Method Article

Handling of the Cotton Rat in Studies for the Pre-clinical Evaluation of Oncolytic Viruses

DOI:

10.3791/52232

November 24th, 2014

In This Article

Summary

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Cotton rats are extremely excitable and have a strong flight-or-fight response. A handling method optimized to reduce the stress of the animals is described which will make cotton rats more accessible as a preclinical model.

Abstract

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Oncolytic viruses are a novel anticancer therapy with the ability to target tumor cells, while leaving healthy cells intact. For this strategy to be successful, recent studies have shown that involvement of the host immune system is essential. Therefore, oncolytic virotherapy should be evaluated within the context of an immunocompetent model. Furthermore, the study of antitumor therapies in tolerized animal models may better recapitulate results seen in clinical trials. Cotton rats, commonly used to study respiratory viruses, are an attractive model to study oncolytic virotherapy as syngeneic models of mammary carcinoma and osteosarcoma are well established. However, there is a lack of published information on the proper handling procedure for these highly excitable rodents. The handling and capture approach outlined minimizes animal stress to facilitate experimentation. This technique hinges upon the ability of the researcher to keep calm during handling and perform procedures in a timely fashion. Finally, we describe how to prepare cotton rat mammary tumor cells for consistent subcutaneous tumor formation, and how to perform intratumoral and intraperitoneal injections. These methods can be applied to a wide range of studies furthering the development of the cotton rat as a relevant pre-clinical model to study antitumor therapy.

Introduction

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Oncolytic viruses (OV) selectively replicate in tumor cells by exploiting biochemical differences between normal and tumor cells 1,2. There are two types of OVs: those that do not require a mutation to achieve selective oncolysis, referred to as naturally occurring wild-type viruses and those which must be engineered to achieve selective oncolysis. The collection of mutations within a given tumor type determines the nature of the selective growth advantage over normal cells for an OV 2. The safety and benefit of using OVs has been demonstrated in clinical trials 3-7. Despite advancements in the field of oncolytic virotherapy there exis....

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Protocol

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NOTE: The protocols used have been approved by our institutional Animal Research Ethics Board at McMaster University according to Canadian Council on Animal Care guidelines. Experiments were performed at the McMaster University Central Animal Facility.

1. Culturing LCRT Cells

  1. Culture LCRT cells in Dulbecco’s modified Eagle’s medium (DMEM) supplemented with 10% fetal bovine serum (FBS), 2 mM L-glutamine, 100 U/ml penicillin and 100 µg/ml streptomycin. Maintain cells in T-150 tissue culture flasks at 37 °C and 5% CO2. Passage cells when they form a 90% confluent monolayer (every 2-3 days, <....

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Results

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Due to the extremely excitable nature of cotton rats, being familiar with and utilizing procedures optimized to reduce the stress of the animals will ease in their use as a pre-clinical animal model. Use of proper handling techniques will also minimize risk to the researcher.

When using cotton rats it is imperative to stay calm. The rats are highly excitable and will attempt to escape their cage. Use of an enrichment tube and nestlets will minimize escape attempts. Figure 2 sh.......

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Discussion

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Cotton rats are highly excitable and have a strong flight response. Therefore, special care should be taken to minimize any undue stress on the animal. The cage setup described will allow for safe and easy capture of the animals, with the placement of the enrichment tube being of the utmost importance. When setting up cages, ensure that the enrichment tubes meet the size and shape requirements, and are placed in proper orientation in the cage. It is also important to ensure that any technicians who might be aiding in ani.......

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Disclosures

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The authors acknowledge there are no financial conflicts of interest related to this research.

Acknowledgements

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Breanne Cuddington holds a fellowship from the Canadian Breast Cancer Foundation. This work was sponsored by operating grants from the Cancer Research Society and the Canadian Cancer Society Research Institute (formerly the Canadian Breast Cancer Research Alliance). We thank Ann Tollefson (Saint Louis University School of Medicine) for LCRT cells and Dr. Kathleen Delaney and Marion Corrick for technical assistance with cotton rat housing and sedation.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Dulbecco’s modified Eagle’s medium Gibco11965-092May use any brand 
1X Phosphate Buffered Saline Can prepare in lab, filter to sterilize
200 mM L-glutamineGibco25030164May use any brand
100x Antibiotic-Antimycotic Gibco15240-062May use any brand
Fetal bovine serumQuality Biological Inc.110-001-101HIMay use any brand
T-150cm2 tissue culture flaskFisher Scientific14-826-80May use any brand
1X TypLE ExpressLife Technologies12604-013
12-well cell culture plate, flat bottomFisher Scientific08-772-29May use any brand, must be tissue culture treated
alamarBlueLife TechnologiesDAL1025May use an alternative reagent for determination of cell viability
8640 Teklad 22/5 Rodent dietHarlan 8640
1/8” corncob rodent beddingHarlan7092
NestletsAncare-Made of pulped virgin cotton fiber, dust-free and autoclavable
50 mL Conical tubesFisher Scientific14-432-22May use any brand, must be sterile
Isoflurane USP, 99.9 %, inhalation anestheticPharmaceutical Partners of Canada Inc.M60302
70% EthanolCan prepare in lab
10 % Neutral Buffered FormalinSigma-AldrichHT501128May use any brand
NAPCO NapFlow 1200 Class II A/B3 Biosafety Microbiological Safety Cabinet (cell culture hood)NAPCOModel used not currently availableMay use any brand
Thermo Fisher Scientific Precision Heated Water BathFisher ScientificModel used not currently available May use any brand
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Reichert Bright-line HemacytometerSigma-AldrichZ359629May use any brand
Typhoon Trio BioAnalyzer GE Healthcare Life SciencesModel used not currently available May use any fluorescence plate reader
Tecan Safire2 Multi-detection Microplate ReaderTecanModel used not currently available May use any fluorescence plate reader
Allegra 6R benchtop centrifugeBeckman Coulter366816May use any brand
Table Top Anaesthesia machineVetEquipModel used not currently available May use any brand, must be portable
Wahl Peanut Mini ClippersWahlMay use any brand of small clippers
Insulin syringes 29 G x 1/2', 0.3 mLBD329464May use any brand. Insulin syringes are recommended as they make injections easier through the rat’s tough skin. 
Cotton swabsMedPro018-425May use any brand
Sharp-Pointed Dissecting ScissorsFisher Scientific8940May use any brand
Dissecting Tissue ForcepsFisher Scientific13-812-41May use any brand

References

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  1. Cervantes-Garcia, D., Ortiz-Lopez, R., Mayek-Perez, N., Rojas-Martinez, A. Oncolytic virotherapy. Ann Hepatol. 7 (1), 34-45 (2008).
  2. Vaha-Koskela, M. J., Heikkila, J. E., Hinkkanen, A. E. Oncolytic viruses in cancer therapy. Cancer Lett. 254 (2), 178-216 (2007).
  3. Abril, C., et al.

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Tags

Cotton Rat HandlingOncolytic VirotherapyPreclinical EvaluationAnimal Stress ReductionEnrichment Tube MethodAnesthetic Induction ChamberTumor Cell InjectionSubcutaneous Tumor FormationIntratumoral InjectionIntraperitoneal Injection

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