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Article

Prevalence and Loads of Fecal Pollution Indicators and the Antibiotic Resistance Phenotypes of Escherichia coli in Raw Minced Beef in Lebanon

by
Issmat I. Kassem
1,2,*,
Nivin A Nasser
1 and
Joanna Salibi
2
1
Center for Food Safety, Department of Food Science and Technology, University of Georgia (UGA), Athens, GA 30223-1797, USA
2
Department of Nutrition and Food Sciences, Faculty of Agricultural and Food Sciences, American University of Beirut (AUB), Beirut 1107 2020, Lebanon
*
Author to whom correspondence should be addressed.
Foods 2020, 9(11), 1543; https://doi.org/10.3390/foods9111543
Submission received: 29 September 2020 / Revised: 19 October 2020 / Accepted: 23 October 2020 / Published: 26 October 2020
(This article belongs to the Special Issue Microbiological Safety and Quality of Food)
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Abstract

:
Meat is an important source of high biological value proteins as well as many vitamins and minerals. In Lebanon, beef meats, including raw minced beef, are among the most consumed of the meat products. However, minced beef meat can also be an important source of foodborne illnesses. This is of a major concern, because food safety in Lebanon suffers from well-documented challenges. Consequently, the prevalence and loads of fecal coliforms and Escherichia coli were quantified to assess the microbiological acceptability of minced beef meat in Lebanon. Additionally, antibiotic resistance phenotypes of the E. coli were determined in response to concerns about the emergence of resistance in food matrices in Lebanon. A total of 50 meat samples and 120 E. coli isolates were analyzed. Results showed that 98% and 76% of meat samples harbored fecal coliforms and E. coli above the microbial acceptance level, respectively. All E. coli were resistant to at least one antibiotic, while 35% of the isolates were multidrug-resistant (MDR). The results suggest that Lebanon needs to (1) update food safety systems to track and reduce the levels of potential contamination in important foods and (2) implement programs to control the proliferation of antimicrobial resistance in food systems.

1. Introduction

Meat is an integral component of a balanced diet, providing proteins, essential amino acids and various micronutrients such as vitamin B12, niacin, vitamin B6, iron, zinc and phosphorous [1]. Consequently, meat production has increased rapidly over the past 50 years worldwide [2]. Cattle meat production has more than doubled since the 1960s, increasing from 28 million tons in 1961 to 68 million tons in 2014 [2]. In Lebanon, beef meat is among the most consumed meats [3]. The average consumption of beef meat was 39.63 kg/capita in Lebanon [2] and the mean intake was 47.6 g/day in surveyed consumers in Beirut, the capital of Lebanon [3]. Lebanon produced 47,484 tons of beef meat in 2014 [2]; however, beef meat in the Lebanese market is mainly imported from Brazil and India [4]. Beef meat constitutes a popular and economically important food in Lebanon. Notably, beef meat can also be consumed raw as part of famous Lebanese dishes. However, Lebanon has been witnessing challenges in food safety that have received media attention and raised national public health concerns. This was not surprising, because food safety can severely impact the health of a population [5], especially in developing countries with weakened infrastructure and limited resources [6]. Foodborne illnesses have been estimated to affect almost 1 in 10 people (~600 million individuals), while 420,000 die every year [5]. Notably, children less than 5 years old constitute a third of the deaths associated with foodborne diseases [5]. In developing countries, the detrimental manifestations of foodborne disease are highly expressed, claiming or debilitating the lives of the most vulnerable populations such as the children, the elderly, the nutritionally deprived, and the immunocompromised [7]. Foodborne diseases in these countries perpetuate the cycle of poverty and damage budding national brands and already-fragile economies. Taken together, this necessitated a closer examination of the safety of popular and essential foods, including minced beef meat, in Lebanon.
Beef meat can be contaminated by different foodborne pathogens that can cause severe illnesses in consumers and have been implicated in foodborne outbreaks [8]. Studies have detected Escherichia coli (E. coli), including E. coli O157:H7, Salmonella spp., Listeria monocytogenes and Campylobacter spp. in minced beef. Minced beef can be contaminated in a variety of ways. For example, during mincing, bacteria that contaminate the surface of the meat/carcass can be mixed into the minced product. Adding leftover cuts and trims during mincing can also increase bacterial loads in comparison to the original fresh carcass or cut. Lack of hygienic practices during processing and the cleanliness of the equipment can contribute to the contamination of the meat [9]. Furthermore, mincing might cause a slight increase in the temperature of the product allowing bacteria to grow faster [9]. Being a nutrient-rich matrix, minced beef becomes a favored environment for the growth of various microorganisms that can be harmful to consumers [10]. Therefore, the microbial quality of minced beef should be closely monitored, especially when the meat will be consumed undercooked or raw, which heightens the risks of infections in consumers.
Foodborne infections are becoming increasingly problematic because of the rise of foodborne bacterial pathogens that have acquired resistance to antibiotics. This can lead to hard-to-treat and complicated infections in consumers [11]. The occurrence of antibiotic resistant bacterial pathogens in various foods, including poultry- and beef products is well documented [12,13,14,15]. In fact, food and food production have been implicated in the emergence and spread of antimicrobial resistance (AMR); largely due to the misuse and/or overuse of clinically important antibiotics in food-animal farming practices [16,17,18,19]. Antibiotics have been used heavily in food-animals to treat (therapy) or prevent (prophylaxis) diseases and for growth promotion. While this has received considerable scrutiny, the use of antibiotics in growth promotion has been the most controversial, because of its potential role in facilitating the emergence of AMR in food animal operations [16]. Currently, the World Health Organization (WHO) recognizes AMR as an imminent crisis, which is predicted to have a devastating impact on health and economy across the globe [16,17,18,19]. However, AMR bacteria in Lebanon in food and environmental matrices have received little attention [17,20]. Therefore, it is important to investigate AMR in minced beef and other foods in Lebanon.
In developing countries, such as Lebanon, it is difficult to estimate the burden of foodborne diseases because of inconsistent and weak monitoring and surveillance systems. The country is also facing a severe economic crisis that has limited these systems further. Although Lebanon has a modern Food Safety Law (issued in 2016), it has not been implemented because of weak governmental oversight. Currently, there are Lebanese standard specifications of minced beef meat (standard 503:2004) that were set by the Lebanese Standards Institution (LIBNOR). However, the standard is outdated (issued in 2004) and should reflect current data collected in the country [21,22]. Admittedly, original data on microbiological criteria that affect the acceptability of many foods are scant in Lebanon. Therefore, we launched an investigation to monitor potential microbial contaminations of different foods in Lebanon. Here, we focused on the prevalence and loads of fecal indicators, fecal coliforms and E. coli, in raw minced beef in the Lebanese market. Indicator organisms are widely used to assess the microbiological criteria of foods and the detection of fecal indicators, such as E. coli and fecal coliforms, suggests the presence of enteric pathogens in foods [23]. Furthermore, acquired resistance in E. coli can reflect the use of antibiotics because of the selection pressure that is needed for the persistence of AMR strains [24]. Indeed, E. coli has been used as an indicator for monitoring antibiotic resistance in foods [24]. Therefore, we also analyzed the AMR profiles of the E. coli associated with minced beef meat.

