Sequence: NC_000003), functional SNPs, Thr29Ala and Arg47Lys (rs1126477 and rs1126478, respectively) were genotyped by real time polymerase chain reaction (PCR) using C___9698511_10 and C___9698521_10 fluorogenic allele-specific TaqMan SNPs genotyping assay probes (Applied Biosystems-Life Technologies, USA) on the ABI7900HT Real Time PCR platform (Applied Biosystems), following manufacturer instructions: an initial step for Taq polymerase activation at 95ºC for 10 min followed by 40 cycles with 15 s of 95ºC for denaturation and 1 min at 60ºC for extension.
Allelic discrimination was done both manually and automatically with the SDS detection software (Applied Biosystems).
Real time allele specific PCRs results were double checked by direct sequencing performed on 50 randomly chosen samples and 100% of concordance was found.
Statistical analysis - LTF gene polymorphisms, allele and genotype frequencies were calculated by direct counting, while haplotype frequencies were computed using the Arlequin software v.3.1 (Excoffier & Lischer 2010).
The Fisher’s exact test for pairwise comparison of allele, genotype and haplotype frequencies (using contingency tables as appropriate) was performed with the open-source R v.3.1.0 (R Development Core Team 2014). Only p values < 0.01 were considered to be significant.
p values for linkage disequilibrium (LD) analysis were calculated using the permutation test with the EM algorithm, Arlequin software (Excoffier & Lischer 2010), whereas D, D’ and r2 measures were computed with SNPstat (Sole et al. 2006, Clayton 2013). Post-hoc power calculations were performed through G*Power software v.3.1.9.2 (Faul et al. 2007).
Ethics - Two independent ethical committees, one from IRCCS Burlo Garofolo (protocol L-1106, 1 May 2010), the other from Prof Fernando Figueira Integral Medicine Institute (registration 2273-11), responsible for all patients’ biological samples (from 4 populations), approved the retrospective study.
All study experiments and procedures have been performed in accordance with the ethical standards of the Declaration of Helsinki.
RESULTS
The genotype frequencies of Thr29Ala and Arg47Lys polymorphisms of the LTF gene were assessed in 238 HIV-1 positive children (EI) and 99 HIV-1 negative (EU) children all born from HIV-1 positive women from four different populations. The polymorphisms were in Hardy-Weinberg equilibrium in all groups, except for the Thr29Ala in the EU Indians group and Arg47Lys in the EI African group (Tables I, II).
The Thr29Ala A allele was the major allele in the African population (76% in the EU and 77% in the EI) and in the Brazilian one (51% in the EU and 52% in the EI), whereas in Indians and Italians, the A allele was the minor one (47% in EU and 39% in the EI in Indians and 25% in EU and 21% in EI in Italians, respectively) (Table I).
TABLE I. LTF Thr29Ala polymorphism allele, genotype frequencies (and counts) in human immunodeficiency virus (HIV) positive (+) and negative (-) children in the four different populations analysed.
