Salmonella intervention strategies at the farm Scott M. Russell, Ph.D. Professor Poultry Science Department The University of Georgia Introduction: It is often difficult to ascertain how Salmonella issues in poultry begin and what measures should be implemented to prevent them. Chickens may become colonized through both vertical (from parent stock) and horizontal (environmental) means. This purpose of this article is to detail how Salmonella colonize poultry and to explain effective measures for preventing or controlling colonization. Breeder chicken origin: Many scientists have implicated breeder chickens as vehicles for vertical transmission of Salmonella from the breeder chickens to the fertile egg. In 1991, Cox et al. evaluated egg fragments, paper pads from chick boxes, and chick fluff from six commercial broiler breeder hatcheries for the presence and level of salmonellae. Overall, 42 of 380 samples (11.1%) from those hatcheries were contaminated with salmonellae. Salmonella were detected in 22 of 145 (15.2%), 5 of 100 (4.6%), and 15 of 125 (12%) samples of egg fragments, chick fluff, and paper pads, respectively. The percentage of salmonellae-positive samples from each of the six hatcheries were 1.3, 5.0, 22.5, 11.4, 36.0, and 4.3% respectively (Cox et al., 1991). Of the 140 samples randomly selected for enumeration, salmonellae were found in 11 samples. Four of these 11 samples had greater than 103 salmonellae per sample, 3 others had greater than 102 but less than 103, and the remaining 4 had less than 102. Salmonella serotypes isolated were S. berta, S. california, S. give, S. hadar, S. mbandaka, S. senftenberg, and S. typhimurium, all of which have previously been isolated from poultry. The authors found that, the incidence and extent of salmonellae-positive samples found in the breeder hatcheries were much less than that previously found in broiler hatcheries, meaning that overall, the industry is reducing Salmonella in breeder chicken populations. Cox et al. (1991) concluded by stating that the cycle of salmonellae contamination will not likely be broken until contamination at these critical points is eliminated. Cox et al. (2000) reported that numerous publications show that Salmonellacontaminated eggs can be produced by artificially inoculating breeding chickens (Photo 1) Photo 1: Cobb broiler breeder chicken (http://www.wattagnet.com/uploadedImages/WattAgNet/Products/Manufacturer/Poultry/Poultry _International/0711PIproductsCobb.jpg) Timoney et al. (1989) reported that oral inoculation of laying hens resulted in infection of the reproductive tract. Challenging the breeder hen with 106 Salmonella cells caused the ovary and oviduct to become infected. Cox et al. (2000) observed that the egg production rate for infected chickens was unaffected, and Salmonella was not detected in all fecal samples; therefore an breeders infected with salmonellae may not always be easily detectable on the farm. For the contaminated breeder hens, the yolks of 10% of the eggs laid were contaminated with S. enteritidis. However, when hens were inoculated with Salmonella at levels of 108 cells, a noticeable drop in egg production and signs of pathogenesis occurred (Cox et al., 2000). In 2002, Bailey et al. stated that, although the widespread presence of Salmonella (Photo 2) in all phases of broiler chicken production and processing is well documented, little information is available to indicate the identity and movement of specific serotypes of Salmonella through the different phases of an integrated operation. In the study by Bailey et al. (2002), samples were collected from the breeder farm, the hatchery, the previous grow-out flock, the flock during grow-out, and carcasses after processing. Salmonella were recovered from 6, 98, 24, 60, and 7% of the samples, respectively, in the first trial and from 7, 98, 26, 22, and 36% of the samples, respectively, in the second trial. Seven different Salmonella serotypes were identified in the first trial, and 12 different serotypes were identified in the second trial (Bailey et al. 2002). Interestingly, for both trials, there was poor correlation between the serotypes found in the breeder farms and those found in the hatchery. Photo 2. Picture of attached Salmonella with flagella. (http://upload.wikimedia.org/wikipedia/commons/thumb/b/b4/SalmonellaNIAID.jpg/715pxSalmonellaNIAID.jpg) Semen implicated Studies have been conducted to determine how vertical transmission from the breeder to the baby broiler chick occurs. In 