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 papersWhich 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
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.
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 models | 3 | |
| Intrinsic and extrinsic factors controlling microbial growth | 2 | |
| Molecular methods: PCR, qPCR and whole-genome sequencing | 2 | |
| Microbiological criteria and sampling plans | 2 | |
| Spoilage of canned, bakery and beverage products | 1 | |
| Bacterial food-borne pathogens: Salmonella, Listeria, E. coli (STEC), Campylobacter, Shigella, Vibrio and Yersinia | 1 | |
| Spore-formers and toxin producers: Clostridium botulinum, C. perfringens, Bacillus cereus and Staphylococcus aureus | 1 | |
| Mycotoxigenic moulds: Aspergillus, Penicillium and Fusarium | 1 | |
| Food-borne viruses and parasites | 1 | |
| Rapid methods: ATP bioluminescence, immunoassays and lateral flow | 1 | |
| Biofilms in food plants | 1 | |
| Conventional methods: plate count, MPN, selective media and confirmation | 1 |
Choose an answer, then open the working. Each explanation says why the right answer is right and why the others are not.
Hurdle technology, as developed by Leistner, is best described as:
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
Canned strawberries soften and disintegrate after a normal pasteurisation process. The organisms most likely responsible are:
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
Salmonella has caused large outbreaks from chocolate, peanut butter and milk powder although it cannot grow in these foods. The best explanation is that:
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
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:
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
Why is sampling, rather than analysis, the largest source of error in determining aflatoxin in a lot of groundnuts?
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
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?
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
In the Weibull inactivation model, a shape parameter p less than 1 describes:
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
Milk powder plants often find thermophilic spore-formers in the product even though the milk was pasteurised. A common source is:
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
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?
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
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?
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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