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Journal of Bacteriology, February 2000, p. 1080-1088, Vol. 182, No. 4
0021-9193/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Departments of Microbiology1 and Crop Sciences,2 University of Illinois at Urbana-Champaign, Urbana, Illinois 61801
Received 13 September 1999/Accepted 19 November 1999
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ABSTRACT |
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Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
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Conjugal transfer of the Ti plasmids from Agrobacterium tumefaciens is controlled by autoinduction via the transcriptional activator TraR and the acyl-homoserine lactone ligand, Agrobacterium autoinducer (AAI). This control process is itself regulated by opines, which are small carbon compounds produced by the crown gall tumors that are induced by the bacteria. Opines control autoinduction by regulating the expression of traR. Transfer of pTiC58 from donors grown with agrocinopines A and B, the conjugal opines for this Ti plasmid, was detected only after the donors had reached a population level of 107 cells per cm2. Donors incubated with the opines and AAI transferred their Ti plasmids at population levels about 10-fold lower than those incubated with opines only. Transcription of the tra regulon, as assessed by monitoring a traA::lacZ reporter, showed a similar dependence on the density of the donor population. However, even in cultures at low population densities that were induced with opines and AAI, there was a temporal lag of between 15 and 20 h in the development of conjugal competence. Moreover, even after this latent period, maximal transfer frequencies required several hours to develop. This lag period was independent of the population density of the donors but could be reduced somewhat by addition of exogenous AAI. Quorum-dependent development of conjugal competence required control by the opine regulon; donors harboring a mutant of pTiC58 deleted for the master opine responsive repressor accR transferred the Ti plasmid at maximum frequencies at very low population densities. Similarly, an otherwise wild-type derivative of pTiC58 lacking traM, which codes for an antiactivator that inhibits TraR activity, transferred at high frequency in a population-independent manner in the absence of the conjugal opines. Thus, while quorum sensing is dependent upon autoinduction, the two phenomena are not synonymous. We conclude that conjugal transfer of pTiC58 is regulated in a quorum-dependent fashion but that supercontrol of the TraR-AAI system by opines and by TraM results in a complex control process that requires not only the accumulation of AAI but also the expression of TraR and the synthesis of this protein at levels that overcome the inhibitory activity of TraM.
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INTRODUCTION |
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Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
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Conjugal transfer of the Ti plasmids from Agrobacterium tumefaciens is regulated directly by the transcriptional activator TraR and its acyl-homoserine lactone (acyl-HSL) ligand, Agrobacterium autoinducer [AAI; N-(3-oxo-octanoyl)-L-homoserine lactone] (16, 34, 40; reviewed in reference 12). TraR, in its interaction with AAI, controls conjugation by autoinduction, a process by which the bacteria induce gene sets in response to signals they themselves produce. This regulatory strategy is believed to tie plasmid transfer to the population density of the donor in what has come to be called the quorum-sensing effect (reviewed in reference 18). The acyl-HSL autoinducers, which are produced by the bacteria themselves, are released into the environment, where they accumulate to ever higher concentrations. Moreover, because these molecules apparently can exchange between the intracellular and extracellular compartments, they transduce the signal among the individual members of the population. The quorum-sensing phenomenon results from the need for the accumulation of the autoinducer to some threshold concentration within the habitat. Not until it reaches this critical level does the autoinducer productively interact with the transcriptional activator, thereby initiating expression of the target genes. Thus, the bacteria gauge their population size by sensing the amount of the autoinducer present in the environment.
Expression of bioluminescence in Vibrio fischeri, the paradigm quorum-sensing system, is controlled by the transcriptional activator LuxR and the acyl-HSL signal molecule, Vibrio autoinducer [VAI; N-(3-oxo-hexanoyl)-L-homoserine lactone] (reviewed in reference 7). At low population densities, the lux operon is not expressed. However, luminescence is strongly induced when, due to population growth, VAI accumulates to its threshold level. Experimentally, the quorum dependence of lux gene activation can be circumvented by adding the acyl-HSL signal to cultures of cells at low population density (8, 10). LuxR is produced at a relatively high basal level during growth (reviewed in reference 36); under such conditions, the activator is not limiting and the lux operon is almost immediately induced.
