Next Article in Journal
Transcriptome Studies Reveal the N6-Methyladenosine Differences in Testis of Yaks at Juvenile and Sexual Maturity Stages
Previous Article in Journal
African Swine Fever in Wild Boar: German Hunters’ Perception of Surveillance and Control—A Questionnaire Study
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Salmonella Control in Fattening Pigs through the Use of Esterified Formic Acid in Drinking Water Shortly before Slaughter

by
María Bernad-Roche
1,
Clara María Marín-Alcalá
2,
Juan Pablo Vico
3 and
Raúl Carlos Mainar-Jaime
1,*
1
Departamento de Patología Animal, Facultad de Veterinaria, Instituto Agroalimentario de Aragón-IA2, Universidad de Zaragoza-CITA, 50013 Zaragoza, Spain
2
Departamento de Ciencia Animal, Centro de Investigación y Tecnología Agroalimentaria de Aragón, Instituto Agroalimentario de Aragón-IA2, Universidad de Zaragoza-CITA, 50059 Zaragoza, Spain
3
IRNASUS-CONICET-Universidad Católica de Córdoba, Facultad de Ciencias Agropecuarias, Universidad Católica de Córdoba, Córdoba 5000, Argentina
*
Author to whom correspondence should be addressed.
Animals 2023, 13(18), 2814; https://doi.org/10.3390/ani13182814
Submission received: 14 August 2023 / Revised: 28 August 2023 / Accepted: 4 September 2023 / Published: 5 September 2023
(This article belongs to the Section Pigs)

Abstract

:

Simple Summary

Salmonellosis is a public health concern, and Salmonella-shedding pigs at the abattoir are one of the main sources of human infection. In this study, an esterified formic acid was applied as an on-farm treatment at a dose of 10 kg of product per 1000 L of water five days before slaughter. It was found that it could significantly reduce the proportion of Salmonella-shedding pigs arriving at the slaughterhouse and the Salmonella loads in the guts of the shedder pigs. These promising results suggest that this esterified formic acid could be used in farm drinking water a few days before slaughter as a complementary mitigation strategy for Salmonella control.

Abstract

The presence of Salmonella in pig feces is a major source of abattoir and carcass contamination, and one of the main sources of human salmonellosis. This study assessed whether using a form of esterified formic acid (30% formic acid) in drinking water (10 kg/1000 L) 5 days before slaughter could be a helpful strategy to mitigate this public health issue. Thus, 240 pigs from three Salmonella-positive commercial fattening farms were selected. From each farm, 40 pigs were allocated to a control group (CG) and 40 to a treatment group (TG). At the abattoir, fecal samples from both groups were collected for Salmonella detection (ISO 6579-1:2017) and quantification (ISO/TS 6579-2:2012). Salmonella was present in 35% (95% IC = 29.24–41.23) of the samples collected. The prevalence was significantly higher in the CG than in the TG (50% vs. 20%; p < 0.001). In all farms, the TG showed a lower percentage of shedders than the CG. A random-effects logistic model showed that the odds of shedding Salmonella were 5.63 times higher (95% CI = 2.92–10.8) for the CG than for the TG. Thus, the proportion of pigs shedding Salmonella that was prevented in the TG due to the use of this form of organic acid was 82.2%. In addition, a Chi-squared analysis for trends showed that the higher the Salmonella count, the higher the odds of the sample belonging to the CG. These results suggest that adding this type of acid to drinking water 5 days before slaughter could reduce the proportion of Salmonella-shedding pigs and the Salmonella loads in the guts of shedder pigs.

1. Introduction

Salmonella infection is a major cause of foodborne outbreaks in the European Union and the second most frequently reported zoonosis in humans [1]. Although most Salmonella-infected pigs may not display any symptoms, they act as carriers of the infection, and contaminated pork and product thereof are among the most common sources of human infection [1].
Pork usually becomes contaminated at the abattoir, and the primary source of the contamination of abattoirs is the presence of Salmonella in the feces of slaughter pigs [2,3]. The proportion of slaughter pigs showing high loads of Salmonella in the cecal content appears to be directly related to the number of contaminated carcasses in the abattoir [4]. Therefore, reducing the number of pigs shedding Salmonella, and/or their intestinal loads of these bacteria, at the time they arrive to the abattoir can be foreseen as an important step to reduce overall abattoir environmental contamination and the proportion of contaminated carcasses.
Most shedding pigs become infected when still on the farm; thus, different approaches have been suggested to reduce the transmission of Salmonella infection within farms. For instance, enhancing farm biosecurity and improving cleaning and disinfection are considered some of the most important measures to control Salmonella in indoor settings [5,6]. However, proper levels of biosecurity will not necessarily reduce farm Salmonella prevalence [7,8,9], likely because its routine implementation and maintenance depend upon the farmers’ perception of the problem [10,11], and pig salmonellosis is considered of low concern for pig producers.
Vaccination has also been proposed for on-farm Salmonella control, and there are some commercially available vaccines against Salmonella infection in pigs [12]. Results from vaccine studies suggest that they may help to somehow reduce Salmonella shedding from specific serotypes [13], but cross-protection against different serotypes is unlikely [12]. Since pigs may be infected by many of them [14], vaccination alone may not be enough.
Another general on-farm strategy against Salmonella is the administration of organic acids (OAs) through feed or water. However, their efficacy against Salmonella has been found to be very variable, with a number of studies showing some positive results [15,16,17,18,19,20,21,22,23,24] but others not observing any effect [25,26,27]. This variability may be attributed to several factors, such as the type, form, dose, and duration of the treatment applied; the pig’s age [28]; or even infections occurring during transport or lairage in the slaughterhouse [29].
The efficacy of OAs is based on their presence, in appropriate amounts, along the gastrointestinal tract, particularly in its distal parts (the cecum and large intestine), where Salmonella is more commonly found [30,31,32]. Lowering the pH in both the extra- and intra-cellular environment is the main mechanism by which OAs prevent Salmonella viability [33,34]. However, as mentioned before, most fattening pigs usually become infected with Salmonella while on the farm and, to a lesser extent, during transport or lairage [35,36]. After infection, pigs may shed large amounts of bacteria for a few days, after which Salmonella may remain silent within tonsils and lymph nodes, with no shedding until after a stressful situation occurs, such as the transport to the abattoir or while pigs are held in lairage [37,38,39]. Since a 12–18 h fasting is usually required before slaughtering, any in-feed treatment may not be effective to control Salmonella shedding when pigs arrive at the abattoir, as not enough OA is left within the intestine. In-feed treatments may then help to reduce the level of shedding while pigs are on the farm, but they may not prevent shedding during transport or at the slaughter of pigs already infected on the farm [21].
On the contrary, administering OA through farm water may have the advantage that pigs would have access to OA even during fasting, thus receiving the treatment until the moment that they are loaded onto the truck. Thus, depending upon the duration of the transport, treatment through drinking water could prolong the presence of OA in the gastrointestinal tract almost until the time of slaughter. However, as noted earlier, the effectiveness of OA treatment in this way may also vary depending on various factors. To optimize the effectiveness of OA treatment through water, researchers have investigated different types, forms, and doses of OA. Short- and medium-chain fatty acid glycerides combined with glycerol present an amphipathic structure that makes them soluble in water while maintaining their in vitro and in vivo efficacy against Gram-negative bacteria [40]. In addition, due to their glyceride form, these OAs are odorless and non-corrosive.
A previous study suggested that the esterified form of formic acid could be effective in decreasing the prevalence of pigs shedding Salmonella at slaughter when administered in drinking water during lairage at the abattoir. Although the treatment was applied overnight and for only a few hours before slaughter, a significant reduction in the prevalence of shedders in the TG was observed (16.4%; [41]). This finding suggests that on-farm water treatment for a longer time with this esterified OA could be a useful strategy to decrease the prevalence of Salmonella shedding at slaughter. Thus, this research aimed to investigate the efficacy of this OA when administered in drinking water a few days before slaughter as a potential strategy for reducing the number of pigs shedding Salmonella at slaughter and the Salmonella loads in the gastrointestinal tract of fattening pigs.

