Senior Scientist Traditional Microbiology
Merck KGaA, Darmstadt, Germany
Barbara is a microbiologist with many years of industry experience who has been at Merck KGaA since 2008. She is a member of several ISO/CEN committees and Chair of IDF Standing Committee for Harmonization of Microbiological Methods and Chair of German DIN NAL Working Group “Microbiology in the Food Chain”.
Microbiology of the food chain — Horizontal method for the enumeration of coagulase-positive staphylococci (Staphylococcus aureus and other species) — Part 1: Method using Baird-Parker agar medium
Microbiology of the food chain — Horizontal method for the enumeration of coagulase-positive staphylococci (Staphylococcus aureus and other species) — Part 2: Method using rabbit plasma fibrinogen agar medium
These recently published documents specify horizontal methods for the enumeration of coagulase-positive staphylococci by counting the colonies obtained on a solid medium after aerboc incubation at 34 °C to 38 °C.
Part 1 uses the solid medium Baird-Parker medium and part 2 uses the solid medium Rabbit plasma fibrinogen medium.
Both parts are applicable to:
Because of the large variety of products in the food chain, it is possible that these horizontal methods are not appropriate in every detail for all products. Nevertheless, it is expected that the required modifications are minimized so that they do not result in a significant deviation from this horizontal method.
Based on the information available at the time of publication of this document, the methods are not considered to be (fully) suited to the examination of fermented products or other products containing technological flora based on Staphylococcus spp. (e.g. S. xylosus) (such as cheeses made from raw milk and certain raw meat products) likely to be contaminated by:
Nevertheless, (EN) ISO 6888-1 and (EN) ISO 6888-2 are given equivalent status.
It is stated in the Introduction of both parts, that the main technical changes listed in the Foreword, introduced in these documents compared with the previous editions (of part 1 and part 2) are considered as minor. They have a minor impact on the performance characteristics of this method.
Results of the interlaboratory study and tested samples are described in Annex C of part 1 and part 2.
The second edition of ISO 6888-1:2021 cancels and replaces the first edition (ISO 6888-1:1999), which has been technically revised. It also incorporates the amendments ISO 6888-1:1999/Amd 1:2003 and ISO 6888-1:1999/Amd 2:2018.
This second edition of ISO 6888-1:2021 cancels and replaces the first edition (ISO 6888-2:1999), which has been technically revised. It also incorporates the Amendment ISO 6888-2:1999/Amd 1:2003.
The main changes of part 1 and part 2 compared with the previous editions are as follows:
Microbiology of the food chain — Horizontal method for the enumeration of coagulase-positive staphylococci (Staphylococcus aureus and other species) — Part 3: Detection and MPN technique for low numbers is currently under revision, the revised documents is planned to be published by mid 2022.
Microbiology of the food chain — Horizontal method for the determination of Vibrio spp. — Part 2: Enumeration of total and potentially enteropathogenic Vibrio parahaemolyticus in seafood using nucleic acid hybridization
This document specifies a method for the direct enumeration of potentially enteropathogenic V. parahaemolyticus (tdh and/or trh positive) and/or the enumeration of total V. parahaemolyticus in seafood.
Potentially enteropathogenic strains of Vibrio parahaemolyticus possess thermostable direct haemolysin (TDH) and/or thermostable direct hemolysin-related hemolysin (TRH). TDH positive strains manifest Kanagawa phenomenon (KP). This characteristic is traditionally utilized in the identification of enterotoxigenic strains of V. parahaemolyticus. Strains possessing TRH do not share the haemolytic characteristics of TDH positive isolates and no conventional identification assay has been reported for TRH identification. Pathogenic strains in the environment are a minority and differentiation between enteropathogenic and total V. parahaemolyticus presence is therefore useful.
This new webpage contains various sections to cover news (hot topic), on-going projects, guidelines and relevant information to contact committee manager as well as chairperson. Relevant additional information is given, for example, for the validation and verification of methods including some background information and links to a document for the transition period for the implementation of (EN) ISO 16140-3.
Another section is dedicated to (EN) ISO 11133 on culture media including a table containing a complete list of culture media and reagents used in ISO food and water microbiology standards with the names of the control strains which should be used for the performance testing.
There is also a part on (EN) ISO 19036 “Estimation of measurement uncertainty for quantitative determinations” which gives answers to the questions on this complex topic in the presentation of the approach of the recently revised standard ISO 19036:2019. A link to an Excel tool enables the user to implement the calculations of this standard is also provided.