| LTF SNP Thr29Ala (rs1126477) | HIV- | HIV+ | HIV- vs. HIV+ p (CI) OR |
|---|---|---|---|
| Africa | n = 15 | n = 26 | |
| A | 0.76 (23) | 0.77 (40) | Reference |
| G | 0.23 (7) | 0.23 (12) | 1.00 (0.30-3.40) 0.99 |
| A/A | 0.60 (9) | 0.61 (16) | Reference |
| A/G | 0.33 (5) | 0.31 (8) | 1.00 (0.19-4.64) 0.90 |
| G/G | 0.07 (1) | 0.08 (2) | 1.00 (0.05-73.62) 1.12 |
| HWE (χ2; p) | 0.07; 0.79 | 0.46; 0.50 | - |
| India | n = 31 | n = 45 | |
| A | 0.47 (29) | 0.39 (35) | Reference |
| G | 0.53 (33) | 0.61 (55) | 0.40 (0.68-2.80) 1.38 |
| A/A | 0.13 (4) | 0.16 (7) | Reference |
| A/G | 0.68 (21) | 0.47 (21) | 0.51 (0.11-2.68) 0.58 |
| G/G | 0.19 (6) | 0.38 (17) | 0.69 (0.25-9.53) 1.59 |
| HWE (χ2; p) | 4.03; 0.04 | 0.01; 0.90 | - |
| Brazil | n = 35 | n = 78 | |
| A | 0.51 (36) | 0.52 (81) | Reference |
| G | 0.49 (34) | 0.48 (75) | 1.00; (0.54-1.79) 0.98 |
| A/A | 0.31 (11) | 0.32 (25) | Reference |
| A/G | 0.40 (14) | 0.40 (31) | 1.00 (0.34-2.78) 0.97 |
| G/G | 0.29 (10) | 0.28 (22) | 1.00 (0.31-3.09) 0.97 |
| HWE (χ2; p) | 1.39; 0.24 | 3.24; 0.07 | - |
| Italy | n = 18 | n = 89 | |
| A | 0.25 (9) | 0.31 (55) | Reference |
| G | 0.75 (27) | 0.69 (123) | 0.55 (0.56-3.46) 1.34 |
| A/A | 0.06 (1) | 0.12 (11) | Reference |
| A/G | 0.39 (7) | 0.37 (33) | 1.00; (0.32-3.61) 1.05 |
| G/G | 0.56 (10) | 0.51 (45) | 0.67 (0.28-115.53) 2.42 |
| HWE (χ2; p) | 0.02; 0.87 | 1.54; 0.21 | - |
CI: confidence interval; HWE: Hardy Weinberg equilibrium; LTF: lactoferrin encoding gene; OR: odds ratio; SNP: single nucleotide polymorphism.
The Arg47Lys A allele was the major allele in the Italian population (64% in the EU and 60% in the EI), while it was the minor allele in the African population (3% in the EU and 4% in the EI), among Indians (34% in the EU and 36% in the EI) and Brazilian individuals (43% in the EU and 33% in the EI) (Table II).
TABLE II. LTF Arg47Lys polymorphism allele, genotype frequencies (and counts) in human immunodeficiency virus (HIV) positive (+) and negative (-) children in the four different populations analysed.
| LTF SNP Arg47Lys (rs1126478) | HIV- | HIV+ | HIV- vs. HIV+ p (CI) OR |
|---|---|---|---|
| Africa | n = 15 | n = 26 | |
| G | 0.97 (29) | 0.96 (50) | Reference |
| A | 0.03 (1) | 0.04 (2) | 1.00 (0.06-70.74) 1.16 |
| G/G | 0.93 (14) | 0.96 (25) | Not calculable |
| A/G | 0.07 (1) | 0.00 (0) | Not calculable |
| A/A | 0.00 (0) | 0.04 (1) | Not calculable |
| HWE (χ2; p) | 0.02; 0.89 | 26; 3.41E-07 | |
| India | n = 31 | n = 45 | - |
| G | 0.66 (41) | 0.64 (58) | Reference |
| A | 0.34 (21) | 0.36 (32) | 0.86 (0.52-2.26) 1.08 |
| G/G | 0.39 (12) | 0.38 (17) | Reference |
| A/G | 0.55 (17) | 0.53 (24) | 1.00 (0.34-2.90) 0.99 |
| A/A | 0.06 (2) | 0.09 (4) | 1.00 (0.17-17.82) 1.40 |
| HWE (χ2; p) | 1.56; 0.21 | 1.21; 0.27 | - |
| Brazil | n = 35 | n = 78 | |
| G | 0.57 (40) | 0.67 (104) | Reference |
| A | 0.43 (30) | 0.33 (52) | 0.18 (0.36-1.24) 0.67 |
| G/G | 0.40 (14) | 0.49 (38) | Reference |
| A/G | 0.34 (12) | 0.36 (28) | 0.82 (0.31-2.38) 0.86 |
| A/A | 0.26 (9) | 0.15 (12) | 0.26 (0.15-1.64) 0.50 |
| HWE (χ2; p) | 3.15; 0.08 | 2.88; 0.09 | - |
| Italy | n = 18 | n = 89 | |
| G | 0.36 (13) | 0.40 (71) | Reference |
| A | 0.64 (23) | 0.60 (107) | 0.71 (0.53-2.70) 1.17 |
| G/G | 0.06 (1) | 0.16 (14) | Reference |
| A/G | 0.61 (11) | 0.48 (43) | 0.79 (0.20-2.45) 0.73 |
| A/A | 0.33 (6) | 0.36 (32) | 0.66 (0.27-129.16) 2.58 |
| HWE (χ2; p) | 1.89; 0.17 | 0.005; 0.94 | - |
CI: confidence interval; HWE: Hardy Weinberg equilibrium; LTF: lactoferrin encoding gene; OR: odds ratio; SNP: single nucleotide polymorphism.