2. Materials and Methods

2.1. Experimental Design and Farm Sampling

Three replicates of a field trial were carried out between May and November 2022 on three different commercial pig farms located in the NE of Spain. Each farm was composed of different fattening units (average size of 1000 animals/fattening unit), two of which were selected for this study. One was assigned as the treatment group (TG) and the other as the control group (CG). Within each farm, the selection of the two fattening units to be included was based on the following criteria: (i) animals came from the same sow herd and had a similar age (less than a one-week difference) and (ii) both fattening units were Salmonella-positive. Within a farm, the TG was always assigned to the fattening unit with the highest seroprevalence.
To confirm the presence of Salmonella in the fattening units and to assess their Salmonella status before starting the trial, pooled floor fecal samples (PFFs) from 10 representative pens and 30 individual blood samples from pigs distributed along the fattening unit (1 pig per pen) were collected in each unit approximately one month before slaughter.

2.2. Product Used

A formic acid (30% formic acid) esterified in the form of mono-, di-, and tri-glyceride with glycerol (MOLI-M C1, Molimen SL, Barcelona, Spain) was selected for the treatment group. It was applied at a dose of 10 kg of product per 1000 L of farm drinking water (EMEC AMS PLUS dosing pump, EMEC, Fitchburg, MA, US). This dose of product (10 g/kg) was below the maximum threshold value of 12 g/kg formic acid approved for the use in pigs in the European Union [42]. The treatment began 5 days before slaughter. Pigs fasted for an average of 18 h before being transported to the abattoir, but the treatment in the drinking water supply was continued until the moment that they were loaded onto the truck.

2.3. Slaughter Sampling

Animals from each group (CG and TG) were slaughtered separately, always beginning with the CG on one day and the TG one or two days later. The farms were less than 2 h from the abattoir, and all animals were transported on the day of slaughter. At the slaughter line, individual gastrointestinal tracts were collected from 40 pigs from each group. They were selected among all the pigs sent for slaughter in that batch (around 200 pigs), following a systematic sampling (one every three–four pigs) and avoiding any pig showing intestinal rupture during evisceration. Intestinal (colon) content (IC) samples were further collected and submitted to the laboratory for immediate processing.

2.4. Isolation and Quantification of Salmonella

Salmonella isolation from the PFF and IC samples was carried out according to the standard ISO 6579-1:2017 method [43]. The quantification of Salmonella was performed on 10 IC samples selected randomly per group and per trial (except for farm 1, where only 9 were analyzed due to 1 being inadvertently forgotten) following the miniaturized Most Probable Number (MPN) enumeration method (ISO/TS 6579-2:2012 [44]). Briefly, in a 4 × 3-well microtiter plate, 2.5 mL of the initial 1:10 buffered peptone water (BPW) suspension used for isolation was transferred to each of the three wells of the first column. Then, 500 µL from each well was transferred and mixed with 2 mL of BPW in the wells from the second column. Dilutions were performed in the same way in the third and fourth columns making a total of 4 dilutions (1:10, 1:50, 1:250, 1:1250) for each sample to be analyzed. Each sample was analyzed in triplicate. Dilutions were incubated at 37 °C ± 1 °C for 18 h ± 2 h. Then, 20 µL of each BPW dilution was transferred onto MRSV plates and incubated at 41.5 °C ± 1 °C for 24 h ± 3 h for selective enrichment. Negative wells after 24 h were further incubated for up to 48 h. Suspect wells of (at least) the highest dilution(s) were plated out on selective isolation medium XLD at 37 °C ± 1 °C for 24 h ± 3 h. From each plate, a characteristic colony was biochemically tested (indole reaction, urea and triple sugar iron agar tests, and L-lysine decarboxylation) (Panreac Química SAU, Castellar del Vallés, Spain) for definitive confirmation. The MPN characteristic number was obtained by counting the number of positive wells in the 4 dilution × 3 repetition system used. Then, MPN was generated using the MPN calculation program version 6 [45]. The results are expressed as MPN per mL or g. The detection limit of the mini-MSRV method is approximately 1 CFU/g.

