Occurrence of some probiotic bacteria in ewe's and goat's milk in Assuit City with regarding to genes responsible for production of bacteriocins.

Document Type : Original researches

Abstract

Small ruminant's milk is recognized as one kind of nutritious food owed to its originality and medicinal values. 100 samples collected from raw ewe and goat milk (50 of each) reared in Assiut City, Egypt. Milk samples were screened for probiotics Lactobacillus, Bifidobactria and Enterococcus spp. as well as their differentiation especially those harboring bacteriocin genes. On the other hand, milk samples were tested for the existence of total aerobic bacteria and total coliforms. Goat's milk showed higher existence of total aerobic and total coliforms count more than ewe's milk which showed higher existence of Lactobacillus, Bifidobacteria and Enterococcus spp. The study detected Enterococcus faecium as more in ewe's milk (40%) than goat's milk (25%) and tested for harboring bacteriocin genes (mes Y &Plantaricin E/F). Our study concluded that goat's milk had more total pathogenic parameters than ewe's milk, but ewe's milk had more probiotic lactic acid bacteria (LAB); Lactobacillus, Bifidobactria and Enterococcus spp., also, contained Enterococcus faecium strains harboring bacteriocin genes mesY& Plantaricin E/F genes more than those of goat's milk. Both of them have its value and uses in dairy industry. Further studies are needed and caring produce of these types of milk and their products in Egypt and could be assessed in several models in a similar manner to what is studied with bovine milk.

Keywords

Main Subjects


Occurrence of some probiotic bacteria in ewe's and goat's milk in Assuit City with regarding to genes responsible for production of bacteriocins.

Zeinab M. Abd-Elhamed1 and Dina N. Ali1

1 Certified Food Hygiene Lab., Animal Health Research Institute (AHRI), Agriculture Research Center (ARC), Egypt.

*corresponding author e-mail: Dr.dinaahri@ahri.gov.eg

 

Abstract

Small ruminant's milk is recognized as one kind of nutritious food owed to its originality and medicinal values. 100 samples collected from raw ewe and goat milk (50 of each) reared in Assiut City, Egypt. Milk samples were screened for probiotics Lactobacillus, Bifidobactria and Enterococcus spp. as well as their differentiation especially those harboring bacteriocin genes. On the other hand, milk samples were tested for the existence of total aerobic bacteria and total coliforms. Goat's milk showed higher existence of total aerobic and total coliforms count more than ewe's milk which showed higher existence of Lactobacillus, Bifidobacteria and Enterococcus spp. The study detected Enterococcus faecium as more in ewe's milk (40%) than goat's milk (25%) and tested for harboring bacteriocin genes (mes Y &Plantaricin E/F). Our study concluded that goat's milk had more total pathogenic parameters than ewe's milk, but ewe's milk had more probiotic lactic acid bacteria (LAB); Lactobacillus, Bifidobactria and Enterococcus spp., also, contained Enterococcus faecium strains harboring bacteriocin genes mesY& Plantaricin E/F genes more than those of goat's milk. Both of them have its value and uses in dairy industry. Further studies are needed and caring produce of these types of milk and their products in Egypt and could be assessed in several models in a similar manner to what is studied with bovine milk.

Keywords: Ewe, Goat, Milk, Lactobacilli, Bacteriocins, Bifidobacteria, Enterococcus spp.

 

Introduction

Ewe's and goat's milk are gaining worldwide interest for their nutritional and functional characteristics (Manis et al. 2023). They have high nutritive value comparing with bovine milk, it can be considered as a useful strategy to stop the problems of poor nutrition and increasing the economic status of many developing countries in Africa and Asia (Guerreiro et al. 2013) especially countries in Medeterrarian region, where be manufactured getting wide variety of products providing consumers prebiotic substances or probiotic bacteria (Kondyli et al. 2012, Balthazar et al. 2017 and Verruck et al. 2019). But ovine milk has been implicated as an important source of infection owing to poor hygienic conditions (milking methods, subclinical mastitis and contamination during or post milking) (Aqib et al. 2019). So, to reduce the bacterial contamination continuous monitoring and improvement of the hygienic quality of milk by ensuring proper handling and production is important (Praja et al. 2023).

