2. muscle to meat SDL Flashcards

(27 cards)

1
Q

What factors contribute to the presentation of dark, firm and dry beef (DFD) also known as dark cutting beef (DCB)?

A

Combination of factors that stress the animal and deplete glycogen stores in muscle:
- rapid fluctuations in temperature
- excessive use of growth promotive implants
- genetic factors
- rough handling
- bulls have more dark cutters than steers, cows or heifers

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2
Q

What factors contribute to the presentation of pale, soft exudate (PSE)?

A
  • Rough handling causes overheating of the pigs
  • rough handling and electric prods also cause increased lactate levels which damage meat quality
  • poor chilling causes internal temperature of pig meat to drop too slowly
  • pig genetics - pigs with a positive PSS (porcine stress syndrome) gene
  • In spring - water temperature increases
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3
Q

How can DFD be prevented?

A
  • Don’t mix strange cattle together prior to slaughter at the plant (to prevent fighting)
  • Handle animals quietly and reduce or eliminate prod usage
  • Unload trucks promptly
  • Cattle should not be held overnight in the stockyards of the plant
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4
Q

How can PSE be prevented?

A
  • Provide adequate pen space in holding pens at the plant
  • During hot weather wet animals down with sprinklers
  • Allow 2-4 hours of rest prior to stunning
  • Handle and drive quietly and reduce or eliminate electric prod use
  • Never fill pens more than one half to three quarters full
  • Access to water
  • Measure levels of lactate in blood to monitor handling in stunning area
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5
Q

What problems result of DFD?

A
  • Economic losses (reduced market value)
  • Quality issues (appearance - dark, texture and taste - tougher and stronger off-putting flavour due to high pH levels, reduced shelf life - High pH can interfere with the curing process)
  • Processing problems (water - holding capacity - higher water-holding capacity, challenges in curing and smoking - higher pH can interfere).
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6
Q

What problems result of PSE?

A
  • Economic losses (reduced market value - meat is less desirable due to poor appearance and texture, often sold at a lower price, increased waste - higher rates of meat rejection and trimming)
  • Quality issues (appearance - meat is pale and unattractive , texture, moisture loss - meat is soft and exudates a lot of moisture and can can become dry and tough when cooked, poor binding - protein structure is compromised leading to poor binding in products like sausages and ham)
  • Processing problems (yield and efficiency - high moisture loss during processing, poor emulsification - in products that require emulsification e.g. sausages, PSE can cause issues with fat and water binding. Shelf life (spoils easily due to exudative properties)
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7
Q

what does it mean that the slaughterhouse dresses the carcasses according to European Union (EU) specifications in pigs?

A

Before weighing the carcase, you must remove the:
- tongue
- bristle (hair)
- hooves
- genital organs
- flare fat
- kidneys
- diaphragm

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8
Q

Why is 2% of carcase weight deducted?

A

Calculating the cold weight requires a 2% deduction on top of the deductions that are made when calculating warm weight

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9
Q

What does it mean when a pig carcase is classified as ‘E’?

A

A grade (SEUROP) refers to the lean meat as a percentage of recorded carcase cold weight.
Grade E - 55% or more but less than 60%

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10
Q

What is the typical outbreak investigation scenario involving broiler chickens?

A

• A Salmonella outbreak affects humans (e.g., children in Rutland)
• Two potential sources: poultry abattoir or open broiler farm (e.g., ‘Blackwater Open Farm’)
• Investigators must sample both sites, use microbiological methods to detect Salmonella, and perform typing methods to determine strain similarity and outbreak linkage.

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11
Q

What are the key questions guiding the investigation?

A

Presence/absence: Is the pathogen there? Prevalence: How widespread is it? Source attribution: Where did it originate? Risk: What is the threat to public health? Typing choice: What typing/genotyping techniques best answer the questions?

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12
Q

What equipment is needed for conducting a zoonotic disease outbreak investigation?