2.5. Serological Analysis

The Herdcheck Swine Salmonella ELISA test (IDEXX Laboratories, Westbrook, ME, USA) was employed according to the manufacturer’s guidelines to detect specific antibodies (IgG) directed against Salmonella. For seroprevalence estimates, and due to the test’s limited sensitivity and specificity on field samples (73% and 95%, respectively; [46]), a cut-off value of OD% ≥ 40 was used to deem a pig seropositive.

2.6. Statistical Analyses

To assess the efficacy of the treatment in each trial, Fischer’s exact test was used to compare the prevalence of Salmonella shedding at slaughter between the CG and the TG. Further, a random-effects logistic regression analysis, considering the results from all the trials together, was carried out to obtain an overall estimate of the effect of the treatment on the prevalence of Salmonella shedding at slaughter. For this purpose, the presence of Salmonella in the IC samples was considered as the dependent variable and the treatment as the independent one. The farm was considered as the random (grouping) variable to account for the likely correlation among individuals within the same farm. The Odds Ratio (OR) between the CG and TG and its corresponding 95% confidence interval (95% CI) were estimated, and from these, an estimate of the proportion of pigs that may have been prevented from shedding because of the use of the OA, that is, the attributable fraction (AF), was calculated as OR-1/OR [47].
The Most Probable Number results were categorized into four groups: (1) ND, not detected (below the limit of detection); (2) between 0.02 and 20.00 CFU/g; (3) between 21 and 200; and (4) exceeding the limits for counting (∞). A Chi-square analysis for linear trends was applied to compare the MPN categories between the CG and TG for all the trials together. These statistical analyses were performed using STATA software (STATA/IC 12.1. Stata-Corp. LP, College Station, TX, USA).

3. Results

3.1. Farm Salmonella Status Prior to the Trial

One month before starting the trials, the Salmonella status of all the farms was assessed, and the fattening units were selected. In all of the units included in this study, Salmonella was detected, with all presenting 10% of pens positive for Salmonella (Table 1). With regard to the serological results, the farms’ overall seroprevalences (considering the two selected fattening units) were 21.6% in farm 1, 38.3% in farm 2, and 48.3% in farm 3. In two farms (1 and 2), no significant differences in seroprevalence were found between the two selected fattening units. In farm 3, however, in one of the units, the seroprevalence was significantly higher than that of the other one (63.3% vs. 33.3%) (Table 1).

3.2. Salmonella Shedding at Slaughter

In farm 1, a high proportion of Salmonella shedders was observed in both groups, but this proportion was significantly higher in the CG than in the TG (65% vs. 27.5%, respectively; p = 0.0015) (Table 2). The odds of Salmonella shedding in the CG were almost 5 times higher than in the TG (OR = 4.9; 95% CI = 1.9–12.7). The MPN results showed higher counts of Salmonella in the CG than in the TG. Salmonella was not detected in 88.9% (eight out of nine) of the samples from the TG or in 55.6% (five out of nine) of the samples from the CG, while there was one sample exceeding the limits for counting in both groups (Table 3).
In farm 2, an overall low Salmonella-shedding prevalence was observed. Salmonella was not detected in the TG, while the CG showed few pigs shedding Salmonella (0% vs. 12.5%; p = 0.055) (Table 2). Regarding the MPN results, in the CG, only one positive Salmonella sample was detected, with low counts (3.8 MPN/g). No Salmonella-positive samples were detected in the TG (Table 3).
In farm 3, a high Salmonella-shedding prevalence was observed in both groups. More shedder pigs were found in the CG than in the TG (72.5% vs. 32.5%, respectively; p = 0.0007) (Table 2). The odds of Salmonella shedding in the control group were more than 5 times higher than in the TG (OR = 5.5; 95% CI = 2.1–14.3). The MPN results showed higher counts of Salmonella in the CG than in the TG. Salmonella was not detected in 77.8% (seven out of nine) of the samples from the TG or in 44.4% (four out of nine) of the samples from the CG. There were no samples exceeding the limits for counting in the TG, while there were three samples in the CG.

3.3. Overall Results for the Three Farms

In 84 out of the 240 IC samples collected, Salmonella was present (35%; 95% IC = 29.24–41.23), and the prevalence was significantly higher in the CG than in the TG (50% vs. 20%; p < 0.001).
An overall significant reduction in the proportion of Salmonella shedders was observed in the TG after adjusting for the effect of the farm. The odds of shedding Salmonella at slaughter were almost 6 times higher for the CG than for the TG (Table 4). Thus, the proportion of pigs shedding Salmonella that had been prevented due to the use of this OA in the TG (the AF) was 82.2%.
From the 58 samples recovered for the MPN analysis, Salmonella was detected (>1 CFU/g) in 15 of them (51.7%). Out of these 15, 11 (73.3%) belonged to the CG and 4 (13.8%) to the TG (p = 0.069). In addition, 13.8% (4/29) of the samples from the CG and 3.4% (1/29) of the samples from the TG were above the limit of counting. In general, and despite the low number of samples analyzed, a significant linear trend was observed: the higher the MPN count, the higher the odds of the sample belonging to the CG (Table 5).