Genus Lactobacillus, together with Bifidobacterium species are most commonly used as probiotic, when be present in adequate amounts confer a health benefit (FAO/WHO, 2001). Some of the isolate of Enterococci exhibited probiotic activity against several food spoilage bacteria and food-borne pathogens (Nami et al 2019). Among food-associated lactic acid producing bacteria (LAB), Enterococci are the most controversial group and important discrepancies exist between studies about their function in foods (Ruiz et al. 2016) as it may have a relevant role in dairy fermentation due to their interesting proteolytic and lipolytic activities (Foulquié Moreno et al. 2006). Although, Enterococcus. faecium has long been recognized for its probiotic benefits (Hu et al. 2019 and Popovic´ et al. 2019), and Enterococcus. faecalis may have antibacterial activity (El Halfawy et al. 2019, El-Sayed et al. 2019). Bacteriocins are considered as ideal candidates for several health care applications due to their limited range of activity and rapid degradability by proteolytic enzymes (Ahmed et al. 2023) So, Several previous studies have focused on the production of bacteriocins by gram-positive bacteria(Staphylococcus aureus)  with lactic acid bacteria (Zommiti et al. 2016; Wyszyńska and Godlewska, 2021). While, our work aimed to screen the bacteriocin production from Enterococcus. faecium and Enterococcus. faecalis and to evaluate the small ruminant's milk through estimating the existence of total aerobic bacteria and total coliforms count as well probiotics bacteria as Lactobacillus, Bifidobacterium and Enterococci spp.

Material and methods

Sampling:

     A total of 100 samples of raw ewe and goat’s milk from clinically healthy sheep and goat were collected from different farms located in Assiut City: 50 samples each, Before a manual milking, teats were carefully cleaned with cotton wool impregnated with 70% of ethanol. After, the three first streams of milk were discarded; udders and mammary secretions were examined for macroscopic signs of abnormality. The samples were collected in sterile tubes and then placed in isotherm cool box (4°C) and transported to the laboratory of food hygiene in animal health research institute at Assiut city. The samples were analyzed for their microbiological and hygienic quality as well as the prevalence of some probiotic bacteria.

Microbiological examination:

  • Total Bacterial Count (TBC): carried out on plate count agar (APHA, 2004).
  • Coliforms count: enumerated by the most probable number (MPN) (FDA, 2002).
  • Enumeration, isolation and identification of Lactobacillus : isolation on DeMan, Rogosa and Sharpe (MRS) plates (DifcoTM) and characterized by the methodology described in the Bergey’s Manual of Determinative Bacteriology (Hammes and Hertel, 2009).
  • Enumeration, isolation and identification of Bifidobactria spp. On Bifidobacterium media (Nebra and Blanch, 1999).
  • Enumeration, isolation and identification of Enterococci spp. (Maia et al., 2017)
  • Identification of Enterococcus faecuim and Enterococcus faecalis: (Morrison et al., 1997 and Manero and Blanch, 1999).
  • Extraction of bacteriocin by growing the strains in MRS broth at 37°C for 48 hours, cells separated by centrifugation at 5000 rpm for 10 minutes. The pH of supernatant was adjusted to 5.5 and the bacteriocin activity in the supernatant was evaluated by agar well diffusion method (Ogaki et al. 2016) using aureus (reference strain) (NCTC No. 7447) it was obtained from High Quality Media unit (HQM) in Animal Health Research Institute in Dokki, Egypt.
  • PCR detection of some bacteriocin genes (Mesentericin Y and Plantaricin E/F) from the previous Enterococci This part was done in Research Laboratory for veterinary quality control on poultry production in Animal Health Research Institute, Dokki, Giza. The samples were performed using the QIAamp DNA Mini kit (Qiagen, Germany, GmbH) with modifications from the manufacturer’s recommendations. Primers used were supplied from Metabion (Germany) are listed in Table (A).

Table (A): Primers, sequences, target genes, amplicon sizes and cycling conditions.

Target gene

Primers sequences

Amplified segment (bp)

Primary

Denatur-ation

Amplification (35 cycles)

Final extension

Reference

Secondary denaturation

Annealing

Extension

Mesentericin Y (mesY)

ATGACGAATATGAAGTC

186

94˚C

5 min.