2. Materials and Methods

2.1. Sampling of Minced Beef

During the spring and summer of 2018, a total of 50 samples of raw minced beef were collected from 50 different butcheries and grocery stores in Beirut, Lebanon. The samples were immediately placed on ice, transported to the laboratory, and processed within 2–3 h of collection.

2.2. Enumeration of Fecal Coliforms and E. coli

For each sample, minced beef meat was weighed, and 25 g were aseptically placed in a sterile stomacher bag (Fisher Scientific, New Hampshire, USA). The sample was then diluted 1:10 with 225 mL of sterile buffered peptone water (BPW) (Oxoid, Hampshire, UK) and homogenized for 1 min using a stomacher (Thomas Scientific, New Jersey, USA). The suspension was then serially diluted (10-fold) in BPW and 3 dilutions (10−1, 10−2, 10−4) were plated on RAPID’E. coli 2 agar plates (BioRad, Hercules, California, USA) in duplicates. The plates were incubated at 44 °C for 18–24 h under aerobic conditions. Colony forming units (CFU) that matched the diagnostic phenotypes (violet to pink E. coli colonies and blue to green colonies for other fecal coliforms) were counted and bacteria densities were determined by averaging the counts from the duplicates. Data were reported as averages of CFU per gram of raw minced beef. BPW without meat was used as control throughout the experiment. E. coli DH5α was used to test the quality of the RAPID’E. coli 2 agar plates. Average CFU counts of E. coli and fecal coliforms were compared using the Student’s t-test. A p < 0.05 was used to identify statistically significant differences.