4. Discussion

Three pig farms were selected based on serological and bacteriological evidence indicating that Salmonella was present. The mean serological values before the trial for these farms (21.6% in farm 1; 38.3% in farm 2; and 48.3% in farm 3) were within levels that would classify them within a category of risk, according to some national control programs [48,49,50,51]. In addition, the bacteriological study of the pens showed that Salmonella was present in the three farms, and this factor, along with medium–high levels of seroprevalence, has been directly related to Salmonella shedding at slaughter [9]. Thus, under this scenario, a considerable proportion of pigs were expected to shed Salmonella at slaughter. Indeed, 35% of the pigs in this study shed Salmonella, with this figure being even higher than that found in a previous large-scale study carried out in the same region (23.6%; [9]). Finding fattening pig farms with significant levels of seroprevalence and Salmonella in the pens is quite common in Spain [9,52]. Considering the risk that this situation poses for the contamination of carcasses at slaughterhouses [2,3], and the difficulties (and lack of cost-effectiveness) of the strategies in reducing the overall level of Salmonella infection at farms [53,54], the search for new and affordable on-farm interventions that mitigate this problem seems unavoidable.
OAs in the form of salts, and in particular formic acid, have been commonly used in livestock production to promote growth, improve feed conversion, and reduce the prevalence of specific bacterial infections [42,55,56]. Their application in esterified form is less known, but in recent years, there has been increasing interest in the potential of esterified acids to reduce the shedding of Salmonella in pigs [41,57]. Their enhanced antimicrobial effects against Gram-negative pathogens would arise from their diminished pH sensitivity and increased resistance to enzymatic breakdown compared to other acidic formulations. This would lead to their efficacy being observed throughout the entire gastrointestinal tract [58].
Ref. [41] showed that this esterified form of formic acid was somewhat effective when administrated for a short period of time (an average of 14 h); thus, it was expected that using the same dose (10 L/1000 L of drinking water) but increasing the time of exposure (5 days) would improve its effect.
When analyzing the results by farm, a common trend was observed; that is, on all the farms, the TG showed a lower percentage of shedders than the CG, which could be considered an indication of the positive effect of this treatment on the control of Salmonella shedding. On two of the farms (1 and 3), the reductions achieved were around 40% when compared to the CG (Table 2), but on farm 2, the differences were not so obvious, with a reduction of just 12.5%. However, the latter was likely a consequence of the low overall proportion of shedders from this farm. Although this farm presented a high seroprevalence when tested prior to the beginning of the trial, different unregistered factors could help to explain this situation, i.e., those associated with lower levels of pig stress.
An analysis of the raw data suggested an overall reduction in shedding of about 30% (20% in the TG vs. 50% in the CG). However, because of the likely differences that could be found among pig farms, a statistical analysis accounting for the grouping effect of the farm was considered. According to the results of the random-effects logistic model, pigs from the CG had 5.63 (95% CI = 2.92–10.8) higher odds of shedding Salmonella at slaughter than pigs from the TG. This result indicates that the efficacy of this treatment to reduce the proportion of pigs shedding Salmonella may reach up to 82.2%. These figures are much higher than those obtained in the previous study carried out (OR = 2.8; AF = 64.3%; [41]), indicating that an increased time of exposure to the OA had a larger beneficial effect.
The amount of Salmonella shedding is also another parameter that should be influenced by the treatment, as OA would kill many salmonellae in the gut. Therefore, a lower number of them would be expected in animals from the TG. The Most Probable Number (MPN) enumeration method was used to determine whether this OA had some effect on the number of bacteria shed. This method is time-consuming and requires the analysis of the sample to be started before knowing whether it is Salmonella-positive. For that reason, only 10 random samples per group were considered (except for farm 1, where only 9 were used).
As expected, and despite the limited number of samples analyzed, the number of negative ones (below the level of detection for the MPN analysis) was higher in the TG than in the CG (86.2% vs. 62.1%, respectively; p = 0.069). But also, among the positive samples, the load of Salmonella was lower in the TG. Only one sample exceeded the limits for counting (∞), and the other three samples were within the lower MPN category (0.02–20 CFU/g). By contrast, in the CG, most of the positive samples (6 out of 11) had counts above 21 CFU/g. As shown in the analysis for trends, higher MPN counts were more likely to belong to the CG (Table 5). These results support the effectiveness of this treatment to reduce the load of Salmonella in the pig’s gut. Since there appears to be a positive association between high cecal Salmonella loads in pigs and carcass contamination [4], the use of this esterified form of formic acid should be considered as a potential alternative to decrease the risk of Salmonella carcass contamination at slaughter.
In a previous study, it was shown that the risk, for a batch of fattening pigs, of shedding Salmonella at slaughter could be predicted before the pigs were sent to slaughter [9]. Therefore, this product could be applied in the drinking water of the farm, five days prior to slaughter, for batches of pigs identified as at risk of shedding Salmonella. It could also be included in the drinking water of the abattoir, helping to reduce the probability of shedding even more [41]. However, further studies applying different treatment protocols should be conducted to try to reduce treatment time or product dose in order to minimize the cost associated with this strategy.

5. Conclusions

On Salmonella-positive farms, the administration to fattening pigs of this esterified formic acid through water, five days prior to slaughter, decreased the proportion of pigs shedding Salmonella at slaughter and the loads of Salmonella in the guts of pigs still shedding. Thus, this intervention may likely help to reduce abattoir and carcass contamination. These findings highlight the potential of esterified formic acid as an on-farm strategy for Salmonella control in pig production, being a feasible mitigation measure to be applied as a complement to other measures in the farm–slaughterhouse interface.

Author Contributions

Conceptualization, R.C.M.-J.; methodology, R.C.M.-J., M.B.-R. and C.M.M.-A.; formal analysis, R.C.M.-J. and M.B.-R.; investigation, R.C.M.-J., M.B.-R., J.P.V. and C.M.M.-A.; writing—original draft preparation, M.B.-R., R.C.M.-J. and J.P.V.; writing—review and editing, M.B.-R., R.C.M.-J., J.P.V. and C.M.M.-A.; supervision, R.C.M.-J.; project administration and funding acquisition, R.C.M.-J. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by grant RTI2018-093915-B-I00 funded by MCIN/AEI/10.13039/501100011033 and “ERDF A way of making Europe” from the European Union.

Institutional Review Board Statement

This study was approved by the Ethical Advisory Commission for Animal Experimentation of the University of Zaragoza (permit no. PI13/20).

Informed Consent Statement

Not applicable.

Data Availability Statement

Data available upon request.

