Table of Contents Author Guidelines Submit a Manuscript
BioMed Research International
Volume 2018, Article ID 5327450, 9 pages
https://doi.org/10.1155/2018/5327450
Research Article

Antibiotics Resistance Genes Screening and Comparative Genomics Analysis of Commensal Escherichia coli Isolated from Poultry Farms between China and Sudan

1College of Veterinary Medicine, Nanjing Agricultural University, Nanjing 210095, Jiangsu Province, China
2College of Animal Production, Bahri University, Khartoum, Sudan
3College of Food Science and Technology, Nanjing Agricultural University, Nanjing 210095, Jiangsu Province, China

Correspondence should be addressed to Wei Zhang; nc.ude.uajn@wzsv

Received 5 May 2018; Revised 26 July 2018; Accepted 9 August 2018; Published 26 August 2018

Academic Editor: Stanley Brul

Copyright © 2018 Sheikheldin A. Abdelgader et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Escherichia coli (E. coli) strains, from the gut of animals and humans, harbor wide range of drug resistance genes. A comparative study is conducted on the intestinal E. coli from fecal samples of healthy chicken from China and Sudan in order to monitor the antimicrobial sensitivity pattern. A number of 250 E. coli isolates from chicken farms, including 120 from China and 130 from Sudan, were isolated and identified. All isolates were subjected to susceptibility tests against 10 antibiotics and the distribution of antibiotic resistant genes was confirmed by PCR amplification, involving genes such as ampC, tetA, pKD13, acrA, ermA, ermB, ermC, tetB, mphA, aadA14, aadA1, aac3-1, and aac3- III. Many isolates were found to exhibit resistance against more than one antibiotic. However, the Chinese isolates showed more antibiotics resistance and resistance genes compared to the Sudanese isolates. For better understanding of the multidrug resistance factors, we conducted whole genome analyses of E. coli D107 isolated from China, which revealed that the genome possesses multiple resistance genes including tetracycline, erythromycin, and kanamycin. Furthermore, E. coli D4 isolate from Sudan was more sensitive to antibiotics such as erythromycin, tetracycline, and gentamicin. After analysis by RAST and MAUVE, the two strains showed 89% average nucleotide identity. However, the genomes mostly differed at the number of antibiotics-related genes, as the genome of D107 revealed a considerable number of antibiotics resistance genes such as ermA and mphD which were found to be absent in D4 genome. These outcomes provided confirmation that the poultry farms environment in different countries (China and Sudan) may serve as a potential reservoir of antimicrobial resistance genes and also indicated the evolutionary differences of strains in terms of resistant genes expression.

1. Introduction

Antibiotic resistance is one of the upcoming crucial concerns to global health care [1], and the spread of antibiotic-resistant bacteria stands as one of the most dangerous global health care issues to human health [2]. This resistance among bacteria is now recognized to have a considerable effect in rising morbidity, mortality, and costs associated with major public health problems [3]. Increasing antimicrobial resistance problems do not only affect developed countries but also affect nonindustrialized countries, where antibiotics resistance issues are more challenging, because of the lack of well-organized antimicrobial usage policies and the need for optimal hygiene situation and contagion control practices [4]. The use of antimicrobials in animal farm does not only induce the resistance in the pathogens but also produce resistance in the commensal bacterial of individuals or groups [5, 6]. Description of antimicrobial resistance determinants in bacteria at the genetic level plays a critical role in understanding and possibly controlling the resistance [7]. Moreover, it is clear that genetic exchange system and the ability of E. coli to transfer and propagate genes between humans and animals may make it a significant vector for the spread of rapidly dispersed resistance genes [8, 9].

Genomes resistant to antimicrobials might have emerged from continuous accumulation of multiple mutations [12]. Hence, whole-genome sequence (WGS) of microorganisms has become an important tool for antibiotics resistance screening and, thus, provides rapid identification of antibiotic resistance mechanisms. Moreover, WGS also enables evaluating the number of mutations and functions of the mutated genes [13, 14]. Sequencing the entire genome is found to be helpful in many antimicrobial applications such as new antibiotics development, diagnostic tests, the management of presently available antibiotics, and clarifying the factors promoting the emergence and resistance of pathogenic bacteria [15, 16]. During the last two decades, the use of antibiotics in poultry farming has changed, as the utilization of antibiotics as growth promoters is banned or severely restricted in some countries, which caused distinctive differences between countries in regard to prevalence of antibiotic resistance [17, 18].