The frequency data of each population were compared using Fisher’s exact test with the most similar ethnic group reported by the HapMap project (International HapMap Consortium 2003) and 1000 Genomes project (GPC et al. 2012). The Italian population was compared with the HapMap-TSI population, Tuscans in Italy; the African population with the Sub-Saharan Africa HapMap-YRI population, Yoruba in Ibadan, Nigeria; the Brazilian population with 1000 Genomes-AMR population, an admixture of Colombian from Medellin, Colombia, Mexican ancestry from Los Angeles, United States of America, Puerto Ricans from Puerto Rica; the Indian population with 1000 Genomes-ASN population, an admixture from Han-Chinese in Beijng, China, Southern Han Chinese, Japanese in Tokyo, Japan.
The Thr29Ala and Arg47Lys frequencies were similar (p > 0.05) for the populations from Africa, Italy and India. Comparing the Brazilian population of our study with an admixed population from 1000 Genomes, AMR population (to serve as a proxy to the admixed Brazilian populations), the Thr29Ala A allele was more frequent in the Brazilian sample (52%) respect to AMR (41%). The Arg47Lys G allele was more represented among our Brazilian population than AMR population (57% and 47% respectively). Moreover the G/G genotype was more frequent in our Brazilian population, whereas A/G and A/A genotype were more frequent in the AMR population (Tables III, IV).
TABLE III. LTF Thr29Ala polymorphism allele, genotype frequencies (and counts) in human immunodeficiency virus (HIV) positive (+) plus negative (-) children in the four different populations compared with the most similar ethnic group reported by HapMap and 1000 Genomes project.
| LTF SNP Thr29Ala (rs1126477) | Total (HIV+ plus HIV-) | HapMap/ 1000 Genomes | Total vs. Hapmap/ 1000 Genomes p (CI) OR |
|---|---|---|---|
| Africa (n = 41) | HapMap-YRIa (n = 113) | ||
| A | 0.77 (63) | 0.85 (192) | Reference |
| G | 0.23 (19) | 0.15 (34) | 0.12 (0.85-3.32) 1.70 |
| A/A | 0.61 (25) | 0.70 (79) | Reference |
| A/G | 0.32 (13) | 0.30 (34) | 0.69 (0.50-2.80) 1.21 |
| G/G | 0.07 (3) | 0.00 (0) | Not calculable |
| India (n = 76) | 1000 Genomes-ASNb (n = 286) | ||
| A | 0.42 (64) | 0.40 (229) | Reference |
| G | 0.58 (88) | 0.60 (343) | 0.64 (0.63-1.34) 0.92 |
| A/A | 0.14 (11) | 0.17 (49) | Reference |
| A/G | 0.55 (42) | 0.46 (131) | 0.38 (0.65-3.32) 1.43 |
| G/G | 0.30 (23) | 0.37 (106) | 1.00 (0.41-2.38) 0.97 |
| Brazil (n = 113) | 1000 Genomes-AMRc (n = 199) | ||
| A | 0.52 (117) | 0.41 (149) | Reference |
| G | 0.48 (109) | 0.59 (213) | 0.01 (0.46-0.92) 0.65 |
| A/A | 0.32 (36) | 0.19 (34) | Reference |
| A/G | 0.40 (45) | 0.45 (81) | 0.03 (0.28-0.99) 0.53 |
| G/G | 0.28 (32) | 0.36 (66) | 0.02 (0.23-0.90) 0.46 |
| Italy (n = 107) | HapMap-TSId (n = 88) | ||
| A | 0.30 (64) | 0.26 (46) | Reference |
| G | 0.70 (150) | 0.74 (130) | 0.43 (0.52-1.32) 0.83 |
| A/A | 0.11 (12) | 0.06 (5) | Reference |
| A/G | 0.37 (40) | 0.41 (36) | 0.27 (0.12-1.60) 0.47 |
| G/G | 0.51 (55) | 0.53 (47) | 0.29 (0.13-1.63) 0.49 |
a: Yoruba, Ibadan, Nigeria; b: an admixture from Han-Chinese in Beijng, China, Southern Han Chinese, Japanese in Tokyo, Japan; c: an admixture of Colombian from Medellin, Colombia, Mexican ancestry from Los Angeles, United States of America, Puerto Ricans, from Puerto Rico; d: Toscans, Italy; CI: confidence interval; LTF: lactoferrin encoding gene; OR: odds ratio; SNP: single nucleotide polymorphism.