Acknowledgments

We thank the pig production companies and their technical staff, the farmers, and the abattoirs for their support and collaboration in carrying out the fieldwork.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. European Food Safety Authority (EFSA) and European Centre for Disease Prevention and Control (ECDC). The European Union One Health 2021 Zoonoses Report. EFSA J. 2022, 20, 7666. [Google Scholar]
  2. Argüello, H.; Alvarez-Ordoñez, A.; Carvajal, A.; Rubio, P.; Prieto, M. Role of slaughtering in Salmonella spreading and control in pork production. J. Food Prot. 2013, 76, 899–911. [Google Scholar] [CrossRef] [PubMed]
  3. Swart, A.N.; Evers, E.G.; Simons, R.L.; Swanenburg, M. Modeling of Salmonella Contamination in the Pig Slaughterhouse. Risk Anal. 2016, 36, 498–515. [Google Scholar] [CrossRef]
  4. Pesciaroli, M.; Cucco, L.; De Luca, S.; Massacci, F.R.; Maresca, C.; Medici, L.; Paniccià, M.; Scoccia, E.; Staffolani, M.; Pezzotti, G.; et al. Association between pigs with high caecal Salmonella loads and carcass contamination. Int. J. Food Microbiol. 2017, 242, 82–86. [Google Scholar] [CrossRef] [PubMed]
  5. De Lucia, A.; Ostanello, F. On-farm risk factors associated with Salmonella in pig herds. Large Anim. Rev. 2020, 26, 133–140. [Google Scholar]
  6. Galipó, E.; Zoche-Golob, V.; Sassu, E.L.; Prigge, C.; Sjölund, M.; Tobias, T.; Rzeżutka, A.; Smith, R.P.; Burow, E. Prioritization of pig farm biosecurity for control of Salmonella and hepatitis E virus infections: Results of a European expert opinion elicitation. Porc. Health Manag. 2023, 9, 8. [Google Scholar] [CrossRef]
  7. Alarcón, L.V.; Allepuz, A.; Mateu, E. Biosecurity in pig farms: A review. Porc. Health Manag. 2021, 7, 5. [Google Scholar] [CrossRef] [PubMed]
  8. Youssef, D.M.; Wieland, B.; Knight, G.M.; Lines, J.; Naylor, N.R. The effectiveness of biosecurity interventions in reducing the transmission of bacteria from livestock to humans at the farm level: A systematic literature review. Zoonoses Public Health 2021, 68, 549–562. [Google Scholar] [CrossRef]
  9. Bernad-Roche, M.; Marín-Alcalá, C.M.; Cebollada-Solanas, A.; de Blas, I.; Mainar-Jaime, R.C. Building a prediction model for assessing the risk of Salmonella shedding at slaughter in fattening pigs. Front. Microbiol. 2023, 14, 1232490. [Google Scholar] [CrossRef]
  10. Fraser, R.W.; Williams, N.T.; Powell, L.F.; Cook, A.J. Reducing Campylobacter and Salmonella infection: Two studies of the economic cost and attitude to adoption of on-farm biosecurity measures. Zoonoses Public Health 2010, 57, e109–e115. [Google Scholar] [CrossRef]
  11. Marier, E.; Piers Smith, R.; Ellis-Iversen, J.; Watson, E.; Armstrong, D.; Hogeveen, H.; Cook, A.J.C. Changes in perceptions and motivators that influence the implementation of on-farm Salmonella control measures by pig farmers in England. Prev. Vet. Med. 2016, 133, 22–30. [Google Scholar] [CrossRef]
  12. Bearson, S.M.D. Salmonella in Swine: Prevalence, Multidrug Resistance, and Vaccination Strategies. Annu. Rev. Anim. Biosci. 2022, 10, 373–393. [Google Scholar] [CrossRef] [PubMed]
  13. De La Cruz, M.L.; Conrado, I.; Nault, A.; Perez, A.; Dominguez, L.; Alvarez, J. Vaccination as a control strategy against Salmonella infection in pigs: A systematic review and meta-analysis of the literature. Res. Vet. Sci. 2017, 114, 86–94. [Google Scholar] [CrossRef] [PubMed]
  14. Garrido, V.; Sánchez, S.; San Román, B.; Zabalza-Baranguá, A.; Díaz-Tendero, Y.; de Frutos, C.; Mainar-Jaime, R.C.; Grilló, M.J. Simultaneous infections by different Salmonella strains in mesenteric lymph nodes of finishing pigs. BMC Vet. Res. 2014, 10, 59. [Google Scholar] [CrossRef] [PubMed]
  15. Van der Wolf, P.J.; Wolbers, W.B.; Elbers, A.R.; van der Heijden, H.M.; Koppen, J.M.; Hunneman, W.A.; van Schie, F.W.; Tielen, M.J. Herd level husbandry factors associated with the serological Salmonella prevalence in finishing pig herds in The Netherlands. Vet. Microbiol. 2001, 78, 205–219. [Google Scholar] [CrossRef] [PubMed]
  16. Papenbrock, S.; Stemme, K.; Amtsberg, G.; Verspohl, J.; Kamphues, J. Investigations on prophylactic effects of coarse feed structure and/or potassium diformate on the microflora in the digestive tract of weaned piglets experimentally infected with Salmonella Derby. J. Anim. Physiol. Anim. Nutr. 2005, 89, 84–87. [Google Scholar] [CrossRef]
  17. Creus, E.; Pérez, J.F.; Peralta, B.; Baucells, F.; Mateu, E. Effect of acidified feed on the prevalence of Salmonella in market-age pigs. Zoonoses Public Health 2007, 54, 314–319. [Google Scholar] [CrossRef]
  18. Boyen, F.; Haesebrouck, F.; Vanparys, A.; Volf, J.; Mahu, M.; Van Immerseel, F.; Rychlik, I.; Dewulf, J.; Ducatelle, R.; Pasmans, F. Coated fatty acids alter virulence properties of Salmonella Typhimurium and decrease intestinal colonization of pigs. Vet. Microbiol. 2008, 132, 319–327. [Google Scholar] [CrossRef]