94˚C

30 sec.

45˚C

30 sec.

72˚C

30 sec.

72˚C

7 min.

Xiraphi et al., 2008

TTACCAAAATCCATTTCC

Plantaricin E/F

GGCATAGTTAAAATTCCCCCC

428

94˚C

5 min.

94˚C

30 sec.

53.2˚C

40 sec.

72˚C

45 sec.

72˚C

10 min.

Rizzello et al., 2014

CAGGTTGCCGCAAAAAAAG

Statistical Analysis

The statistical analysis was performed using programs GraphPadPrism 5.04 (GraphPad, Inc., San Diego, USA) and Statistical 12.0 (Dell, Inc., Tulsa, USA). The bacterial count represented by mean±SD (standard deviation value). The data represented by using the Microsoft Excel Spreadsheet. Also Kolmogorov-Smirnov D test, Chi-square test and Fishers exact test

Results

Table (1). Statistical analytical results of microbial count in the examined ewe’s and goat's milk samples (n=50 each CFU/mL).

Samples

Ewe's milk

N=50

Goat's milk

N=50

Positive samples

Min.

Max.

mean±SD

Positive samples

Min.

Max.

mean±SD

No.

%

No.

%

TBC

50

100

1×101

9×105

13x103± 16x102

50

100

2×101

3×107

23x103± 2.1x103

Coliforms**

34

68

>10

3×103

27.3x102 ±4.3x102

32

64

>10

4×105

2x103± 3.1x102

**High significant statistical variation in coliforms count between Ewe's milk and Goat's milk (Kolmogorov-Smirnov D = 0.3725, p< 0.01)

Table (2). Occurrence of Lactobacillus spp. among the examined ewe’s and goat's milk samples (n=50).

 

Lactobacillus spp.

Positive samples

Ewe's milk

Goat's milk

40

36

Lact.acidophilus

4

4

Lact.fermentis

22

20

Lact.bulgaricus

4

3

Lact.brevis

2

2

Lact.plantarium

4

3

Lact.casei

4

4

 

Table (3). Occurrence of Bifidobacteria spp. among the examined ewe’s and goat's milk samples (n=50).

 

Bifidobacteria spp.

Positive samples

Ewe's milk

Goat's milk

27

18

Bifido.bifidium **

18

5

Bifido.breve

4

3

Bifido.subtile**

5

10

Bifido.infantis

0

0

** High significant statistical variation in Bifido.bifidium between Ewe's milk and Goat's milk (Chi-square = 6.537, p< 0.01)

** High significant statistical variation in Bifido. subtile between Ewe's and Goat's milk ( Chi-square = 6.667, p < 0.01)

 

Table (4). Occurrence of some Enterococci spp. among the examined ewe’s and goat's milk samples (n=50).

 

Entero.faecium

Entero.faecalis

Types of samples

ewe's milk

goat's milk

ewe's milk

goat's milk

No.

%

No.

%

No.

%

No.

%

Positive samples

10

20

5

10

4

8

2

4

Photo 1.The amplified (mesY) gene of Entero.fecalis and Entero.faecium recovered from ewe’s and goat's milk.

Lane L: Molecular marker; Lane pos: Positive control; Lane Neg: Negative control; Lanes 2, 4, 6, 8, 10: negative for Mesentericin Y; Lane 1, 3, 5, 7, 9: positive isolates for Mesentericin Y

 

Photo 2.The amplified Plantaricin E/F gene of Entero.fecalis and Entero.faecium recovered from ewe’s and goat's milk.

 

Lane L: Molecular marker; Lane pos: Positive control; Lane Neg: Negative control; Lanes 1,2,4-7,9,10: negative for Plantaricin E/F; Lane 3,8: positive isolates for Plantaricin E/F.

