Enhancement of murine sarcoma virus (Moloney) infection and tumorigenesis in vivo by coinfection with Rauscher leukemia virus.

نویسندگان

  • W Turner
  • M A Chirigos
چکیده

Dual infection of mice with murine sarcoma virus (Moloney) [MSV(M)] and Rauscher leukemia virus (RLV) resulted in an enhanced MSV(M) infection, reflected by increased mortality with tumor. Significant increases in tumor incidence, induced by low concentrations of MSV(M) when inoculated into RLV-infected mice, demonstrated that RLV enhanced MSV(M) oncogenicity. Temporal studies indicated that RLV-mediated enhancement of MSV(M) infection appeared to be independent of the time of RLV challenge. Inoculation with RLV, as early as 5 days prior to or as late as 6 days after MSV(M) infection, resulted in significant increases in incidence of tumor deaths over MSV(M) controls. The level of enhancement of MSV(M) infection produced in mice coinfected with MSV(M) and RLV was maintained over 4 cell-free passages in normal adult mice by MSV(M) originally extracted from tumors induced in dually infected animals. The possible mechanisms by which RLV enhanced MSV(M) infection and oncogenicity are discussed.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Increased oncogenicity of the murine sarcoma virus (Moloney) by co-infection with murine leukemia viruses.

The high incidence of spontaneous regressions of primary tu mors induced by the Moloney sarcoma virus in adult mice was significantly altered by co-infection with Rauscher, Moloney, and Friend leukemia viruses. Intramuscular, intraperitoneal, or subcutaneous inoculation of sarcoma extracts, prepared from progressively growing tumors obtained from dually infected animals, resulted in extensive m...

متن کامل

Alteration of the syncytium-forming property of XC cells by productive Moloney leukemia virus infection.

The effect of productive murine leukemia virus (MuLV) infection of the syncytium-forming property of XC cells was studied MuLV-Moloney-infected XC cells, designated XC(M), initially went through a period of spontaneous syncytium formation. The syncytia then disappeared, and XC(M) cells continued to propagate and produce both infectious MuLV and MuLV group-specific antigens. However, XC(M) cells...

متن کامل

Infection of human embryonic cell cultures with the Rauscher murine leukemia virus.

Although infection of mouse cell lines with murine leukemia and sarcoma viruses can be achieved with relative ease (4, 6, 12), similar infection of human cell cultures has not been reported until very recently. Boiron et al. (2) have described the successful infection of a diploid human embryonic lung culture, WI-38, with the murine sarcoma virus Moloney strain (MSV-M). Infection and continuous...

متن کامل

Purification of the Moloney and Rauscher murine leukemia viruses by use of zonal ultracentrifuge systems.

The B-IV and B-IX zonal ultracentrifuge rotors were applied to the concentration and purification of the Moloney and Rauscher murine leukemia viruses from large volumes of infected tissue culture fluids and animal materials. Potassium tartrate, potassium citrate and sucrose gradients were used to obtain viral concentrates from the density 1.16 to 1.18 zone. Proteolytic enzyme digestion of tissu...

متن کامل

Studies on the Biological and Antigenic Properties of ESP-1 Type C Virus Particles1

ESP-1 virus provides a helper function to defective Friend spleen focus-forming virus (SFFV). This helper activity is demonstrable only in B-type mice (Fv-lbb) under conditions in which the N-tropic lymphatic leukemia-inducing virus contained in the Friend virus complex is inhibited. ESP-1 virus therefore expresses a B-tropic host range in vivo with respect to its ability to provide a helper fu...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Cancer research

دوره 29 11  شماره 

صفحات  -

تاریخ انتشار 1969