The objective of our study was to comparatively determine the antibiotic resistance in commensal E. coli isolated from chicken’s farms between China and Sudan. We utilized WGS and polymerase chain reaction (PCR) techniques to study antimicrobial resistance genes and highlighted the importance of identifying the antibiotics resistance changes in the natural microbiota due to the overuse of antimicrobials by commercial poultry meat producers.

2. Materials and Methods

2.1. Samples Collection

A total of 500 cloacal swab samples were collected from commercial chicken farms located in Khartoum, Sudan (n=250), and Nanjing, China (n=250), in June, 2016. All samples were swabbed with a sterile cotton swab (Xuzhou Kanger Company, Xuzhou, China). After collection, samples were stored in ice-cold sterile containers during transportation from the farm to the laboratory. The samples collected from Sudan were transferred in LB medium (Sigma Aldrich, China) to the College of Veterinary Medicine Nanjing Agriculture University, China, within two days after collection; for isolation and identification. All the samples collected from China and Sudan were handled at the same time.

2.2. Bacterial Isolation

Samples collected from both countries were inoculated (5 μL inoculums) in LB medium and stored at 4°C. Fecal coliform isolates were further characterized by streaking on MacConkey agar (Qingdao hope bio-technology co. ltd., China) and incubated overnight at 37°C. The phylogenetic classification of the bacteria isolates was conducted by multiplex PCR and assigned to the 4 major E. coli bacteria groups A, B1, B2, and group D according to the 16S rRNA analysis.

Based on the initial biochemical tests, a total of 250 E. coli isolates (120 samples from China and 130 samples from Sudan) were selected and stored in sterile containers for further tests.

2.3. Antibiotics Agents

All the bacterial isolates were tested for antibiotics resistance including ampicillin, cefotaxime, kanamycin, erythromycin, doxycycline, ciprofloxacin, tetracycline, gentamicin, streptomycin, and spectinomycin. All antimicrobials were purchased from Sigma-Aldrich, China. Antibiotics were prepared and diluted in the LB medium to concentrations ranging from 0.01 μg/mL to 128 μg/mL (Table 1). Isolates which showed resistance to two or more antimicrobial agents were defined as multidrug-resistant.

Table 1: Class, concentration range, and resistant breakpoints of tested antibiotics.
2.4. Antibiotics Testing

Antibiotic susceptibilities of the E. coli isolates were determined by minimum inhibitory concentration (MIC) test and were carried out by the agar dilution method according to Clinical and Laboratory Standards Institute (CLSI) recommendations [19].

The MIC was reported as the lowest test concentration extract that showed no visible bacterial growth. The plate wells with a complete inhibition of macroscopic growth were recorded as MIC against the tested strain. The density of the suspension to contain colony forming units (CFU)/mL was adjusted by comparison with a 0.5 McFarland turbidity standard. Tested antibiotics, concentration ranges, and resistance MIC points are listed in Table 1, and E. coli ATCC 25922 was used as the control organism.

2.5. Detection of Antibiotics Resistance Genes

The PCR amplifications were carried out using PCR primers listed in Table 2, for the detection of 13 different antibiotics resistance genes ARGs, such as ampicillin ampC, tetracycline tetA, kanamycin pKD13, ciprofloxacin acrA, erythromycin ermA, ermB, ermC, doxycycline tetB, cefotaxime mphA, spectinomycin aadA14, streptomycin aadA1, and gentamicin aac3-1, aac3- III.