 

Discussion

As the small ruminant's milk lacks detail evaluation, the present study aimed to assess the total viable bacteria and coliforms, that reflect its hygienic and environmental conditions at which the small ruminant's pasture as well as its probiotic volubility by assessment of Lactobacilli, Bifidobactria spp. and Enterococcus spp. Where Table (1) showed the mean values with standard deviation for total bacterial count and coliforms count existence as (13x103± 16x102, 27.3x102 ±4.3x102, CFU/ml, respectively) for ewe's milk while higher results for goat's milk (23x103± 2.1x103, 2x103± 3.1x102, respectively). In addition, there was high significant statistical variation in coliforms count between Ewe's milk and Goat's milk (Kolmogorov-Smirnov D = 0.3725, p< 0.01). Our results in this study showed that all the examined samples were contaminated with aerobic plate count but the count was lower than (Morgan et al. 2003; Muehlherr et al. 2003 and Ombarak and Elbagory, 2017) who investigated the aerobic plate count was 9.11±2.47×106 and 2.04±0.91×106 CFU/ml for goat’s and ewe’s milk, respectively and the incidences of coliforms was similar to our findings which was 68.57% and 60%, for raw goat’s and ewe’s milk, respectively. In Egypt, the microbial quality of raw caprine's and ovine's milk may be affected by unhygienic milking procedures, bad handling, contaminated animals water supply, keeping environments, storage and transportation of milk (Chye et al. 2004, Hicham et al. 2009, Saad et al. 2013 and Bogdanovičová et al. 2016) but there is no evidence of health hazards from raw goat’s or ewe’s milk (Mcintyre et al. 2002).  Presence of coliforms bacterial count in milk may be returned to the unsanitary conditions practices during milk manipulation (Kondyli et al. 2012). A reference according the Malaysians Food Act 1983 and Food Regulations 1985, the total aerobic bacteria concentration in milk, which safe for consumed should not exceed 5.0 log cfu/ml (Food Act 1983 and Food Regulations 1985 – Act 281, 2005) which means that our results detected that most of examined samples were safe.

The higher microbial counts in goat's than ewe's milk samples may be related to the anatomical structure differ between ewe's udder as it have higher, smaller udder with short rapidly closed teat canal than goat's one (Carretero et al. 1999), environmental surroundings, milk manipulation and feeding manner also have effect on microbial count (Eman et al. 2009 and Abo El-Makarem, 2016). 

Our work also scopes on the economic important of using these types of milk in dairy industry especially in our developing country. So, we examine the samples for presence of probiotic bacteria Tables (1& 2) were showed the presence of different species from Lactobacillus and Bifidobacterium spp. isolated from ewe's and goat's milk. Lactobacillus spp. detected in ewe's milk (40 samples) in higher percentages than goat's milk (36 samples) and vice versa with Bifidobacterium spp. (27 and 18, respectively). Lact.fermentis, Lact.bulgaricus and Lact.acidophilus were the most isolated Lactobacillus spp. from milk samples and Bifido.bifidium, Bifido.subtile and Bifido.breve from Bifidobacterium spp. It is worth to be mentioned that was high significant statistical variation in Bifidobacteria spp. between Ewe's and Goat's milk (Kolmogorov-Smirnov D = 0.5185, p< 0.01).

In addition, there was high significant statistical variation in Bifido.bifidium isolates between Ewe's and Goat's milk (Chi-square = 6.537, p< 0.01) and high significant statistical variation in Bifido.subtile isolates between the both types of milk (Chi-square = 6.667, p< 0.01).

Bifidobacteria are considered the primary probiotic bacteria associated with milk and dairy products (Rodrigues et al. 2011). Raw ewe’s and goat’s milk is a good source for isolation of wild lactobacilli which are able to bring unique processing properties in development of dairy products, cheeses or fermented dairy products (Miroslav et al. 2014) and there are many studies isolated lactic acid bacteria (LAB) from Ewe's and Goat's milk (Chen et al. 2020; Tanaka et al. 2023). So, In Egypt, deeply in need for new economic sources of probiotic products manifested in sheep and goat milk production is nearly not used. The beneficial effects of probiotic consumption include antibacterial activity (El Halfawy et al. 2019)  

Among the Lactic Acid Bacteria (LAB), Enterococcous spp.,which reported to goodwill to produce antimicrobial compounds including bacteriocins, bacteriocin - like substances, or metabolites with antibacterial activity, which made them potential candidates for biopreservative agents for a wide range of food products, promotion of human and animal health by improving the intestinal microbial balance and is now being considered as a probiotic trait (Franz et al. 2011, Yang et al. 2014 and Bali et al. 2016).

