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Table 1 Bacterial strains and plasmids used in this work

From: Mutants in the lipopolysaccharide of Brucella ovis are attenuated and protect against B. ovis infection in mice

Bacterial strains/Plasmids

Characteristic

Source/Reference

Brucella ovis

  

PA

virulent strain, natural NalR

CITA collection

BoΔwadA

PA in frame deletion mutant in wadA Δ58-679

This work

BoΔwadB

PA in frame deletion mutant in wadB Δ49-195

This work

BoΔwadC

PA in frame deletion mutant in wadC Δ17-306

This work

BoPA-Gm

challenge strain, PA GmR

UN collection

Brucella melitensis

  

Rev 1

reference vaccine

CITA collection

E. coli

  

S17-1 λpir

mating strain with plasmid RP4 inserted into the chromosome

Simon et al. [[19]]

TOP10 F’

FlacI q Tn 10 (TetR) mcrA Δ(mrr-hsdRMS-mcrBC) 80lacZ ΔM15 ΔlacX74 recA1alaD139 endA1 nupG

Invitrogen

Plasmids

  

pCR2.1

cloning vector

Invitrogen

pJQK

derivated of pJQ200KS+; KmR, GmS

Scupham and Triplett [[20]]

pYRI-12

913-bp of B. abortus parental chromosomal DNA containing the wadA deletion allele, generated by PCR and cloned into pCR2.1

This work

pYRI-13

BamHI-XbaI fragment from pYRI-12 cloned into the corresponding sites of pJQK

This work

pYRI-1

570-bp of B. abortus parental chromosomal DNA containing the wadB deletion allele, generated by PCR and cloned into pCR2.1

Gil-Ramírez et al. [[7]]

pYRI-2

BamHI-XbaI fragment from pYRI-1 cloned into the corresponding sites of pJQK

Gil-Ramírez et al. [[7]]

pYRI-14

934-bp of B. ovis parental chromosomal DNA containing the wadC deletion allele, generated by PCR and cloned into pCR2.1

This work

pYRI-15

BamHI-XbaI fragment from pYRI-14 cloned into the corresponding sites of pJQK

This work

  1. CITA, Centro de investigación y tecnología agroalimentaria; UN, Universidad de Navarra.