  19. Taube, V.A.; Neu, M.E.; Hassan, Y.; Verspohl, J.; Beyerbach, M.; Kamphues, J. Effects of dietary additives (potassium diformate/organic acids) as well as influences of grinding intensity (coarse/fine) of diets for weaned piglets experimentally infected with Salmonella Derby or Escherichia coli. J. Anim. Physiol. Anim. Nutr. 2009, 93, 350–358. [Google Scholar] [CrossRef]
  20. Visscher, C.F.; Winter, P.; Verspohl, J.; Stratmann-Selke, J.; Upmann, M.; Beyerbach, M.; Kamphues, J. Effects of feed particle size at dietary presence of added organic acids on caecal parameters and the prevalence of Salmonella in fattening pigs on farm and at slaughter. J. Anim. Physiol. Anim. Nutr. 2009, 93, 423–430. [Google Scholar] [CrossRef]
  21. Argüello, H.; Carvajal, A.; Costillas, S.; Rubio, P. Effect of the addition of organic acids in drinking water or feed during part of the finishing period on the prevalence of Salmonella in finishing pigs. Foodborne Pathog. Dis. 2013, 10, 842–849. [Google Scholar] [CrossRef] [PubMed]
  22. Lynch, H.; Leonard, F.C.; Walia, K.; Lawlor, P.G.; Duffy, G.; Fanning, S.; Markey, B.K.; Brady, C.; Gardiner, G.E.; Argüello, H. Investigation of in-feed organic acids as a low cost strategy to combat Salmonella in grower pigs. Prev. Vet. Med. 2017, 139, 50–57. [Google Scholar] [CrossRef] [PubMed]
  23. Walia, K.; Argüello, H.; Lynch, H.; Leonard, F.C.; Grant, J.; Yearsley, D.; Kelly, S.; Duffy, G.; Gardiner, G.E.; Lawlor, P.G. Effect of strategic administration of an encapsulated blend of formic acid, citric acid, and essential oils on Salmonella carriage, seroprevalence, and growth of finishing pigs. Prev. Vet. Med. 2017, 137, 28–35. [Google Scholar] [CrossRef]
  24. Casanova-Higes, A.; Andrés-Barranco, S.; Mainar Jaime, R.C. Use of a new form of protected sodium butyrate to control Salmonella infection in fattening pigs. Span. J. Agric. Res. 2019, 16, e05SC02. [Google Scholar] [CrossRef]
  25. De Busser, E.V.; Dewulf, J.; Nollet, N.; Houf, K.; Schwarzer, K.; De Sadeleer, L.; De Zutter, L.; Maes, D. Effect of organic acids in drinking water during the last 2 weeks prior to slaughter on Salmonella shedding by slaughter pigs and contamination of carcasses. Zoonoses Public Health 2009, 56, 129–136. [Google Scholar] [CrossRef]
  26. Martín-Peláez, S.; Costabile, A.; Hoyles, L.; Rastall, R.A.; Gibson, G.R.; La Ragione, R.M.; Woodward, M.J.; Mateu, E.; Martín-Orúe, S.M. Evaluation of the inclusion of a mixture of organic acids or lactulose into the feed of pigs experimentally challenged with Salmonella Typhimurium. Vet. Microbiol. 2010, 142, 337–345. [Google Scholar] [CrossRef]
  27. De Ridder, L.; Maes, D.; Dewulf, J.; Pasmans, F.; Boyen, F.; Haesebrouck, F.; Méroc, E.; Butaye, P.; Van der Stede, Y. Evaluation of three intervention strategies to reduce the transmission of Salmonella Typhimurium in pigs. Vet. J. 2013, 197, 613–618. [Google Scholar] [CrossRef]
  28. Nguyen, D.H.; Seok, W.J.; Kim, I.H. Organic Acids Mixture as a Dietary Additive for Pigs-A Review. Animals 2020, 10, 952. [Google Scholar] [CrossRef]
  29. Isaacson, R.E.; Firkins, L.D.; Weigel, R.M.; Zuckermann, F.A.; DiPietro, J.A. Effect of transportation and feed withdrawal on shedding of Salmonella Typhimurium among experimentally infected pigs. Am. J. Vet. Res. 1999, 60, 1155–1158. [Google Scholar]
  30. Darwin, K.H.; Miller, V.L. Molecular basis of the interaction of Salmonella with the intestinal mucosa. Clin. Microbiol. Rev. 1999, 12, 405–428. [Google Scholar] [CrossRef]
  31. Uribe, J.H.; Collado-Romero, M.; Zaldívar-López, S.; Arce, C.; Bautista, R.; Carvajal, A.; Cirera, S.; Claros, M.G.; Garrido, J.J. Transcriptional analysis of porcine intestinal mucosa infected with Salmonella Typhimurium revealed a massive inflammatory response and disruption of bile acid absorption in ileum. Vet. Res. 2016, 47, 11. [Google Scholar] [CrossRef]
  32. Cevallos-Almeida, M.; Martin, L.; Houdayer, C.; Rose, V.; Guionnet, J.M.; Paboeuf, F.; Denis, M.; Kerouanton, A. Experimental infection of pigs by Salmonella Derby, S. Typhimurium and monophasic variant of S. Typhimurium: Comparison of colonization and serology. Vet. Microbiol. 2019, 231, 147–153. [Google Scholar] [CrossRef] [PubMed]
  33. Ricke, S.C. Perspectives on the use of organic acids and short chain fatty acids as antimicrobials. Poult. Sci. 2003, 82, 632–639. [Google Scholar] [CrossRef] [PubMed]
  34. Hirshfield, I.N.; Terzulli, S.; O’Byrne, C. Weak organic acids: A panoply of effects on bacteria. Sci. Prog. 2003, 86, 245–269. [Google Scholar] [CrossRef] [PubMed]
  35. Berends, B.R.; Urlings, H.A.; Snijders, J.M.; van Knapen, F. Identification and quantification of risk factors in animal management and transport regarding Salmonella spp. in pigs. Int. J. Food Microbiol. 1996, 30, 37–53. [Google Scholar] [CrossRef]
