In 1971, Paul Berg asked Francis Crick about his views on a controversial proposed experiment involving recombinant DNA; to Berg's surprise, Crick had no comment to make. This article first describes the multiple reasons why Crick did not respond to Berg, including psychological factors that affected Crick at the time, the limits of his unstated reflexively positivist approach to social issues, and his reluctance to pursue social or political issues when challenged. Crick's lack of involvement in discussions about recombinant DNA, including in the Asilomar process, is then used to explore two other notable absences from Asilomar: the immunologist Niels Jerne, who was invited to be on the organizing committee but was not involved for reasons that are unclear; and molecular biologist and biological weapons campaigner Matthew Meselson, whose presence would have added a layer of understanding to the discussions, particularly regarding the threat of bioweapons. These enigmatic absences raise questions about the representativeness of Asilomar and suggest future investigations as to how the legacy of Asilomar was shaped both by those who were present-and by those who were not.
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http://dx.doi.org/10.1007/s10739-025-09805-y | DOI Listing |
Biotechnol Prog
March 2025
Amgen Bioprocessing Center, Henry E. Riggs School of Applied Life Sciences, Keck Graduate Institute, California, USA.
One of the widely used techniques for producing recombinant adeno-associated virus serotype 2 (rAAV2) particles, as viral vectors for gene therapy applications, is the triple transient (TT) transfection of human embryonic kidney 293 (HEK293) cells. It is desirable to optimize this transfection process for more efficient manufacturing of rAAV viral vectors for gene therapy purposes. We examined the application of dimethyl sulfoxide (DMSO) as an additive to this transfection technique to improve the expression yield of rAAV2 particles with HEK293 cells in adherent and suspension cell culture modalities.
View Article and Find Full Text PDFArch Microbiol
March 2025
Tianjin Key Laboratory of Agricultural Animal Breeding and Healthy Husbandry, College of Animal Science and Veterinary Medicine, Tianjin Agricultural University, No. 22, Jinjing Road, Xiqing District, Tianjin, 300392, People's Republic of China.
Avian infectious bronchitis (IB) is one of the major respiratory diseases in poultry. At present, attenuated vaccines are the main commercial vaccines, but they have many defects. We aimed to construct a novel multi-epitope DNA vaccine based on avian infectious bronchitis virus (IBV) S1 and N proteins for the prevention of IBV infection.
View Article and Find Full Text PDFBackground: Alkhumra hemorrhagic fever virus is a newly discovered tick-borne flavivirus that was first identified in 1994 - 1995 in the Alkhumra district of Jeddah, Kingdom of Saudi Arabia. AHFV was detected in a butcher who developed severe hemorrhagic fever. Since then, a total of 604 confirmed cases have been reported in KSA between 1995 - 2020.
View Article and Find Full Text PDFHum Reprod Open
February 2025
Department of Obstetrics and Gynecology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Study Question: Does FSH induce free radical generation with substantial oxidative damage in human cumulus granulosa cells (cGCs) and mural granulosa cells (mGCs)?
Summary Answer: FSH of both physiological and supraphysiological concentrations induced free radical generation on subcellular levels, most notably in the mitochondria, while the elevated free radical load caused neglectable oxidative damage in both cGCs and mGCs.
What Is Known Already: FSH is fundamental for regulation of granulosa cell (GC) function and oocyte maturation, during which a physiological level of reactive oxygen species (ROS) is essential, while excessive amounts lead to oxidative damage. Potential adverse effects of high FSH doses on GCs may be mediated by ROS.
Sci Rep
March 2025
Department of Neurology, China-Japan Union Hospital of Jilin University, 130033, Changchun, Jilin, China.
As an infectious disease that poses a significant threat to the rapidly growing pig breeding industry, the detection of Haemophilus parasuis (HPS) is often compromised by various interfering substances present in the test sample during quantitative real-time PCR (qPCR). The rapid detection of HPS is important for the isolation of infectious pigs and their treatment. We designed and optimized a rapid qPCR test to detect the INFB gene of HPS in clinical and environmental samples on pig farms.
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