Quarantine Biosecurity

Quarantine biosecurity is the use of controlled isolation and protective procedures to prevent infectious agents, pests, or other biological hazards from entering, spreading within, or leaving a population or facility. It works by separating newly introduced or potentially exposed organisms, restricting movement of people, animals, materials, and equipment, and applying monitoring, sanitation, and decontamination measures during a defined observation period. In biology, these practices help identify infection before contact with established populations and reduce transmission in laboratories, animal facilities, agriculture, aquaculture, and wildlife management. Effective quarantine supports safer research, protects animal and plant health, and limits the ecological and economic consequences of biological disease outbreaks.

Quarantine Biosecurity - Related Videos

Research

JoVE Journal - Biology
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Environmental Screening of Aeromonas hydrophila, Mycobacterium spp., and Pseudocapillaria tomentosa in Zebrafish Systems

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Cited by 17 •

2017

This protocol describes the use of sump swabs and sludge analysis of zebrafish systems, which leads to increased detection compared to the sole use of sentinels to detect pathogens such as Aeromonas hydrophila, Mycobacterium spp., and Pseudocapillaria tomentosa. A system to monitor P. tomentosa eggs in quarantine is also proposed.

Research

JoVE Journal - Biology
Free Sample

Using Unfixed, Frozen Tissues to Study Natural Mucin Distribution

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Cited by 39 •

2012

Unfixed frozen tissue samples embedded in Optimal Cutting Temperature medium (OCT) can be used to study natural distribution and glycosylation of secreted mucus. In this approach tissue processing is minimal and the natural presentation of glycolipids, mucins and glycan-epitopes is preserved. Tissue sections can be analyzed by immunohistochemistry using fluorescence or chromogenic detection.

Research

JoVE Journal - Chemistry

Resolving Water, Proteins, and Lipids from In Vivo Confocal Raman Spectra of Stratum Corneum through a Chemometric Approach

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Cited by 1 •

2019

Here, we present a protocol for collection of confocal Raman spectra from human subjects in clinical studies combined with chemometric approaches for spectral outlier removal and the subsequent extraction of key features.

In Vitro Bioluminescence Assay to Characterize Circadian Rhythm in Mammary Epithelial Cells

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Cited by 12 •

2017

An in vitro bioluminescence assay to determine cellular circadian rhythm in mammary epithelial cells is presented. This method utilizes mammalian cell reporter plasmids expressing destabilized luciferase under the control of the PERIOD 2 gene promoter. It can be adapted to other cell types to evaluate organ-specific effects on circadian rhythm.

Cutaneous Leishmaniasis in the Dorsal Skin of Hamsters: a Useful Model for the Screening of Antileishmanial Drugs

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Cited by 40 •

2012

Optimization of the experimental hamster model for cutaneous leishmaniasis by intradermal injection of Leishmania promastigotes at the dorsal skin. This approach is useful during inoculation, follow-up, characterization of lesions, application of treatments and obtaining of clinical samples. Locomotion, search for food and water, play and social activities are preserved.

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