High-resolution melting-curve analysis for serotyping of Salmonella spp. group B isolated from minced pork in the Northern part of Thailand
Main Article Content
Abstract
Background: Nontyphoidal Salmonella spp. is the major bacterial cause of food poisoning. Conventional serotyping is complicated and time consuming.
Objectives: To establish a rapid molecular - based screening for Salmonella serotypes
Materials and methods: Several aspects of Salmonella isolates were characterized by both rapid multiplex real-time PCR and high-resolution melting-curve (HRM) analysis. Group B Salmonella isolates (n=29) were isolated from 165 of minced pork samples randomly collected from local markets in six provinces of the Northern Thailand. Several genetic determinants responsible to specific phenotypes were selected, including Salmonella spp. (InvA), Salmonella Serotypes (fljB, gyrB and ycfQ), Beta lactam resistance including serious ESBL determinants (blaTEM, blaCTX-M).
Results: HRM serotyping successfully revealed the epidemiological prevalence of three Salmonella serotypes from all group B Salmonella isolates, including 38% S. Stanley, 24% S. Typhimurium, and 17% S. Monophasic. Further conventional serotyping showed five unknown HRM patterns as S. Agona, S. Schwarzengrund, S. Saintpaul, S. Brandenburg and one unknown serotype. Fifty-five percent of the isolates showed multidrug-resistant phenotype. The high prevalence of blaTEM gene totally corresponded to the observed ampicillin-resistant phenotype. However, the presence of blaCTX-M group 1 was widely observed but not corresponded to its expected ESBL phenotype. Melt curve analysis of the observed blaCTX-M group 1 amplicons compared with the positive ESBL gene (blaCTX-M -55) showed the high difference in the melting temperature (Tm) of those amplicons which indicated that the observed blaCTX-M group 1 amplicons were less likely to be ESBL gene. Only one ESBL Salmonella isolate from Nan province showed the presence of blaCTX -M group 9 with ESBL phenotype. The highly virulent ESBL Salmonella serovar Typhimurium encoding blaCTX-M group 9 in contaminated minced pork from the Nan province suggested the high alert for the rapid screening of ESBL producing Salmonella spp. in meat and animals to prevent a potential future outbreak.
Conclusion: By performing the molecular analysis, this study successfully revealed the importantly epidemiological aspects of the Salmonella isolates group B collected from the Northern Thailand. This approach should simplify the screening for Salmonella serotypes in minced pork.
Article Details
This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Personal views expressed by the contributors in their articles are not necessarily those of the Journal of Associated Medical Sciences, Faculty of Associated Medical Sciences, Chiang Mai University.
References
[2]. A.D.Grimont, Patrick F-XW. Antigenic formulae of the Salmonella serovars, 9th edition. 9th ed. France; 2007.
[3]. BUREAU OF EPIDEMIOLOGY. DISEASES SURVEILLANCE [Internet]. [cited 2021 Jun 7]. Available from: https://203.157.15.110/boe/home.php
[4]. Pulsrikarn C, Pornreongwong S, Tribuddharat C, Meethai C, Srifuengfung S. Serogroup and Serovar Distribution of Salmonella in Siriraj Hospital. Siriraj Med J 2013; 65(Suppl): s34–7.
[5]. Bangtrakulnonth A, Pornreongwong S, Pulsrikarn C, Sawanpanyalert P, Hendriksen RS, Lo Fo Wong DM a. Salmonella Serovars from Humans and Other Sources in Thailand, 1993-2002. Emerg Infect Dis. 2004; 10(1): 131–6.
[6]. Kim S. Salmonella serovars from foodborne and waterborne diseases in Korea, 1998-2007: Total isolates decreasing versus rare serovars emerging. J Korean Med Sci 2010; 25(12): 1693–9.
[7]. Hendriksen RS, Bangtrakulnonth A, Pulsrikarn C, Pornreongwong S, Hasman H, Song SW. Antimicrobial Resistance and Molecular Epidemiology of Salmonella Rissen from Animals, Food Products, and Patients in Thailand and Denmark. Foodborne Pathog Dis [Internet]. 2008;5(5):605–19. Available from: https://www.liebertonline.com/doi/abs/10.1089/fpd.2007.0075
[8]. Padungtod P, Kaneene JB. Salmonella in food animals and humans in northern Thailand. Int J Food Microbiol 2006; 108(3): 346–54.
