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Journal of Clinical Microbiology, October 2000, p. 3908-3909, Vol. 38, No. 10
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
LETTERS TO THE EDITOR
Bacteriocin Production by Lactobacillus salivarius
of Animal Origin
 |
LETTER |
Bacteriocins are secreted oligopeptides, proteins or protein
complexes with antimicrobial activity against strains taxonomically related to the producer organism (2, 10). In recent years, numerous reports have been published on antimicrobial peptides or
proteins produced by gram-positive bacteria, including lactic acid
bacteria (LAB) (4, 7), and bacteriocins for lactobacilli from different environments have been described (3).
However, only two reports mention bacteriocin production in
Lactobacillus salivarius isolates, which were obtained from
Japanese grass leaves (1) and from a human vaginal sample
(8). The objective of this study was to detect bacteriocin
production in LAB isolated from animal fecal samples in order to
determine their spectrum of action, including human pathogens, and
their significance in the ecology of the gastrointestinal environment.
Twenty-nine LAB isolates recovered from fecal samples of 20 pigs and 9 pets (cats and dogs) were tested for antimicrobial activity (one LAB
isolate per fecal sample). These isolates were the following: 18 Lactobacillus salivarius, 1 Lactobacillus
fructivorans, 3 Lactobacillus fermentum, 1 Lactobacillus viridescens, 1 Lactobacillus brevis, 2 Lactobacillus spp., 2 Pediococcus
pentosaceus, and 1 Pediococcus acidilactici. Fifty-two
bacterial isolates belonging to eight different genera and 26 different
species were used as indicators for bacteriocin production. Human
pathogens and LAB of animal fecal origin were included, among others,
in the group of indicator strains (Table
1). Bacteriocin production was evaluated by a method previously described (5).
Bacteriocin activity was detected in 11 of 18 (61%) L. salivarius isolates tested (all of them recovered from pigs) but
not among the other species of LAB studied. Table 1 shows the spectrum of antimicrobial activity of these 11 isolates against the 52 indicator
isolates used. All bacteriocin-producing L. salivarius isolates strongly inhibited the growth of the three clinical
Staphylococcus aureus isolates tested as indicators (two
methicillin resistant and one methicillin susceptible), and for five of
them, antimicrobial activity was also detected against clinical
Staphylococcus epidermidis isolates (methicillin resistant
and susceptible). None of these 11 bacteriocin-producing L. salivarius isolates showed growth inhibition activity against
Enterococcus spp., Bacillus spp., or E. coli. Two of these isolates (X13 and X61) showed the widest range
of action, inhibiting the growth of nine and seven different species of
indicators tested, respectively. Curiously, both strains inhibited the
growth of four different LAB species of animal intestinal origin, and
X13 also inhibited the growth of Listeria murrayi and
Micrococcus luteus.
A negative PCR result was obtained with these 11 bacteriocin-producing
L. salivarius isolates when the specific plnA
primers for plantaricine A were used (9). Bacteriocin
activity of X13 and X61 could not be demonstrated after filtration
(Millipore filter; 45-µm pore size), and this fact could be explained
by its adsorption to the cell membrane.
Therefore, antimicrobial peptides constitute a potent adaptation
advantage for those strains that dominate in a medium and could play an
important role in the ecology of the gastrointestinal tract. In fact,
L. salivarius is a species frequently found in the
intestinal tract of pigs (6), and this could be
explained by the production of bacteriocins in fecal L. salivarius isolates active against other animal fecal LAB.
On the other hand, the high inhibitory activity of these bacteriocins
against methicillin-resistant and -susceptible staphylococci could be
of clinical interest.
 |
ACKNOWLEDGMENTS |
We thank Carmen Tenorio for providing us with lactic acid bacteria
for this study.
This work was financed in part by a grant of the Fondo de
Investigaciones Sanitarias (00/0545), and Beatriz Robredo has a fellowship from the University of La Rioja, Logroño, Spain.
 |
FOOTNOTES |
*
Phone:
34-941-299284 Fax: 34-941-299274 E-mail:
carmen.torres{at}daa.unirioja.es
 |
REFERENCES |
| 1.
|
Arihara, K.,
S. Ogihara,
T. Mukai,
M. Itoh, and Y. Kondo.
1996.
Salivacin 140, a novel bacteriocin from Lactobacillus salivarius subsp. salicinius T140 active against pathogenic bacteria.
Lett. Appl. Microbiol.
22:420-424[Medline].
|
| 2.
|
Jack, R. W.,
J. R. Tag, and B. Ray.
1995.
Bacteriocins of gram-positive bacteria.
Microbiol. Rev.
59:171-200[Abstract/Free Full Text].
|
| 3.
|
Klaenhammer, T. R.
1988.
Bacteriocin of lactic acid bacteria.
Biochimie
70:337-340[Medline].
|
| 4.
|
Klaenhammer, T. R.
1993.
Genetics of bacteriocins produced by lactic acid bacteria.
FEMS Microbiol. Rev.
12:39-86[Medline].
|
| 5.
|
Navarro, L.,
M. Zarazaga,
J. Sáenz,
F. Ruiz-Larrea, and C. Torres.
2000.
Bacteriocin production by lactic acid bacteria isolated from Rioja red wines.
J. Appl. Microbiol.
88:44-51[CrossRef][Medline].
|
| 6.
|
Nemcova, R.,
A. Laukova,
S. Gancarcikova, and R. Kastel.
1997.
In vitro studies of porcine lactobacilli for possible probiotic use.
Berl. Muench. Tieraerztl. Wochenschr.
110:413-417.
|
| 7.
|
Nissen-Meyer, J., and I. F. Nes.
1997.
Ribosomally synthesized antimicrobial peptides: their function, structure, biogenesis, and mechanism of action.
Arch. Microbiol.
167:67-77[CrossRef][Medline].
|
| 8.
|
Ocaña, V. S.,
A. A. Pesce de Ruiz Holgado, and M. E. Nader-Macías.
1999.
Characterization of a bacteriocin-like substance produced by a vaginal Lactobacillus salivarius strain.
Appl. Environ. Microbiol.
65:5631-5635[Abstract/Free Full Text].
|
| 9.
|
Remiger, A.,
M. A. Ehrmann, and R. F. Vogel.
1996.
Identification of bacteriocin genes in lactobacilli by polymerase chain reaction (PCR).
Syst. Appl. Microbiol.
19:28-34.
|
| 10.
|
Tagg, J. R.,
A. S. Dajani, and L. W. Wannamaker.
1976.
Bacteriocins of gram-positive bacteria.
Bacteriol. Rev.
40:722-756[Free Full Text].
|
| | | | |
Beatriz Robredo
Carmen Torres*
Area de Bioquimica y Biologia Molecular Universidad de
La Rioja 26004 Logroño, Spain
|
Journal of Clinical Microbiology, October 2000, p. 3908-3909, Vol. 38, No. 10
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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