Autoinduction of Ti plasmid transfer is somewhat more complex than that of lux-mediated bioluminescence. Expression of the tra regulon also is controlled by a second set of exogenous signals, highly specific compounds called the conjugal opines that are produced by the crown gall tumors induced by the phytopathogen (reviewed in reference 12). These compounds, the production of which is coded for by genes inherited from the bacterium by the transformed plant cells, control conjugation by regulating the expression of traR (15, 35). Thus, unlike lux, autoinduction of tra is tightly controlled at the transcriptional level by regulating the expression of traR. Furthermore, the activity of TraR itself is modulated by the antiactivator, TraM (17, 21). This small protein interacts with TraR to form a complex that no longer can bind to promoters of the tra regulon (22, 26a). Like the lux system, the expression of traI, the gene responsible for the production of AAI, requires activated TraR (23). However, given that the expression of traR requires the opine signal, only very small amounts of AAI are produced when donor populations are growing in the absence of crown gall tumors. Thus, autoinduction of the tra regulon first requires the induction of the expression of traR. Then, the activator must accumulate to levels sufficient to overcome the inhibitory activity of TraM. In the meantime, autoinduction and its attendant quorum dependence require that AAI accumulate to the levels necessary to activate the newly synthesized TraR.
The requirements for TraR and AAI indicate that conjugal transfer is controlled by autoinduction and predict that transfer is regulated in a quorum-dependent manner. This appears to be the case; transfer of the octopine-type Ti plasmid pTiR10 occurs only when the donor population has reached a critical size (14). Moreover, density dependence could be circumvented by addition of exogenous AAI to the culture. However, how the hierarchical control exerted by the opine regulon influences the TraR-dependent quorum-sensing system has not been critically examined, nor has the role of TraM, if any, in quorum dependence been determined. In this study, we analyzed the influence of regulation by the conjugal opine on the expression of the quorum-sensing system of the nopaline-type Ti plasmid, pTiC58. We also examined the roles of the opine-responsive regulatory protein AccR and the antiactivator TraM in controlling Ti plasmid transfer. Our results indicate that these regulatory components, while not required for TraR-AAI-mediated autoinduction, are essential for the quorum-dependent character of Ti plasmid transfer.
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MATERIALS AND METHODS |
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Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
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Bacterial strains and plasmids.
All strains of A. tumefaciens used in this study are derivatives of the
nopaline-agrocinopine-type pathogen C58 (Table
1). The Ti plasmids used in this study
are derivatives of pTiC58 and are described in Table 1.
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Media and growth conditions. Bacteria were grown in Luria-Bertani broth (Gibco-BRL, Gaithersburg, Md.), on nutrient agar plates (Difco Laboratories, Detroit, Mich.), or in AB minimal medium containing 0.2% mannitol (ABM) (5). AB medium solidified with 1.5% agar and containing 1 mM nopaline (Sigma Chemical Co., St. Louis, Mo.) and 9 mM arginine, along with rifampin (50 µg per ml) and streptomycin (200 µg per ml), was used as the selection medium for conjugation assays (2). In this medium, nopaline allows Ti plasmid-dependent utilization of arginine as the sole source of carbon (2). A preparation containing a mixture of agrocinopines A and B was partially purified from extracts of crown gall tumors induced on tomato plants by A. tumefaciens C58 as described by Hayman et al. (19). The concentration of the opines in the mixture, expressed as arabinose equivalents, was determined by the phloroglucinol assay as previously described (19). All cultures were incubated at 28°C. Cultures in liquid medium were incubated with shaking to ensure aeration. Growth of liquid cultures was followed by Klett colorimetry (red filter) or by turbidity measurements at 600 nm with a Spectronic 20 spectrophotometer.
Preparation of AAI.
Crude preparations of AAI were prepared
by growing cells of strain NT1(pTiC58
accR) to saturation
in ABM medium. The cells were removed by centrifugation, and the
culture supernatant was sterilized by filtration. The preparation was
stored at 4°C. Pure synthetic AAI was the gift of David Lynn,
University of Chicago.