TABLE IV. LTF Arg47Lys polymorphism allele, genotype frequencies (and counts) in human immunodeficiency virus (HIV) positive (+) plus negative (-) children in the four different populations compared with the most similar ethnic group reported by HapMap and 1000 Genomes project.
| LTF SNP Arg47Lys (rs1126478) | Total (HIV+ plus HIV-) | HapMap/ 1000 Genomes | Total vs. Hapmap/ 1000 Genomes p (CI) OR |
|---|---|---|---|
| Africa (n = 41) | HapMap-YRIa (n = 113) | ||
| G | 0.97 (79) | 0.99 (223) | Reference |
| A | 0.03 (3) | 0.01 (3) | 0.19 (0.37-21.43) 2.81 |
| G/G | 0.93 (39) | 0.97 (110) | Reference |
| A/G | 0.07 (1) | 0.03 (3) | 1.00 (0.02-12.11) 0.94 |
| A/A | 0.00 (1) | 0.00 (0) | Not calculable |
| India (n = 76) | 1000 Genomes-ASNb (n = 286) | ||
| G | 0.66 (99) | 0.65 (371) | Reference |
| A | 0.34 (53) | 0.35 (201) | 1.00 (0.66-1.46) 0.99 |
| G/G | 0.39 (29) | 0.43 (124) | Reference |
| A/G | 0.55 (41) | 0.43 (123) | 0.22 (0.81-2.54) 1.42 |
| A/A | 0.06 (6) | 0.14 (39) | 0.51 (0.21-1.78) 0.66 |
| Brazil (n = 113) | 1000 Genomes-AMRc (n = 199) | ||
| G | 0.57 (144) | 0.47 (169) | Reference |
| A | 0.43 (82) | 0.53 (193) | 0.00006 (0.35-0.71) 0.50 |
| G/G | 0.40 (52) | 0.24 (44) | Reference |
| A/G | 0.34 (40) | 0.45 (81) | 0.002 (0.23-0.75) 0.42 |
| A/A | 0.26 (21) | 0.31 (56) | 0.0004 (0.16-0.63) 0.32 |
| Italy (n = 107) | HapMap-TSId (n = 88) | ||
| G | 0.36 (84) | 0.33 (59) | Reference |
| A | 0.64 (130) | 0.67 (117) | 0.25 (0.50-1.21) 0.78 |
| G/G | 0.06 (15) | 0.10 (9) | Reference |
| A/G | 0.61 (54) | 0.47 (41) | 0.65 (0.28-2.16) 0.79 |
| A/A | 0.33 (38) | 0.43 (38) | 0.35 (0.20-1.68) 0.60 |
a: Yoruba, Ibadan, Nigeria; b: an admixture from Han-Chinese in Beijng, China, Southern Han Chinese, Japanese in Tokyo, Japan; c: an admixture of Colombian from Medellin, Colombia, Mexican ancestry from Los Angeles, United States of America, Puerto Ricans, from Puerto Rico; d: Toscans, Italy; CI: confidence interval; LTF: lactoferrin encoding gene; OR: odds ratio; SNP: single nucleotide polymorphism.
Therefore, the allele and genotype frequencies of both polymorphisms were not statistically different when comparing EI with EU children in our populations (Tables I, II).
