Multi-drug resistance and biofilm production among diarrheagenic Escherichia coli pathotypes isolated from stools of children with acute diarrheal disease

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Abstract

Background. Diarrheagenic E. coli (DEC) is an etiological agent of childhood diarrhea. Resistance against commonly used drugs in the empirical treatment of enteric infections has increased among DEC. Relationship between antibiotic resistance and biofilm formation in microorganisms have been widely reported. This study was aimed to determine the antibiotic resistance and biofilm production pattern among DEC pathotypes isolated from stools of children aged 0–5 years with acute diarrheal disease in Abakaliki, Nigeria. Materials and methods. Diarrheal stool samples were obtained from 60 children and E. coli were isolated and identified using standard guidelines provided for laboratory diagnosis of enteric pathogens. Molecular identification was done by amplification of E. coli universal stress protein A (uspA) using polymerase chain reaction (PCR) method. Detection of virulent genes of DEC pathotypes was performed in a group of multiplex PCR using their specific primers. Kirby–Bauer disk diffusion method was used to determine the antibiotic susceptibility patterns of the isolates while biofilms production was detected by thiazolyl blue tetrazolium bromide dye in a 96-well plate. Results. DEC was isolated in 40 stools among which EIEC [40% (n = 16)] was commonly detected followed by ETEC [30% (n = 12)], EAEC [20% (n = 8)] and typical EPEC [10% (n = 4)]. Half of EAEC showed the highest multidrug resistance against ampicillin, cefoxitin, ciprofloxacin, levofloxacin, and tetracycline with the strongest biofilm production followed by all the EPEC which were resistant to ampicillin, ciprofloxacin, levofloxacin, and tetracycline with moderate biofilm production. All the LT-ETEC exhibited the least resistance to ampicillin and tetracycline with the weakest biofilm production. Conclusion. High frequency of the EIEC pathotype suggests its role as the primary etiological agent of diarrhea in children. Correlation between high drug resistance and biofilm production among the pathotype may indicate that biofilms may provide compatible uptake of resistance genes.

About the authors

E. E. David

Alex Ekwueme Federal University Ndufu-Alike

Author for correspondence.
Email: david.ebuka@funai.edu.ng
ORCID iD: 0000-0001-6903-6392