[9]. Padungtod P, Kadohira M, Hill G. Livestock production and foodborne diseases from food animals in Thailand. J Vet Med Sci [Internet]. 2008;70(9):873–9. Available from: https://www.ncbi.nlm.nih.gov/pubmed/18840959
[10]. Akyala AI, Alsam S. Extended Spectrum Beta Lactamase Producing Strains of Salmonella species - A Systematic Review. J Microbiol Res 2015; 5(2): 57–70.
[11]. Liebana E, Gibbs M, Clouting C, Barker L, Clifton-Hadley F a, Pleydell E, et al. Characterization of beta-lactamases responsible for resistance to extended-spectrum cephalosporins in Escherichia coli and Salmonella enterica strains from food-producing animals in the United Kingdom. Microb Drug Resist 2004; 10(1): 1–9.
[12]. Cantón R, González-Alba JM, Galán JC. CTX-M enzymes: Origin and diffusion. Front Microbiol 2012; 3: 1–19.
[13]. ISO. 2007. ISO 6579:2007. Microbiology of food and animal feeding stuffs — Horizontal method for the detection of Salmonella spp. Fourth edi. Geneva, Switzerland; 2002.
[14]. O’Regan E, McCabe E, Burgess C, McGuinness S, Barry T, Duffy G, et al. Development of a real-time multiplex PCR assay for the detection of multiple Salmonella serotypes in chicken samples. BMC Microbiol [Internet]. 2008;8(156):1–11. Available from: https://bmcmicrobiol.biomedcentral.com/articles/10.1186/1471-2180-8-156
[15]. Bee KL, Kwai LT. Application of PCR-based serogrouping of selected Salmonella serotypes in Malaysia. J Infect Dev Ctries 2009; 3(6): 420–8.
[16]. Masek BJ, Hardick J, Won H, Yang S, Hsieh YH, Rothman RE, et al. Sensitive detection and serovar differentiation of typhoidal and nontyphoidal Salmonella enterica species using 16S rRNA gene PCR coupled with high-resolution melt analysis. J Mol Diagnostics [Internet]. 2014;16(2):261–6. Available from: https://dx.doi.org/10.1016/j.jmoldx.2013.10.011
[17]. Zeinzinger J, Pietzka AT, Stöger A, Kornschober C, Kunert R, Allerberger F, et al. One-step triplex high-resolution melting analysis for rapid identification and simultaneous subtyping of frequently isolated Salmonella serovars. Appl Environ Microbiol 2012; 78(9): 3352–60.
[18]. CLSI. M100S: Performance Standards for Antimicrobial Susceptibility Testing. 27th ed. M100S, 26th Edition. Wayne, PA, USA: Clinical and Laboratory Standards Institute; 2016.
[19]. Cheng HR, Jiang N. Extremely rapid extraction of DNA from bacteria and yeasts. Biotechnol Lett 2006; 28(1): 55–9.
[20]. Eng S-K, Pusparajah P, Ab Mutalib N-S, Ser H-L, Chan K-G, Lee L-H. Salmonella: A review on pathogenesis, epidemiology and antibiotic resistance. Front Life Sci 2015; 8(3): 284–93.
[21]. Sinwat N, Angkittitrakul S, Coulson KF, Pilapil FMIR, Meunsene D, Chuanchuen R. High prevalence and molecular characteristics of multidrug-resistant Salmonella in pigs, pork and humans in Thailand and Laos provinces. J Med Microbiol [Internet]. 2016;65(10):1182–93. Available from: https://jmm.sgmjournals.org/%0Ahttps://www.cabdirect.org/cabdirect/abstract/20173008111
[22]. Shafini AB, Son R, Mahyudin NA, Rukayadi Y, Tuan Zainazor TC. Prevalence of Salmonella spp. in chicken and beef from retail outlets in Malaysia. Int Food Res J 2017; 24(1): 437–49.
[23]. Bale J, Meunier D, Weill FX, DePinna E, Peters T, Nair S. Characterization of new Salmonella serovars by whole-genome sequencing and traditional typing techniques. J Med Microbiol 2016; 65(10): 1074–8.