Entero.faecium could be detected in (20 and 10%) and Entero.faecalis (8 and 4%) in ewes and goats' milk, respectively (Table 4). while, The isolated Entero.faecium and Entero.faecalis strains in this study investigated for bacteriocin production by the antibacterial activity of it through extraction of bacteriocin by cold centrifugation and using the supernatant (which contain bacteriocin) against Staph.aureus by well diffusion method. We choose Staphylococcus aureus because it is a significant and costly public health concern since it may enter the human nourishment chain and usually causing foodborne illness (Liu et al., 2022). Also, milk and milk products are known to be a source of S. aureus contamination whether they are collected from dairy animals or from food handlers carrying the organism because of poor individual cleanliness (Bingol et al., 2012). Five strains from ewe's milk and five from goat's milk were bacteriocin producers then these strains subjected to PCR for detection the presence of some bacteriocin genes as Mesentericin Y (mesY) and Plantaricin E/F and found that 5 strains of Entero.faecium have mesY (3 isolated from ewe's, 2 from goat's milk origin), one of them have both genes (returned to goat's milk) and one have only Plantaricin E/F (from ewe's milk) while, no strain of Entero.faecalis have any of both genes.

Enterococcus spp. carries many bacteriocin-related genes that PCR array allowed quick and easy identification of the presence of these genes (Henning et al. 2015). Plantaricin E/F containing natural substances against foodborne pathogenic, as well as spoilage bacteria has raised considerable interest for their application in food preservation (Todorov, 2009). Also, mesY bacteriocin genes provide antimicrobial activity and may also be useful in activity against spoilage and pathogenic organisms in select food applications. Many strains of Enterococcus spp. encode more than one bacteriocin, although it remains to be seen which ones might be actively expressing bacteriocin proteins (He´chard et al., 1992 and Henning et al., 2015).

It is now relatively simple to use specific PCR screening techniques to determine whether bacteriocin genes are present in the bacterial isolates especially when multiple species are present in the samples (Kubašová et al., 2020).

 

Conclusion

It is concluded that small ruminant raw milk samples contained different types of probiotics which carry a lot of benefits to human in both health and economic importance. Goat's milk had more total pathogenic studied parameters than ewe's milk and ewe's milk had more probiotic LAB; Lactobacillus, Bifidobactria and Enterococcus spp. and contained Enter. Faecium strains harboring bacteriocin genes mesY & Plantaricin E/F genes more than those of goat's milk.

It is recommended that further intensive studies should be carried out for the production of dairy products from these valuable economic types of milk to fulfill the needs of local markets.

