Minimal infective dose
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The concept of minimal infective dose (MID) has traditionally been used for bacteria that contaminate foods that cause infection in or from the digestive tract. MID was defined as the number of bacteria ingested (the dose) from which a pathology is observed in the consumer. Examples such as this are found in textbooks:[which?] to cause gastrointestinal disorders, the food must contain more than 100,000 Salmonella per gram. However, in such a formulation, we immediately see an inaccuracy: to know the dose ingested, concentration is not enough. It is also necessary to know the mass of the portion:
- = number of bacteria i.e. dose
- = concentration of bacteria
- = mass
Nevertheless, this formulation has served as a basis for very useful reasoning to establish the maximum concentrations permitted by the microbiological regulatory criteria intended to protect the health of consumers. Thus in 1992, as the outbreaks previously caused by Listeria monocytogenes involved only food containing more than 1000 L. monocytogenes cells per gram, lawmakers on both sides of the Atlantic - keeping a margin of safety - fixed its maximum concentration at 100 L. monocytogenes per gram.
Dose-effect relationship and dose-response relationship
The concept of a dose-response relationship developed from 1995 onward, as quantitative risk assessment matured as a discipline within the field of food safety. An infectious bacterium in a food can cause various effects: diarrhea, vomiting, sepsis, meningitis, abortion, Guillain-Barré syndrome, death, etc. As the dose increases, the severity of the pathological effects increases, and a "dose-response relationship" can often be established. For example, the higher the dose of Salmonella, the more diarrhea occurs soon after ingestion and the more stressful it is. However, among people who have ingested the same dose, not all are affected. The proportion of people affected is called response. The dose-response relationship for a given effect (e.g., diarrhea) is therefore the relationship between the dose and the likelihood of experiencing this effect. When the response is less than about 10%, it is observed that there is a strictly proportional relationship between dose and response:
- = probability of the effect considered
- = response
Do not confuse the dose-effect relationship with the dose-response relationship.
The existence of this relation has a first important consequence: the proportionality factor, symbolized by the letter r, corresponds precisely to the probability of the effect considered when the dose is equal to one bacterial cell. As a result, the minimum infective dose is exactly equal to one bacterial cell: it is far from the traditional notion recalled at the beginning of this article. Proportionality has a second consequence, which is obvious: when the dose is divided by ten, the probability of observing the effect is also divided by ten. And it has a third consequence, which is not obvious: it is a relationship without threshold. Of course, if a portion of food does not contain the bacterium, there will be no effect. But in industrial practice, everything is done to reduce the probability that a serving contains the bacterium. There is therefore on the market food in which, for example, only one serving in a hundred is contaminated. The probability of the effect considered is then r / 100. If one in ten thousand is contaminated, the probability goes to r / 10,000, and so on. The line representing the relation can be extended to minus infinity: there is no threshold. For readers familiar with the notion of D50 (the dose that causes the effect in 50% of consumers exposed to the hazard), in most cases the following relationship applies:
To compare the dose-response relationships for different effects caused by the same bacterium, or for the same effect caused by different bacteria, we can of course directly compare the values of r. However, experience shows that it may be easier for the mind to compare the doses causing the effect in 50% or 1% of consumers. Here are some values of D1 (dose causing the effect considered in 1% of consumers exposed to the hazard):
- Escherichia coli (EHEC), haemolytic-uremic syndrome in children under 6 years: 8.4 bacterial cells;
- Escherichia coli (EHEC), haemolytic-uraemic syndrome in children aged 6 to 14 years: 41.9 bacterial cells;
- Listeria monocytogenes, severe listeriosis in the general population: 4.2.1011 bacterial cells;
- Listeria monocytogenes, severe listeriosis in the susceptible population: 9.5.109 bacterial cells.
These examples highlight two important things:
- D1 and r depend not only on the bacterium and the effect considered, but also on the belonging to categories of consumers susceptible to the disease; therefore, there are as many dose-response curves as there are pathogens, health effects and sensitivities of exposed individuals;
- For the bacteria of the examples above, the orders of magnitude of the values of D1 are profoundly different. The hygiene practices and control measures that food chain businesses must implement against these bacteria are therefore not comparable.
It may seem that if the contamination of food with a pathogenic bacterium is low and infrequent, the risk of becoming ill is such that there will be no public health problem. Such a view is incomplete: admittedly, consuming a low dose of this bacterium is associated with a low probability of disease. But this probability is not zero. This explains the sporadic cases observed in the population. And that is also why there is no concentration in food below which there will be no epidemic.
In the foregoing, there was mention of bacteria contaminating foods that cause infection in or from the digestive tract. Other food-borne bacteria can cause disease by producing toxins. It is no longer about infection, but toxication. Among these bacteria, some synthesize a toxin only when their concentration in the food before ingestion exceeds a threshold. This is the case of Staphylococcus aureus and Bacillus cereus, for example. The concept of MID does not apply to them, but there is indeed a concentration (not a dose) below which they do not constitute a danger to the health of the consumers.
- Stella, P., Cerf, O., Koutsoumanis, KP, Nguyen-The, C., Sofos, JN, Valero, A. & Zwietering, MH (2013) Ranking the microbiological safety of foods: a new tool and its application to composite products. Trends in Food Science & Technology 33 (2): 124-138.
- ANSES, the French Agency for Food, Environmental and Occupational Health and Safety, classifies in susceptible populations 'persons with a higher than average probability of developing, after exposure to the food hazard, symptoms of the disease, or serious forms of the disease'