2.3. Assessing Antimicrobial Resistance (AMR) of E. coli Using the Disk Diffusion Assay

Antimicrobial resistance analysis was performed on E. coli isolated from the minced beef samples using the disk diffusion assay [25]. Briefly, 120 E. coli were isolated from contaminated meat samples (1 to 3 isolates per sample). E. coli isolates were suspended in Mueller-Hinton (MH) broth (Oxoid, Hampshire, UK) and their turbidity was adjusted using a 0.5 McFarland standard and a spectrophotometer (Thermo Fisher Scientific, Massachusetts, USA) [25]. The bacterial suspensions were then spread on MH agar (MH) plates. Nineteen different antibiotic discs (Oxoid, Hampshire, UK) belonging to 9 classes of antibiotics were then added on top of the MH agar plates. The antibiotic classes and discs used were: (1) penicillins (class): penicillin (PEN; 6 µg) and ampicillin (AMP; 10 μg); (2) β-lactam/β-lactamase inhibitor combinations: amoxicillin/clavulanic acid (AMC; 20 μg/10 μg); (3) cephalosporins: cefepime (FEP; 30 μg), cefotaxime (CTX; 30 μg), cefalexin (LEX; 30 μg), and cefixime (CFM; 6 μg); (4) carbapenems: doripenem (DOR; 10 μg), meropenem (MEM; 10 μg), and imipenem (IPM; 10 μg); (5) aminoglycosides: gentamicin (GEN; 10 μg), kanamycin (KAN; 30 μg), and streptomycin (STR; 10 μg); (6) tetracyclines: tetracycline (TET; 30 μg); (7) quinolones and fluoroquinolones: ciprofloxacin (CIP; 5 μg) and norfloxacin (NOR; 10 μg); (8) folate-pathway inhibitors: trimethoprim/sulfamethoxazole (SXT; 25 μg); and (9) phenicols: chloramphenicol (CHL; 30 μg) [26]. These antibiotics are (1) clinically and agriculturally important and (2) used to evaluate acquired resistance in Enterobacteriaceae, including E. coli [27,28]. Erythromycin (ERY; 15 μg) was used for quality control, because E. coli is intrinsically resistant to this antibiotic [29]. Additionally, E. coli DH5α was also used for quality control across the experiments. The MH agar plates were incubated at 37 °C for 18–24 h. The zone of inhibition was measured and the AMR profiles of the isolates were determined using the Clinical and Laboratory Standards Institute (CLSI) and the European Committee on Antimicrobial Susceptibility Testing (EUCAST) standards [27,28]. The AMR phenotypes were analyzed using hierarchical clustering. Briefly, the AMR profile of each strain was coded in Excel® (Microsoft, Washington, USA) as follows: 1 corresponded to resistance, while 0 and −1 replaced intermediate resistance and susceptibility, respectively. This resulted in a matrix comprised of AMR profiles of the strains in rows, while the tested antibiotics were represented in the column. Following this, the matrix was exported to MeV v4.6.2 software (http://www.tm4.org/) [30] to perform hierarchical clustering using the Pearson correlation as a distance metric and the complete linkage method [31]. A graphical presentation of the matrix (heat map) was produced, where the upper limit (1) was colored green, while midpoint (0) and lowest limit (−1) were colored black and red, respectively [31].

3. Results and Discussion

3.1. Prevalence and Loads of Fecal Coliforms and E. coli

We assessed the acceptability of the minced beef samples in Lebanon by quantifying the prevalence and loads of fecal indicators, namely fecal coliforms and E. coli. Fecal coliforms were present in 49 of 50 (98%) raw minced beef samples, while E. coli was detected in 38 samples (76%). Fecal coliform CFU counts in positive samples ranged between 6.3 × 104 CFU/g and 1.62 × 107 CFU/g, while E. coli CFU counts ranged between 4.5 × 103 CFU/g and 3.48 × 106 CFU/g (Figure 1a). The visual distribution of the CFU counts of fecal coliforms in comparison to those of E. coli is presented in Figure 1b, which also shows the median, quartiles (25% and 75%), minimum and maximum values, and outliers.
According to LIBNOR standards, the acceptable limit of fecal coliforms in minced beef is 100 CFU/g [21], which is similar to other countries such as New Zealand that has a limit ranging from 100 to 1000 CFU/g [32], while the USA uses 1000 CFU/g of total coliforms as a critical limit for ground beef [32]. Therefore, using the LIBNOR standards and those from other countries, 98% of the tested minced beef samples in Lebanon exceeded the microbiological criterion based on fecal coliform counts (Figure 1a). The LIBNOR standard [21] for minced raw meat does not include limits on E. coli counts. However, there are many countries and researchers who established an E. coli limit to determine the acceptability of meat. For example, the USA uses 500 E. coli CFU/g as a critical limit for boneless beef [33]. Other studies showed that some states have more strict limits. For example, Oregon State (USA) has set a maximum of 50 CFU/g of E. coli [34], while New York State (USA) adopted 10 CFU/g of E. coli for assessing the acceptability of minced meat products [34]. Furthermore, the European Union (EU) Commission Regulation (EC) No. 2073/2005 set the limit of E. coli at 50 CFU/g [35]. When considering the aforementioned limits, it can be concluded that 76% of the tested minced beef samples in Lebanon exceeded the microbiological criterion based on E. coli counts.
Taken together, the wide prevalence and high loads of fecal indicator bacteria on minced beef samples in Lebanon are concerning, perhaps suggesting the need for better hygienic practices in the minced beef production chain. Admittedly, assessing the hygienic practices and possible sources of contamination of raw minced beef in a sustainable manner can be challenging. Specifically, monitoring must encompass (1) different food iterations that may contain raw beef in Lebanon (a notable example is minced beef with mixed herbs, Middle Eastern spices and onions that are consumed raw or cooked), (2) different types of indicator organisms and pathogens that might be present in each product, (3) differences in the handling and/ or processing procedures in foodservice establishments, butcher shops, and meat processing plants, and (4) a variety of sampling and testing procedures that require specialized laboratories, equipment and trained personnel [36,37]; all of which are difficult to secure in a country that is experiencing severe political and economic crises. However, despite the challenges, the safety of meat as well as other essential foods is critical to maintain public health and should be prioritized by the Lebanese government.
Both fecal coliforms and E. coli are effective indicators of fecal pollution. The latter suggests the presence of a variety of pathogens that can negatively impact human health [23,38]. In this study, 98% and 76% of the meat samples were rejected based on counts of fecal coliforms and E. coli, respectively, showing a difference in the rate of rejection based on the tested indicator. Subsequently, Lebanon would benefit from studies that screen for the best indicators of meat acceptability. This will reduce monitoring costs and will perhaps better reflect the acceptability of the meat. LIBNOR, along with other specialized stakeholders, should work on modifying and updating the current safety guidelines to enable proper assessment of the microbial quality of raw meat products in Lebanon.