Table 2: Primer sequences and annealing temperatures used in the PCR reactions carried out the virulence genes of E. coli isolates in this study.
2.6. Genomic DNA Extraction

The total bacterial DNA was extracted by using commercial bacterial DNA extraction kit (Omega Co., China) according to the kit manufacturer’s instructions. Briefly, 1.5 mL of E. coli isolate (grown overnight in LB medium) was pelleted in Eppendorf tube by microcentrifuge at 10,000×g at max speed for 10 min. The supernatant was discarded followed by addition of 100 μL TE buffer and vortexed to completely resuspended the cell pellet. Lysozyme (10 μL) was added and the solution was incubated at 57°C for 10 minutes. Then, 20 μL of proteinase K solution was added, samples were vortexed, and the cell solution was incubated at 55°C shaking water bath for lysis 6 hrs. After the lysis, 5 μL of the RNase was added and the tubes were incubated at room temperature for 5 minutes. This was followed by the addition of 220 μL of BDL buffer; then, samples were vortexed and incubated at 65°C for 10 minutes. The genomic DNA was concentrated by the addition of 220 μL of 100% ethanol, vortexed for 20 seconds, and centrifuged for 1 min at 10,000×g. Then, 500 μL HBC buffer was added and centrifuged for 1 min at 10,000×g for washing. The purified DNA was eluted in a fresh 1.5 mL microcentrifuge tube using 100 μL elution buffer, 171, and kept at room temperature for 5 minutes, and centrifuged for 1 min at 10,000×g. Finally, the DNA concentration was evaluated using nanodrop spectrophotometer before being stored at −20°C.

2.7. Genome Annotations and Comparison

DNA sequencing runs of E. coli isolates were completed for both genomes of D107 (resistant) strain from China and D4 (sensitive) strain from Sudan. Open reading frames annotation and comparative gene clusters analysis was conducted using the rapid annotation subsystem technology (RAST version 4.0). Gene sequence alignment was performed using Genedoc (version 2.6).

3. Results and Discussion

3.1. Antibiotics Resistance Testing

Antimicrobial resistance test of all E. coli isolates were determined by minimum inhibitory concentration (MIC). Classification and percentage distribution of antibiotic resistance in commensal E. coli isolates against 10 different antibiotics is presented in Table 3. All E. coli isolates were resistant to at least one antibiotic; these results are consistent with other previous studies on commensal E. coli, where commensal E. coli exhibited high prevalence of resistance to commonly used antibiotics in livestock [20, 21] (Miles et al., 2016). Furthermore, about 75.5% of bacterial isolate were resistant to more than two antibiotics (multidrug-resistant). Among examined individual antibiotics, tetracycline resistance was the highest percentage found in both isolates from China and Sudan at of 80% and 54.4%, respectively. This high rate of resistance in commensal E. coli from poultry was also demonstrated in the study of Cizman [22]. Tetracycline is commonly used antibiotic against commensal E. coli from chicken farms in the above studied two countries. Another significantly high resistance was found towards ampicillin at 75.2% of isolates from China; however, the isolates from Sudan were significantly lower in percentage (29.2%). This is followed by the resistance to ampicillin, kanamycin, and erythromycin. Moreover, about 62% of the E. coli isolates resistant to ampicillin also showed resistance against tetracycline.

Table 3: Phenotypic pattern of commensal E. coli isolates from poultry farms in China and Sudan to 10 antibiotics agents, included in this study.

The overall phenotypic resistance comparison reveals significant higher rates of antibiotic resistant E. coli isolates from China compared to the Sudan isolates except in the ciprofloxacin where the Sudanese isolate showed higher resistance, which might be due to the variation of antibiotics overuse between both countries.

3.2. Distribution of E. coli Isolates Resistance Genes

PCR amplifications were performed to detect 13 virulence genes using their appropriate primers. The distribution of identified virulence genes is presented in Figure 1. Tetracycline resistant gene tetA was found to be highly distributed in isolates from China and Sudan at 84% and 54%, respectively, which is comparable to some studies reporting higher frequencies of tetA and tetB [23, 24]. This percentage is followed by the ampicillin resistance gene (ampC) at 75% and 27.6%, respectively. The detection of resistance genes was found to be in agreement with the phenotypic resistance data in Table 3, suggesting that these genes play significant role in the tolerance against the tested antibiotic. Moreover, about 72% of the tetA resistance isolates were also resistant to ampC, and around 35% of isolates possessing ampC/pKD13 genes in their genome were found to possess tetA gene, indicating significantly high prevalence of these multidrug resistance isolates. The occurrence of remaining genes in the genome of tested isolates was present in a range from 34% to 66%, except for erythromycin ermA in Sudan isolates and gentamicin (aac3- III) in both countries which were not detected, while the pKD13 genes were identified in 65% and 42% of isolates from China and Sudan, respectively. Therefore, this indicates that local and the geographical localization factors can play a major role in the appearance of some antimicrobial resistance genes. It has been mentioned that sensitive strains harbor antibiotic(s) resistant gene(s) might express this resistant and generate strains that are likely to be resistant to those antibiotics [25].