APHA (American Public Health Association) 2001. In: Frances, P.D., Keith,I. (Eds.), Compendium of methods for the microbiological examination of foods.
Ahmed MH, Rasha MA, Yasser E, Wael SE. 2023. Diversity of Bacteriocin-encoding Gene Families and the Activity Spectrum among Bacillus amyloliquefaciens Isolates. Egyptian Journal of Botany http://ejbo.journals.ekb.eg/ Egypt. J. Bot. Vol. 63, No. 1, pp. 69-83.
Aqib AI, Nighat S, Ahmed R, Sana S, Jamal MA, Kulyar MF, Khan NU, Sarwar MS, Muhammad AH, Asadullah AR, Sadeeq R. 2019. Drug Susceptibility Profile of Staphylococcus aureus Isolated from Mastitic Milk of Goats and Risk Factors Associated with Goat Mastitis in Pakistan. Pakistan J. Zool., vol. 51(1), pp 307-315.
Abo El-Makarem, HS 2016. Chemical and microbiological quality of ewe’s milk. 3rd International Food Safety Conference, Damanhur University, 10/10/2016.
Bali V, Panesar PS, Bera MB, Kennedy JF. 2016. Bacteriocins: Recent Trends and Potential Applications. Crit Rev Food SciNutr.56(5):817–34. doi: 10.1080/10408398.2012.729231.
Balthazar CF, Pimentel TC, Ferr˜ao LL, Almada CN, Santillo A, Albenzio M, Mollakhalili N, Mortazavian AM, Nascimento JS, Silva MC, Freitas MQ, Sant’Ana AS, Granato D, Cruz AG. 2017. Sheep Milk: Physicochemical Characteristics and Relevance for Functional Food Development. Comprehensive Reviews in Food Science and Food Safety. 16: 247-262.
Bingol EB, Cetin O, Colak H, Hampikyan H. 2012. Presence of enterotoxin and verotoxin in Turkish cheeses sold in Istanbul. Turkish J. Vet. Anim. Sci., 36: 424–432. https://doi.org/10.3906/vet-1105-5
Bogdanovičová K, Marcela VK, Vladimír B, Libor K, Ivana K, Renáta K. 2016. Microbiological Quality of Raw Milk in the Czech Republic. Czech J. Food Sci., 34, 2016 (3): 189–196.
Carretero A J, Ruberte G, Caja F, Pérez-Aparicio X, Such S, Peris et al. 1999. Study on the structure and the development of the canalicular system of the mammary gland during lactation in Manchega and Lacaune dairy sheep. p. 35-40. In Barillet, F., and N.P. Zervas (eds.) Milking and milk production of dairy sheep and goats. European Federation of Animal Science (EAAP) Publication nr 95, Wageningen Press, Wageningen, the Netherlands.
Chen T, Leli W, Qinxin L, Yingjie L, Yuming L, Jie Y, Yan Z, Le H, Tingyu Y, Muhammad NA, Huansheng Y, Qiye W, Congjia T, Tahir AK, Qiuyue L, Jia Y, Qiang T, Yulong Y. 2020. Functional probiotics of lactic acid bacteria from Hu sheep milk. BMC Microbiology (2020) 20:228.
Chye, F. Y., Abdullah, A., & Ayob, M. K. (2004). Bacteriological quality and safety of raw milk in Malaysia. Food microbiology, 21(5), 535-541.‏
El Halfawy NM, El-Naggar MY, Simon CA. 2019. Draft Genome Sequence of an Enterococcus faecalis Strain (24FS) That Was Isolated from Healthy Infant Feces and Exhibits High Antibacterial Activity, Multiple-Antibiotic Resistance, and Multiple Virulence Factors. Microbiol. Resource Announcement.  8(13):1-3.
El-Sayed H, Aly Y, Elgamily H, Mohamed MN. 2019. A Promising Probiotic Irrigant: An In Vitro Study. Macedonian Journal of Medical Sciences, 7(3):407-411.
Eman M, El-Demerdash ME, Hashem ME. 2009. Survey study on goat’s milk from different breeds raised under Egyptian conditions, Egyptian J. Sheep & Goat Sci., 4 (1), 89-98.
FAO/WHO. 2001. Evaluation of health and nutritional properties of powder milk and live lactic acid bacteria. Cordoba, Argentina: Food and Agriculture Organization of the United Nations and World Health Organization Expert Consultation Report. 1-34.
FDA 2002. Bacteriological analytical manual online. Enumeration of Escherichia coli and the coliform bacteria. Retrieved on March 22, 2011 from FDA Website:
http://www.fda.gov/Food/FoodScienceResearch/ LaboratoryMethods/ucm064948.htm