The Thr29Ala and Arg47Lys polymorphisms were in LD (p < 0.07, D’statistic > 0.72; r2 statistic > 0.11 for all groups) and combined to form three major haplotypes (AG, GG and GA, with frequencies > 0.01) and one minor (AA, with frequency ≤ 0.01). Comparing the haplotype frequencies between EU and EI in the four populations, no statistically significant differences were observed when using Fisher test with 4 x 2 table (Table V). The same results were obtained considering the most frequent haplotype as reference and analysing all other haplotypes vs. that reference (data not shown).
TABLE V. LTF haplotype frequencies (and counts) in human immunodeficiency virus (HIV) positive (+) and negative (-) children in the four different populations analysed.
| LTF haplotypes (Thr29Ala-Arg47Lys) | HIV- | HIV+ | HIV- vs. HIV+ (p) |
|---|---|---|---|
| Africa | n = 30 | n = 52 | |
| AG | 0.77 (23) | 0.77 (40) | 1.00 |
| GG | 0.20 (6) | 0.19 (10) | |
| GA | 0.03 (1) | 0.04 (2) | |
| AA | 0.00 (0) | 0.00 (0) | |
| LD (p; D’; r2) | 0.07; 0.99; 0.11 | 0.01; 0.99; 0.13 | - |
| India | n = 62 | n = 90 | |
| AG | 0.47 (29) | 0.39 (35) | 0.56 |
| GG | 0.19 (12) | 0.25 (23) | |
| GA | 0.34 (21) | 0.36 (32) | |
| AA | 0.00 (0) | 0.00 (0) | |
| LD (p; D’; r2) | < 0.01; 0.99; 0.45 | < 0.01; 0.99; 0.35 | - |
| Brazil | n = 70 | n = 156 | |
| AG | 0.46 (32) | 0.51 (79) | 0.19 |
| GA | 0.37 (26) | 0.32 (50) | |
| GG | 0.11 (8) | 0.16 (25) | |
| AA | 0.06 (4) | 0.01 (2) | |
| LD (p; D’; r2) | < 0.01; 0.72; 0.41 | < 0.01; 0.91; 0.45 | - |
| Italy | n = 36 | n = 178 | |
| GA | 0.64 (23) | 0.60 (106) | 0.85 |
| AG | 0.25 (9) | 0.30 (54) | |
| GG | 0.11 (4) | 0.10 (17) | |
| AA | 0.00 (0) | 0.01 (1) | |
| LD (p; D’; r2) | < 0.01; 0.99; 0.59 | < 0.01; 0.97; 0.63 | - |
LD: linkage disequilibrium; LTF: lactoferrin encoding gene.
DISCUSSION
Several biological activities of lactotransferrin against HIV-1 have been described so far, ranging from the inhibition of virus-cell interaction through CXCR4 and CCR5 binding or viral gp120 V3 loop blocking (Berkhout et al. 2002), to inhibit viral processes within the host cells (Ng et al. 2001). Recently, Wong et al. (2014) have shown the inhibitory activity of lactotransferrin fragments lactoferricin and lactoferrampin against HIV-1 reverse transcriptase and integrase, respectively.
A reduction of the serum lactotransferrin concentration has previously been associated with increased HIV-1 infection susceptibility (Defer et al. 1995, Semba et al. 1998, Dapsanse et al. 2001) and AIDS progression (van der Strate et al. 2001). Additionally, recent works have explored the role of lactotransferrin in the oral health among HIV-1 infected subjects. Alves et al. (2014) observed higher salivary lactotransferrin levels in HIV-1 infected children during Candida sp. oral colonisation. Ferreira et al. (2014) reported no lactotransferrin level alterations in gingival crevicular fluid and saliva from HIV-1 infected subjects with chronic periodontitis.
To the best of our knowledge, no studies so far investigated the possible association between LTF genetic variants and susceptibility to HIV-1 infection or with progression to AIDS and its clinical manifestations.
Two functional polymorphisms within LTF gene, named Thr29Ala and Arg47Lys, were previously associated with an increased susceptibility to periodontitis development (Velliyagounder et al. 2003, Jordan et al. 2005, Wu et al. 2009), dental caries (Azevedo et al. 2010, Fine et al. 2013), ovarian cancer (Cao et al. 2011), nasopharyngeal carcinoma (Zhou et al. 2012), dyslipidaemia (Moreno-Navarrete et al. 2008) and coronary artery stenosis (Videm et al. 2012). In our study, the Thr29Ala and Arg47Lys polymorphisms were analysed in order to investigate the possible role of these LTF genetic variants on HIV-1 MTCT.