Figure 1: Distribution of resistance genes among commensal Escherichia coli isolates, from poultry farms (China and Sudan).
3.3. Comparative Genomes Sequence

In order to determine the extent of DNA sequencing coverage, TBLASTN searches were performed against the whole genome sequences of D107 strain from China and D4 strain from Sudan. In general, among these two E. coli genomes, the chromosomes of Sudanese strain (more antibiotic sensitive) were found to have smaller genome size (4,742,490 bp) and consisted of 4179 coding DNA sequences (CDS), whereas the Chinese strain has 5,111,357 bp and 5193 CDS. Figure 2 represents different gene groups categorized by RAST (RAST.nmpdr.org) annotation tool. The genome sequence of commensal E. coli strain D107 isolated from China revealed a wide array of antimicrobial resistance genes compared with the whole genome of the E. coli D4 strain.

Figure 2: Genomic maps showing deferent group of genes functions categories, annotated by RAST. (a) E. coli D107 (China strain); (b) E. coli D4 (Sudan strain). The number of shared genes and the number of unique genes and genes shared between two strains are shown.

The antimicrobial resistance genes identified in whole genomes sequence of E. coli D107 and D4 are listed in Table 4. The comparative sequence analysis of both D107 and D4 genomes (Figure 3) revealed that erythromycin (ermA) and cefotaxime gene (mphD) antibiotics resistant genes were found in the D107 while being absent in the E. coli from the D4 isolate. The missing resistance genes from antimicrobial susceptible strain (D4) suggests that it has various plasmid complement that any antimicrobial resistance determinants were either missing or never obtained. However, quinolone (qnrA1) and gentamicin (aac3- III) resistance genes were not found in both genomes.

Table 4: Inventory of antibiotic resistance genes identified in whole E. coli genomes (D107 and D4).
Figure 3: Circular map of D107 and D4 Genomic comparison. The outer circle shows identity position of both genomes. The second circle shows the D107 genome and inner circle shows D4 genome. Gaps seen in D4 indicate that sequence is missing in this isolate but present in D107.

The detection of the differences between the two genomes holds a great potential for understanding the development of risky E. coli resistant strains from the Chinese isolate. The chromosomal backbones of the two E. coli strains are different as in Figure 3. Although D107 and D4 (both are commensal bacteria) have highly various antimicrobial profiles of high and low susceptibility, respectively, this suggests that transferring exogenous or horizontal genes is a key mechanism for the acquisition of antimicrobial resistance. This is implication is reasonable, since many antimicrobial resistance genes determinants are transmitted by moving plasmids or mobile elements, particularly for gut microorganisms [26].

The specific gene sequence comparison in between D107 and D4 strains is exemplified for the ampC gene (Figure 4). Although the gene was present in the genome of both strains, the phenotypic resistance varied significantly which could indicate a strong engagement between antibiotics resistance genes and an elevated mutation rate. Moreover, many studies have observed that the acquisition of a mutation provides antibiotic resistance genes [26].

Figure 4: Alignment result of AmpC gene in the genomes of China strain (D107) and Sudan strain (D4).

4. Conclusion

Herein we report a comparative study on the antibiotic resistance isolates of commensal E. coli, evaluating genes associated with antibiotic resistance from Chinese and Sudanese poultry farms. Clear variation in phenotypic resistance patterns was found, as isolates from China were significantly more tolerant to a wide array of antibiotics, which is supported by the detection of specific genes and genome-wide comparative analysis. The results indicate the variations of irrational utilization of these antimicrobial agents in animal farms for treatments or as growing promoters. We are currently exploring the interplay between the genetic makeup of resistant strains and their expressed phenotypic resistance.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Acknowledgments

The authors thank Dr. Faisal Nureldin Awad (National Food Research Centre, Sudan) for the valuable comments and language editing of this manuscript. This work was supported by grants from the National Natural Science Foundation of China (no. 31322054) and the Priority Academic Program Development of Jiangsu Higher Education Institutions.

