Infectivity of adeno-associated virus serotypes in mouse testis

被引:14
|
作者
Rajasekaran, Santhanasabapathy [1 ]
Thatte, Jayashree [1 ]
Periasamy, Jayaprakash [1 ]
Javali, Alok [1 ,2 ]
Jayaram, Manjunath [1 ]
Sen, Dwaipayan [3 ,4 ,5 ]
Krishnagopal, Akshaya [3 ,4 ]
Jayandharan, Giridhara R. [3 ,4 ,6 ]
Sambasivan, Ramkumar [1 ]
机构
[1] Inst Stem Cell Biol & Regenerat Med, GKVK Campus,Bellary Rd, Bengaluru 560065, India
[2] TIFR, Natl Ctr Biol Sci, GKVK Campus,Bellary Rd, Bengaluru 560065, India
[3] Christian Med Coll & Hosp, Dept Haematol, Vellore 632004, Tamil Nadu, India
[4] Christian Med Coll & Hosp, Ctr Stem Cell Res, Vellore 632004, Tamil Nadu, India
[5] VIT, Cellular & Mol Therapeut Lab, CBCMT, Vellore 632014, Tamil Nadu, India
[6] Indian Inst Technol, Dept Biol Sci & Bioengn, Kanpur 208016, Uttar Pradesh, India
来源
BMC BIOTECHNOLOGY | 2018年 / 18卷
关键词
Adeno-associated viruses (AAV); Germline transmission; Tropism; Mouse testis injection; Myoid cell; Leydig cell; Sertoli cell; Spermatogonia; GENE-TRANSFER EFFICIENCY; IN-VIVO; STEM-CELLS; TRANSMISSION; TRANSDUCTION; IMPROVES; VECTORS; DELIVERY; TROPISM; BINDING;
D O I
10.1186/s12896-018-0479-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
BackgroundRecombinant adeno-associated viruses (AAVs) are emerging as favoured transgene delivery vectors for both research applications and gene therapy. In this context, a thorough investigation of the potential of various AAV serotypes to transduce specific cell types is valuable. Here, we rigorously tested the infectivity of a number of AAV serotypes in murine testis by direct testicular injection.ResultsWe report the tropism of serotypes AAV2, 5, 8, 9 and AAVrh10 in mouse testis. We reveal unique infectivity of AAV2 and AAV9, which preferentially target intertubular testosterone-producing Leydig cells. Remarkably, AAV2 TM, a mutant for capsid designed to increase transduction, displayed a dramatic alteration in tropism; it infiltrated seminiferous tubules unlike wildtype AAV2 and transduced Sertoli cells. However, none of the AAVs tested infected spermatogonial cells.ConclusionsIn spite of direct testicular injection, none of the tested AAVs appeared to infect sperm progenitors as assayed by reporter expression. This lends support to the current view that AAVs are safe gene-therapy vehicles. However, testing the presence of rAAV genomic DNA in germ cells is necessary to assess the risk of individual serotypes.
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页数:9
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