A

• Sampling equipment: sterile swabs, peptone water, faecal pots
• PPE: gloves, masks
• Transport: cool boxes, documentation
• Lab tools: incubators, selective media, PCR machines, ELISA kits, serotyping reagents.

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13
Q

What are the sample handling and transport regulations (EU Regulation 200/2012)?

A

• Samples must be collected aseptically
• maintained at 4°C during transport
• processed within 48 hours
• clearly labelled
• and traceable with proper documentation.

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14
Q

What sample types are typically collected in poultry-related investigations?

A

• Faeces
• carcass swabs
• feed and water
• bedding/litter swabs
• slaughterhouse equipment
• carcass rinse
• meat surface swabs
• cloacal swabs.

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15
Q

How do you isolate Salmonella from samples?

A

• Pre-enrichment in buffered peptone water
• selective enrichment (Rappaport-Vassiliadis or Selenite broth)
• plating on XLD or Hektoen agar
• incubation at 37°C
• colony identification via biochemical tests
• and confirmation by typing.

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16
Q

How are pathogens enumerated from farm/food samples?

A

• Plate Count (CFU)
• Most Probable Number (MPN)
• membrane filtration
• qPCR for DNA copy number
• and direct microscopic count.

17
Q

What is serotyping and how is it performed?

A

• Serotyping detects surface antigens (O, H) by mixing bacterial suspension with specific antisera
• Agglutination indicates a positive result
• Fast and specific, but expensive and lacks strain-level resolution.

18
Q

What is genotyping and why is it important in tracing pathogens?

A

• Genotyping uses DNA analysis to distinguish bacterial strains
• Includes PCR, WGS, PFGE, and MLST
• Provides high-resolution source tracking during outbreaks.

19
Q

How does PCR work in outbreak investigations?

A

• PCR amplifies specific DNA targets
• It is sensitive, rapid, and specific but cannot distinguish live from dead cells and only samples small genomic regions.

20
Q

What is PFGE and when is it used?

A

• PFGE cuts bacterial DNA with rare enzymes, separates fragments on a pulsed gel, and creates a DNA fingerprint
• Highly accurate but expensive and labour-intensive.

21
Q

What is phage typing?

A

• Tests bacterial sensitivity to a panel of bacteriophages
• Generates unique profiles, but sensitivity may vary and requires expert interpretation.

22
Q

What is whole genome sequencing (WGS) and what are its benefits?

A

• WGS reads the entire DNA sequence of an organism
• Extremely accurate, allows creation of phylogenetic trees, but expensive and requires bioinformatics support.

23
Q

What is the IMViC test and what does it assess?

A

• Biochemical test panel (Indole, Methyl Red, Voges-Proskauer, Citrate) to differentiate coliforms
• Easy and low-cost but lacks strain specificity.

24
Q

What are the key requirements for transporting samples in a zoonotic outbreak investigation?

A

• Samples must be transported aseptically
• Must be kept at 4°C to prevent bacterial overgrowth or degradation
• Samples should be processed within 48 hours
• Ensure accurate labelling and traceability
• Avoid contamination during handling and transit.

25
What regulation governs sample handling and transport in the EU?
• EU Regulation 200/2012 • Specifies procedures for collection, handling, and transport of animal-origin samples • Enforces aseptic technique, temperature control, and timely testing.
26
What transport media can be used to preserve microbial samples?
• Buffered Peptone Water • Stuart's or Amies transport medium for swabs • Sterile saline for dilution or surface swabs • Broths for selective enrichment depending on target organism (e.g., Rappaport-Vassiliadis for Salmonella).
27
What precautions must be taken when transporting zoonotic samples to the lab?
• Maintain cold chain (4°C) using ice packs or cool boxes • Use leak-proof, labelled containers • Apply biosafety protocols (e.g., PPE and contamination control) • Log samples in a tracking system or chain-of-custody form • Deliver samples within 48 hours to maintain viability.