References

  1. S. Schjørring and K. A. Krogfelt, “Assessment of Bacterial Antibiotic Resistance Transfer in the Gut,” International Journal of Microbiology, vol. 2011, Article ID 312956, 10 pages, 2011. View at Publisher · View at Google Scholar
  2. D. L. Paterson, W.-C. Ko, A. Von Gottberg et al., “Antibiotic therapy for Klebsiella pneumoniae bacteremia: implications of production of extended-spectrum β-lactamases,” Clinical Infectious Diseases, vol. 39, no. 1, pp. 31–37, 2004. View at Publisher · View at Google Scholar · View at Scopus
  3. C. A. Bunner, B. Norby, P. C. Bartlett, R. J. Erskine, F. P. Downes, and J. B. Kaneene, “Prevalence and pattern of antimicrobial susceptibility in Escherichia coli isolated from pigs reared under antimicrobial-free and conventional production methods,” Journal of the American Veterinary Medical Association, vol. 231, no. 2, pp. 275–283, 2007. View at Publisher · View at Google Scholar · View at Scopus
  4. G. M. Rossolini and M. C. Thaller, “Coping with antibiotic resistance: Contributions from genomics,” Genome Medicine, vol. 2, no. 2, 2010. View at Google Scholar · View at Scopus
  5. L. J. Piddock, “Does the use of antimicrobial agents in veterinary medicine and animal husbandry select antibiotic-resistant bacteria that infect man and compromise antimicrobial chemotherapy?” Journal of Antimicrobial Chemotherapy, vol. 38, no. 1, pp. 1–3, 1996. View at Publisher · View at Google Scholar · View at Scopus
  6. A. E. Van Den Bogaard and E. E. Stobberingh, “Antibiotic usage in animals. Impact on bacterial resistance and public health,” Drugs, vol. 58, no. 4, pp. 589–607, 1999. View at Publisher · View at Google Scholar · View at Scopus
  7. C. T. Archer, J. F. Kim, H. Jeong et al., “The genome sequence of E. coli W (ATCC 9637): comparative genome analysis and an improved genome-scale reconstruction of E. coli,” BMC Genomics, vol. 12, article 9, 2011. View at Publisher · View at Google Scholar · View at Scopus
  8. P. B. Eckburg, E. M. Bik, C. N. Bernstein et al., “Microbiology: diversity of the human intestinal microbial flora,” Science, vol. 308, no. 5728, pp. 1635–1638, 2005. View at Publisher · View at Google Scholar · View at Scopus
  9. G. D. Wright, “The antibiotic resistome: the nexus of chemical and genetic diversity,” Nature Reviews Microbiology, vol. 5, no. 3, pp. 175–186, 2007. View at Publisher · View at Google Scholar · View at Scopus
  10. N. Woodford and D. M. Livermore, “Infections caused by Gram-positive bacteria: a review of the global challenge,” Infection, vol. 59, supplement 1, pp. S4–S16, 2009. View at Publisher · View at Google Scholar · View at Scopus
  11. G. J. Velicer, G. Raddatz, H. Keller et al., “Comprehensive mutation identification in an evolved bacterial cooperator and its cheating ancestor,” Proceedings of the National Acadamy of Sciences of the United States of America, vol. 103, no. 21, pp. 8107–8112, 2006. View at Publisher · View at Google Scholar · View at Scopus
  12. L. L. Marcusson, N. Frimodt-Møller, D. Hughes, and B. R. Levin, “Interplay in the Selection of Fluoroquinolone Resistance and Bacterial Fitness,” PLoS Pathogens, vol. 5, no. 8, p. e1000541, 2009. View at Publisher · View at Google Scholar
  13. L. Friedman, J. D. Alder, and J. A. Silverman, “Genetic changes that correlate with reduced susceptibility to daptomycin in Staphylococcus aureus,” Antimicrobial Agents and Chemotherapy, vol. 50, no. 6, pp. 2137–2145, 2006. View at Publisher · View at Google Scholar · View at Scopus
  14. C. D. Herring, A. Raghunathan, C. Honisch et al., “Comparative genome sequencing of Escherichia coli allows observation of bacterial evolution on a laboratory timescale,” Nature Genetics, vol. 38, no. 12, pp. 1406–1412, 2006. View at Publisher · View at Google Scholar · View at Scopus
