Recoding anaerobic regulator fnr of Salmonella Typhimurium attenuates it's pathogenicity.


Journal

Microbial pathogenesis
ISSN: 1096-1208
Titre abrégé: Microb Pathog
Pays: England
ID NLM: 8606191

Informations de publication

Date de publication:
Jul 2022
Historique:
received: 11 02 2022
revised: 12 05 2022
accepted: 13 05 2022
pubmed: 25 5 2022
medline: 18 6 2022
entrez: 24 5 2022
Statut: ppublish

Résumé

How recoding of fnr, an anaerobic regulatory gene, affects pathogenicity related parameters of Salmonella Typhimurium (STM). The fnr gene was recoded by substituting all of it's codons with synonymous rare codons of STM. Recoding fnr gene severely reduced the ability of the recoded mutant to compete with wild strain under nutrient depletion condition. Mutants were also less motile than the wild strain and their biofilm forming ability was significantly decreased as compared to wild strain. The recoded strain showed significant reduced survival within murine macrophages (RAW264.7) and monocyte derived macrophage of poultry origin. The colonisation ability of recoded mutant in liver and spleen of mice on day 5 of post infection was significantly reduced. The recoded strain exhibited significant reduction in faecal shedding on day 1 and 5 after infection. Our study showed that recoding the anaerobic regulator fnr of STM significantly compromised its growth, decreased motility, biofilm forming ability and survival within macrophages. Further, the recoded fnr strain showed reduced colonisation ability and faecal shedding in mice. Thus, these findings highlight that recoding the global anaerobic regulator fnr of Salmonella Typhimurium attenuates its pathogenicity.

Identifiants

pubmed: 35609767
pii: S0882-4010(22)00204-2
doi: 10.1016/j.micpath.2022.105591
pii:
doi:

Substances chimiques

Bacterial Proteins 0
Codon 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

105591

Informations de copyright

Copyright © 2022 Elsevier Ltd. All rights reserved.

Auteurs

K C Nikhil (KC)

Division of Animal Biochemistry, Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar Pradesh, 243122, India.

Laxmi Noatia (L)

Department of Veterinary Physiology & Biochemistry, College of Veterinary Sciences & A.H., Central Agricultural University, Selesih, Aizawl, Mizoram, 796014, India.

Swagatika Priyadarsini (S)

Division of Animal Biochemistry, Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar Pradesh, 243122, India.

M Pashupathi (M)

Division of Animal Biochemistry, Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar Pradesh, 243122, India.

Jagan Mohanarao Gali (JM)

Department of Veterinary Physiology & Biochemistry, College of Veterinary Sciences & A.H., Central Agricultural University, Selesih, Aizawl, Mizoram, 796014, India.

M Ayub Ali (MA)

Department of Veterinary Physiology & Biochemistry, College of Veterinary Sciences & A.H., Central Agricultural University, Selesih, Aizawl, Mizoram, 796014, India.

S K Behera (SK)

Department of Veterinary Medicine, College of Veterinary Sciences & A.H., Central Agricultural University, Selesih, Aizawl, Mizoram, 796014, India.

Bhaskar Sharma (B)

Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar Pradesh, 243122, India.

Parimal Roychoudhury (P)

Department of Veterinary Microbiology, College of Veterinary Sciences & A.H., Central Agricultural University, Selesih, Aizawl, Mizoram, 796014, India.

Ajay Kumar (A)

Division of Animal Biochemistry, Indian Veterinary Research Institute, Izatnagar, Bareilly, Uttar Pradesh, 243122, India. Electronic address: ajayivri@gmail.com.

Parthasarathi Behera (P)

Department of Veterinary Physiology & Biochemistry, College of Veterinary Sciences & A.H., Central Agricultural University, Selesih, Aizawl, Mizoram, 796014, India. Electronic address: partha_vet@yahoo.co.in.

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