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. 2009 Sep 22;4(9):e7122.
doi: 10.1371/journal.pone.0007122.

Compartmentalization of HIV-1 within the female genital tract is due to monotypic and low-diversity variants not distinct viral populations

Affiliations

Compartmentalization of HIV-1 within the female genital tract is due to monotypic and low-diversity variants not distinct viral populations

Marta Bull et al. PLoS One. .

Abstract

Background: Compartmentalization of HIV-1 between the genital tract and blood was noted in half of 57 women included in 12 studies primarily using cell-free virus. To further understand differences between genital tract and blood viruses of women with chronic HIV-1 infection cell-free and cell-associated virus populations were sequenced from these tissues, reasoning that integrated viral DNA includes variants archived from earlier in infection, and provides a greater array of genotypes for comparisons.

Methodology/principal findings: Multiple sequences from single-genome-amplification of HIV-1 RNA and DNA from the genital tract and blood of each woman were compared in a cross-sectional study. Maximum likelihood phylogenies were evaluated for evidence of compartmentalization using four statistical tests. Genital tract and blood HIV-1 appears compartmentalized in 7/13 women by >/=2 statistical analyses. These subjects' phylograms were characterized by low diversity genital-specific viral clades interspersed between clades containing both genital and blood sequences. Many of the genital-specific clades contained monotypic HIV-1 sequences. In 2/7 women, HIV-1 populations were significantly compartmentalized across all four statistical tests; both had low diversity genital tract-only clades. Collapsing monotypic variants into a single sequence diminished the prevalence and extent of compartmentalization. Viral sequences did not demonstrate tissue-specific signature amino acid residues, differential immune selection, or co-receptor usage.

Conclusions/significance: In women with chronic HIV-1 infection multiple identical sequences suggest proliferation of HIV-1-infected cells, and low diversity tissue-specific phylogenetic clades are consistent with bursts of viral replication. These monotypic and tissue-specific viruses provide statistical support for compartmentalization of HIV-1 between the female genital tract and blood. However, the intermingling of these clades with clades comprised of both genital and blood sequences and the absence of tissue-specific genetic features suggests compartmentalization between blood and genital tract may be due to viral replication and proliferation of infected cells, and questions whether HIV-1 in the female genital tract is distinct from blood.

