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ICAR AICE-JRF/SRF Food Microbiology: Spoilage, Pathogens & Detection: practice questions

ICAR AICE-JRF/SRF (PhD) — Food Processing Technology, Food Safety & Quality, Processing and Food Engineering · India · ICAR through the National Testing Agency

Original practice questions written to the published syllabus · not past papers
10worked here, free
17written to this exam in this subject
12syllabus units

What this subject covers

Which microorganisms grow in which foods and why, the pathogens and toxins behind food-borne disease, and the methods — conventional, rapid and molecular — used to find them. The PG units on predictive microbiology and genomic surveillance carry it beyond the hygiene-focused milk and meat microbiology in the Veterinary track (milk-meat-hygiene-food-safety).

In the exams: GATE XE-G and XL-U Section 2 (spoilage, toxins from microbes); ICAR AIEEA-PG Code 18 Unit IV; ICAR AICE 35.b Units 2–4

What ICAR AICE-JRF/SRF asks from it

ICAR AICE-JRF/SRF (PhD) — Food Processing Technology, Food Safety & Quality, Processing and Food Engineering

35.b Units 2–4: risk analysis, food law with two- and three-class sampling plans and FSSAI microbiological criteria, rapid methods, and food microbiology in depth. Deeper questions on predictive models, qPCR interpretation, WGS in outbreak investigation, biofilm control and the probability of lot acceptance.

Where the 17 questions fall

How our questions for ICAR AICE-JRF/SRF spread across the units of Food Microbiology: Spoilage, Pathogens & Detection. Difficulty: 0 easy, 2 medium, 15 hard.

Predictive microbiology: primary and secondary models3
Intrinsic and extrinsic factors controlling microbial growth2
Molecular methods: PCR, qPCR and whole-genome sequencing2
Microbiological criteria and sampling plans2
Spoilage of canned, bakery and beverage products1
Bacterial food-borne pathogens: Salmonella, Listeria, E. coli (STEC), Campylobacter, Shigella, Vibrio and Yersinia1
Spore-formers and toxin producers: Clostridium botulinum, C. perfringens, Bacillus cereus and Staphylococcus aureus1
Mycotoxigenic moulds: Aspergillus, Penicillium and Fusarium1
Food-borne viruses and parasites1
Rapid methods: ATP bioluminescence, immunoassays and lateral flow1
Biofilms in food plants1
Conventional methods: plate count, MPN, selective media and confirmation1

10 practice questions, worked

Choose an answer, then open the working. Each explanation says why the right answer is right and why the others are not.

1 · Intrinsic and extrinsic factors controlling microbial growth · hard

Hurdle technology, as developed by Leistner, is best described as:

  1. Applying one severe preservation step that is sufficient on its own to sterilise the food completely
  2. Combining mild preservation factors that together prevent growth with less damage to quality
  3. Adding a sequence of chemical preservatives at doses each high enough to stop growth individually
  4. Storing a food under a fluctuating temperature regime that repeatedly shocks the microflora
Answer and working

B. Combining mild preservation factors that together prevent growth with less damage to quality

The idea is that factors such as reduced aw, low pH, mild heat, preservatives and chilling, each sub-inhibitory alone, combine to stabilise the food. A single severe step is the opposite approach.

Further reading: Jay, Loessner and Golden, Modern Food Microbiology, ch. 3

2 · Spoilage of canned, bakery and beverage products · hard

Canned strawberries soften and disintegrate after a normal pasteurisation process. The organisms most likely responsible are:

  1. Heat-resistant moulds such as Byssochlamys with ascospores that survive mild heat
  2. Pseudomonas species entering through the seam during water cooling of the cans
  3. Lactic acid bacteria that grow in the syrup and produce dextran from sucrose
  4. Proteolytic Clostridium botulinum that grows because the fruit is a low-acid food
Answer and working

A. Heat-resistant moulds such as Byssochlamys with ascospores that survive mild heat

Byssochlamys fulva and B. nivea produce heat-resistant ascospores and pectinolytic enzymes that soften fruit. Strawberries are acid, so C. botulinum is not the concern.

Further reading: Adams, Moss and McClure, Food Microbiology; Stumbo, Thermobacteriology in Food Processing

3 · Bacterial food-borne pathogens: Salmonella, Listeria, E. coli (STEC), Campylobacter, Shigella, Vibrio and Yersinia · hard

Salmonella has caused large outbreaks from chocolate, peanut butter and milk powder although it cannot grow in these foods. The best explanation is that:

  1. It survives for long periods at low water activity, and fat may protect it during digestion
  2. It grows slowly at water activities down to 0.60 when the storage temperature is high
  3. It produces a preformed heat-stable toxin in the raw ingredients before processing
  4. It forms heat-resistant spores that may germinate once the product is reconstituted with water
Answer and working

A. It survives for long periods at low water activity, and fat may protect it during digestion

Salmonella does not grow below about 0.93–0.95 aw but survives drying for months; in fatty foods the infectious dose can be very low. It is not a spore-former and does not cause intoxication.

Further reading: Doyle, Diez-Gonzalez and Hill, Food Microbiology: Fundamentals and Frontiers

4 · Spore-formers and toxin producers: Clostridium botulinum, C. perfringens, Bacillus cereus and Staphylococcus aureus · hard

Enterotoxin-producing Clostridium perfringens strains were classically called type A. Under the revised toxinotyping scheme published in 2018, most such food-poisoning strains are placed in:

  1. Type B
  2. Type G
  3. Type F
  4. Type D
Answer and working

C. Type F

The 2018 scheme created type F for strains carrying the enterotoxin gene without beta, epsilon or iota toxin, and type G for NetB-producing strains linked to necrotic enteritis in poultry.