Ebuka Elijah David,  MSc (Biochemstry), Department of Chemistry/Biochemistry 

1010, Ebonyi State, Abakaliki

Phone: +234 803 318-88-23 

Nigeria

M. A. Yameen

COMSATS University Islamabad, Abbottabad Campus

Email: arfatyameen@gmail.com

PhD (Microbial Pharmacology), Department of Pharmacy 

Abbottabad

Pakistan

I. Igwenyi

Ebonyi State University

Email: igweyike@yahoo.com

PhD (Biochemistry), Associate Professor, Department of Biochemistry 

Ebonyi State

Nigeria

A. C. Okafor

Edo University, Iyamho

Email: arthur.okafor@edouniversity.edu.ng

PhD (Microbiology), Department of Microbiology 

Edo State

Nigeria

U. N. Obeten

Alex Ekwueme Federal University Ndufu-Alike

Email: uketgabriel@gmail.com

MSc (Biochemstry), Department of Chemistry/Biochemistry 

Ikwo, Ebonyi State

Nigeria

D. O. Obasi

Alex Ekwueme Federal University Ndufu-Alike

Email: obasidoris19@gmail.com

MSc (Biochemstry), Department of Chemistry/Biochemistry 

Ikwo, Ebonyi State

Nigeria

U. R. Ezeilo

Alex Ekwueme Federal University Ndufu-Alike

Email: ucmgbenka@gmail.com

PhD (Enzymology), Department of Chemistry/Biochemistry 

Ikwo, Ebonyi State

Nigeria

M. N. Emeribole

Alex Ekwueme Federal University Ndufu-Alike

Email: mnnanyere@gmail.com

MSc (Biochemstry), Department of Chemistry/Biochemistry 

Ikwo, Ebonyi State

Nigeria

C. N. David

Ebonyi State University

Email: nnenne.nnaji@gmail.com

MSc (Biochemstry), Department of Microbiology 

Ebonyi State

Nigeria

References

  1. Adefisoye M.A., Okoh A.I. Identification and antimicrobial resistance prevalence of pathogenic Escherichia coli strains from treated wastewater effluents in Eastern Cape, South Africa. Microbiologyopen., 2016, vol. 5, pp. 143–151. doi: 10.1002/mbo3.319
  2. Akinrotoye K.P., Uzal U. Combating diarrhoea in Nigeria: the way forward. J. Microbiol. Exp., 2018, vol. 6, no. 4, pp. 191–197. doi: 10.15406/jmen.2018.06.00213
  3. Alikhani M.Y., Hashemi S.H., Aslani M.M., Farajnia S. Prevalence and antibiotic resistance patterns of diarrheagenic Escherichia coli isolated from adolescents and adults in Hamedan, Western Iran. Iran J. Microbiol., 2013, vol. 5, no. 1, pp. 42–47.
  4. Behiry I.K., Abada E.A., Ahmed E.A., Labeeb R.S. Enteropathogenic Escherichia coli associated with diarrhea in children in Cairo, Egypt. Sci. World J., 2011, vol. 11, pp. 2613–2619. doi: 10.1100/2011/485381
  5. Bollinger R.R., Everett M.L., Wahl S.D., Lee Y.H., Orndorff P.E., Parker W. Secretory IgA and mucin-mediated biofilm formation by environmental strains of Escherichia coli: role of type 1 pili. Mol. Immunol., 2006, vol. 43, no. 4, pp. 378–387. doi: 10.1016/j.molimm.2005.02.013
  6. Cepas V., López Y., Muñoz E., Rolo D., Ardanuy C., Martí S., Xercavins M., Horcajada J.P., Bosch J., Soto S.M. Relationship between biofilm formation and antimicrobial resistance in gram-negative bacteria. Microb. Drug Resist., 2019, vol. 25, no. 1, pp. 72–79. doi: 10.1089/mdr.2018.0027
  7. Cheesbrough M. District laboratory practice in tropical countries. Part 2 (2nd ed.). Cambridge: Cambridge University Press, 2006. doi: 10.1017/CBO9780511543470
  8. Chellapandi K., Dutta T.K., Sharma I., De Mandal S., Kumar N.S., Ralte L. Prevalence of multi drug resistant enteropathogenic and enteroinvasive Escherichia coli isolated from children with and without diarrhea in Northeast Indian population. Ann. Clin. Microbiol. Antimicrob., 2017, vol. 16, no. 1: 49. doi: 10.1186/s12941-017-0225-x
  9. Chen D., Zhao T., Doyle M.P. Single- and mixed-species biofilm formation by Escherichia coli O157:H7 and Salmonella, and their sensitivity to levulinic acid plus sodium dodecyl sulfate. Food Control, 2015, vol. 57, pp. 48–53. doi: 10.1016/j.foodcont.2015.04.006
