Open Access
Research (Published online: 29-06-2018)
21. Extended-spectrum β-lactamases producing multidrug resistance Escherichia coli, Salmonella and Klebsiella pneumoniae in pig population of Assam and Meghalaya, India
A. Lalruatdiki, T. K. Dutta, P. Roychoudhury and P. K. Subudhi
Veterinary World, 11(6): 868-873

A. Lalruatdiki: Department of Veterinary Microbiology, College of Veterinary Science and A.H., Central Agricultural University, Selesih, Aizawl - 796 014, Mizoram, India.
T. K. Dutta: Department of Veterinary Microbiology, College of Veterinary Science and A.H., Central Agricultural University, Selesih, Aizawl - 796 014, Mizoram, India.
P. Roychoudhury: Department of Veterinary Microbiology, College of Veterinary Science and A.H., Central Agricultural University, Selesih, Aizawl - 796 014, Mizoram, India.
P. K. Subudhi: Department of Veterinary Microbiology, College of Veterinary Science and A.H., Central Agricultural University, Selesih, Aizawl - 796 014, Mizoram, India.

doi: 10.14202/vetworld.2018.868-873

Share this article on [Facebook] [LinkedIn]

Article history: Received: 19-02-2018, Accepted: 16-05-2018, Published online: 29-06-2018

Corresponding author: T. K. Dutta

E-mail: tapandutta@rediffmail.com

Citation: Lalruatdiki A, Dutta TK, Roychoudhury P, Subudhi PK (2018) Extended-spectrum β-lactamases producing multidrug resistance Escherichia coli, Salmonella and Klebsiella pneumoniae in pig population of Assam and Meghalaya, India, Veterinary World, 11(6): 868-873.
Abstract

Aim: The present study was conducted to record the prevalence of extended spectrum β-lactamases (ESBLs) producing Escherichia coli, Salmonella spp., and Klebsiella pneumoniae from pig population of Assam and Meghalaya and to record the ability of the resistant bacteria to transfer the resistance genes horizontally.

Materials and Methods: Fecal samples (n=228), collected from pigs of Assam (n=99) and Meghalaya (n=129), were processed for isolation and identification of E. coli and Salmonella spp. All the isolates were tested for ESBLs production by double disc synergy test (DDST) followed by screening for ESBLs producing genes (blaTEM, blaSHV, blaCTX-M, and blaCMY) by polymerase chain reaction (PCR). Possible transfer of resistance encoding genes between enteric bacterial species was carried out by in vitro and in vivo horizontal gene transfer (HGT) method.

Results: A total of 897 enteric bacteria (867 E. coli and 30 Salmonella) were isolated and identified. Altogether 25.41% isolates were confirmed as ESBL producers by DDST method. Majority of the isolates were E. coli followed by Salmonella. By PCR, 9.03% isolates were found positive for at least one of the target resistance genes. blaSHV was absent in all the isolates. blaCMY was the most prevalent gene. All the E. coli isolates from Assam were negative for blaTEM. A total of 2.76% isolates were positive for blaTEM + blaCMY. On the other hand, 0.67% isolates were positive for blaCTX-M + blaCMY genes. Only 0.33% isolates carried all the three genes. Altogether, 4.68% bacteria carried the resistance encoding genes in their plasmids. blaTEM gene could be successfully transferred from Salmonella (donor) to E. coli (recipient) by in vitro (5.5-5.7x10-5) and in vivo (6.5x10-5 to 8.8x10-4) methods. In vivo method was more effective than in vitro in the transfer of resistance genes.

Conclusion: The pig population of Assam and Meghalaya are carrying multidrug resistance and ESBLs producing E. coli and Salmonella. The isolates are also capable to transfer their resistance trait to other bacterial species by HGT. The present finding could be considered as a serious public health concern as similar trait can also be transmitted to the human commensal bacteria as well as pathogens.

Keywords: Enterobacteriaceae, multidrug resistance, North East India, pigs.

References

1. Davis, G.S. and Price, L.B. (2016), Recent research examining links among Klebsiella pneumoniae from food, food animals and human extraintestinal infections. Curr. Environ. Health Rep. 3(2): 128-135. [Crossref] [PubMed]

2. Blaak, H., De Kruijf, P., Hamidjaja, R.A., Van Hoek, A.H.A.M., De Roda Husman, A.M. and Schets, F.M. (2014) Prevalence and characteristics of ESBL producing E. coli in Dutch recreational waters influenced by wastewater treatment plants. Vet. Microbiol., 171(3-4): 448-459. [Crossref] [PubMed]

3. Hamilton, W.L. and Wenlock, R. (2016) Antimicrobial resistance: A major threat to public health. http://cambridgemedicine.org/hamilton2016/. Last accessed on 29-04-2018.

4. Rather, I.A., Kim, B.C., Bajpai, V.K. and Park, Y.H. (2017) Self-medication and antibiotic resistance: Crisis, current challenges, and prevention. Saudi. J. Biol. Sci., 24: 808-812. [Crossref] [PubMed] [PMC]

5. Mandakini, R., Dutta, T.K., Chingtham, S., Roychoudhury, P., Samanta, I., Joardar, S.N., Pachauau, A.R. and Chandra, R. (2014) ESBL-producing Shiga-toxigenic E. coli (STEC) associated with piglet diarrhoea in India. Trop. Anim. Health Prod., 47(2): 377-381. [Crossref] [PubMed]

6. CLSI. (2014) Performance Standards for Antimicrobial Susceptibility Testing, 18th Informational Supplement. M100-S18. Clinical and Laboratory Standards Institute, Wayne, PA.