3.2. AMR Profiles of E. coli Isolated from Minced Beef Meat

AMR analysis revealed that the E. coli isolates (n = 120) were resistant to PEN (100% of isolates), AMP (22.5%), FEP (0.8%), CTX (1.7%), LEX (37.5%), DOR (0.8%), GEN (2.5%), KAN (5.8%), STR (30%), TET (34.2%), CIP (10.8%), NOR (10%), SXT (15.8%), and CHL (10%) (Table 1). All isolates were sensitive to AMC, CFM, IPM, and MEM. Furthermore, 35% of the E. coli were classified as multi-drug resistant (resistance to ≥three classes of antibiotics) [39] (Table 1). Notably, three and 12 isolates exhibited resistance to six and five classes of antibiotics, respectively (Table 1). Hierarchal clustering organized the AMR profiles into four distinct clusters (Figure 2). Resistance to CIP and NOR was notable in the AMR profiles of isolates in Cluster 1 (C1). Similarly, resistance to STR–TET and resistance to LEX were notable in C2 and C4, respectively (Figure 2). The majority of multi-drug resistant (MDR) E. coli were grouped in C1 and C2, while C3 and C4 were mainly comprised of E. coli that were resistant to one or two antibiotics (Figure 2).
In comparison, 55% of E. coli isolated from raw beef preparations in Northwest Spain were resistant to TET [40]. Additionally, 6.67% of the E. coli isolated from beef muscles in Ghana were resistant to AMC, CHL, and GEN, respectively [41]. In the same study, 40% and 0% of the isolates were resistant to TET and CIP, respectively [41]. In Egypt, 25% of the E. coli isolated from raw samples were resistant to TET, STR, and AMP, respectively [42]. This suggested that the resistance in Lebanon was comparable to those in other countries. However, it should be noted that beef growing operations are limited in Lebanon in comparison to the aforementioned countries. Furthermore, the size of Lebanon and its human population are much smaller in comparison to these countries. Taken together, this suggested that (1) there is an overreliance on the use of antibiotics in Lebanese farming [17,43,44] and/or (2) the resistance percentages are masked by the beef imported from other countries. Regardless, given that E. coli is an indicator for monitoring antibiotic resistance in foods, the AMR detected in Lebanese raw minced beef samples is a cause of concern. Therefore, the prevalence of multi-drug resistant E. coli isolates in the raw beef meat samples in Lebanon should be monitored periodically to assess the dissemination of these bacteria and the potential proliferation of transmissible genetic determinants of resistance [43,44,45]. Given the potential negative impacts on consumers, environment, and farmed animals, decreasing the incidences of multi-drug resistance in cattle and particularly in beef is a necessity.
Many studies have reported a high number of MDR pathogens associated with foods, food-animals and food-environment, including E. coli, Campylobacter spp., and Salmonella spp. [42,43,44,45,46,47]. The emergence and proliferation of resistance have been linked to the improper use of antibiotics in medical and agricultural practices [16,17,48,49]. In the latter, AMR bacteria and genes encoding resistance can be transmitted to humans via (1) the food chain, (2) direct farm exposure, and/or (3) environmental contamination with farm waste and products [48,49,50]. As a result, recalcitrant AMR infections associated with food and/or agriculture have become a global risk [11,16,17,18,19]. This is predicted to be more severe in developing countries that have challenges in infrastructure and antimicrobial stewardship [17,18,19]. Lebanon is one of these countries that have also been affected by wide-spread pollution. Therefore, the emergence and dissemination of resistance in Lebanon should receive national and global attention, because AMR bacteria and genes can spread locally and beyond national borders, affecting other countries [43,51].

4. Conclusions

This study revealed a high occurrence of fecal coliforms and E. coli in raw minced beef in the Lebanese market. The high loads of these indicator bacteria are worrying, especially because beef meat is a major food item in the Lebanese cuisine and is consumed raw or minimally cooked in many instances. The occurrence of multi-drug resistant E. coli in the meat highlights the importance of adopting and implementing policies for reducing the use of antibiotics in food animal production in Lebanon and countries of importation. Furthermore, it might be beneficial to investigate and monitor the genetic bases of AMR in E. coli isolated from minced beef in order to assess the possibility of the persistence and dissemination of resistance to other vital matrices in Lebanon. Here, we call for updating national food safety systems in Lebanon and for investing in infrastructure and expertise that allow sustainable monitoring of food safety and the spread of AMR. This will greatly benefit public health and the economy in Lebanon.

Author Contributions

Conceptualization, I.I.K.; methodology, I.I.K.; validation, I.I.K.; formal analysis, I.I.K., N.A.N. and J.S.; investigation, I.I.K., N.A.N. and J.S.; resources, I.I.K.; data curation, I.I.K., N.A.N. and J.S.; writing—original draft preparation, I.I.K., N.A.N. and J.S.; writing—review and editing, I.I.K.; visualization, I.I.K.; supervision, I.I.K.; project administration, I.I.K.; funding acquisition; I.I.K. All authors have read and agreed to the published version of the manuscript.

Funding

This work was funded by a University Research Board (URB) grant from the American University of Beirut (AUB) and seed funding from the Center for Food Safety, the University of Georgia (UGA).

