Journals / Turkish Journal of Veterinary and Animal Sciences / 2018 / Cilt: 42 - Sayı: 4

Avian Salmonella enteritidis serovar Enteritidis with ClpP deletion is attenuated and highly immunogenic in chickens

Pages
269–276
Publication Date
2022-11-05
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The survival rate of 7-day-old SPF chickens immunized with SM-6/ΔClpPagainst homologous challenge and antibody kinetics indicated that SM-6/ΔClpP provided efficient protection from lethal challenge andinduced robust antibody immune responses, demonstrating the potential of live, attenuated SE as a vaccine candidate.

📌 3 Key Takeaways

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Objective & Hypothesis:Salmonella enterica subsp. enterica serovars are leading causative agents of gastroenteritis in humans and numerous animalspecies worldwide.
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Key Findings & Data:Therefore,SM-6/ΔClpP, deletion of the ClpP gene from a wild-type SE-6 (SM-6) strain, was generated using the phage λ Red homologousrecombination.
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Conclusion & Impact:The survival rate of 7-day-old SPF chickens immunized with SM-6/ΔClpPagainst homologous challenge and antibody kinetics indicated that SM-6/ΔClpP provided efficient protection from lethal challenge andinduced robust antibody immune responses, demonstrating the potential of live, attenuated SE as a vaccine candidate.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Salmonella enterica subsp. enterica serovars are leading causative agents of gastroenteritis in humans and numerous animalspecies worldwide. The ClpP from Salmonella enterica is responsible for regulation under various stress conditions. We were interested inthe effect of ClpP deletion mutation on attenuation of Salmonella enterica subsp. enterica serovar Enteritidis (SE) in chickens. Therefore,SM-6/ΔClpP, deletion of the ClpP gene from a wild-type SE-6 (SM-6) strain, was generated using the phage λ Red homologousrecombination. Compared with SM-6, SM-6/ΔClpP represented a retarded growth rate and lower concentration in LB broth with andwithout 5% NaCl or lower pH values, indicating that it is sensitive to conventional disinfectants. SM-6/ΔClpP represented reducedinvasion into macrophages in vitro and an approximate 400-fold attenuation based on cell invasion assay and median lethal dose (LD50)in specific pathogen-free (SPF) chickens. Furthermore, SM-6/ΔClpP showed reduced colonization in the liver and spleen and fasterclearance compared with SM-6, indicating a short discharge. The survival rate of 7-day-old SPF chickens immunized with SM-6/ΔClpPagainst homologous challenge and antibody kinetics indicated that SM-6/ΔClpP provided efficient protection from lethal challenge andinduced robust antibody immune responses, demonstrating the potential of live, attenuated SE as a vaccine candidate.

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Cite This Article

LIU, S., WEN, X., RAN, X., NI, H., YANG, Z., SHAO, G. (2022). Avian Salmonella enteritidis serovar Enteritidis with ClpP deletion is attenuated and highly immunogenic in chickens. Turkish Journal of Veterinary and Animal Sciences, Cilt: 42 - Sayı: 4, 269–276. https://ajindex.com/articles/614981

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References (13)

  1. Guo Z, Su C, Huang J, Niu J. A food-borne outbreak of gastroenteritis caused by different Salmonella serotypes in 2 universities in Xiamen, Fujian, China, in 2012. Jpn J Infect Dis 2015; 68: 187-191
  2. Lutful Kabir SM. Avian colibacillosis and salmonellosis: a closer look at epidemiology, pathogenesis, diagnosis, control and public health concerns. Int J Environ Res Public Health 2010; 7: 89-114
  3. Gantois I, Ducatelle R, Pasmans F, Haesebrouck F, Gast R, Humphrey TJ, Van Immerseel F. Mechanisms of egg contamination by Salmonella Enteritidis. FEMS Microbiol Rev 2009; 33: 718-738
  4. Van Doren JM, Neil KP, Parish M, Gieraltowski L, Gould LH, Gombas KL. Foodborne illness outbreaks from microbial contaminants in spices, 1973-2010. Food Microbiol 2013; 36: 456-464
  5. Thompson Bastin ML, Neville NR, Parsons RE, Flannery AH, Tennant SJ, Johnson CA. An unusual case of Salmonella Enteritidis causing pneumonia, septic shock and multiple organ failure in an immunocompetent patient. IDCases 2016; 6: 85-89
  6. Hendriksen RS, Vieira AR, Karlsmose S, Lo Fo Wong DM, Jensen AB, Wegener HC, Aarestrup FM. Global monitoring of Salmonella serovar distribution from the World Health Organization Global Foodborne Infections Network Country Data Bank: results of quality assured laboratories from 2001 to 2007. Foodborne Pathog Dis 2011; 8: 887-900
  7. Morales-Barrera E, Calhoun N, Lobato-Tapia JL, Lucca V, Prado-Rebolledo O, Hernandez-Velasco X, Merino-Guzman R, Petrone-Garcia VM, Latorre JD, Mahaffey BD et al. Risks involved in the use of enrofloxacin for Salmonella Enteritidis or Salmonella Heidelberg in commercial poultry. Front Vet Sci 2016; 3: 72
  8. Fernandez Marquez ML, Burgos MJ, Pulido RP, Galvez A, Lopez RL. Biocide tolerance and antibiotic resistance in Salmonella isolates from hen eggshells. Foodborne Pathog Dis 2017; 14: 89-95
  9. Bolan NS, Szogi AA, Chuasavathi T, Seshadri B, Rothrock MJ, Panneerselvam P. Uses and management of poultry litter. World’s Poultry Science Journal 2010; 66: 673-698
  10. Cogan TA, Humphrey TJ. The rise and fall of Salmonella Enteritidis in the UK. J Appl Microbiol 2003; 94 (Suppl.): 114S-119S
  11. MacLennan CA. Antibodies and protection against invasive salmonella disease. Front Immunol 2014; 5: 635
  12. Lillehoj EP, Yun CH, Lillehoj HS. Vaccines against the avian enteropathogens Eimeria, Cryptosporidium and Salmonella. Anim Health Res Rev 2000; 1: 47-65
  13. Penha Filho RA, de Paiva JB, Arguello YM, da Silva MD, Gardin Y, Resende F,