1995 Reiber et al. conducted three experiments to determine the bacteriological quality of rooster semen. The most frequently isolated genera of bacteria from rooster semen included Escherichia, Staphylococcus, Micrococcus, Enterococcus, and Salmonella. Most of the bacteria that were isolated were endemic to poultry and were commonly found in the environment of chickens (Reiber et al., 1995). Thus, during mating, female breeders may become inoculated with Salmonella during semen transmission. Buhr et al. (2005) reported the recovery of Campylobacter (naturally colonized) from the ductus deferens of 5 of 101 broiler breeder roosters, and four of those five positive roosters had previously produced Campylobacter-positive semen samples. Those results prompted further evaluation to determine if inoculation route influenced the prevalence or level of Campylobacter contamination of semen, the digestive tract, or reproductive organs. Individually caged roosters, confirmed to be feces and semen negative for Campylobacter, were challenged with a marker strain of Campylobacter jejuni either orally, by placing Campylobacter onto the everted phallus immediately after semen collection, or by dip coating an ultrasound probe in Campylobacter and inserting the probe through the vent into the colon. Six days after inoculation, individual feces and semen samples were again collected and cultured for Campylobacter. Seven days postinoculation, roosters were killed, the abdomen aseptically opened to expose the viscera, and one cecum, one testis, and both ductus deferens were collected. Campylobacter was recovered 6 days after challenge from feces in 82% of samples (log104.1 colony-forming units [CFU]/g sample), 85% of semen samples (log102.9 CFU/ml), and on the seventh day after challenge from 88% of cecal samples (log105.8 CFU/g sample). These results demonstrate that male breeders exposed to Salmonella and Campylobacter may pass these bacteria on to the female during mating. This helps to explain how vertical transmission with these pathogens occurs. The effect of disinfection and rodents In a study to determine the effect of disinfection on Salmonella in breeders, three broiler breeder houses at three different locations were sampled before and after cleansing and disinfection (Davies and Wray, 1996). None of the farms were able to achieve total elimination of Salmonella Enteritidis from the poultry house environment. The authors concluded that, in each of the three breeder houses, failure to eliminate mice from the house that was infected with S. Enteritidis was likely to be the most important hazard for transmission to the next flock (Davies and Wray, 1996). These studies demonstrate that both vertical and horizontal transmission of Salmonella from breeders and from the environment may occur. Any potential intervention at this stage of production must focus on controlling Salmonella in breeders and in the environment of the breeder chickens. Interventions for breeders: Over the years, a number of methods have been used to eliminate Salmonella from breeder chicken populations. One method employed in Denmark, Sweden, and the Netherlands is to test breeder flocks and, if found to be positive for Salmonella, slaughter them. Slaughtering positive flocks: Rapid increases in the incidence in human salmonellosis in the second half of the 1980s in Denmark was attributed to the spread of Salmonella in broiler chickens. Because of this link to poultry, a targeted national control program was initiated. Initally, the aim of the program was to reduce Salmonella in broiler flocks to less than 5% prevalence (Wegener et al., 2003). The program was developed based on the concept of eliminating Salmonella from the breeders, which will then theoretically ensure that broilers and processed products would be free from Salmonella. Wegener et al. (2003) reported that infected flocks of breeder chickens are destroyed, and infected birds are slaughtered. The intensive testing program developed gradually over time. Birds from Salmonella positive flocks are slaughtered on separate slaughter lines or late in the day to avoid crosscontamination of Salmonella negative birds. One incentive the Danes give poultry growers is that farmers get a better price for birds from Salmonella-free flocks, and slaughterhouses can use the label “Salmonella-free” for birds that meet criteria determined by the authorities (Wegener et al., 2003). The effect of this program may be seen in Figure 1 presented below. Figure 1. Effect of slaughtering Salmonella positive breeder flocks on Salmonella positive chickens arising from processing operations. 