Acknowledgments

We thank the personnel of the Laboratory of Food Microbiology (AUB, NFSC) for their support.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Williams, P.G. Nutritional Composition of Red Meat. 2007. Available online: https://ro.uow.edu.au/hbspapers/48 (accessed on 18 September 2018).
  2. Ritchie, H.; Roser, M. Meat and Seafood Production & Consumption. Our World in Data. 2017. Available online: https://ourworldindata.org/grapher/meat-production-tonnes (accessed on 20 October 2018).
  3. Nasreddine, L.; Hwalla, N.; Sibai, A.; Hamzé, M.; Parent-Massin, D. Food consumption patterns in an adult urban population in Beirut, Lebanon. Public Health Nutr. 2006, 9, 194–203. [Google Scholar] [CrossRef]
  4. USDA FAS. Global Agricultural Information Network (GAIN): Lebanese Market Overview. 2016. Available online: https://gain.fas.usda.gov/Recent%20GAIN%20Publications/Lebanese%20Market%20Overview_Cairo_Lebanon_6-26-2016.pdf (accessed on 10 December 2018).
  5. WHO. Food Safety. 2017. Available online: http://www.who.int/news-room/fact-sheets/detail/food-safety (accessed on 29 October 2018).
  6. UNHCR. UNHCR Lebanon-Operational Fact Sheet-January 2020. Available online: https://www.unhcr.org/lb/wp-content/uploads/sites/16/2020/02/UNHCR-Lebanon-Operational-Fact-sheet-January-2020.pdf (accessed on 11 September 2020).
  7. Todd, E. Foodborne diseases: Overview of biological hazards and foodborne diseases. Encycl. Food Saf. 2014, 1, 221–242. [Google Scholar] [CrossRef]
  8. Jay, J.M.; Loessner, M.J.; Golden, D.A. Foodborne gastroenteritis. In Modern Food Microbiology, 7th ed.; Springer: Boston, MA, USA, 2005; pp. 619–655. [Google Scholar]
  9. FSIS. FSIS Microbiological Hazard Identification Guide for Meat and Poultry Components of Products Produced by very Small Plants. 1999. Available online: https://www.fsis.usda.gov/wps/wcm/connect/0b96c2cf-ffdc-4dc5-92f0-bdfd181b8368/higuide.pdf?MOD=AJPERES (accessed on 18 September 2020).
  10. NSAI. IS 340:2007 Hygiene in the Catering Sector; National Standards Authority of Ireland: Dublin, Ireland, 2007; Available online: https://www.nsai.ie/images/uploads/standards/I-S-340-2007-A1-2015.pdf (accessed on 18 September 2020).
  11. Economou, V.; Gousia, P. Agriculture and food animals as a source of antimicrobial-resistant bacteria. Infect. Drug Resist. 2015, 8, 49–61. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Johnson, J.R.; Sannes, M.R.; Croy, C.; Johnston, B.; Clabots, C.; Kuskowski, M.A.; Bender, J.; Smith, K.E.; Winokur, P.L.; Belongia, E.A. Antimicrobial drug–resistant Escherichia coli from humans and poultry products, Minnesota and Wisconsin, 2002–2004. Emerg. Infect. Dis. 2007, 13, 838. [Google Scholar] [CrossRef] [PubMed]
  13. Moawad, A.A.; Hotzel, H.; Awad, O.; Tomaso, H.; Neubauer, H.; Hafez, H.M.; El-Adawy, H. Occurrence of Salmonella enterica and Escherichia coli in raw chicken and beef meat in northern Egypt and dissemination of their antibiotic resistance markers. Gut. Pathog. 2017, 9, 57. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Nekouei, O.; Checkley, S.; Waldner, C.; Smith, B.A.; Invik, J.; Carson, C.; Avery, B.; Sanchez, J.; Gow, S. Exposure to antimicrobial-resistant Escherichia coli through the consumption of ground beef in Western Canada. Int. J. Food Microbiol. 2018, 272, 41–48. [Google Scholar] [CrossRef]
  15. Rasheed, M.U.; Thajuddin, N.; Ahamed, P.; Teklemariam, Z.; Jamil, K. Antimicrobial drug resistance in strains of Escherichia coli isolated from food sources. Rev. Inst. Med. Trop. Sao Paulo 2014, 56, 341–346. [Google Scholar] [CrossRef]
  16. Kassem, I.I.; Helmy, Y.A.; Kashoma, I.P.; Rajashekara, G. The Emergence of Antibiotic Resistance in Poultry Farms. In Achieving Sustainable Production of Poultry Meat Volume 1: Safety, Quality and Sustainability; Ricke, S., Ed.; Burleigh Dodds Science Publishing Limited: Cambridge, UK, 2016; ISBN 978 1 78676 064 7. [Google Scholar]
  17. Kassem, I.I.; Hijazi, M.A.; Saab, R. On a collision course: The availability and use of colistin-containing drugs in human therapeutics and food-animal farming in Lebanon. J. Glob. Antimicrob. Resist. 2019, 16, 162–164. [Google Scholar] [CrossRef]
  18. WHO. Antimicrobial Resistance. 2020. Available online: https://www.who.int/news-room/fact-sheets/detail/antimicrobial-resistance (accessed on 21 September 2020).
