Original Article Detecting Virulence Genes Among Salmonella Serovar Infantis Isolated From Poultry Sources

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Introduction
almonella is one of the most important pathogens that cause different illnesses in humans and animals worldwide.This pathogen belongs to the family of Enterobacteriaceae (Lamas et al., 2018).Salmonella is highly prevalent in broilers, poultry feed, and the environment.Moreover, most Salmonella isolates are resistant to many antimicrobials and disinfectants used in medical and poultry practices (Sevilla-Navarro et al., 2019;Jovčić et al., 2020;Belachew et al., 2021;Li et al., 2021).So far, more than 2600 Salmonella serovars have been identified.Some serovars, such as Enteritidis, Infantis, and Typhimurium, have been the most reported isolated serovars throughout the world in recent years (Almeida et al., 2013;Shi et al., 2015;Mishra et al., 2020;Quino et al., 2020;Shome et al., 2020;Yu et al., 2021).Salmonella enterica subspecies enterica serovar Infantis (S.Infantis) can infect humans and animals, including poultry (Wajid et al., 2019).Salmonella Infantis has been one of the most reported serovars from different parts of the world, including Asian, African, European, and American countries (Hendriksen et al., 2011;Fuche et al., 2016;Mejía et al., 2020).The main source of salmonellosis in humans is food-producing animals such as cattle, pig, and poultry (Thorns, 2000;Wessels et al., 2021).Salmonella is transferred to eggs and poultry meat via fecal contamination, and humans are infected with Salmonella when they consume contaminated poultry products (Samiullah et al., 2013).Salmonella infection may cause enteritis and subclinical infections in humans (Antunes et al., 2016;Hindermann et al., 2017;Rincón-Gamboa et al., 2021).
According to the EFSA report (2017), about 50% of all Salmonella isolates reported by all European Union member states were S. Infantis.Moreover, the most common pathogenic serovars for humans were S. Typhimurium, Salmonella Enteritidis, S. Infantis, and Salmonella Derby (EFSA, 2017).More prevalence of S. Infantis among diverse environmental sources suggests that this pathogen can survive in various environmental situations and is still considered a public health concern (EFSA, 2017).
Salmonella serovars can encode and express virulence genes which help the microorganism interact with the host immune system.Various virulence properties play different roles in the pathogenesis of Salmonella in humans and animals.These virulence factors include capsule, flagella, adhesins, virulence plasmids, iron scavenging mechanisms, and the pathogenicity island (PAIs) (Wilharm & Heider, 2014;Elkenany et al., 2019;Lapierre et al., 2020).
Effector proteins, including Salmonella outer protein E (sopE), Salmonella outer protein B (sopB), and Salmonella inner protein A (sipA), are translocated from type III secretion system-1 (T3SS-1), which play a significant role in the attachment and invasion of Salmonella to the host cell.The plasmid-encoded fimbriae A (pefA) has also been reported as another important virulence element at this stage (Fabrega & Vila, 2013).Salmonella iron transporter C (sitC) is needed for the survival and spread of Salmonella in an iron-deficient environment, and its gene (sitC) is expressed from the sitABCD operon in SPI-I (Moest & Méresse, 2013).Salmonella virulence plasmid C (spvC) gene expressed from the operon of spv, which is composed of 5 genes (spvRABCD), is related to the spread of Salmonella serovars in the reticuloendothelial system and the expansion of systemic infection in different hosts (Foley et al., 2013).It may also be necessary to investigate the virulence properties of Salmonella serovars present in poultry intestinal tract during different production phases.
In this study, the presence or absence of 6 important virulence genes, including sipA, sopB, sopE, spvC, pefA, and sitC, were detected among S. Infantis isolates originating from poultry sources and analyzed.