80 70 60 50 40 30 20 10 0 89 90 91 92 93 94 95 96 97 98 99 00 01 However, it is important to note that due to the sheer size of the poultry industry in the U.S., this approach would be impossible. For example, we produced roughly twice as much poultry in Athens, GA last year than they produced in all of Sweden. When we compare the rate of human salmonellosis between Sweden and the U.S. we find 42.8 per 100,000 people in Sweden versus the U.S. where it is 14.9 per 100,000 people. The question is, “In a country where extraordinarily expensive measures are used to eliminate Salmonella from the flocks prior to processing, what are they getting for their money?” Medications and competitive exclusion: Scientists have been working for decades in an attempt to control Salmonella colonization of chickens using bacterial cultures that will colonize the baby chick and thus, prevent Salmonella from colonizing the chick. Another approach has been to use antibiotics to prevent colonization of the chickens with Salmonella. In 1997, Reynolds et al. medicated breeding flocks of domestic fowl (Gallus gallus) using an antimicrobial treatment followed by competitive exclusion in 13 trials between February and September 1993. This approach was being used as an alternative to the Swedish model such that positive flocks would not have to be slaughtered, but would be treated instead. In each trial, the flock had been confirmed as naturally infected with Salmonella enterica serovar Enteritidis and the effect of treatment was determined on Salmonella isolation from internal tissues. Of the 11 trials where enrofloxacin was used to medicate the flocks, a long-term reduction of Salmonella was observed in two and a short-term reduction was measured in birds from another five trials. Salmonella Enteritidis was isolated from birds after treatment in four other trials with enrofloxacin and in two trials of medication with amoxycillin. The authors of this study concluded that enrofloxacin significantly reduced the prevalence of S. Enteritidis in tissues from birds, and reduced the level and prevalence of Salmonella in the bird’s environment. No Salmonella was identified in statutory meconium samples taken from the hatched chicks derived from the flocks after treatment. The program of antibiotic treatment and competitive exclusion offers an alternative to slaughter, but the approach must be part of a coordinated program, which will effect a decrease in the prevalence of S. Enteritidis over time by contemporary use of disease security measures (Reynolds et al., 1997). This approach in the U.S. may not be acceptable as many companies are trying to decrease the use of prophylactic antibiotics in order to preclude development of antibiotic resistant bacteria. Vaccination: A number of poultry companies have investigated the use of vaccines for eliminating Salmonella in breeder flocks. Inoue et al. (2008) stated that young poultry are very susceptible to Salmonella Enteritidis (SE) infections because of the absence of complete intestinal flora colonization and an immature immune system in baby chicks. The authors conducted a study to evaluate the role of passive immunity on the resistance of young birds against early infections caused by SE. The progeny of broiler breeders were vaccinated compared to the progeny of unvaccinated birds. The efficacy of the vaccine was determined by challenging birds at Days 1 and 14 with SE. After challenge at 1 day of age, the progeny of vaccinated birds presented a significantly lower number (log10) of SE in liver (2.21), spleen (2.31), and cecal contents (2.85) compared with control groups (2.76, 3.02, and 6.03, respectively). This means that vaccination in these breeders reduced SE colonization by greater than 99%. Inoue et al. (2008) observed that examination of the internal organs, 3 days after infection, revealed that 28% of the birds (7/25) from vaccinated breeders were positive, whereas 100% (25/25) of the chicks derived from unvaccinated birds were positive. Moreover, birds that were challenged at 14 days of age showed a lower number of positive samples compared with those challenged at 1 day of age, and the progeny of vaccinated birds presented statistically lower numbers (2.11 vs. 2.94). In this study, age influenced the susceptibility of birds to SE infections: in control groups, the number of positive birds at 14 days