  19. WHO. Antimicrobial Resistance in the Food Chain. 2017. Available online: https://www.who.int/foodsafety/areas_work/antimicrobial-resistance/amrfoodchain/en/ (accessed on 21 September 2020).
  20. Osman, M.; Al Mir, H.; Rafei, R.; Dabboussi, F.; Madec, J.-Y.; Haenni, M.; Hamze, M. Epidemiology of antimicrobial resistance in Lebanese extra-hospital settings: An overview. J. Glob. Antimicrob. Resist. 2019, 17, 123–129. [Google Scholar] [CrossRef]
  21. LIBNOR. Lebanese Specification Standard No. 503: Minced Meat; Lebanese Standards Institution: Beirut, Lebanon, 2004; p. 12. [Google Scholar]
  22. El-Jardali, F.; Hammoud, R.; Kamleh, R.; Jurdi, M. K2P Briefing Note: Protecting Consumers in Lebanon: The Need for Effective Food Safety System; American University of Beirut: Beirut, Lebanon, 2014; Available online: https://eventscal.lau.edu.lb/conferences/nfrd2014/abstracts/food/food-abstract13.pdf (accessed on 18 September 2020).
  23. Erkmen, O.; Bozoglu, T.F. Indicators of Foodborne Pathogens; Chapter 12 in Food Microbiology, 2 Volume Set: Principles into Practice; John Wiley & Sons: Hoboken, NJ, USA, 2016. [Google Scholar]
  24. EFSA. Report from the Task Force on Zoonoses Data Collection including guidance for harmonized monitoring and reporting of antimicrobial resistance in commensal Escherichia coli and Enterococcus spp. from food animals. EFSA J. 2008, 6, 1–44. [Google Scholar] [CrossRef]
  25. Balouiri, M.; Sadiki, M.; Ibnsouda, S.K. Methods for in vitro evaluating antimicrobial activity: A review. J. Pharm. Anal. 2016, 6, 71–79. [Google Scholar] [CrossRef] [Green Version]
  26. Sourenian, T.; Mann, D.; Li, S.; Deng, X.; Jaafar, H.; Kassem, I.I. Dissemination of multidrug-resistant Escherichia coli harboring the mobile colistin resistance gene mcr-1.1 on transmissible plasmids in the Mediterranean Sea. J. Glob. Antimicrob. Resist. 2020, 22, 84–86. [Google Scholar] [CrossRef]
  27. Nguyen, M.C.P.; Woerther, P.L.; Bouvet, M.; Andremont, A.; Leclercq, R.; Canu, A. Escherichia coli as reservoir for macrolide resistance genes. Emerg. Infect. Dis. 2009, 15, 1648–1650. [Google Scholar] [CrossRef] [PubMed]
  28. CLSI. Performance Standards for Antimicrobial Susceptibility Testing; Clinical and Laboratory Standards Institute: Wayne, PA, USA, 2016. [Google Scholar]
  29. European Committee on Antimicrobial Susceptibility Testing (EUCAST). Breakpoint Tables for Interpretation of MICs and Zone Diameters; EUCAST, Version 8.1. 2018. Available online: http://www.eucast.org (accessed on 20 September 2020).
  30. Multiple Experiment Viewer (MEV). Available online: http://mev.tm4.org/#/welcome (accessed on 14 October 2020).
  31. Berrazeg, M.; Drissi, M.; Medjahed, L.; Rolain, J.M. Hierarchical clustering as a rapid tool for surveillance of emerging antibiotic-resistance phenotypes in Klebsiella pneumoniae strains. J. Med. Microbiol. 2013, 62, 864–874. [Google Scholar] [CrossRef] [PubMed]
  32. Government of New Zealand. Microbiological Reference Criteria for Food. 1995. Available online: https://www.mpi.govt.nz/dmsdocument/21185/direct (accessed on 21 September 2020).
  33. AMS USDA. Microbiological Testing of Ams Purchased Meat, Poultry and Egg Commodities. 2020. Available online: https://www.ams.usda.gov/resources/microbiological-testing (accessed on 21 September 2020).
  34. Goepfert, J. The aerobic plate count, coliform and Escherichia coli content of raw ground beef at the retail level. J. Milk Food Technol. 1976, 39, 175–178. [Google Scholar] [CrossRef]
  35. EC. Commission Regulation (EC) No 2073/2005 of 15 November 2005 on microbiological criteria for foodstuffs. OJEU 2005, 50, 1–26. [Google Scholar]
  36. National Research Council. Application of microbiological criteria to foods and food ingredients. In An Evaluation of the Role of Microbiological Criteria for Foods and Food Ingredients; National Academies Press: Washington, DC, USA, 1985. [Google Scholar]
  37. National Research Council. Current status of microbiological criteria and legislative bases. In An Evaluation of the Role of Microbiological Criteria for Foods and Food Ingredients; National Academies Press: Washington, DC, USA, 1985. [Google Scholar]
  38. Ekici, G.; Dümen, E. Escherichia coli and food safety. In The Universe of Escherichia coli; Starčič Erjavec, M., Ed.; IntechOpen: London, UK, 2019. [Google Scholar] [CrossRef]