  36. Stärk, K.D.; Wingstrand, A.; Dahl, J.; Møgelmose, V.; Lo Fo Wong, D.M. Differences and similarities among experts’ opinions on Salmonella enterica dynamics in swine pre-harvest. Prev. Vet. Med. 2002, 53, 7–20. [Google Scholar] [CrossRef]
  37. Hurd, H.S.; McKean, J.D.; Griffith, R.W.; Wesley, I.V.; Rostagno, M.H. Salmonella enterica infections in market swine with and without transport and holding. Appl. Environ. Microbiol. 2002, 68, 2376–2381. [Google Scholar] [CrossRef]
  38. Mannion, C.; Egan, J.; Lynch, B.P.; Fanning, S.; Leonard, N. An investigation into the efficacy of washing trucks following the transportation of pigs—A Salmonella perspective. Foodborne Pathog. Dis. 2008, 5, 261–271. [Google Scholar] [CrossRef]
  39. Ferrer Savall, J.; Bidot, C.; Leblanc-Maridor, M.; Belloc, C.; Touzeau, S. Modelling Salmonella transmission among pigs from farm to slaughterhouse: Interplay between management variability and epidemiological uncertainty. Int. J. Food Microbiol. 2016, 229, 33–43. [Google Scholar] [CrossRef]
  40. Cantini. Compositions Containing C1 to C7 Organic Acid Monoglycerides and Glycerol, Their Preparation and Use as Antibacterials and Anti-Mould Agents. 2015. Available online: https://patents.google.com/patent/WO2010106488A2/en (accessed on 15 July 2023).
  41. Bernad-Roche, M.; Casanova-Higes, A.; Marín-Alcalá, C.M.; Mainar-Jaime, R.C. Salmonella Shedding in Slaughter Pigs and the Use of Esterified Formic Acid in the Drinking Water as a Potential Abattoir-Based Mitigation Measure. Animals 2022, 12, 1620. [Google Scholar] [CrossRef]
  42. Luise, D.; Correa, F.; Bosi, P.; Trevisi, P. A Review of the Effect of Formic Acid and Its Salts on the Gastrointestinal Microbiota and Performance of Pigs. Animals 2020, 10, 887. [Google Scholar] [CrossRef] [PubMed]
  43. ISO 6579-1:2017; Microbiology of the Food Chain—Horizontal Method for the Detection, Enumeration and Serotyping of Salmonella—Part 1: Detection of Salmonella spp. ISO: Geneva, Switzerland, 2017.
  44. ISO/TS 6579-2:2012; Microbiology of Food and Animal Feed—Horizontal Method for the Detection, Enumeration and Serotyping of Salmonella—Part 2: Enumeration by a Miniaturized Most Probable Number Technique. ISO: Geneva, Switzerland, 2012.
  45. Jarvis, B.; Wilrich, C.; Wilrich, P.T. Reconsideration of the derivation of Most Probable Numbers, their standard deviations, confidence bounds and rarity values. J. Appl. Microbiol. 2010, 109, 1660–1667, Erratum in J. Appl. Microbiol. 2015, 119, 905. [Google Scholar] [CrossRef] [PubMed]
  46. Mainar-Jaime, R.C.; Atashparvar, N.; Chirino-Trejo, M.; Blasco, J.M. Accuracy of two commercial enzyme-linked immunosorbent assays for the detection of antibodies to Salmonella spp. in slaughter pigs from Canada. Prev. Vet. Med. 2008, 85, 41–51. [Google Scholar] [CrossRef]
  47. Dohoo, I.R.; Martin, W.; Stryhn, H.E. Veterinary Epidemiologic Research; University of Prince Edward Island: Charlottetown, PE, Canada, 2003; p. 127. [Google Scholar]
  48. Anonymous. S.I. No. 165/2002—Abattoirs Act 1988 (Veterinary Examination) (Amendment) Regulations 2002. 2002. Available online: https://www.irishstatutebook.ie/eli/2002/si/165/made/en/print (accessed on 21 July 2023).
  49. Anonymous. Koninklijk Besluit tot Opheffing van het Koninklijk en het Ministerieel Besluit van 27 April 2007 Betreffende de Bewaking van Salmonella bij Varkens. Voedselketen, F.A.v.d.V.v.d., Ed. 2015. Available online: https://etaamb.openjustice.be/nl/koninklijk-besluit-van-27-april-2007_n2007022865 (accessed on 21 July 2023).
  50. Van der Wolf, P.J. Monitoring for Salmonella in Swine in the Netherlands. Pig333. 2017. Available online: https://www.pig333.com/articles/monitoring-forsalmonella-in-swine-in-the-netherlands_12866/ (accessed on 17 July 2023).
  51. QS. Guidelines Salmonella Monitoring Pigs. 2023. Available online: https://www.q-s.de/services/files/downloadcenter/h-salmonellenmonitoring/2023/leitfaeden/englisch/Guideline_Salmonella_Monitoring_Pigs01.01.2023.pdf (accessed on 17 July 2023).
  52. Teng, K.T.; Martinez Avilés, M.; Ugarte-Ruiz, M.; Barcena, C.; de la Torre, A.; Lopez, G.; Moreno, M.A.; Dominguez, L.; Alvarez, J. Spatial Trends in Salmonella Infection in Pigs in Spain. Front. Vet. Sci. 2020, 7, 345. [Google Scholar] [CrossRef]
  53. Anonymous. FCC Consortium, Final Report. Analysis of the Costs and Benefits of Setting a Target for the Reduction of Salmonella in Breeding Pigs for European Commission Health and Consumers Directorate-General SANCO/2008/E2/056. Brussels: SANCO/2008/E2/056. 2011. Available online: https://food.ec.europa.eu/system/files/2016-10/biosafety_food-borne-disease_salmonella_fattening-pigs_slaughthouse-analysis-costs.pdf (accessed on 17 July 2023).
  54. Gavin, C.; Simons, R.R.L.; Berriman, A.D.C.; Moorhouse, D.; Snary, E.L.; Smith, R.P.; Hill, A.A. A cost-benefit assessment of Salmonella-control strategies in pigs reared in the United Kingdom. Prev. Vet. Med. 2018, 160, 54–62. [Google Scholar] [CrossRef] [PubMed]