of age (9/25) was lower when compared with the group infected at 1 day of age (25/25). The number of positive fecal samples of the progeny of vaccinated birds was significantly lower (36) than those of the control group (108) after challenge at 1 day of age. The authors showed that vaccinating breeders helped to increase the resistance of the progeny against early SE infections. However, the bacteria were not completely eliminated, suggesting that additional procedures are needed to effectively control SE infections (Inoue et al., 2008). Most efforts to control Salmonella in breeder flocks in the U.S. have been concentrated on vaccination programs. In some cases, they are very effective; however, in others they do not have any effect. In working with one company that was vaccinating 100% of their breeders, plants receiving the broilers from these flocks reported a 100% Salmonella positive rate. These data indicate that the vaccination program in these operations was having no impact and highlights the importance of identifying the serotypes of Salmonella that are most frequently isolated and targeting those serotypes in the vaccine (Russell, unpublished data). Hatchery origins: Many opportunities exist for Salmonella to be transferred from contaminated eggs to uninfected baby chicks during the hatching process. Cox et al. (2000) published an excellent review on this subject. Salmonella may be found in the nest boxes where breeders lay eggs, in the cold storage egg room at the breeder farm, on the truck that transports baby chicks to the growout houses, or in the hatchery environment. All of these situations may cause horizontal contamination of the eggs with Salmonella. Once transferred, the Salmonella is carried on the surface of the shell or just beneath the shell if it is able to penetrate the shell. One mechanism for natural contamination of the eggs is when moist, freshly laid eggs are cooled from the body temperature of the hen to the air temperature, the internal contents of the egg shrink, pulling bacteria into the shell through pores (Cox et al., 2000). The breeder hen’s nest becomes contaminated Salmonella when she brings soil and feces into it. Smeltzer et al. (1979) demonstrated that eggs laid in wet, dirty nests or on the floor are more likely to be contaminated with bacteria. It has been known for over 100 years that salmonellae are able to penetrate egg shells. Moreover, numerous studies have shown the ability of Salmonella to penetrate and multiply within the contents of both chicken and turkey hatching eggs (Cox et al., 2000). There exists significant variability in terms of how well Salmonella can penetrate eggs (Stokes et al., 1956; Humphrey et al., 1989, 1991). Shell attributes (Sauter and Petersen, 1974), pH (Sauter et al., 1977), number of pores on an egg shell (Walden et al., 1956), temperature (Graves and Maclaury, 1962), humidity (Gregory, 1948), and vapor pressure (Graves, and Maclaury, 1962) are all factors that may effect penetration (Cox et al., 2000). In spite of the protective effect of the inner and outer egg shell membranes (Baker, 1974), several researchers have demonstrated that Salmonella and other bacteria may penetrate these membranes rapidly. Studies have have shown that bacteria were able to penetrate 25 to 60% of inner membranes and 10 to 15% of albumen in eggs that were inoculated (Muira et al., 1964; Humphrey et al., 1989, 1991). Other scientists observed that penetration of the cuticle and shell of eggs by salmonellae occurred almost immediately in some eggs. In fact, in one egg, penetration below both membranes was detected as early as 6 min following shell exposure (Williams et al., 1968). The authors found that, once bacteria get past the membranes of hatching eggs, there is no way to prevent their further invasion of the egg contents or developing embryo. Hatchery Intervention: The most common approaches to eliminate Salmonella from hatcheries and to control cross-contamination from contaminated eggs to uncontaminated eggs during hatching involve disinfection of the surfaces in the incubator and hatching cabinets and disinfecting the hatching eggs. The problem with disinfecting hatching eggs is that it is very difficult to get the sanitizer to coat the egg effectively and it is not advisable to wet the egg during this process. Thus, Russell (2003) conducted a study to determine if electrostatic spraying was effective for disinfecting hatching eggs contaminated with Salmonella. Fertile hatching eggs were