[24]. Poonchareon K, Chaiwat Pulsrikarn, Sukon Khamvichai PT, Pakpoom Tadee. The feasibility study of High-Resolution Melting curve analysis and real-time PCR method for a rapid serotyping of frequently isolated Salmonella serovar from hospitalized patients. J Assoc Med Sci 2019; 52(1): 36-40
[25]. Vugia DJ, Samuel M, Farley MM, Marcus R, Shiferaw B, Shallow S, et al. Invasive Salmonella Infections in the United States, FoodNet, 1996–1999: Incidence, Serotype Distribution, and Outcome. Clin Infect Dis 2004; 38(Supplement_3): S149–56.
[26]. Shimoni Z, Pitlik S, Leibovici L, Samra Z, Konigsberger H, Drucker M, et al. Nontyphoid Salmonella Bacteremia: Age‐Related Differences in Clinical Presentation, Bacteriology, and Outcome. Clin Infect Dis 1999; 28(4): 822–7.
[27]. Neuert S, Nair S, Day MR, Doumith M, Ashton PM, Mellor KC, et al. Prediction of phenotypic antimicrobial resistance profiles from whole genome sequences of non-typhoidal Salmonella enterica. Front Microbiol 2018; 9: 1–11.
[28]. Tadee P, Boonkhot P, Pornruangwong S, Patchanee P. Comparative phenotypic and genotypic characterization of Salmonella spp. in pig farms and slaughterhouses in two provinces in northern Thailand. PLoS One 2015; 10(2): 1–11.
[29]. Huoy L, Pornruangwong S, Pulsrikarn C, Chaturongakul S. Molecular Characterization of Thai Salmonella enterica Serotype Typhimurium and Serotype 4,5,12:i:- Reveals Distinct Genetic Deletion Patterns. Foodborne Pathog Dis [Internet]. 2014;11(8):589–92. Available from: https://online.liebertpub.com/doi/abs/10.1089/fpd.2013.1723
[30]. Yang X, Wu Q, Zhang J, Huang J, Guo W, Cai S. Prevalence and characterization of Salmonella serovar 1,4,[5],12:i:-of food origin in China. PLoS One 2015; 10(9): 1–10.
[31]. Soyer Y, Switt a. M, Davis M a., Maurer J, McDonough PL, Schoonmaker-Bopp DJ, et al. Salmonella enterica serotype 4,5,12:i:-, an emerging Salmonella serotype that represents multiple distinct clones. J Clin Microbiol 2009; 47(11): 3546–56.
[32]. Guerra B, Junker E, Miko a, Helmuth R, Mendoza MC. Characterization and Localization of Drug Resistance 2004; 10(2): 83–91.
[33]. Phu Huong Lan N, Le Thi Phuong T, Nguyen Huu H, Thuy L, Mather AE, Park SE, et al. Invasive Non-typhoidal Salmonella Infections in Asia: Clinical Observations, Disease Outcome and Dominant Serovars from an Infectious Disease Hospital in Vietnam. PLoS Negl Trop Dis 2016; 10(8): 1–13.
[34]. Noda T, Murakami K, Etoh Y, Okamoto F, Yatsuyanagi J, Sera N, et al. Increase in Resistance to Extended-Spectrum Cephalosporins in Salmonella Isolated from Retail Chicken Products in Japan. PLoS One [Internet]. 2015;10(2):e0116927. Available from: https://dx.plos.org/10.1371/journal.pone.0116927
[35]. Zhang WH, Lin XY, Xu L, Gu XX, Yang L, Li W, et al. CTX-M-27 producing Salmonella enterica serotypes typhimurium and Indiana are prevalent among food-producing animals in China. Front Microbiol 2016; 7:1-11.
[36]. Dallenne C, da Costa A, Decré D, Favier C, Arlet G. Development of a set of multiplex PCR assays for the detection of genes encoding important β-lactamases in Enterobacteriaceae. J Antimicrob Chemother 2010; 65(3): 490–5.
[37]. Rahn K, Grandis A De, Clarke RC, McEwen S. A, Galin JE, Ginocchio C, et al. Amplification of invA gene of Salmonella by polymerase chain reaction (PCR) as a specific method for detection of Salmonellae. Mol Cell Probes 1992; 6(2): 271–9