  55. Suiryanrayna, M.V.; Ramana, J.V. A review of the effects of dietary organic acids fed to swine. J. Anim. Sci. Biotechnol. 2015, 6, 45. [Google Scholar] [CrossRef] [PubMed]
  56. Pearlin, B.V.; Muthuvel, S.; Govidasamy, P.; Villaban, M.; Alagawany, M.; Farag, M.R.; Dhama, K.; Gopi, M. Role of acidifiers in livestock nutrition and health: A review. J. Anim. Physiol. Anim. Nutr. 2020, 104, 558–569. [Google Scholar] [CrossRef]
  57. Kuterna, L. A Combined Strategy to Reduce Salmonella in Pigs. PigProgress. 2015. Available online: https://www.pigprogress.net/health-nutrition/a-combined-strategy-to-reduce-salmonella-in-pigs-2/ (accessed on 18 July 2023).
  58. Gomez-Osorio, L.M.; Yepes-Medina, V.; Ballou, A.; Parini, M.; Angel, R. Short and Medium Chain Fatty Acids and Their Derivatives as a Natural Strategy in the Control of Necrotic Enteritis and Microbial Homeostasis in Broiler Chickens. Front. Vet. Sci. 2021, 8, 773372. [Google Scholar] [CrossRef]
Table 1. Bacteriological and serological results for Salmonella prevalence at the farms prior to trial for the control (CG) and treatment (TG) groups.
Table 1. Bacteriological and serological results for Salmonella prevalence at the farms prior to trial for the control (CG) and treatment (TG) groups.
FarmGroupNo.Seroprevalence (%)p-ValueNo.Pen Prevalence (%)p-Value 1
1CG3016.670.5310101
TG3026.701010
2CG3030.000.2910101
TG3046.671010
3CG3033.330.0410101
TG3063.331010
1 Fischer’s exact test, two-tailed.
Table 2. Bacteriological results for Salmonella isolation from fecal samples at slaughter for the control (CG) and treatment (TG) groups.
Table 2. Bacteriological results for Salmonella isolation from fecal samples at slaughter for the control (CG) and treatment (TG) groups.
FarmGroupNNo. Salmonella-Positive Samples (%)p-Value 1
1CG4026 (65.0)0.0015
TG4011 (27.5)
2CG405 (12.5)0.0547
TG400 (0.0)
3CG4029 (72.5)0.0007
TG4013 (32.5)
TotalCG12060 (50.0)<0.001
TG12024 (20.0)
1 Fisher’s exact test, two-tailed.
Table 3. Prevalence and concentration of Salmonella (MPN/g) in fecal samples at slaughter for the control (CG) and treatment (TG) groups using the MPN method.
Table 3. Prevalence and concentration of Salmonella (MPN/g) in fecal samples at slaughter for the control (CG) and treatment (TG) groups using the MPN method.
FarmGroupNNo. Salmonella-Positive Samples (%)No. Samples in Salmonella MPN/g Ranges (%)
ND 10.02–2021–2002
1CG94 (44.4)5 (55.6)3 (33.3)0 (0.0)1 (11.1)
TG91 (11.1)8 (88.9)0 (0.0) 0 (0.0)1 (11.1)
2CG101 (10.0)9 (90.0)1 (10.0)0 (0.0)0 (0.0)
TG100 (0.0)10 (100.0)0 (0.0)0 (0.0)0 (0.0)
3CG106 (60.0)4 (40.0)1 (10.0)2 (20.0)3 (30.0)
TG103 (30.0)7 (70.0)3 (30.0)0 (0.0)0 (0.0)
TotalCG2911 (37.9)18 (62.1)5 (17.2)2 (6.9)4 (13.8)
TG294 (13.8)25 (86.2)3 (10.3)0 (0.0)1 (3.4)
1 ND: not detected, below the limit of detection (<1 CFU/g). 2 ∞: exceeding the limit for counting.
Table 4. Results of the random-effects logistic regression analysis * to predict Salmonella shedding at the abattoir.
Table 4. Results of the random-effects logistic regression analysis * to predict Salmonella shedding at the abattoir.
Coefficient (β)Std Error (β)Odds Ratio (OR)95% CI (OR)p-Value
Group
  Control 1--
  Treatment1.730.335.632.92–10.8<0.001
Constant−1.860.840.150.29–0800.026
* Farm considered as grouping (random) variable. Intraclass correlation coefficient (ICC): 0.36 (95% CI = 0.09–0.76).
Table 5. Results for the analysis for linear trends in proportions for the control (CG) and treatment (TG) groups according to Most Probable Number (MPN) results.
Table 5. Results for the analysis for linear trends in proportions for the control (CG) and treatment (TG) groups according to Most Probable Number (MPN) results.
MPN CategoryCG (%)TG (%)OR *95% CI (OR)p
Not detected18 (62.1)25 (86.2)1--
0.02–20.00 CFU/g5 (17.2)3 (10.3)2.320.47–11.30.28
21–∞ CFU/g *6 (20.7)1 (3.5)8.330.80–8.620.03
Chi-squared for linear trend = 5.11 p = 0.023. * MNP categories “21–200 CFU/g” and “∞ CFU/g” were merged for the sake of the calculation (to avoid zeros).
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Bernad-Roche, M.; Marín-Alcalá, C.M.; Vico, J.P.; Mainar-Jaime, R.C. Salmonella Control in Fattening Pigs through the Use of Esterified Formic Acid in Drinking Water Shortly before Slaughter. Animals 2023, 13, 2814. https://doi.org/10.3390/ani13182814

AMA Style

Bernad-Roche M, Marín-Alcalá CM, Vico JP, Mainar-Jaime RC. Salmonella Control in Fattening Pigs through the Use of Esterified Formic Acid in Drinking Water Shortly before Slaughter. Animals. 2023; 13(18):2814. https://doi.org/10.3390/ani13182814

Chicago/Turabian Style

Bernad-Roche, María, Clara María Marín-Alcalá, Juan Pablo Vico, and Raúl Carlos Mainar-Jaime. 2023. "Salmonella Control in Fattening Pigs through the Use of Esterified Formic Acid in Drinking Water Shortly before Slaughter" Animals 13, no. 18: 2814. https://doi.org/10.3390/ani13182814

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop