Abstract:Listeria monocytogenes continues to pose a food safety risk in ready‐to‐eat foods, including fresh and soft/semisoft cheeses. Despite L. monocytogenes being detected regularly along the cheese production continuum, variations in cheese style and intrinsic/extrinsic factors throughout the production process (e.g., pH, water activity, and temperature) affect the potential for L. monocytogenes survival and growth. As novel preservation strategies against the growth of L. monocytogenes in susceptible cheeses, rese… Show more
“…Conversely, at abusive (>7–12 °C) temperatures L. lactis and other Bac+ mesophilic dairy LAB strains affect the desirable sensory quality characteristics of high-pH ready-to-eat (RTE) whey cheeses by a simultaneous high production of organic acids during retail storage. To overcome low-pH defects, bioprotective strains of non-aciduric LAB species/genera or Nis+/Bac+ mutant lactose-negative dairy LAB strains may be applied [ 28 , 29 , 30 ]. An alternate option is the addition of commercial nisin (Nisaplin ® ), pediocins or various crude LAB bacteriocin concentrates in fresh whey cheeses [ 3 , 10 , 28 , 30 ].…”
Section: Introductionmentioning
confidence: 99%
“…To overcome low-pH defects, bioprotective strains of non-aciduric LAB species/genera or Nis+/Bac+ mutant lactose-negative dairy LAB strains may be applied [ 28 , 29 , 30 ]. An alternate option is the addition of commercial nisin (Nisaplin ® ), pediocins or various crude LAB bacteriocin concentrates in fresh whey cheeses [ 3 , 10 , 28 , 30 ]. However, Nisaplin ® added as an antilisterialbiopreservative to the whey (100 or 500 IU/g) before heating, or to the fresh cheese curd (500 IU/g) before VP, reversed the natural predominant spoilage microbiota of traditional Anthotyros from Gram-positive LAB in the control cheeses without nisin to Gram-negative bacteria during storage at 4 °C for up to 45 days, particularly in the most effective Nisaplin ® treatments [ 3 ].…”
Section: Introductionmentioning
confidence: 99%
“…The best candidates are selected safe Ent+ strains of Enterococcus faecium , Enterococcus durans and Enterococcus faecalis without β-hemolytic activity, virulence genes, vancomycin resistance genes and other undesirable traits. An increasing number of promising experimental applications of Ent+ strains or enterocin preparations in dairy foods, particularly active against L. monocytogenes , are summarized in recent reviews [ 28 , 30 , 31 ], including a few studies on fresh whey cheeses [ 32 ]. Most enterococci are naturally non-aciduric LAB, which is advantageous for Ent+ strain applications in fresh RTE whey cheeses.…”
Section: Introductionmentioning
confidence: 99%
“…Most enterococci are naturally non-aciduric LAB, which is advantageous for Ent+ strain applications in fresh RTE whey cheeses. Moreover, apart from L. monocytogenes , the antimicrobial spectrum of several enterocins and/or Ent+ strains has been reported to include a wide range of Gram-positive sporoforming as well as Gram-negative bacteria [ 28 , 29 , 30 , 31 , 33 ]. On the other hand, most enterococci promote negligible or poor growth at refrigeration temperatures [ 33 ], which is against outnumbering other psychrotrophic spoilage or pathogenic bacteria with sufficient in situ enterocin production in fresh cold-stored whey cheeses [ 14 ].…”
Although fresh whey cheeses are prone to rapid deterioration, mainly by psychrotrophic Gram-negative bacteria and lactic acid bacteria (LAB), data on the specific spoilage species in traditional Greek whey cheeses are scarce. Therefore, this study quantified growth and characterized the primary spoilage bacteria in fresh Anthotyros whey cheeses stored at 4 °C in a vacuum for 40 days, without or with an added 5% (v/w) of an enterocin A-B-P crude extract (CEntE). Psychrotrophic Pseudomonas spp., Aeromonas spp., Hafnia spp. and Serratia spp. grew faster than LAB during early storage. However, LAB outgrew the Gram-negative bacteria and prevailed by mid to late storage in all cheese batches, causing a strong or milder batch-dependent natural acidification. Two major non-slime-producing and two minor biotypes of Leuconostoc-like bacteria, all identified as Leuconostoc mesenteroides by 16S rRNA sequencing, dominated the LAB association (76.7%), which also included four subdominant Carnobacterium maltaromaticum biotypes (10.9%), one Leuconostoc lactis biotype (3.3%) and few Lactococcus (1.6%), mesophilic Lactobacillus (0.8%) and Enterococcus (0.8%). Growth and distribution of LAB and Gram-negative species were strongly batch-dependent and plant-dependent. The CEntE neither retarded growth nor altered the whey cheese spoilage association but enhanced LAB growth and the declines of Gram-negative bacteria by late storage.