Study samples
A total of 54 S. Infantis isolates recovered from broiler feces, poultry processing, and broiler carcasses from different regions of Iran were chosen from the culture collection of the university (Table 1) (Peighambari et al., 2015).Samples were cultured for regeneration under sterile conditions, next to the flame, by a sterile loop in a brain-heart broth (BHI), which had already been prepared and sterilized in a test tube with the number of each sample written on it and in a shaker incubator.The samples were incubated for 18 to 24 hours.After this time, the samples were taken out of the incubator, and most showed turbidity in the medium, which is a sign of bacterial growth.The samples were cultured again on McConkey's agar (MC) medium, and after 24 hours in the incubator, the samples were removed from the incubator, and single Salmonella colonies were observed.A single colony of these media was cultured again on a brain-heart broth medium with a sterile loop and flame, incubated, and then refrigerated for the next step, DNA extraction.Haghighatnezhad., et al. (2023).Virulence Genes of Salmonella Infantis.Iran J Vet Med, 17(4):363-374.

Salmonella isolation and identification
The genomic DNA of each of the 54 isolates was extracted by boiling method, and the DNA concentration was determined.A total of 500 µL of BHI broth culture was suspended in 350 µL sterile water and placed in boiling water at 100°C for 15 min.Then, the suspension was spun for 5 min, and 70 µL of the supernatant containing chromosomal DNA was used as a template DNA in polymerase chain reaction (PCR) to reconfirm the Salmonella serovar Infantis strains (Kardos et al., 2007;Peighambari et al., 2015).

Molecular detection of genes
A conventional PCR was used to detect the presence or absence of 6 important virulence genes (sopB, sopE, sitC, pefA, sipA, and spvC) in 54 S. Infantis isolates.The primer sequences designed for detecting 6 virulence genes are shown in Table 2.For each isolate, an amplification reaction was prepared in a 25-µL reaction volume containing 2.5 μL 10x PCR buffer, 3 μL of 50 mM MgCl 2 , 0.5 μL of 10 mM dNTPs, 1 μL of each primer, 0.2 μL of Taq DNA polymerase and 14.8 μL of sterile deionized H 2 O. Also, 2 μL of extracted DNA template was added to the mixture.Positive and negative (deionized H 2 O instead of template DNA) controls were included in all reactions (Peighambari et al., 2015;Taheri et al., 2018).Amplification was programmed in a thermocycler (SensoQuest, Germany) as follows: 95 °C for 3 min followed by 30 cycles of denaturation at 94 °C for 1 min, annealing at 61 °C (sitC, sipA, and sopB), 51 °C (spvC), 65 °C (sopE) for 1 min, extension at 72 °C for 1 min and a final extension at 72 °C for 3 min.To detect the pefA gene, the PCR reaction was performed as previously described by Skyberg et al. (2006).All amplified products were detected by gel electrophoresis in 1.5% agarose gel in 1x TAE buffer with the addition of DNA Safe Stain ® (SinaClon) and visualized under UV illumination.Where appropriate, two markers including 100 bp DNA ladder (Yekta Tajhiz Azma, Tehran, Iran) and 100 bp Plus DNA ladder II (Dana Zist Asia, Mashhad, Iran), were employed as MW markers in each gel running.All materials used in PCR reactions were purchased from SinaClon (Tehran, Iran).

Results
All isolates showed the amplified band of 413 bp as a confirmation for the S. Infantis (Figure 1).The 6 virulence genes of S. Infantis, ie, sopB, sopE, sitC, pefA, sipA, and spvC, were detected by conventional PCR in 54 isolates and the results have been demonstrated in Table 3.The sopE gene was identified as the most prevalent virulence gene (Figure 2).The sopE gene was detected in 96.7% of fecal isolates (30/31 isolates), 90% of processing isolates (18/20 isolates), and all of the carcasses' isolates (3/3 isolates).The sitC virulence gene was the second-highest prevalent virulence gene (Figure 3).This virulence gene was positive in 93.5% of fecal isolates (29/31 isolates), 85% of processing isolates (17/20 isolates), and all other isolates.The pefA virulence gene was the third most prevalent virulence gene among isolates (Figure 4).Unlike the previous 2 genes, the highest detection percentage of this gene (52.38%) was in processing isolates (11/20).This gene was detected in 48.3% of fecal isolates (15 isolates out of 31 isolates).But this gene was negative in carcasses' isolates.The sipA gene was the fourth most prevalent virulence gene (Figure 5).This gene was detected in 33.3% of carcass isolates, 32.2% of fecal isolates, and 20% of slaughter isolates.It is noteworthy that the sopB gene was detected only in 16.12% of fecal isolates (10/31) (Figure 6).The spvC virulence gene was not detected in any of the isolates (Table 3).In summary, in the present study, sopE, sitC, pefA, sipA, and sopB virulence genes were detected in 51(94.4%),49(90.7%),26(48.1%),15(27.7%),and 5(9.2%) isolates, respectively.The spvC gene was not found in any of the isolates.

Discussion
Salmonellosis is an important disease that affects human and poultry health.Salmonella Infantis has recently been among the most reported Salmonella serovars worldwide (Mejía et al., 2020).Characterization and detection of virulence genes among S. Infantis isolates obtained from various sources have been the subject of investigations by many researchers worldwide, leading to different findings (Skyberg et al., 2006;Gole et al., 2013;Krawiec et al., 2015;Karacan Sever & Akan, 2019;Garcia-Soto et al., 2020).In Iran, due to a lack of information on the virulence genes of S. Infantis isolates originating from poultry sources, the present study was conducted to determine the presence of the 6 most important virulence genes among S. Infantis isolates recovered from poultry flocks.The investigated virulence genes included sopB, sopE, sitC, pefA, sipA, and spvC among 54 S. Infantis isolates.There were similarities and differences in the presence of virulence genes among our isolates with those of previous investigations, as is described below.
The high prevalence of the sopE virulence gene among S. Infantis isolates was compatible with the previous findings (Hopkins & Threlfall, 2004;Karasova et al., 2009;Karacan Sever & Akan, 2019).Earlier, Hopkins and Threlfall (2004) emphasized the role of the sopE  protein in altering the actin structure that facilitates invasion to the host cell.Also, it has been indicated that mutation in the sopE gene leads to an inability to attack nonpolarized epithelial cell lines (Raffatellu et al., 2005).High frequency (90%) of sope gene presence among S. Infantis isolates originating from poultry processing plants may be considered an intimidating factor because there is a chance of human infection with these isolates due to the consumption of infected poultry products.
The presence of the sitC virulence gene was very high among isolates which were comparable with the find-ings of previous investigations (Skyberg et al., 2006;Gole et al., 2013;Krawiec et al., 2015;Karacan Sever & Akan, 2019;Dantas et al., 2020).Previous works have emphasized the importance of the sitC virulence gene for the survival and multiplication of Salmonella in irondeficient environments (Zhou et al., 1999;Elemfareji & Thong, 2013).sipA protein is encoded by genes located on Salmonella pathogenicity island I, and also, this protein is a main virulence property of Salmonella that accelerates the entry of Salmonella into the host cell (Raffatellu et   , 2005).The absence of sipA in the early stage of the pathogenesis of Salmonella usually reduces the invasion of this bacteria to host cells (Perrett & Jepson, 2009).Unlike the findings reported previously (Almeida et al., 2013;Figueiredo et al., 2015;Karacan Sever & Akan, 2019;Dantas et al., 2020;Lapierre et al., 2020), a somewhat low positive rate of sipA gene presence (27.7%) was observed among the isolates of this study.
Both sopB and pefA proteins have important roles in host recognition and invasion (Tarabees et al., 2017).Contrary to the previously reported investigations (Karasova et al., 2009;Huehn et al., 2010;Almeida et al., 2013;Gole et al., 2013;Karacan Sever & Akan, 2019;Dantas et al., 2020), the presence of sopB gene, in the present study, was found in 5 S. Infantis isolates (9.2%) only.The role of fimbria, encoded by the pefA gene, in the adhesion phase of Salmonella and the ability of this pathogen to adhere to different sites of the host cells and pathogenicity have been previously reported by other researchers (Elemfareji & Thong, 2013;Figueiredo et al., 2015).Our findings for the presence of the pefA gene among S. Infantis isolates were compatible with those of Figueiredo et al. (2015) and Krawiec et al. (2015) but not with results reported by Karacan Sever & Akan (2019).In the present investigation, in 26 isolates (48.1%), the pefA gene was detected, but Karacan Sever and Akan (2019) reported 1 positive isolate (0.44%) only.
The contribution of Salmonella virulence plasmid C to the spread of Salmonella serovars in the reticuloendothelial system and the expansion of systemic infection in different hosts have been documented by some researchers (Foley et al., 2013;Krzyzanowski et al., 2014).In this study, no S. Infantis isolate was positive for the presence of the spvC gene, unlike the findings of previous researchers (Huehn et al., 2010;Krzyzanowski et al., 2014;Figueiredo et al., 2015;Karacan Sever & Akan, 2019).The reason for this difference may be related to the fact that the number of our tested isolates was lower than those of previous studies.