coated with Salmonella and separated into 2 groups. The groups were hatched in two separate hatching cabinets. In one hatching cabinet, water was electrostatically applied to the eggs during hatching to serve as a control. In the other cabinet, electrolyzed oxidative (EO) water was electrostatically applied to the hatching eggs to kill Salmonella. Photos 3 and 4 clearly illustrates how much more effective coating a round object using electrostatic spraying is when compared to using standard misters. In this photo, 2 black balls were coated with a white powder solution. The one in the foreground was coated using a traditional sprayer. The one in the background was coated using an electrostatic sprayer. Note the difference in coverage. Photo 3. Traditional versus electrostatic application of powder to black balls, simulating an egg. Photo 4. Traditional versus electrostatic application of powder to black balls, simulating an egg (different view). Photo 5 shows the electrostatic application of sanitizer in a hatching cabinet. Photo 5. Electrostatic application of sanitizer to a hatching cabinet. This photo indicates that very little material is sprayed into the cabinet during the electrostatic spraying. Because of this, the eggs do not become wet and relative humidity does not increase significantly. Hatchability results for fertile eggs sprayed using electrostatic spraying in commercial situations (Table 1) and experimental conditions (Table 2) are presented below. Results for Salmonella typhimurium prevalence in the lower intestines of broiler chickens from hatching eggs treated electrostatically with tap water or EO water during hatch are presented in Table 3. These results are extremely encouraging in that 65 to 95 % (Replicate 1 and 2, respectively) of the chickens were colonized when only tap water was used to treat the fertile hatching eggs, indicating that our method for inducing colonization was appropriate; however, for electrostatically treated eggs using EO water, Salmonella was only able to colonize one chicken out of forty tested over two repetitions under actual growout conditions. This research has tremendous industrial application because many of the companies that are experiencing failures due to high Salmonella prevalence at the poultry plant are receiving flocks of birds that are 80 – 100% positive for Salmonella as they enter the plant. It would seem logical to suppose that if the number of chickens in field that are colonized with Salmonella could be reduced to the levels observed in this study, the industry would be able to meet the Salmonella performance standard required by the USDA-FSIS. This research describes a method that should have tremendous value to the poultry industry for reducing Salmonella in flocks arriving to the processing plant, which, according to our research, will translate directly into lower numbers of processed carcasses that are positive for Salmonella. Moreover, the electrostatic spraying system is not expensive to incorporate into a commercial hatchery. Table 1. Results for hatchability of commercial broiler-breeder chicks from hatching eggs treated electrostatically with tap water or EO water during hatch under commercial conditions. Normal Hatch* Tap Water EO Water Treated Treated Hatchability 85 % 82 % 79 % n 15,000 15,000 *Fertile eggs used in this study for the EO water treatment were older and expected hatchability was lower than the normally expected hatch. Table 2. Results for hatchability of chicks from hatching eggs treated electrostatically with tap water or EO water during hatch under research conditions at the University of Georgia Poultry Research Center. Normal Hatch Tap Water EO Water Treated Treated Hatchability 92 % 93 % 93 % n 160 160 Table 3. Results for Salmonella typhimurium prevalence (%) in the lower intestines, ceca, or cloacae of broiler chickens from hatching eggs treated electrostatically with tap water or EO water during hatch. Treatment Repetition 1 Repetition 2 Tap Water 65 % 95 % Control EO Water 0% 5% Treated n 20 20 Growout origins: Even if “Salmonella-free” birds are delivered to the growout house, it is still possible for them to become colonized during growout. The USDA-Agricultural Research Service (ARS) to conducted a large epidemiological study to determine the relative importance of all known sources of Salmonella from the hatchery through growout and processing in high- and low- production flocks from four integrated operations located in four states across four seasons (Bailey et al., 2001-Table 4). Table 4. Salmonella detection percentage from all sample types, times, and integrators across all seasons and high and low production houses (32 houses and 8,739 samples). Sample Total 50.8 6.6 1.4 1.9 10.5 2.3 Integrator A 32.5 0.8 0.0 0.5 1.6 1.6 Integrator B 47.4 10.3 1.3 1.3 15.4 3.9 Integrator C 26.6 9.2 0.0 2.7 15.0 0.0 Integrator D 96.0 5.2 3.7 3.1 9.4 3.2 Paper pads Feces Water line Water cup Litter Feed hopper Feeder Drag swab Wall swab Fan swab Mouse samples Wild-bird feces Animal feces Insects Dirt, near entrance Standing water Boot swab Fly strip Cecal droppings Total 2.3 14.2 3.4 3.4 6.1 0.0 2.1 3.1 1.6 12.5 3.9 21.1 2.6 1.3 0.0 0.0 16.7 7.8 7.8 3.7 4.8 15.6 0.0 3.1 0.0 6.6 6.1 14.3 4.3 4.8 3.0 3.8 0.0 0.0 2.6 2.8 6.1 6.1 6.3 0.8 13.5 4.2 3.3 1.9 0.0 5.1 4.8 4.2 8.3 4.5 12.0 18.7 4.4 14.3 25.0 1.0 16.7 5.3 9.2 11.8 29.6 5.0 6.5 17.1 1.1 9.8 5.2 10.8 9.7 13.4 Reprinted from Bailey et al. (2001) These data show that Salmonella may be transferred to birds during growout from rodents, wild birds, and insect vectors, such as beetles and flies. This table makes it clear that controlling Salmonella during growout requires a comprehensive approach. Due to the high level detected in the litter and incoming chick paper pads, it is also clear that vertical transmission is occurring from breeders to hatchery to the baby chicks. Therefore, any intervention must be able to comprehensively prevent Salmonella colonization from environmental sources and prevent vertical transmission. Growout interventions: Competitive exclusion: Researchers have conducted studies using cecal cultures from healthy, Salmonella free birds in an attempt to develop colonization of the bird’s intestines with good bacteria that will preclude later colonization of the bird by Salmonella. Hofacre (2000) reported that establishment of adult intestinal flora in day-old turkeys using competitive exclusion has been shown highly effective in reducing Salmonella colonization. The efficacy of two commercial products, a chicken-origin lyophilized culture (Aviguard, Bayer Animal Health. Merriam, KS) and a probiotic culture (Avian Pac Soluble Plus, Loveland Industries, Greeley, CO) containing only Lactobacillus acidophilus, was compared with that of fresh and 24-hr-old turkey cecal material using the challenge Mead model. The Aviguard was protective, but fresh turkey cecal material (undefined cecal culture from healthy turkeys) was significantly more protective in three of the four trials. Another approach to competitively excluding Salmonella has been to use starches such as isomaltooligosaccharide (IMO) to enrich cecal bifidobacterial populations and thus, reduce colonization levels of Salmonella in the ceca of broiler chickens. Thitaram et al. (2005) prepared broiler starter diets with final IMO concentrations of 1% (wt/wt), 2% (wt/wt), and 4% (wt/wt) and a control diet without IMO supplementation. Chickens were divided into 4 groups and challenged with 108 cell of Salmonella. The IMO-supplemented diets resulted in significantly higher cecal bifidobacteria compared with the control diet. Chickens fed diets with 1% IMO had a significant 2-log reduction in the level of inoculated S. Typhimurium present in the ceca compared with the control group. No differences in feed consumption, feed conversion, or feed efficiency compared with the control group were observed; however, the result showed a significant reduction in weight for birds fed 1% IMO diet compared with those fed the control diet. Higgins in 2007 evaluated the ability of a commercially available lactic acid bacteria-based probiotic culture (LAB) to reduce Salmonella Enteritidis or Salmonella Typhimurium in day-of-hatch broiler chicks. In these experiments, LAB significantly reduced the incidence of Salmonella Enteritidis (60 to 70% reduction) or Salmonella Typhimurium (89 to 95% reduction) recovered from the cecal tonsils of day-old broiler chicks 24 h following treatment as compared with controls. In these studies, LAB treatment significantly reduced recovery of Salmonella in day-ofhatch broilers. Vaccination: Many companies have been investigating the use of vaccination of broiler chickens at the hatchery or during growout to reduce Salmonella colonization of the live birds. Babu et al. (2004) showed that cell-mediated immunity (CMI) was enhanced by live Salmonella vaccine (LV). A study to evaluate the impact of live and killed Salmonella vaccines on Salmonella enteritidis (SE) clearance. Chickens