Further reading: Doyle, Diez-Gonzalez and Hill, Food Microbiology: Fundamentals and Frontiers

5 · Mycotoxigenic moulds: Aspergillus, Penicillium and Fusarium · hard

Why is sampling, rather than analysis, the largest source of error in determining aflatoxin in a lot of groundnuts?

  1. Aflatoxin moves between kernels during storage, so the lot changes after sampling
  2. The toxin is concentrated in a few highly contaminated kernels, so its distribution is very uneven
  3. Immunoaffinity columns retain the toxin unpredictably between replicate extractions of one ground sample
  4. Aflatoxin degrades rapidly in ground samples before they reach the laboratory
Answer and working

B. The toxin is concentrated in a few highly contaminated kernels, so its distribution is very uneven

A small fraction of kernels can carry most of the toxin, so small samples give highly variable results. Regulations therefore require large aggregate samples that are ground and subsampled.

Further reading: Adams, Moss and McClure, Food Microbiology; Codex General Standard for Contaminants and Toxins in Food and Feed

6 · Rapid methods: ATP bioluminescence, immunoassays and lateral flow · hard

A food contains 1 Salmonella cell in a 25 g portion homogenised in 225 mL of enrichment broth. The organism doubles every 30 min with no lag, and a lateral flow test detects 10^5 CFU/mL. About how long must the enrichment run?

  1. 12.3 h
  2. 8.3 h
  3. 6.1 h
  4. 24.6 h
Answer and working

A. 12.3 h

Starting concentration = 1/250 mL = 0.004 CFU/mL. Doublings = log2(10^5/0.004) = log2(2.5 × 10^7) = 24.6. Time = 24.6 × 0.5 h = 12.3 h. 24.6 h treats doublings as hours.

Further reading: Jay, Loessner and Golden, Modern Food Microbiology, rapid methods chapter

7 · Predictive microbiology: primary and secondary models · medium

In the Weibull inactivation model, a shape parameter p less than 1 describes:

  1. A survivor curve with a shoulder
  2. A survivor curve with tailing
  3. A curve showing regrowth after heating
  4. A straight log-linear survivor curve
Answer and working

B. A survivor curve with tailing

p < 1 gives an upward-concave curve that tails; p > 1 gives a shoulder; p = 1 reduces to the log-linear (D value) model.

Further reading: McKellar and Lu, Modeling Microbial Responses in Food

8 · Biofilms in food plants · hard

Milk powder plants often find thermophilic spore-formers in the product even though the milk was pasteurised. A common source is:

  1. Growth of Listeria in the finished powder during dry storage at room temperature for months
  2. Biofilms of Pseudomonas in the raw milk silos that survive spray drying
  3. Biofilms of lactic acid bacteria on the outer packaging of the powder
  4. Biofilms of thermophilic bacilli such as Anoxybacillus and Geobacillus in evaporators
Answer and working

D. Biofilms of thermophilic bacilli such as Anoxybacillus and Geobacillus in evaporators

Thermophilic bacilli form biofilms on warm surfaces in evaporators and shed spores into the product during long runs.

Further reading: Doyle, Diez-Gonzalez and Hill, Food Microbiology: Fundamentals and Frontiers, biofilm chapter

9 · Microbiological criteria and sampling plans · hard

A lot has 10% of its units contaminated. Using a two-class plan with c = 0, how does increasing n from 5 to 60 change the probability of acceptance?

  1. From 0.59 to about 0.002
  2. From 0.50 to about 0.05
  3. From 0.90 to about 0.54
  4. From 0.59 to about 0.10
Answer and working

A. From 0.59 to about 0.002

Pa = 0.9^5 = 0.59 and 0.9^60 = 0.0018. 0.90 to 0.54 uses p = 0.01 and n = 60 for the second value only.

Further reading: ICMSF, Microorganisms in Foods 7; Codex CXG 21-1997; Regulation (EC) No 2073/2005

10 · Intrinsic and extrinsic factors controlling microbial growth · hard

Non-proteolytic Clostridium botulinum has a minimum growth temperature of about 3 °C. A chilled vacuum-packed fish product is stored at 2 °C. Which statement best describes the safety position?

  1. The product is safe because vacuum packing raises the redox potential above the organism's limit
  2. The product is unsafe because non-proteolytic strains grow fastest at refrigeration temperatures
  3. Safe only while 2 °C is held throughout; abuse makes shelf-life limits or extra hurdles necessary
  4. The product is safe indefinitely because spores of non-proteolytic strains cannot survive storage at 2 °C or below
Answer and working

C. Safe only while 2 °C is held throughout; abuse makes shelf-life limits or extra hurdles necessary

Storage below 3 °C prevents growth, but chill chains are rarely perfect, so regulators combine temperature with shelf-life limits or hurdles such as salt or pH. Vacuum packing lowers, not raises, the redox potential.

Further reading: Jay, Loessner and Golden, Modern Food Microbiology, ch. 3

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Food Microbiology: Spoilage, Pathogens & DetectionThe full study manual, free ICAR AICE-JRF/SRFFormat, sections and how it has changed

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Food Microbiology: Spoilage, Pathogens & Detection for other exams

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