Induction of conjugation with agrocinopines. Donors were grown on sterile filters (diameter, 13 mm; Millipore Corp., Bedford, Mass.) on small towers (5 mm [diameter] by 8 mm [height]) of ABM agar medium impregnated with a mixture of agrocinopines A and B (2 mM). When required, the towers also were impregnated with an aqueous solution of AAI. At the appropriate time intervals, cells were removed from the filters by vortexing them in 500-µl volumes of 0.9% NaCl.
Conjugation assays. Conjugal transfer was assessed by the spot plate mating method, which measures only initial transfer events (2). The recipient was spread as a confluent lawn over the surfaces of the selection plates. Five-microliter volumes of donor cells at decreasing cell concentrations were spotted onto the surface of the recipient lawn, and the cultures were incubated at 28°C for 48 h. Transconjugant colonies appearing within the donor inoculum spots were enumerated with the aid of a dissecting microscope. In all cases, A. tumefaciens C58C1RS was used as the recipient. Titers of donor cultures were determined by dilution plating in triplicate on NA plates at the time of mating.
Alternatively, when it was necessary to control the numbers of both donors and recipients, matings were performed on nitrocellulose filters essentially as described by Cook and Farrand (6). Donor and recipient bacteria grown in liquid ABM medium were adjusted to the desired population densities. Volumes were mixed, the cells were collected onto sterile nitrocellulose filters (diameter, 25 mm; Millipore Corp.), and the filters were incubated on ABM plates for 2 h at 28°C. The cells were resuspended from the filters in 1-ml volumes of 0.9% NaCl and diluted, and 10-µl volumes of appropriate dilutions were spotted in triplicate onto the surface of the selection medium. Following incubation for 48 h, transconjugant colonies appearing within the spots were enumerated as described above. Titers of donor and recipient cultures were determined by dilution plating in triplicate on NA plates at the time of mating. To assess the effects of Ti plasmid mutations on quorum sensing, a series of 1:2 dilutions of an early-exponential-phase culture of the appropriate donor was prepared in 1-ml volumes of ABM medium and the cultures were incubated overnight at 28°C with shaking. The next morning, the culture showing the faintest turbidity (ca. 106 to 107 CFU per ml) was chosen, and the cells were collected by centrifugation, washed twice with AB medium lacking mannitol, and resuspended in a 1-ml volume of ABM medium. A 750-µl volume of this preparation was used to inoculate 200 ml of ABM medium, and the culture was incubated at 28°C with shaking. At intervals of time, appropriate volumes were removed and the cells were concentrated by filtration onto nitrocellulose membranes if needed and mated on filters with C58C1RS as described above. Titers of the donor were determined by dilution plating in triplicate on NA plates at the time of mating.
-Galactosidase assays.
-Galactosidase activity,
expressed as units per 109 cells, was quantified as
described previously (13).
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RESULTS |
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Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
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Conjugal transfer of pTiC58 is dependent upon donor population size. The transfer of wild-type pTiC58 (Fig. 1) requires induction by the sugar phosphodiester opines agrocinopines A and B (1, 9) and also activation of TraR by AAI (35). Since TraR and AAI comprise the two components of a typical quorum-sensing system, we determined whether the frequency of transfer of wild-type pTiC58 is influenced by the size of the donor population. Filters inoculated with cultures of NT1(pTiC58) at low density were placed on agar towers impregnated with agrocinopines A and B with or without AAI, and the filter-bound cultures were incubated at 28°C. At intervals of time, a filter of each culture set was removed, the cells were resuspended in buffer and diluted, and volumes of appropriate dilutions were spot-mated with a confluent culture of the recipient strain, C58C1RS, as described in Materials and Methods. As shown in Fig. 2, the two culture sets, one with AAI and the other without, grew exponentially at similar rates from beginning titers of about 106 CFU per cm2. In the set induced with agrocinopines alone, transfer was first detected after 22 h of growth, when the donors had reached a density of 1.6 × 107 CFU per cm2 (Fig. 2A). Transfer frequencies increased steadily as the density of the donor population increased and plateaued when the culture reached a population density of close to 108 CFU per cm2. Adding AAI at the time of inoculation onto opine induction medium resulted in detectable transfer after 8 h of incubation at a donor population density of 2 × 106 CFU per cm2 (Fig. 2B). Transfer frequencies increased rapidly over the next 10 h as the density of the donor population increased to about 3 × 107 CFU per cm2. From that point, transfer frequencies increased more slowly as the donor population reached a density of 1.1 × 108 CFU per cm2. When examined as a function of population density, the donor set incubated with opines and AAI initiated conjugal transfer at a significantly lower density compared to the culture set incubated with the conjugal opine only (Fig. 2C). Thus, a threshold donor population density is required to initiate conjugation, and this density can be lowered by addition of exogenous AAI.