  10. CLSI. Performance standards for antimicrobial disk susceptibility tests. 13th ed. CLSI standard M02. Wayne, PA: Clinical and Laboratory Standard Institute, 2018. 13 p.
  11. David E.E., Udedi S.C., Ekwealor K.E., Igwilo I.O., Enemali M.O., Ifemeje T.O., Asogw A. Antidiarrhoeal activity of cashew (Anacardium occidentale) leaf extract enriched with zinc in wistar albino rats. SJBR, 2013, vol. 2, pp. 37–41.
  12. David E.E., Yameen M.A., Igwenyi I.O., Okafor A.Ch., Obeten U.N., Obasi D.O., Ezeilo U.R., David Ch.N. The frequency of virulent genes and antimicrobial resistance patterns of diarrheagenic Escherichia coli isolated from stools of children presenting with diarrhea in a tertiary hospital in Abakaliki, Nigeria. Int. J. One Health, 2020, vol. 6, no. 2, pp. 147–152. doi: 10.14202/ IJOH.2020.147-152
  13. Dumaru R., Baral R., Shrestha L.B. Study of biofilm formation and antibiotic resistance pattern of gram-negative bacilli among the clinical isolates at BPKIHS, Dharan. BMC Res. Notes, 2019, vol. 12, no. 1: 38. doi: 10.1186/s13104-019-4084-8
  14. DuPont H.L., Steffen R. Use of antimicrobial agents for treatment and prevention of travellers’ diarrhoea in the face of enhanced risk of transient fecal carriage of multi-drug resistant enterobacteriaceae: setting the stage for consensus recommendations. J. Travel Med., 2016, 23, no. 6: taw054. doi: 10.1093/jtm/taw054
  15. Dutta S., Guin S., Ghosh S., Pazhani G.P., Rajendran K., Bhattacharya M.K., Takeda Y., Nair G.B., Ramamurthy T. Trends in the prevalence of diarrheagenic Escherichia coli among hospitalized diarrheal patients in Kolkata, India. PLoS One, 2013, vol. 8, no. 2: e56068. doi: 10.1371/journal.pone.0056068
  16. Healey A., Furtado A., Cooper T., Henry R.J. Protocol: a simple method for extracting next-generation sequencing quality genomic DNA from recalcitrant plant species. Plant Methods, 2014, vol. 10: 21. doi: 10.1186/1746-4811-10-21
  17. Ifeanyi C.I., Ikeneche N.F., Bassey B.E., Al-Gallas N., Ben Aissa R., Boudabous A. Diarrheagenic Escherichia coli pathotypes isolated from children with diarrhea in the Federal Capital Territory Abuja, Nigeria. J. Infect. Dev. Ctries., 2015, vol. 9, no. 2, pp. 165–174. doi: 10.3855/jidc.5528
  18. Levels and trends in child mortality: report 2020. URL: https://data.unicef.org/resources/levels-and-trends-in-child-mortality
  19. Magiorakos A.P., Srinivasan A., Carey R.B., Carmeli Y., Falagas M.E., Giske C.G., Harbarth S., Hindler J.F., Kahlmeter G., Olsson-Liljequist B., Paterson D.L., Rice L.B., Stelling J., Struelens M.J., Vatopoulos A., Weber J.T., Monnet D.L. Multidrugresistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin. Microbiol. Infect., 2012, vol. 18, no. 3, pp. 268–281. doi: 10.1111/j.1469-0691.2011.03570.x
  20. Mah T.-F. Biofilm-specific antibiotic resistance. Future Microbiol., 2012, vol. 7, pp. 1061–1072. doi: 10.2217/fmb.12.76
  21. Molecular characterization of enterotoxigenic Escherichia coli: effect on intestinal nitric oxide in diarrheal disease. J. Bacteriol. Parasitol., vol. 9: 339. doi: 10.4172/2155-9597.1000339
  22. Moyo S.J., Maselle S.Y., Matee M.I., Langeland N., Mylvaganam H. Identification of diarrheagenic Escherichia coli isolated from infants and children in Dar es Salaam, Tanzania. BMC Infect. Dis., 2007, vol. 7: 92. doi: 10.1186/1471-2334-7-92
  23. Nguyen T.V., Le Van P., Le Huy C., Gia K.N., Weintraub A. Detection and characterization of diarrheagenic Escherichia coli from young children in Hanoi, Vietnam. J. Clin. Microbiol., 2005, vol. 43, no. 2, pp. 755–760. doi: 10.1128/JCM.43.2.755-760.2005
  24. Nweze E.I. Aetiology of diarrhoea and virulence properties of diarrhoeagenic Escherichia coli among patients and healthy subjects in southeast Nigeria. J. Health Popul. Nutr., 2010, vol. 28, no. 3, pp. 245–252. doi: 10.3329/jhpn.v28i3.5551