  15. H. Hasman, D. Saputra, T. Sicheritz-Ponten et al., “Rapid whole-genome sequencing for detection and characterization of microorganisms directly from clinical samples,” Journal of Clinical Microbiology, vol. 52, no. 1, pp. 139–146, 2014. View at Publisher · View at Google Scholar · View at Scopus
  16. S. Niemann, C. U. Köser, S. Gagneux et al., “Genomic diversity among drug sensitive and multidrug resistant isolates of Mycobacterium tuberculosis with identical DNA fingerprints,” PLoS ONE, vol. 4, no. 10, Article ID e7407, 2009. View at Publisher · View at Google Scholar · View at Scopus
  17. A. E. van den Bogaard, N. London, C. Driessen, and E. E. Stobberingh, “Antibiotic resistance of faecal Escherichia coli in poultry, poultry farmers and poultry slaughterers,” Journal of Antimicrobial Chemotherapy, vol. 47, no. 6, pp. 763–771, 2001. View at Publisher · View at Google Scholar · View at Scopus
  18. O. O. Adelowo, F. A. Ojo, and O. E. Fagade, “Prevalence of multiple antibiotic resistance among bacterial isolates from selected poultry waste dumps in Southwestern Nigeria,” World Journal of Microbiology and Biotechnology, vol. 25, no. 4, pp. 713–719, 2009. View at Publisher · View at Google Scholar · View at Scopus
  19. P. M. Hawkey and A. M. Jones, “The changing epidemiology of resistance,” Journal of Antimicrobial Chemotherapy, vol. 64, supplement 1, pp. i3–i10, 2009. View at Publisher · View at Google Scholar · View at Scopus
  20. T. D. Miles, W. McLaughlin, and P. D. Brown, “Antimicrobial resistance of Escherichia coli isolates from broiler chickens and humans,” BMC Veterinary Research, vol. 2, article 7, pp. 1–9, 2006. View at Publisher · View at Google Scholar · View at Scopus
  21. M. Marchant, L. Vinué, C. Torres, and M. A. Moreno, “Change of integrons over time in Escherichia coli isolates recovered from healthy pigs and chickens,” Veterinary Microbiology, vol. 163, no. 1-2, pp. 124–132, 2013. View at Publisher · View at Google Scholar · View at Scopus
  22. M. Čižman, “The use and resistance to antibiotics in the community,” International Journal of Antimicrobial Agents, vol. 21, no. 4, pp. 297–307, 2003. View at Publisher · View at Google Scholar · View at Scopus
  23. V. I. Enne, C. Cassar, K. Sprigings, M. J. Woodward, and P. M. Bennett, “A high prevalence of antimicrobial resistant Escherichia coli isolated from pigs and a low prevalence of antimicrobial resistant E. coli from cattle and sheep in Great Britain at slaughter,” FEMS Microbiology Letters, vol. 278, no. 2, pp. 193–199, 2008. View at Publisher · View at Google Scholar · View at Scopus
  24. B. Guerra, E. Junker, A. Schroeter, B. Malorny, S. Lehmann, and R. Helmuth, “Phenotypic and genotypic characterization of antimicrobial resistance in German Escherichia coli isolates from cattle, swine and poultry,” Journal of Antimicrobial Chemotherapy, vol. 52, no. 3, pp. 489–492, 2003. View at Publisher · View at Google Scholar · View at Scopus
  25. F. Martineau, F. J. Picard, N. Lansac et al., “Correlation between the resistance genotype determined by multiplex PCR assays and the antibiotic susceptibility patterns of Staphylococcus aureus and Staphylococcus epidermidis,” Antimicrobial Agents and Chemotherapy, vol. 44, no. 2, pp. 231–238, 2000. View at Publisher · View at Google Scholar
  26. L. P. Randall, S. W. Cooles, M. K. Osborn, L. J. V. Piddock, and M. J. Woodward, “Antibiotic resistance genes, integrons and multiple antibiotic resistance in thirty-five serotypes of Salmonella enterica isolated from humans and animals in the UK,” Journal of Antimicrobial Chemotherapy, vol. 53, no. 2, pp. 208–216, 2004. View at Publisher · View at Google Scholar · View at Scopus