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Induction of tra genes is dependent upon donor
population density.
We determined whether induction of
transcription of the tra regulon is itself dependent upon
donor population density and the accumulation of AAI. Strain
NT1(pTiC58; pJM749), which harbors a wild-type Ti plasmid and a clone
that contains a TraR-dependent traA::lacZ reporter fusion (Table 1),
was induced with agrocinopines on solid medium in the presence and
absence of exogenous AAI as described above. Expression of the reporter
fusion was monitored at different incubation times by assessing levels
of -galactosidase activity. In the absence of AAI, the reporter was
not expressed at detectable levels until the population had reached a
density of between 106 and 107 CFU per
cm2 (Fig. 3). Expression
levels increased almost 10-fold as the population increased to about
2 × 108 CFU per cm2. Adding AAI at the
beginning of growth resulted in expression of the traA
reporter at a population density of between 105 and
106 CFU per cm2, a donor density at least
10-fold lower than that observed for the culture incubated with the
opines alone (Fig. 3). Moreover, expression of the reporter increased
to almost 1,500 U per 109 cells as the culture density rose
to around 107 CFU per cm2. This level of
expression is almost 100 times that seen in cells of the culture not
exposed to exogenous AAI that were at a similar population density.
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Induction of conjugation is dependent upon population density and
induction time.
Transfer of the Ti plasmid from a culture of
NT1(pTiC58) induced with agrocinopines only was undetectable
(<10
6 transconjugants per input donor) for the first
15 h of incubation (Fig. 2A). Like other quorum-sensing systems,
this could reflect the time required for the autoinducer to accumulate
to levels sufficient to activate TraR. However, transfer from a culture of NT1(pTiC58) induced with the opines and AAI simultaneously also was
undetectable for a period of almost 8 h and then steadily increased over a period beginning about 15 h after inoculation (Fig. 2B). This lag is not characteristic of other quorum-sensing systems (8, 10, 38). We suspected that even with sufficient AAI, the donor population requires time to fully express and assemble a
functional transfer system. To differentiate between the time required
to express the transfer system and population density effects, a set of
10-fold serially diluted donor cultures was prepared from an
early-exponential-phase culture of NT1(pTiC58). Two sets of such
diluted cultures were incubated for 15 h on solid ABM medium
supplemented with agrocinopines, one with and the other without AAI.
Two additional sets were incubated for 20 h, on the same two types
of medium. This resulted in sets of donor cultures exposed to opines or
to opines and AAI, one for 15 h, the other for 20 h, each
with increasing initial donor population densities within the set.
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Opine control and TraM are required for quorum-dependent Ti plasmid
transfer.
The quorum-sensing system of pTiC58 is itself controlled
by the opine regulon (35). In the absence of the conjugal
opine, expression of traR is strongly repressed. Opines
induce transfer in part because these signals induce the expression of
traR. Thus, failure to transfer at low densities, even in
the presence of the conjugal opine, may result from the need to produce
adequate levels of TraR. We tested this possibility by examining the
conjugal transfer properties of pTiC58accR at increasing
donor densities in the absence and presence of AAI. This derivative of
pTiC58 contains a deletion mutation in accR, the gene coding
for the opine-responsive repressor that regulates expression of
traR (Fig. 1) (1). As a consequence, strains
harboring this Ti plasmid express traR constitutively,
produce large amounts of AAI, and transfer the plasmid at high
frequency in the absence of the conjugal opine (1, 23, 34).
accR) with an initial population
density of about 104 CFU per ml was prepared from a
low-density (ca. 106 CFU/ml) exponential-phase preculture
as described in Materials and Methods. The culture was split in two,
AAI was added to one subculture, and the two cultures were incubated in
parallel. Samples were removed at intervals, the donor titers were
determined by dilution plating, and the donors were mated with C58C1RS
on filters. As shown in Fig. 4A, the Ti
plasmid transferred at high frequency from all samples, even from those
in which the donor population density was about 105 CFU per
cm2. Furthermore, transfer frequency did not increase as
the donor population density increased. Such high frequency transfer
was not influenced by the addition of exogenous AAI at the beginning of
the culture period.