  25. Okeke I.N., Lamikanra A., Steinrück H., Kaper J.B. Characterization of Escherichia coli strains from cases of childhood diarrhea in provincial southwestern Nigeria. J. Clin. Microbiol., 2000, vol. 38, no. 1, pp. 7–12. doi: 10.1128/JCM.38.1.7-12.2000
  26. Olorunshola I.D., Smith S.I., Coker A.O. Prevalence of EHEC O157:H7 in patients with diarrhoea in Lagos, Nigeria. APMIS, 2000, vol. 108, no. 11, pp. 761–763. doi: 10.1034/j.1600-0463.2000.d01-26.x
  27. Onanuga A., Igbeneghu O., Lamikanra A. A study of the prevalence of diarrhoeagenic Escherichia coli in children from Gwagwalada, Federal Capital Territory, Nigeria. Pan. Afr. Med. J., 2014, vol. 17: 146. doi: 10.11604/pamj.2014.17.146.3369
  28. Pavlickova S., Klancnik A., Dolezalova M., Mozina S.S., Holko I. Antibiotic resistance, virulence factors and biofilm formation ability in Escherichia coli strains isolated from chicken meat and wildlife in the Czech Republic. J. Environ. Sci. Health. B, 2017, vol. 52, no. 8, pp. 570–576. doi: 10.1080/03601234.2017.1318637
  29. Porat N., Levy A., Fraser D., Deckelbaum R.J., Dagan R. Prevalence of intestinal infections caused by diarrheagenic Escherichia coli in Bedouin infants and young children in Southern Israel. Pediatr. Infect. Dis. J., 1998, vol. 17, no. 6, pp. 482–488. doi: 10.1097/00006454-199806000-00010
  30. Protocol: a simple method for extracting next-generation sequencing quality genomic DNA from recalcitrant plant species. Plant Methods, 2014, vol. 10: 21.
  31. Rodas C., Mamani R., Blanco J., Blanco J.E., Wiklund G., Svennerholm A.M., Sjöling A., Iniguez V. Enterotoxins, colonization factors, serotypes and antimicrobial resistance of enterotoxigenic Escherichia coli (ETEC) strains isolated from hospitalized children with diarrhea in Bolivia. Braz. J. Infect. Dis., 2011, vol. 15, no. 2, pp. 132–137. doi: 10.1016/s1413-8670(11)70158-1
  32. Sarowska J., Futoma-Koloch B., Jama-Kmiecik A., Frej-Madrzak M., Ksiazczyk M., Bugla-Ploskonska G., Choroszy-Krol I. Virulence factors, prevalence and potential transmission of extraintestinal pathogenic Escherichia coli isolated from different sources: recent reports. Gut Pathog., 2019, vol. 11: 10. doi: 10.1186/s13099-019-0290-0
  33. Sharma D., Misba L., Khan A.U. Antibiotics versus biofilm: an emerging battleground in microbial communities. Antimicrob. Resist. Infect. Control, 2019, vol. 8: 76. doi: 10.1186/s13756-019-0533-3
  34. Soleimani A., Foroozanfard F., Tamadon M.R. Evaluation of water and electrolytes disorders in severe acute diarrhea patients treated by WHO protocol in eight large hospitals in Tehran: a nephrology viewpoint. J. Renal. Inj. Prev., 2016, vol. 6, no. 2, pp. 109–112. doi: 10.15171/jrip.2017.21
  35. Thakur S., Gray G.C. The Mandate for a Global “One Health” Approach to Antimicrobial Resistance Surveillance. Am. J. Trop. Med. Hyg., 2019, vol. 100, no. 2, pp. 227–228. doi: 10.4269/ajtmh.18-0973
  36. Verma S., Venkatesh V., Kumar R., Kashyap S., Kumar M., Maurya A.K., Dhole T.N., Singh M. Etiological agents of diarrhea in hospitalized pediatric patients with special emphasis on diarrheagenic Escherichia coli in North India. J. Lab. Physicians, 2019, vol. 11, no. 1, pp. 68–74. doi: 10.4103/JLP.JLP_123_18
  37. Vieira N., Bates S.J., Solberg O.D., Ponce K., Howsmon R., Cevallos W., Trueba G., Riley L., Eisenberg J.N. High prevalence of enteroinvasive Escherichia coli isolated in a remote region of northern coastal Ecuador. Am. J. Trop. Med. Hyg., 2007, vol. 76, no. 3, pp. 528–533.

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Copyright (c) 2021 David E.E., Yameen M.A., Igwenyi I., Okafor A.C., Obeten U.N., Obasi D.O., Ezeilo U.R., Emeribole M.N., David C.N.

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