were first immunized at 2 weeks of age followed by a booster dose at 4 weeks, challenged with live SE vaccine 2 weeks later (6-week-old) and tested. The results suggested that the live Salmonella vaccine protected against SE infection, probably by enhancing cell mediated immunity (Babu et al., 2004). Acid in waterers during feed withdrawal: Salmonella in the crops of chickens that have consumed litter may be spread from carcass to carcass during the crop removal process (Hargis et al., 1995, and Barnhart et al., 1999). During cropping, the cropper piston is inserted into the vent area of the carcass and continues through the entire carcass, spinning as it goes. The piston has sharp grooves on the end of it that pick up the crop and wraps the crop around the end of the cropper piston. As the piston moves through the neck opening, the cropper piston comes in contact with a brush that removes the crop from the piston. Then, the piston, while spinning, goes back through the entire carcass. If the crop breaks during this removal process, the contents leak onto the cropper piston and are transferred to the interior and exterior of the carcass, possibly spreading Salmonella. Studies have been conducted by Dr. Allen Byrd of the USDA - Agricultural Research Service (ARS) in which the crops of live birds were filled with fluorescein dye. After thirty minutes, the birds were processed. By examining the carcasses at different stages of processing under a black light, crop contents that were transferred to the inside or outside of the carcass could be clearly visualized. These studies have shown that commercial croppers result in a large amount of contamination of the inside and outside of the carcasses. Thus, efforts should be made to control Salmonella in the crop prior to the crop removal process. Some companies have been successful at controlling Salmonella in the crop by acidifying the bird’s drinking water during the feed withdrawal process. Acetic, citric or lactic acids and Poultry Water Treatment (PWT) have all been used to acidify the crop to the extent that Salmonella are unable to survive. Byrd et al. (2001) found that lactic acid was most effective and that 0.44% lactic acid in the waterers of broilers during the feed withdrawal period reduced Salmonella contaminated crops by 80%. This effect carried over to the pre-chill carcasses on which the prevalence of Salmonella was reduced by 52.4 % (Byrd et al., 2001). When acidifying drinking water using lactic acid, it is best to gradually expose the birds to higher and higher levels of acid in the water the week before birds are to be caught. The key is to make the lactic acid concentration as high as possible while ensuring that the birds continue drinking the water. Conclusions: Preventing colonization of chickens during breeding, hatching, and growout is challenging. This article details a number of methods that may be used to decrease or eliminate Salmonella from broiler chickens. However, each company must balance the cost of implementation of these techniques as there may be more effective methods that can be used at a lower cost to the company during processing, to allow the company to maintain Salmonella at low levels. References: Babu, U., R. A. Dalloul, M. Okamura, H. S. Lillehoj, H. Xie, R. B. Raybourne, D. Gaines, and R. A. Heckert, 2004. Salmonella enteritidis clearance and immune responses in chickens following Salmonella vaccination and challenge. Vet. Immunol. Immunopath. 101(3-4):251-257. Barnhart, E. T., D. J. Caldwell, M. C. Crouch, J. A. Byrd, D. E. Corrier, D.E., and B. M. Hargis, 1999. Effect of lactose administration in drinking water prior to and during feed withdrawal on Salmonella Bailey, J. S., N. A. Cox, S. E. Craven, and D. E. Cosby, 2002. Serotype tracking of Salmonella through integrated broiler chicken operations. J. Food Prot. 65(5):742-745. Baker, R. C., 1974. Microbiology of eggs. J. Milk Food Technol. 