  39. Souli, M.; Galani, I.; Giamarellou, H. Emergence of extensively drug-resistant and pandrug-resistant Gram-negative bacilli in Europe. Eurosurveillance 2008, 13, 19045. [Google Scholar] [CrossRef]
  40. González-Gutiérrez, M.; García-Fernández, C.; Alonso-Calleja, C.; Capita, R. Microbial load and antibiotic resistance in raw beef preparations from northwest Spain. Food Sci. Nutr. 2020, 8, 777–7785. [Google Scholar] [CrossRef]
  41. Adzitey, F. Incidence and antimicrobial susceptibility of Escherichia coli isolated from beef (meat muscle, liver and kidney) samples in Wa Abattoir, Ghana. Cogent Food Agric. 2020, 6, 1718269. [Google Scholar] [CrossRef]
  42. Sabala, R.F.; Usui, M.; Tamura, Y.; Abd-Elghany, S.M.; Sallam, K.I.; Elgazzar, M.M. Prevalence of colistin-resistant Escherichia coli harbouring mcr-1 in raw beef and ready-to-eat beef products in Egypt. Food Control 2021, 119, 107436. [Google Scholar] [CrossRef]
  43. Hmede, Z.; Kassem, I.I. The colistin resistance gene, mcr-1, is prevalent in commensal E. coli isolated from Lebanese pre-harvest poultry. Antimicrob. Agents Chemother. 2018, 62. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  44. Hassan, J.; El-Gemayel, L.; Bashour, I.; Kassem, I.I. On the edge of a precipice: The global emergence and dissemination of plasmid-borne mcr genes that confer resistance to colistin, a last-resort antibiotic. In Antibiotics and Antimicrobial Resistance Genes in the Environment; Elsevier: Amsterdam, The Netherlands, 2020; pp. 155–182. [Google Scholar]
  45. Hmede, Z.; Alhaj Sulaiman, A.; Jaafar, H.; Kassem, I.I. Emergence of plasmid-borne colistin resistance gene mcr-1 in multidrug-resistant Escherichia coli isolated from irrigation water in Lebanon. Int. J. Antimicrob. Agents 2019, 54, 102–104. [Google Scholar] [CrossRef] [PubMed]
  46. Kassem, I.I.; Kehinde, O.; Kumar, A.; Rajashekara, G. Antimicrobial-resistant Campylobacter in organically and conventionally raised layer chickens. Foodborne Pathog. Dis. 2017, 14, 29–34. [Google Scholar] [CrossRef] [PubMed]
  47. Nisar, M.; Kassem, I.I.; Rajashekara, G.; Goyal, S.M.; Lauer, D.; Voss, S.; Nagaraja, K.V. Genotypic relatedness and antimicrobial resistance of Salmonella Heidelberg isolated from chickens and turkeys in the midwestern United States. J. Vet. Diagn. Invest. 2017, 29, 370–375. [Google Scholar] [CrossRef]
  48. Sahin, O.; Kassem, I.I.; Shen, Z.; Lin, J.; Rajashekara, G.; Zhang, Q. Campylobacter in poultry: Ecology and potential interventions. Avian Dis. 2015, 59, 185–200. [Google Scholar] [CrossRef]
  49. Cogliani, C.; Goossens, H.; Greko, C. Restricting antimicrobial use in food animals: Lessons from Europe. Microbe 2011, 6, 274–279. [Google Scholar] [CrossRef]
  50. Kimera, Z.I.; Mshana, S.E.; Rweyemamu, M.M.; Mboera, L.E.; Matee, M.I. Antimicrobial use and resistance in food-producing animals and the environment: An African perspective. Antimicrob. Resist. Infect. Control 2020, 9, 1–12. [Google Scholar] [CrossRef] [Green Version]
  51. Hassan, J.; Kassem, I.I. Audacious hitchhikers: The role of travel and the international food trade in the global dissemination of mobile colistin-resistance (mcr) genes. Antibiotics 2020, 9, 370. [Google Scholar] [CrossRef]
Foods 09 01543 g001a 550Foods 09 01543 g001b 550
Figure 1. (a) The prevalence and loads (colony forming unit (CFU)/g) of fecal coliforms and E. coli in minced beef in Lebanon. The dashed lines show the limit of acceptability based on the Lebanese Standards Institution (LIBNOR) (fecal coliforms; 100 CFU/g), while the black line indicates E. coli limit adopted in other countries (500 CFU/g). NS: indicates no significant difference between the fecal coliforms and E. coli CFU. (b) Box and whisker plot showing the variation in the average CFU/g (circles) of E. coli and fecal coliforms in the minced beef samples.
Figure 1. (a) The prevalence and loads (colony forming unit (CFU)/g) of fecal coliforms and E. coli in minced beef in Lebanon. The dashed lines show the limit of acceptability based on the Lebanese Standards Institution (LIBNOR) (fecal coliforms; 100 CFU/g), while the black line indicates E. coli limit adopted in other countries (500 CFU/g). NS: indicates no significant difference between the fecal coliforms and E. coli CFU. (b) Box and whisker plot showing the variation in the average CFU/g (circles) of E. coli and fecal coliforms in the minced beef samples.
