Fast Dissemination of New HIV-1 CRF02/A1 Recombinants in Pakistan

被引:18
作者
Chen, Yue [1 ]
Hora, Bhavna [1 ]
DeMarco, Todd [1 ]
Shah, Sharaf Ali [2 ]
Ahmed, Manzoor [2 ]
Sanchez, Ana M. [1 ]
Su, Chang [1 ]
Carter, Meredith [1 ]
Stone, Mars [3 ]
Hasan, Rumina [4 ,5 ]
Hasan, Zahra [4 ,5 ]
Busch, Michael P. [3 ]
Denny, Thomas N. [1 ]
Gao, Feng [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Med, Duke Human Vaccine Inst, Durham, NC 27710 USA
[2] Bridge Consultants Fdn, Karachi, Pakistan
[3] Blood Syst Res Inst, San Francisco, CA USA
[4] Aga Khan Univ, Dept Pathol, Karachi, Pakistan
[5] Aga Khan Univ, Dept Microbiol, Karachi, Pakistan
基金
美国国家卫生研究院;
关键词
INJECTION-DRUG USERS; INFECTION; DYNAMICS;
D O I
10.1371/journal.pone.0167839
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A number of HIV-1 subtypes are identified in Pakistan by characterization of partial viral gene sequences. Little is known whether new recombinants are generated and how they disseminate since whole genome sequences for these viruses have not been characterized. Near full-length genome (NFLG) sequences were obtained by amplifying two overlapping half genomes or next generation sequencing from 34 HIV-1-infected individuals in Pakistan. Phylogenetic tree analysis showed that the newly characterized sequences were 16 subtype As, one subtype C, and 17 A/G recombinants. Further analysis showed that all 16 subtype A1 sequences (47%), together with the vast majority of sequences from Pakistan from other studies, formed a tight subcluster (A1a) within the subtype A1 clade, suggesting that they were derived from a single introduction. More in-depth analysis of 17 A/G NFLG sequences showed that five shared similar recombination breakpoints as in CRF02 (15%) but were phylogenetically distinct from the prototype CRF02 by forming a tight subcluster (CRF02a) while 12 (38%) were new recombinants between CRF02a and A1a or a divergent A1b viruses. Unique recombination patterns among the majority of the newly characterized recombinants indicated ongoing recombination. Interestingly, recombination breakpoints in these CRF02/A1 recombinants were similar to those in prototype CRF02 viruses, indicating that recombination at these sites more likely generate variable recombinant viruses. The dominance and fast dissemination of new CRF02a/A1 recombinants over prototype CRF02 suggest that these recombinant have more adapted and may become major epidemic strains in Pakistan.
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