37:265–268. Bailey, J. S., N. J. Stern, P. Fedorka-Cray, S. E. Craven, N. A. Cox, D. E. Cosby, S. Ladely, and M. T. Musgrove, 2001. Sources and movement of Salmonella through integrated poultry operations: A multistate epidemiological investigation. J. Food Prot. 64(11):1690-1697. Buhr, R. J., M. T. Musgrove, L. J. Richardson, N. A. Cox, J. L. Wilson, J. S. Bailey, D. E. Cosby, and D. V. Bourassa, 2005. Recovery of Campylobacter jejuni in feces and semen of caged broiler breeder roosters following three routes of inoculation. Avian Dis. 49(4):577-581. Byrd, J. A., R. C. Anderson, R. L. Brewer, T. R. Callaway, K. M. Bischoff, J. L. McReynolds, D. J. Caldwell, B. M. Hargis, K. L. Herron, and R. H. Bailey, 2001. Effect of lactic acid administration in the drinking water during preslaughter feed withdrawal on Salmonella and Campylobacter contamination of broilers. Poult. Sci. 80(3):278-283. Cox, N. A., J. S. Bailey, J. M. Mauldin, L. C. Blankenship, and J. L. Wilson, 1991. Research note: Extent of salmonellae contamination in breeder hatcheries. Poultry Sci. 70:416-418. Cox, N. A., M. E. Berrang, and J. A. Cason, 2000. Salmonella penetration of egg shells and proliferation in broiler hatching eggs-A review. Poult. Sci. 79:1571-1574. Davies, R. H., and C. Wray, 1996. Studies of contamination of three broiler breeder houses with Salmonella enteritidis before and after cleansing and disinfection. Avian Dis. 40(3):626-633. Graves, R. C., and D. W. Maclaury, 1962. The effects of temperature, vapor pressure, and absolute humidity on bacterial contamination of shell eggs. Poultry Sci. 41:1219–1225. Hargis, B. M., D. J. Caldwell, R. L. Brewer, D. E. Corrier, and J. R. DeLoach, 1995. Evaluation of the chicken crop as a source of Salmonella contamination for broiler carcasses. Poult. Sci. 74(9):15481552. Higgins, J. P., F. E. Higgins, J. L. Vicente, A. D. Wolfenden, G. Tellez, and B. M. Hargis, 2007. Temporal effects of lactic acid bacteria probiotic culture on Salmonella in neonatal broilers. Poult. Sci. 86(8):1662-1666. Hofacre, C. L., 2000. Comparison of a lyophilized chicken-origin competitive exclusion culture, a lyophilized probiotic, and fresh turkey cecal material against Salmonella colonization. J. Appl. Poult. Res. 9:195-203. Humphrey, T. J., A. Baskerville, S. Mawer, B. Rowe, and S. Hopper, 1989. Salmonella enteritidis phage type 4 from the contents of intact eggs: A study involving naturally infected eggs. Epidem. Inf. 103:415–423. Humphrey, T. J., A. Whitehead, A.H.L. Gawler, A. Henley, and B. Rowe, 1991. Numbers of Salmonella enteritidis in the contents of naturally contaminated hens’ eggs. Epidemiol. Infect. 106:489–496. Inoue, A. Y., J. B. Paiva, E. V. Sterzo, A. Berchieri, Jr., A. Bernardino, 2008. Passive immunity of progeny from broiler breeders vaccinated with oil-emulsion bacterin against Salmonella Enteritidis, 2008. Avian Dis. 52(4):567-571. Muira, S., G. Sato, and T. Miyamae, 1964. Occurrence and survival of Salmonella organisms in hatcher chick fluff in commercial hatcheries. Avian Dis. 8:546-554. Reiber, M. A., J. A. McInroy, and D. E. Conner, 1995. Enumeration and identification of bacteria in chicken semen. Poult. Sci. 74(5):795-799. Reynolds, D. J., R. H. Davies, M. Richards, and C. Wray, 1997. Evaluation of combined antibiotic and competitive exclusion treatment in broiler breeder flocks infected with Salmonella enterica serovar Enteritidis. Avian Path. 26(1):83-95. Russell, S. M., 1993. Effect of santizers applied by electrostatic spraying on pathogenic and indicator bacteria attached to the surface of eggs. J. Appl. Poult. Res. 12:183-189. Sauter, E. A., and C. F. Petersen, 1974. The effect of egg shell quality on penetration by various salmonellae. Poultry Sci. 53:2159–2162. Sauter, E. A., C. F. Petersen, J. F. Parkinson, and E. E. Steele, 1977. Effects of pH on egg shell penetration by salmonellae. Poultry Sci. 56:1754–1755. Smeltzer, T. I., K. Orange, B. Peel, and G. Runge, 1979. Bacterial penetration in floor and nest box eggs from meat and layer birds. Aust. Vet. J. 55:592–593. Stokes, J. L., W. W. Osborne, and H. G. Bayne, 1956. Penetration and growth of Salmonella in shell eggs. Food Res. 21:510–518. Thitaram, S. N., C. H. Chung, D. F. Day, A. Hinton, Jr., J. S. Bailey, and G. R. Siragusa, Isomaltooligosaccharide increases cecal Bifidobacterium population in young broiler chickens. Poult. Sci. 84(7):998-1003. Timoney, J. F., H. L. Shivaprasad, R. C. Baker, and B. Rowe, 1989. Egg transmission after infection of hens with Salmonella enteritidis phage type 4. Vet. Rec. 125:600–601. Walden, C. C., I.V.F. Allen, and P. C. Trussell, 1956. The role of the egg shell and shell membranes in restraining the entry of microorganisms. Poultry Sci. 35:1190–1196. Wegener, H. C., T. Hald, D. L. F. Wong, M. Madsen, H. Korsgaard, F. Bager, P. Gerner-Smidt, K. Mølbak, 2003. Salmonella control programs in Denmark. Emerg. Infect. Dis. 9(7):774-80. Williams, J. E., L. H. Dillard, and G. O. Hall, 1968. The penetration patterns of Salmonella typhimurium through the outer structures of chicken eggs. Avian Dis. 12:445–466.