7. Silhavy, T.J., Berman, M.L. and Enquist, L.W. (1984) Experiments with Gene Fusions. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York.

8. Mandakini, R. (2015) Analysis of Multi-Drug Resistance Genes in Escherichia coli Isolates from Pigs of North-Eastern India. Ph.D. Thesis, Submitted to Central Agricultural University, Imphal, Manipur, India.

9. Karuppasamy, C., Dutta, T.K., Sharma, I., Mandal, S.D., Senthilkumar, N. and Ralte, L. (2017) Prevalence of multidrug-resistant enteropathogenic and enteroinvasive Escherichia coli isolated from children with and without diarrhea in Northeast Indian Population. Ann. Clin. Microbiol. Antimicrob., 16: 49. [Crossref] [PubMed] [PMC]

10. Alcaine, S.D., Sukhnanand, S.S., Warnick, L.D., Su, W.L., McGann, P., McDonough, P. and Wiedmann, M. (2005) Ceftiofur-resistant Salmonella strains isolated from dairy farms represent multiple widely distributed subtypes that evolved by independent horizontal gene transfer. Antimicrob. Agents Chemother., 49: 4061-406. [Crossref]

11. Lalzampuia, H., Dutta, T.K., Warjri, I. and Chandra, R. (2013) PCR-based detection of extended-spectrum β-lactamases (blaCTX-M-1 and blaTEM) in Escherichia coli, Salmonella spp. and Klebsiella pneumoniae Isolated from Pigs in North Eastern India (Mizoram). Ind. J. Microbiol., 53(3): 291-296.

12. Wandili, S.A., Onyango, D.M. and Waindi, E.N. (2013) Prevalence and antimicrobial resistance profile of clinical Salmonella isolates from Nandi Central of Rift Valley, Kenya. Intl. J. Innov. Biotechnol. Biochem., 1(1): 1-10.

13. Li, W., Huang, F.Y., Liu, C.P., Weng, L.C., Wang, N.Y., Chiu N.C. and Chiang, C.S. (2005) Ceftriaxone resistant of non-typhoidal Salmonella enterica isolates in Northern Taiwan attributable to production of CTX-M-14 and CMY-2 β-lactamases. J. Clin. Microbiol., 43: 3237-3243. [Crossref] [PubMed] [PMC]

14. Winokur, P.L., Vonstein, D.L., Hoffman, L.J., Uhlenhopp, E.K. and Doern, G.V. (2001) Evidence for transfer of CMY-2 AmpC β-Lactamase plasmids between Escherichia coli and Salmonella isolates from food animals and humans. Antimicrob. Agents Chemother., 45: 2716-2722. [Crossref] [PubMed] [PMC]

15. Faure, S., Guyomard, P.A., Delmas, J.M. and Laurentie, M. (2009) Impact of therapeutic treatment with β-lactam on transfer of the blaCTX-M-9 resistance gene from Salmonella enterica serovar Virchow to Escherichia coli in gnotobiotic Rats. Appl. Environ. Microbiol., 75: 5523-5528. [Crossref]

16. Akortha, E.E. and Filgona, J. (2009) Transfer of gentamicin resistance genes among Enterobacteriaceae isolated from the outpatients with urinary tract infections attending 3 hospitals in Mubi, Adamawa State. Sci. Res. Essay, 4: 745-752.

17. Shoemaker, N.B., Wang, G.R. and Salyers, A.A. (1992) Evidence for natural transfer of a tetracycline resistance gene between bacteria from the human colon and bacteria from the bovine lumen. Appl. Environ. Microbiol., 58: 1313-1320. [PubMed] [PMC]

18. Jenks, P.J., Hu, Y.M., Danel, F., Mehtar, S. and Livermore, D.M. (1995) Plasmid-mediated production of class1 (AmpC) β-lactamase by two Klebsiella pneumoniae. J. Antimicrob. Chemother., 35: 235-236. [Crossref] [PubMed]

19. Harajly, M., Khairallah, M., Corkill, J.E., Araj, G.F. and Matar, G.M. (2010) Frequency of conjugative transfer of plasmid-encoded ISECP-1-blaCTX-M-15 and aac (6')-lb-crgenes in Enterobaccteriaceae at a tertiary care centre in Lebanon- Role of transferases. Ann. Clin. Microbiol. Antimicrob., 9: 19-27. [Crossref] [PubMed] [PMC]

20. Chen, S., Zhao, S., White, D.G., Schroeder, C.M., Lu, R., Yang, H., McDermott, P.F. and Ayers, S. (2004) Characterisation of multiple-antimicrobial-resistant Salmonella serovars isolated from retails meats. Appl. Environ. Microbiol., 70(1): 1-7. [Crossref] [PubMed] [PMC]

21. Al-Jasser, A.M. (2006) Extended spectrum beta- lactamases (ESBLs): A global problem. Kuwait Med. J. 38: 171-185.