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Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. Maximum likelihood phylogenetic analyses of HIV-1 sequences corresponding to the C2-V5 region of env.
Phylograms of blood and genital tract RNA and DNA sequences, derived by single-genome-amplification, are shown. Mixing of genital tract and blood sequences was noted in phylograms of most subjects. Subjects 1 and 2 were studied during effective ART (<50 copies/mL). Subjects 3 and 4 were studied during “failing” (>400 copies/mL) ART. HIV-1 sequences from plasma (gray stars); PBMC (gray circles), cell-free cervical RNA (black stars) and cell-associated cervical DNA (black circles) are shown. Sequences that were predicted to encode X4-tropic virus are indicated with brackets. Bootstrap values of >70% are indicated in each tree. Phylograms were rooted using representative sequences, indicated with the letter B, for the corresponding subtype from GenBank (Clade B: B.US.83.RF, B.US.90.WEAU160, B.FR.83.HXB2, B.US.86.JRFL). The scale bar (horizontal line) indicates the horizontal branch length corresponding to 1 substitution per 100 sites.
Figure 2
Figure 2. Maximum likelihood phylogenetic analyses of HIV-1 sequences corresponding to the C2-V5 region of env.
Phylograms of blood and genital tract RNA and DNA sequences, derived by single-genome-amplification, are shown. Mixing of genital tract and blood sequences was noted in phylograms of most subjects. Subjects 5 and 6 were studied during “failing” (>400 copies/mL) ART. Subjects 7 and 8 were studied while not receiving ART. HIV-1 sequences from plasma (gray stars); PBMC (gray circles), cell-free cervical RNA (black stars) and cell-associated cervical DNA (black circles) are shown. Bootstrap values of >70% are indicated in each tree. Phylograms were rooted using representative sequences, indicated with the letter B, for the corresponding subtype from GenBank (Clade B: B.US.83.RF, B.US.90.WEAU160, B.FR.83.HXB2, B.US.86.JRFL). The scale bar (horizontal line) indicates the horizontal branch length corresponding to 1 substitution per 100 sites.
Figure 3
Figure 3. Maximum likelihood phylogenetic analyses of HIV-1 sequences corresponding to the C2-V5 region of env.
Phylograms of blood and genital tract RNA and DNA sequences, derived by single-genome-amplification are shown. Mixing of genital tract and blood sequences was noted in phylograms of most subjects. Subjects 9, 10, 11, and 12 were studied while not receiving ART. HIV-1 sequences from plasma (gray stars); PBMC (gray circles), cell-free cervical RNA (black stars) and cell-associated cervical DNA (black circles) are shown. Sequences that were predicted to encode X4-tropic virus are indicated with brackets. Bootstrap values of >70% are indicated in each tree. Phylograms were rooted using representative sequences, indicated with the letter B or A, for the corresponding subtype from GenBank (Clade B: B.US.83.RF, B.US.90.WEAU160, B.FR.83.HXB2, B.US.86.JRFL; Clade A1 A1.KE.93.Q23-17, A1.SE.94.SE7253, A1.UG.92.92UG037, A1.UG.85.U455). The scale bar (horizontal line) indicates the horizontal branch length corresponding to 1 substitution per 100 sites.
Figure 4
Figure 4. Maximum likelihood phylogenetic analyses of HIV-1 sequences corresponding to the C2-V5 region of env.
Phylograms of blood and genital tract RNA and DNA sequences, derived by single-genome-amplification are shown. Mixing of genital tract and blood sequences were also noted in the phylogram of Subject 13 who was studied while not receiving ART. HIV-1 sequences from plasma (gray stars); PBMC (gray circles), cell-free cervical RNA (black stars) and cell-associated cervical DNA (black circles) are shown. Bootstrap values of >70% are indicated in each tree. Phylograms were rooted using representative sequences, indicated with the letter B, for the corresponding subtype from GenBank (Clade B: B.US.83.RF, B.US.90.WEAU160, B.FR.83.HXB2, B.US.86.JRFL). The scale bar (horizontal line) indicates the horizontal branch length corresponding to 1 substitution per 100 sites.

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References

    1. Diem K, Nickle DC, Motoshige A, Fox A, Ross S, et al. Male genital tract compartmentalization of human immunodeficiency virus type 1 (HIV). AIDS Res Hum Retroviruses. 2008;24:561–571. - PubMed
    1. Ghosn J, Viard JP, Katlama C, de Almeida M, Tubiana R, et al. Evidence of genotypic resistance diversity of archived and circulating viral strains in blood and semen of pre-treated HIV-infected men. Aids. 2004;18:447–457. - PubMed
    1. Gupta P, Leroux C, Patterson BK, Kingsley L, Rinaldo C, et al. Human immunodeficiency virus type 1 shedding pattern in semen correlates with the compartmentalization of viral Quasi species between blood and semen. J Infect Dis. 2000;182:79–87. - PubMed
    1. Coombs RW, Speck CE, Hughes JP, Lee W, Sampoleo R, et al. Association between culturable human immunodeficiency virus type-1 (HIV-1) in semen and HIV-1 RNA levels in semen and blood: evidence for compartmentalization of HIV-1 between semen and blood. J Infect Dis. 1998;177:320–330. - PubMed
    1. Delwart EL, Mullins JI, Gupta P, Learn GH,, Jr., Holodniy M, et al. Human immunodeficiency virus type 1 populations in blood and semen. J Virol. 1998;72:617–623. - PMC - PubMed

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