Franz CMAP, Huch M, Abriouel H, Holzapfel W, Gálvez A. 2011. Enterococci as probiotics and their implications in food safety. Int. J. Food Microbiol. 151(2):125-140.
Food Regulations 1985. 2005. Food ACT 1983 and Food Regulations 1985 (Act 281), p. 1-265. Kuala Lumpur, Malaysia: MDC Publishers Sdn. Bhd.
 Foulquié Moreno MR, Sarantinopoulos P, Tsakalidou E, De Vuyst L. 2006. The role and application of enterococci in food and health.Int. J. Food Microbiol. 106(1):1-24.
Guerreiro O, Velez Z, Alvarenga N, Matos C, Duarte M. 2013). Molecular screening of ovine mastitis in different breeds, J. Dairy Sci., 96 (2): 752-60.
Hammes WP and Hertel C. 2009. Genus I.  Lactobacillus Beijerink 1901. In. De Vos P, Garrity GM, Jones D, Krieg NR, Ludwig W, Rainey FA, Schleifer KH, Whitman WB, editors. Bergey’s Manual of Systematic Bacteriology, 2nd ed. Springer Science Business Media, New York, pp. 465-510.
Hicham LE, Laarousi B, Abderrahim E, Mohamed BE, Mohammed O. 2009. Étudephysicochimique et microbiologique de laitscrus.Bull. Soc. Pharm. Bordeaux, 148: 7-16.
He´chard Y, De´rijard B, Letellier F, Cenatiempo Y. 1992. Characterization and purification of mesentericin Y105, an anti-Listeria bacteriocin from Leuconostocmesenteroides. J Gen Microbiol 138:2725–2731.
Henning C, Gautam D, Muriana P. 2015. Identification of Multiple Bacteriocins in Enterococcus spp. Using an Enterococcus-Specific Bacteriocin PCR Array.Microorganisms2015, 3, 1-16; doi:10.3390/microorganisms3010001.
Hu C, Xing W, Liu X, Zhang X, Li K, Liu J, Deng B, Deng B, Yong L, Tan C. 2019. Effects of dietary supplementation of probiotic Enterococcus faecium on growth performance and gut microbiota in weaned piglets. AMB Expr (2019) 9:33.
Kondyli E, Svarnas C, Samelis J, Katsiari MC. 2012. Chemical composition and microbiological quality of ewe and goat milk of native Greek breeds. Small Rum. Res, 103: 194-199.
Kubašová I, Diep DB, Ovchinnikov KV, Lauková A, Strompfová V. 2020. Bacteriocin production and distribution of bacteriocin-encoding genes in enterococci from dogs. International Journal of Antimicrobial Agents, 55(2), 105859.
Liu H, Dong L, Zhao Y, Meng L, Wang J, Wang C, Zheng N. 2022. Antimicrobial Susceptibility, and Molecular Characterization of Staphylococcus aureus Isolated From Different Raw Milk Samples in China. Front. Microbiol. 13:840670. https://doi.org/10.3389/fmicb.2022.840670
Maia LF, Giazzi A, Brandalize C, Katsuda S, Rocha KR., Terra MR, Furlaneto MC. 2017. Isolation and characterization of potential probiotic enterococci strains from soft cheese flora. African J. Microbiol. Res. 11(12): 482-487.
Manero A and Blanch AR. 1999. Identification of Enterococcus spp. With a biochemical key. Applied and environmental Microbiology 65(10): 4425-30.
Manis C, Scano P, Garau V, Addis M, Ibba I, Caboni PI. 2023. Mobility–Mass Spectrometry. Approach for the Comparison of Sheep and Goat Milk Lipidomes. Appl. Sci. 2023, 13, 3535.
Mcintyre L, Fung J, Paccagnella A, Isaac-Renton J, Rockwell F, Emerson B, Preston T. 2002. Escherichia coli O157 outbreak associated with the ingestion of unpasteurized goat’s milk in British Columbia, 2001. Canada Communicable Disease Report 28: 6–8.
Miroslav K, Anna S, Maroš D, Lýdia K, Vladimír K, Dobroslava B, Andrea L, Gabriel G, Mária G, Martin T. 2014. Characterization of Lactobacilli from  ewe’s and goat’s milk for their further processing reutilization. Potravinarstvo® Scientific Journal for Food Industry. Potravinarstvo, vol. 8, 2014, no. 1, p. 130-134. doi:10.5219/354.
Morgan F, Massouras T, Barbosa M, Roseiro L, Ravasco F, Kandarakis I, Bonnin V, Fistakoris M, Anifantakis E, Jaubert G, Raynal-Ljutovac D. 2003. Characteristics of goat milk collected from small and medium enterprises in Greece, Portugal and France. Small Ruminant Research 47: 39–49.
Morrison D, Woodford N, Cookson B. 1997. Enterococci as emerging pathogens of humans. Journal of applied microbiology 83(s1),89s-99s.