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Figure 2. Hierarchical clustering of the antimicrobial resistance (AMR) profiles of each E. coli (n = 120) isolated from minced beef meat in Lebanon. The strains were labelled E1 to E120. The green color in the scale and the heat map represents resistance, while black and red indicate intermediate resistance and susceptibility, respectively. The letter C indicates clusters.
Figure 2. Hierarchical clustering of the antimicrobial resistance (AMR) profiles of each E. coli (n = 120) isolated from minced beef meat in Lebanon. The strains were labelled E1 to E120. The green color in the scale and the heat map represents resistance, while black and red indicate intermediate resistance and susceptibility, respectively. The letter C indicates clusters.
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Table
Table 1. Antibiotic resistance profile of E. coli isolated from raw minced meat in Lebanon. Antibiotics in the resistance profile were arranged according to the order of antibiotics/classes listed in the Clinical and Laboratory Standards Institute (CLSI) guidelines. Penicillin (PEN), ampicillin (AMP), cefepime (FEP), cefotaxime (CTX), cephalexin (LEX), doripenem (DOR), gentamicin (GEN), kanamycin (KAN), streptomycin (STR), tetracycline (TET), ciprofloxacin (CIP), norfloxacin (NOR), trimethoprim-sulfamethoxazole (SXT), and chloramphenicol (CHL). All isolates were susceptible to amoxicillin/clavulanic acid (AMC), cefixime (CFM), meropenem (MEM), and imipenem (IPM), so these antibiotics were not listed in the table. Shaded (grey) cells with the letter R indicate resistance.
Table 1. Antibiotic resistance profile of E. coli isolated from raw minced meat in Lebanon. Antibiotics in the resistance profile were arranged according to the order of antibiotics/classes listed in the Clinical and Laboratory Standards Institute (CLSI) guidelines. Penicillin (PEN), ampicillin (AMP), cefepime (FEP), cefotaxime (CTX), cephalexin (LEX), doripenem (DOR), gentamicin (GEN), kanamycin (KAN), streptomycin (STR), tetracycline (TET), ciprofloxacin (CIP), norfloxacin (NOR), trimethoprim-sulfamethoxazole (SXT), and chloramphenicol (CHL). All isolates were susceptible to amoxicillin/clavulanic acid (AMC), cefixime (CFM), meropenem (MEM), and imipenem (IPM), so these antibiotics were not listed in the table. Shaded (grey) cells with the letter R indicate resistance.
Resistance ProfilesPENAMPFEPCTXLEXDORGENKANSTRTETCIPNORSXTCHLNumber of Isolates (%)Number of Antibiotic Classes
P1RR RRRRRRRR1 (0.8)6
P2RR R R RRRRR 1 (0.8)6
P3RR R RRRR R1 (0.8)6
P4RR RRRRR R2 (1.7)5
P5RR RRRRR 1 (0.8)5
P6RR R RRRR 2 (1.7)5
P7R RRRR RR1 (0.8)5
P8RR RR RR1 (0.8)5
P9RR RRRR1 (0.8)4
P10RR R RRR 1 (0.8)4
P11R RRRRR1 (0.8)5
P12R RRRRR 1 (0.8)5
P13RR RR R1 (0.8)4
P14RR R RR 1 (0.8)3
P15RR RR R 7 (5.8)4
P16R RR RR2 (1.7)5
P17R RRR R 1 (0.8)5
P18RR RR 4 (3.3)3
P19RR R R 1 (0.8)3
P20R R R R1 (0.8)4
P21R R RR 1 (0.8)4
P22R R R 1 (0.8)3
P23R R R 1 (0.8)3
P24R R R 1 (0.8)3
P25R R R 5 (4.2)3
P26R RR 1 (0.8)3
P27R RR 1 (0.8)2
P28R RR 1 (0.8)2
P29RR 2 (1.7)1
P30R R 29 (24.2)2
P31R R 5 (4.2)2
P32R R 4 (3.3)2
P33R R 1 (0.8)2
P34R 35 (29.2)1
Total120
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Kassem, I.I.; Nasser, N.A.; Salibi, J. Prevalence and Loads of Fecal Pollution Indicators and the Antibiotic Resistance Phenotypes of Escherichia coli in Raw Minced Beef in Lebanon. Foods 2020, 9, 1543. https://doi.org/10.3390/foods9111543

AMA Style

Kassem II, Nasser NA, Salibi J. Prevalence and Loads of Fecal Pollution Indicators and the Antibiotic Resistance Phenotypes of Escherichia coli in Raw Minced Beef in Lebanon. Foods. 2020; 9(11):1543. https://doi.org/10.3390/foods9111543

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Kassem, Issmat I., Nivin A Nasser, and Joanna Salibi. 2020. "Prevalence and Loads of Fecal Pollution Indicators and the Antibiotic Resistance Phenotypes of Escherichia coli in Raw Minced Beef in Lebanon" Foods 9, no. 11: 1543. https://doi.org/10.3390/foods9111543

APA Style

Kassem, I. I., Nasser, N. A., & Salibi, J. (2020). Prevalence and Loads of Fecal Pollution Indicators and the Antibiotic Resistance Phenotypes of Escherichia coli in Raw Minced Beef in Lebanon. Foods, 9(11), 1543. https://doi.org/10.3390/foods9111543

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