Persistence of a Staphylococcus aureus small-colony variant under antibiotic pressure in vivo

被引:66
作者
Brouillette, E
Martinez, A
Boyll, BJ
Allen, NE
Malouin, F [1 ]
机构
[1] Univ Sherbrooke, Dept Biol, CEVDM, Sherbrooke, PQ J1K 2R1, Canada
[2] Eli Lilly & Co, Elanco Anim Hlth, Greenfield, IN USA
来源
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY | 2004年 / 41卷 / 01期
关键词
Staphylococcus aureus; hemB; small-colony variant; SCV; mastitis; antibiotic resistance;
D O I
10.1016/j.femsim.2003.12.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Staphylococcus aureus small-colony variants (SCVs) have been implicated in chronic and persistent infections. Bovine mastitis induced by S. aureus is an example of an infection difficult to eradicate by conventional antimicrobial therapies. In this study, the ability to colonize mouse mammary glands and persist under antibiotic treatment was assessed for S. aureus Newbould and an isogenic hemB mutant, which exhibited the classical SCV phenotype. The hemB mutant showed a markedly reduced capacity to colonize tissues. However, although the hemB mutant was as susceptible as S. aureus Newbould to cephapirin in vitro, it was over a 100 times more persistent than the parental strain in the mammary glands when 1 or 2 mg kg(-1) doses were administrated. These results suggest that, although the hemB mutant has a reduced ability to colonize mammary glands, the SCV phenotype may account for the persistence of S. aureus under antibiotic pressure in vivo. (C) 2004 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:35 / 41
页数:7
相关论文
共 29 条
[1]   Persistent wound infection after herniotomy associated with small-colony variants of Staphylococcus aureus [J].
Abele-Horn, M ;
Schupfner, B ;
Emmerling, P ;
Waldner, H ;
Göring, H .
INFECTION, 2000, 28 (01) :53-54
[2]   Prevention of diseases caused by Staphylococcus aureus using the peptide RIP [J].
Balaban, N ;
Collins, LV ;
Cullor, JS ;
Hume, EB ;
Medina-Acosta, E ;
da Motta, OV ;
O'Callaghan, R ;
Rossitto, PV ;
Shirtliff, ME ;
da Silveira, LS ;
Tarkowski, A ;
Torres, JV .
PEPTIDES, 2000, 21 (09) :1301-1311
[3]   GENTAMICIN-RESISTANT MENADIONE AND HEMIN AUXOTROPHIC STAPHYLOCOCCUS-AUREUS PERSIST WITHIN CULTURED ENDOTHELIAL-CELLS [J].
BALWIT, JM ;
VANLANGEVELDE, P ;
VANN, JM ;
PROCTOR, RA .
JOURNAL OF INFECTIOUS DISEASES, 1994, 170 (04) :1033-1037
[4]   Staphylococcus aureus menD and hemB mutants are as infective as the parent strains, but the menadione biosynthetic mutant persists within the kidney [J].
Bates, DM ;
von Eiff, C ;
McNamara, PJ ;
Peters, G ;
Yeaman, MR ;
Bayer, AS ;
Proctor, RA .
JOURNAL OF INFECTIOUS DISEASES, 2003, 187 (10) :1654-1661
[5]   Physiology and antibiotic susceptibility of Staphylocoecus aureus small colony variants [J].
Baumert, N ;
Von Eiff, C ;
Schaaff, F ;
Peters, G ;
Proctor, RA ;
Sahl, HG .
MICROBIAL DRUG RESISTANCE, 2002, 8 (04) :253-260
[6]   The fibronectin-binding proteins of Staphylococcus aureus may promote mammary gland colonization in a lactating mouse model of mastitis [J].
Brouillette, E ;
Talbot, BG ;
Malouin, F .
INFECTION AND IMMUNITY, 2003, 71 (04) :2292-2295
[7]  
Bruckner R, 1997, FEMS MICROBIOL LETT, V151, P1
[8]   EXPERIMENTAL BACTERIAL MASTITIS IN MOUSE [J].
CHANDLER, RL .
JOURNAL OF MEDICAL MICROBIOLOGY, 1970, 3 (02) :273-&
[9]   Fibronectin binding protein and host cell tyrosine kinase are required for internalization of Staphylococcus aureus by epithelial cells [J].
Dziewanowska, K ;
Patti, JM ;
Deobald, CF ;
Bayles, KW ;
Trumble, WR ;
Bohach, GA .
INFECTION AND IMMUNITY, 1999, 67 (09) :4673-4678
[10]   Bovine mastitis and intramammary drug delivery: review and perspectives [J].
Gruet, P ;
Maincent, P ;
Berthelot, X ;
Kaltsatos, V .
ADVANCED DRUG DELIVERY REVIEWS, 2001, 50 (03) :245-259