Muehlherr JE, Zweifel C, Corti S, Blanco JE, Stephan R. 2003. Microbiological quality of raw goat’s and ewe’s bulk-tank milk in Switzerland. Journal of Dairy Science 86: 3849-3856.
Nami Y, Bakhshayesh RV, Jalaly HM, Lotfi H, Eslami S, Hejazi MA. 2019. Probiotic Properties of Enterococcus Isolated From Artisanal Dairy Products. Frontiers in Microbiology 10 (300): 1-13.
Nebra Y and Blanch A. 1999. A New Selective Medium for Bifidobacterium spp. Applied and environmental microbiology.Nov., pp. 5173–5176.
Ombarak RA and Elbagory AM. 2017. Bacteriological quality and occurrence of some microbial pathogens in goat’s and ewe’s milk in Egypt. International Food Research Journal 24(2): 847-851 (April 2017). Journal homepage: http://www.ifrj.upm.edu.my.
Ogaki MB, Rocha KR, Terra MR, Furlaneto MC, Furlaneto-Maia L. 2016. Screening of the Enterocin-encoding genes and antimicrobial activity in Enterococcus species. J. Microbiol. Biotechnol. 26(6):1026–1034.
Popovic N, Djokic J, Brdaric´ E, Dinic´ M, Terzic´ -Vidojevic´ A, Nataša G´, Katarina V. 2019. The Influence of Heat-Killed Enterococcus faecium BGPAS1-3 on the Tight Junction Protein Expression and Immune Function in Differentiated Caco-2 Cells Infected with Listeria monocytogenes ATCC 19111. Frontiers in Microbiology 10: 412.
Praja RN, Yudhana A, Saputro AL, Hamonangan JM. 2023. The first study on antimicrobial resistance of Staphylococcus aureus isolated from raw goat milk associated with subclinical mastitis in Siliragung Subdistrict, East Java, Indonesia. Veterinary World, 16(4): 786–791.
Rizzello CG, Filannino P, Di Cagno R, Calasso M, Gobbetti M. 2014. Quorum-sensing regulation of constitutive plantaricin by Lactobacillus plantarum strains under a model system for vegetables and fruits. Appl Environ Microbiol., 80(2):777-87.
Rodrigues D, Rocha-Santos TAP, Pereira CI, Gomes AM, Malcata X, Freitas AC. 2011. The potential effect of FOS and inulin upon probiotic bacterium performance in curdled milk matrices. LWT – Food Science and Technology, 44, 100–108.
Ruiz P, Fátima PM, Susana S, María LP. 2016. Seasonal diversity and safety evaluation of enterococci population from goat milk in a farm. Dairy Sci. & Technol. 96:359–375.
Saad MF, Nagah M, Hafiz A, Salwa A.  2013. Microbiological Quality Evaluation of Raw Goat’s Milk In Egypt. IJBPAS, 2 (10): 1837-1848.
Tanaka Y, Aryantini NPD, Yamasaki E, Saito M, Tsukigase Y, Nakatsuka H, Urashima T, Horiuchi R, Fukuda K. 2023. In Vitro Probiotic Characterization and Safety Assessment of Lactic Acid Bacteria Isolated from Raw Milk of Japanese-Saanen Goat (Capra hircus). Animals, 13, 7.
Todorov DS. 2009. Review. Bacteriocins from Lactobacillus plantarum production, genetic organization and mode of action.Braz. J. Microbiol. 40 (2). São Paulo Apr./June 2009
Verruck S, Dantas A, Prudencio E S. 2019. Functionality of the components from goat’s milk, recent advances for functional dairy products development and its implications on human health. Journal of Functional Foods 52: 243–257.
Wyszyńska AK, Godlewska R. 2021. Lactic acid bacteria - a promising tool for controlling chicken Campylobacter infection. Frontiers in Microbiology, 12, 703441.
Xiraphi N, Georgalaki M, Rantsiou K, Cocolin L, Tsakalidou E, Drosinos EH. 2008. Purification and characterization of a bacteriocin produced by Leuconostoc mesenteroides E131. Meat Science, 80:194–203.
Yang SC, Lin CH, T., Sung, C, Fang, JY. 2014. Antibacterial activities of bacteriocins: application in foods and pharmaceuticals. Front. Microbiol. 5:241. doi: 10.3389/fmicb.2014.00241.
Zommiti M, Almohammed H, Ferchichi M. 2016. Purification and characterization of a novel anti-campylobacter bacteriocin produced by Lactobacillus curvatus DN317. Probiotics Antimicrob Proteins, 8(4), 191-201.