Our association analysis, performed among children born from HIV-1 positive mothers from four different populations, indicates that the LTF Thr29Ala and Arg47Lys allele, genotype and haplotype frequencies, are similar in HIV-1 infected and HIV-1 EU children and are also comparable to those reported by the HapMap project (International HapMap Consortium 2003) and 1000 Genomes project (GPC et al. 2012); the Brazilian population does not follow the same frequency distribution, probably due to the ethnic heterogeneity among Brazilians, that are an admixture of African, Caucasian and native American populations (Alves-Silva et al. 2000), and considering that the AMR population that was used as a comparison is not a Brazilian one, but is an admixture of Colombian from Medellin, Mexican ancestry from Los Angeles and Puerto Ricans.
During descriptive analysis, African and Italian populations seemed to present opposite allelic frequencies. On the other hand, among the Indian and the Brazilian subjects, the frequencies of the two polymorphisms seemed to be similar.
No significant differences were found when comparing HIV-1 positive and HIV-1 negative children, suggesting that the two LTF polymorphisms could be not involved in HIV-1 vertical transmission. However, the data are preliminary and the comparison of the frequencies among the distinct human groups is quite complex to be performed: it is not excluded that the lack of association may be due in part to the small sample size of the populations investigated combined with a small effect of LTF in HIV-1 susceptibility, a multifactorial trait. Indeed, although the total number of analysed individual was 337, the classification in HIV-1 positive and negative and in the four subgroups based on ethnic origins led to a reduction of the power of the study. In fact, except for the haplotype analysis in the Brazilian population (power = 0.96), all other tests had a low power (0.07 for African population; 0.51 for Indian populations and 0.32 for Italian population). The unavailability of other samples did not allow us to increase the sample size; this was a limitation of our study that could affect the evaluation of the potential role of LTF genetic variants in the context of susceptibility to HIV-1 infection.
It is also important to consider the difficulties in comparing LTF SNPs frequencies within the groups, also assuming that the populations studied are sets of individuals from different ethnic origins. However, even if the number of individuals is limited, we tried to replicate the association findings in different ethnic groups, being aware that any replica and comparison within the four analysed groups is quite difficult due to the low frequency of LTF SNPs.
Previous findings suggested that lactotransferrin could play a role in HIV-1 vertical transmission, but no studies have been conducted on the ability of the two LTF variants to prevent HIV-1 entry to the cells or to interfere with the viral processes. Considering our negative results we could speculate that, although the two polymorphisms are not synonymous and result in two amino acidic substitutions, these variations may not modify the antiviral activity of the mature protein; the PolyPhen-2 (Adzhubei et al. 2010) software predicted the two SNPs as benign and thus not able to radically affect the protein. Another hypothesis is that if even the two polymorphisms could influence the antiviral role of the protein, perhaps an increment in gene expression, due to external factors other than genetic variations, may compensate the alterations within the molecule. A study conducted by Moreno-Navarrete et al. (2008) showed that the two LTF polymorphisms did not correlate with the plasma protein level in a Spanish population.
Unfortunately, in this study, being a retrospective one performed on historical groups of HIV-1 patients infected trough vertical transmission, biological samples other than DNA were not available to perform functional studies and investigating the effective influence of LTF genetic variants on protein production or on protein functionality. Other limitations of the study are the lack of information about the mother’s genotypes and regarding breastfeeding occurrence.
Our results suggest that LTF genetic polymorphisms Thr29Ala and Arg47Lys are not associated with susceptibility to HIV-1 MTCT, but our data are preliminary, obtained on low number of individual, also lacking of functional characterisation of the analysed SNPs. Therefore, further large-scale studies and functional analysis are necessary to clarify the potential role of LTF gene polymorphisms in HIV-1 infection susceptibility.
Funding Statement
Financial support: Italian Ministry of Health (RC 2007) (FVG 2006)
Footnotes
Financial support: Italian Ministry of Health (RC 2007) (FVG 2006)
LZ and VP have fellowships from IRCCS Burlo Garofolo.
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