Conclusion
The current investigation examined the presence of 6 virulence genes among 54 Salmonella serovar Infantis isolates originating from poultry sources in Iran.A considerably identical profile was found on virulence genes' presence between isolates recovered from broiler feces and poultry processing plants sources that may be a cause of concern for health authorities.However, more Salmonella serovar Infantis isolates obtained from various poultry sources and human should be examined and analyzed to reinforce these findings.This survey can help the health authorities better understand the pathogenesis and epidemiology of S. Infantis in Iran.

Figure 1 .
Figure 1.Electrophoresis of PCR products on 1% agarose gel to confirm Salmonella Infantis Amplified 413 bp bands of 5 isolates are shown in lanes 3 to 7. Lanes M, C+, and C-indicate commercial 100 bp plus DNA ladder II, positive control, and negative control (dH 2 O instead of DNA), respectively.Other lanes demonstrate negative results for tested Salmonella isolates.

Figure 2 .
Figure 2. Electrophoresis of PCR products on 1% agarose gel to confirm the presence of sopE gene Amplified 376 bp bands of isolates are shown in lanes 1 to 6. Lanes M, C+, and C-indicate commercial 100 bp DNA ladder, positive control, and negative control (dH 2 O instead of DNA), respectively.

Figure 3 .
Figure 3. Electrophoresis of PCR products on 1% agarose gel to confirm the presence of sitC gene Amplified 768 bp bands of isolates are shown in lanes 1 to 7. Lanes M, C+, and C-indicate commercial 100 bp DNA ladder, positive control, and negative control (dH 2 O instead of DNA), respectively.

Figure 4 .
Figure 4. Electrophoresis of PCR products on 1% agarose gel to confirm the presence of pefA gene Amplified 157 bp bands of isolates are shown in lanes 3, 5, and 6.Lanes M, C+, and C-indicate commercial 100 bp DNA ladder, positive control, and negative control (dH 2 O instead of DNA), respectively.Other lanes demonstrate negative results for the tested pefA gene.

Figure 5 .
Figure 5. Electrophoresis of PCR products on 1% agarose gel to confirm the presence of sipA gene.Amplified 2055 bp bands of isolates are shown in lanes 1, 4, and 5. Lanes M, C+, and C-indicate commercial 100 bp Plus DNA ladder II, positive control, and negative control (dH 2 O instead of DNA), respectively.Other lanes demonstrate negative results for the tested sipA gene.

Figure 6 .
Figure 6.Electrophoresis of PCR products on 1% agarose gel to confirm the presence of sopB gene.Amplified 1987 bp bands of isolates are shown in lanes 1, 3, and 5. Lanes M, C+, and C-indicate commercial 100 bp plus DNA ladder II, positive control, and negative control (dH 2 O instead of DNA), respectively.Other lanes demonstrate negative results for the tested sopB gene.

Table 1 .
Origins of Salmonella Infantis isolates of the study

Table 2 .
Primer sequences used for the detecting virulence genes in Salmonella Infantis

Table 3 .
The results for detected virulence genes among 54 Salmonella Infantis isolates