Microbiology of food, animal feed and water — Preparation, production, storage and performance testing of culture media — Amendment 2
This second amendment to the already published (EN) ISO 11133:2014 gives additional information by specifying control strains for the performance testing of confirmation and characterization media, reagents, dyes, stains and materials described in standards for the microbiological examination of samples from the food chain and water. The strains chosen have been selected preferentially those already cited in (EN) ISO 11133:2014. If a suitable strains was not available from this source, a strains from the catalogue of organisms compiled by the World Data Centre for Microorganisms (WDCM) has been selected. In most cases, more than one strain has been listed for both positive and negative reactions. The user may choose any of the strains cited for positive and negative reactions.
Microbiology of the food chain — Horizontal method for the detection, enumeration and serotyping of Salmonella — Part 1: Detection of Salmonella spp. — Amendment 1: Broader range of incubation temperatures, amendment to the status of Annex D, and correction of the composition of MSRV and SC
Amendmend 1:2020 includes an extension of the temperature range for incubation of the selective media from 37 °C ± 1 °´C to 34 °C to 38 °C without further tolerance (e.g. for MKTTn broth, XLD agar, SC medium, BS agar, confirmation media and reagents). This temperature range was already included in (EN) ISO 6579-1:2017 for incubation of non-selective media.
Status of Annex D “Detection of Salmonella enterica subspecies enterica serovars Typhi and Paratyphi” has been changed from “normative” to “informative”.
Composition of MSRV (Modified semi-solid Rappaport-Vassiliadis) agar and SC (Selenite cysteine) medium have been corrected for their preparation from single ingredients.
Microbiology of the food chain — Preparation of test samples, initial suspension and decimal dilutions for microbiological examination — Part 5: Specific rules for the preparation of milk and milk products
This document specifies rules for the preparation of samples of milk and milk products and their suspensions for microbiological examination when the samples require a different preparation from the general methods specified in ISO 6887-1. It excludes the preparation of samples for both enumeration and detection test methods where preparation details are specified in the relevant International Standards.
Besides a list of diluents with their composition and performance testing, it describes general and specific procedures for preparation of the initial suspension and further decimal dilutions, e.g. for milk and liquid milk products, dehydrated milk products, cheese and cheese products, casein products, butter, milk-based products with low pH (e.g. yoghurts, probiotic milk products) and dehydrated milk-based infant foods with or without probiotics.
(EN) ISO 6887-5:2020 is intended to be used in conjunction with (EN) ISO 6887-1:2017 “Microbiology of the food chain — Preparation of test samples, initial suspension and decimal dilutions for microbiological examination — Part 1: General rules for the preparation of the initial suspension and decimal dilutions”.
Microbiology of food and animal feeding stuffs — Horizontal method for the enumeration of presumptive Bacillus cereus — Colony-count technique at 30 °C — Amendment 1: Inclusion of optional tests
Amendmend 1:2020 includes optional tests intended for complemenatry investigations (i.e. epidemiological) on isolated Bacillus cereus group strains obtained from the procedure as described in (EN) ISO 7932:2004.
In this amendmed, the term “B. cereus group” is used instead of “presumptive B. cereus” following the EFSA optinion published in 2016.
New Annex C describes a validated PCR method that targets both cytK gene variants (cytK-1 or cytK-2 gene variants of the gene encoding Cytotoxin K) and, if present, indicates which of the two forms is present. It also allows confirmation of isolates as B. cytotoxicus.
New Annex D describes a rapid and validated PCR method that targets the ces gene. A cereulide peptide synthetase (ces) is involved in the non-ribosomal syntehsis of cereulide. This cereulide, when poduced in food, can cause an emetic food poisoning syndrome.
The motility test described in Annex E allows for screening for presumptive B. anthracis among isolated B. cereus group. This test has strong limitations and it is intended to assist in differentiating B. anthracis from other B. cereus group members. The correct identification of B. anthracis strains is very complex and needs additional tests which are outside the scope of this document.
Microscopic examination of the parasporal crystal from Bacillus thuringiensis is described in Annex F. B. thuringiensis, one of the B. cereus group species, can be distinguished from the other species of this group by the microsocopic examination of the parasporal crystal formation. This method was evaluated through an interlaboratory study and performance characteristics are included in Annex F.