scholarly journals Modeling Intervention Scenarios During Potential Foot-and-Mouth Disease Outbreaks Within U.S. Beef Feedlots

2021 ◽  
Vol 8 ◽  
Author(s):  
Aurelio H. Cabezas ◽  
Michael W. Sanderson ◽  
Victoriya V. Volkova

Foot-and-mouth disease (FMD) is a highly contagious disease of livestock and has severely affected livestock industries during the past two decades in previously FMD-free countries. The disease was eliminated in North America in 1953 but remains a threat for re-introduction. Approximately 44% of the on-feed beef cattle in the U.S. are concentrated in feedlots <32,000 heads, but little information is available on dynamics of FMD in large feedlots. Therefore, there is a need to explore possible management and intervention strategies that might be implemented during potential FMD outbreaks on feedlots. We used a within home-pen stochastic susceptible-latent-infectious-recovered (SLIR) FMD dynamics model nested in a meta-population model of home-pens in a feedlot. The combinatory model was previously developed to simulate foot-and-mouth disease virus (FMDv) transmission within U.S. beef feedlots. We evaluated three intervention strategies initiated on the day of FMD detection: stopping movements of cattle between home-pens and hospital-pen(s) (NH), barrier depopulation combined with NH (NH-BD), and targeted depopulation of at-risk home-pens combined with NH (NH-TD). Depopulation rates investigated ranged from 500 to 4,000 cattle per day. We evaluated the projected effectiveness of interventions by comparing them with the no-intervention FMD dynamics in the feedlot. We modeled a small-size (4,000 cattle), medium-size (12,000 cattle), and large-size (24,000 cattle) feedlots. Implementation of NH delayed the outbreak progression, but it did not prevent infection of the entire feedlot. Implementation of NH-BD resulted in depopulation of 50% of cattle in small- and medium-size feedlots, and 25% in large-size feedlots, but the intervention prevented infection of the entire feedlot in 40% of simulated outbreaks in medium-size feedlots, and in 8% in large-size feedlots. Implementation of NH-TD resulted in depopulation of up to 50% of cattle in small-size feedlots, 75% in medium-size feedlots, and 25% in large-size feedlots, but rarely prevented infection of the entire feedlot. Number of hospital-pens in the feedlot was shown to weakly impact the success of NH-TD. Overall, the results suggest that stopping cattle movements between the home-pens and hospital-pens, without or with barrier or targeted cattle depopulation, would not be highly effective to interrupt FMDv transmission within a feedlot.

Author(s):  
Sydney S. Breese ◽  
Howard L. Bachrach

Continuing studies on the physical and chemical properties of foot-and-mouth disease virus (FMDV) have included electron microscopy of RNA strands released when highly purified virus (1) was dialyzed against demlneralized distilled water. The RNA strands were dried on formvar-carbon coated electron microscope screens pretreated with 0.1% bovine plasma albumin in distilled water. At this low salt concentration the RNA strands were extended and were stained with 1% phosphotungstic acid. Random dispersions of strands were recorded on electron micrographs, enlarged to 30,000 or 40,000 X and the lengths measured with a map-measuring wheel. Figure 1 is a typical micrograph and Fig. 2 shows the distributions of strand lengths for the three major types of FMDV (A119 of 6/9/72; C3-Rezende of 1/5/73; and O1-Brugge of 8/24/73.


Author(s):  
S. S. Breese ◽  
H. L. Bachrach

Models for the structure of foot-and-mouth disease virus (FMDV) have been proposed from chemical and physical measurements (Brown, et al., 1970; Talbot and Brown, 1972; Strohmaier and Adam, 1976) and from rotational image-enhancement electron microscopy (Breese, et al., 1965). In this report we examine the surface structure of FMDV particles by high resolution electron microscopy and compare it with that of particles in which the outermost capsid protein VP3 (ca. 30, 000 daltons) has been split into smaller segments, two of which VP3a and VP3b have molecular weights of about 15, 000 daltons (Bachrach, et al., 1975).Highly purified and concentrated type A12, strain 119 FMDV (5 mg/ml) was prepared as previously described (Bachrach, et al., 1964) and stored at 4°C in 0. 2 M KC1-0. 5 M potassium phosphate buffer at pH 7. 5. For electron microscopy, 1. 0 ml samples of purified virus and trypsin-treated virus were dialyzed at 4°C against 0. 2 M NH4OAC at pH 7. 3, deposited onto carbonized formvar-coated copper screens and stained with phosphotungstic acid, pH 7. 3.


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