“…Conversely, at abusive (>7–12 °C) temperatures L. lactis and other Bac+ mesophilic dairy LAB strains affect the desirable sensory quality characteristics of high-pH ready-to-eat (RTE) whey cheeses by a simultaneous high production of organic acids during retail storage. To overcome low-pH defects, bioprotective strains of non-aciduric LAB species/genera or Nis+/Bac+ mutant lactose-negative dairy LAB strains may be applied [ 28 , 29 , 30 ]. An alternate option is the addition of commercial nisin (Nisaplin ® ), pediocins or various crude LAB bacteriocin concentrates in fresh whey cheeses [ 3 , 10 , 28 , 30 ].…”
Section: Introductionmentioning
confidence: 99%
“…To overcome low-pH defects, bioprotective strains of non-aciduric LAB species/genera or Nis+/Bac+ mutant lactose-negative dairy LAB strains may be applied [ 28 , 29 , 30 ]. An alternate option is the addition of commercial nisin (Nisaplin ® ), pediocins or various crude LAB bacteriocin concentrates in fresh whey cheeses [ 3 , 10 , 28 , 30 ]. However, Nisaplin ® added as an antilisterialbiopreservative to the whey (100 or 500 IU/g) before heating, or to the fresh cheese curd (500 IU/g) before VP, reversed the natural predominant spoilage microbiota of traditional Anthotyros from Gram-positive LAB in the control cheeses without nisin to Gram-negative bacteria during storage at 4 °C for up to 45 days, particularly in the most effective Nisaplin ® treatments [ 3 ].…”
Section: Introductionmentioning
confidence: 99%
“…The best candidates are selected safe Ent+ strains of Enterococcus faecium , Enterococcus durans and Enterococcus faecalis without β-hemolytic activity, virulence genes, vancomycin resistance genes and other undesirable traits. An increasing number of promising experimental applications of Ent+ strains or enterocin preparations in dairy foods, particularly active against L. monocytogenes , are summarized in recent reviews [ 28 , 30 , 31 ], including a few studies on fresh whey cheeses [ 32 ]. Most enterococci are naturally non-aciduric LAB, which is advantageous for Ent+ strain applications in fresh RTE whey cheeses.…”
Section: Introductionmentioning
confidence: 99%
“…Most enterococci are naturally non-aciduric LAB, which is advantageous for Ent+ strain applications in fresh RTE whey cheeses. Moreover, apart from L. monocytogenes , the antimicrobial spectrum of several enterocins and/or Ent+ strains has been reported to include a wide range of Gram-positive sporoforming as well as Gram-negative bacteria [ 28 , 29 , 30 , 31 , 33 ]. On the other hand, most enterococci promote negligible or poor growth at refrigeration temperatures [ 33 ], which is against outnumbering other psychrotrophic spoilage or pathogenic bacteria with sufficient in situ enterocin production in fresh cold-stored whey cheeses [ 14 ].…”
Although fresh whey cheeses are prone to rapid deterioration, mainly by psychrotrophic Gram-negative bacteria and lactic acid bacteria (LAB), data on the specific spoilage species in traditional Greek whey cheeses are scarce. Therefore, this study quantified growth and characterized the primary spoilage bacteria in fresh Anthotyros whey cheeses stored at 4 °C in a vacuum for 40 days, without or with an added 5% (v/w) of an enterocin A-B-P crude extract (CEntE). Psychrotrophic Pseudomonas spp., Aeromonas spp., Hafnia spp. and Serratia spp. grew faster than LAB during early storage. However, LAB outgrew the Gram-negative bacteria and prevailed by mid to late storage in all cheese batches, causing a strong or milder batch-dependent natural acidification. Two major non-slime-producing and two minor biotypes of Leuconostoc-like bacteria, all identified as Leuconostoc mesenteroides by 16S rRNA sequencing, dominated the LAB association (76.7%), which also included four subdominant Carnobacterium maltaromaticum biotypes (10.9%), one Leuconostoc lactis biotype (3.3%) and few Lactococcus (1.6%), mesophilic Lactobacillus (0.8%) and Enterococcus (0.8%). Growth and distribution of LAB and Gram-negative species were strongly batch-dependent and plant-dependent. The CEntE neither retarded growth nor altered the whey cheese spoilage association but enhanced LAB growth and the declines of Gram-negative bacteria by late storage.
“…Although milk is usually subjected to a heating process prior to processing, cheese can become contaminated during several process steps such as pressing, curing, ripening, and during cutting and packaging [22,23].…”
Most Austrian dairies and cheese manufacturers participated in a Listeria monitoring program, which was established after the first reports of dairy product-associated listeriosis outbreaks more than thirty years ago. Within the Listeria monitoring program, up to 800 mL of product-associated liquids such as cheese smear or brine are processed in a semi-quantitative approach to increase epidemiological sensitivity. A sampling strategy within cheese production, which detects environmental contamination before it results in problematic food contamination, has benefits for food safety management. The liquid-based sampling strategy was implemented by both industrial cheese makers and small-scale dairies located in the mountainous region of Western Austria. This report considers more than 12,000 Listeria spp. examinations of liquid-based samples in the 2009 to 2018 timeframe. Overall, the occurrence of L. monocytogenes in smear liquid samples was 1.29% and 1.55% (n = 5043 and n = 7194 tested samples) for small and industrial cheese enterprises, respectively. The liquid-based sampling strategy for Listeria monitoring at the plant level appears to be superior to solid surface monitoring. Cheese smear liquids seem to have good utility as an index of the contamination of cheese up to that point in production. A modelling or validation process should be performed for the new semi-quantitative approach to estimate the true impact of the method in terms of reducing Listeria contamination at the cheese plant level.
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