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Ti plasmid-less A. tumefaciens is an inefficient
conjugal recipient.
We have proposed that autoinduction and TraM
cooperate to prevent the induction of the Ti plasmid tra
system at low donor population levels (21, 22, 35). However,
it is not clear why activation of the transfer system should be avoided
under such conditions. It is possible that the agrobacteria that
comprise the recipient pool are not efficient acceptors of Ti plasmids via conjugation. Delaying expression of the tra apparatus
until donor population levels are high may represent a mechanism that has evolved to overcome such a deficiency. We tested this hypothesis by
determining the efficiency by which a Ti plasmid-less A. tumefaciens strain inherits pTiC58. Late-exponential-phase
cultures of NT1(pTiC58accR) were mated at input densities
of 102 to 108 CFU per cm2 with
C58C1RS at densities between 108 and 102 CFU
per cm2 (33). This yielded ratios of donors to
recipients ranging from 106 to 106. As
expected, transfer frequencies, expressed as the number of transconjugants per input recipient, were highest when donors were
present in numbers equal to or greater than those of the recipients
(Fig. 5). However, even when donors were
in 1,000-fold excess, transfer frequencies never exceeded
102 per input recipient.
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DISCUSSION |
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Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
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Although TraR serves to regulate conjugation in a density-dependent manner, our results indicate that control of plasmid transfer is a complex process involving other environmental inputs. Clearly, the availability of opines constitutes the primary determinant for initiating the induction of the conjugal transfer process. Opines trigger conjugation by controlling the expression of traR (15, 30, 35). Furthermore, the active traR alleles of all Ti plasmids examined to date are expressed as components of opine-regulated operons, suggesting that regulation by these nutrient sources is important to the biology of Ti plasmid transfer (15, 30, 35; reviewed in reference 12).
In the lux system, LuxR is produced at a relatively high level in the absence of VAI (reviewed in reference 36), making the induction of bioluminescence dependent primarily on the accumulation of the autoinducer. Thus, the addition of exogenous signal results in an almost immediate induction of the lux operon. However, with the availability of TraR itself controlled, the Ti plasmid quorum-sensing system is insensitive to exogenous autoinducer in the absence of the conjugal opine. This hierarchical control may represent a protective measure to ensure that, when not influenced by crown gall tumors, the tra regulon will not respond inadvertently to acyl-HSLs produced by other microorganisms present in the soil (32). Furthermore, even upon opine induction, there is a substantial lag period before the tra regulon is induced. Some of this lag can be accounted for by the necessity to accumulate AAI to sufficient levels. Thus, in the presence of opines, the addition of AAI to the cultures results in tra gene induction and a corresponding increase in conjugal transfer frequencies at population levels lower than those in cultures induced with the opines alone (Fig. 2 and 3). However, there remained a temporal lag even when AAI was added early in the culture cycle, and this lag was independent of the population density of the donor culture (Table 2). Thus, in addition to a dependence on the accumulation of AAI for quorum sensing, there is a temporal component to the induction of conjugal transfer. Under these conditions, between 15 and 20 h is required for the development of conjugation competence following addition of the conjugal opine.
We propose that the observed lag in the induction of conjugation
following the addition of opines is multivariate. Clearly, TraR first
must be expressed to levels sufficient to activate transcription.
Concomitantly, AAI must accumulate to its threshold concentration. The
kinetics of autoinducer production and accumulation no doubt contribute
to the lag period although, since growth is occurring, this requirement
establishes the quorum-sensing nature of the system. This conclusion is
supported by our observations that, under conditions in which AAI is
not limiting, high levels of transfer can occur at low donor population
densities as long as sufficient time is allowed, presumably for gene
induction and construction of the conjugal apparatus (Table 2).
Alternatively, the lag may result from changes in culture conditions,
such as oxygen availability or pH, attendant on the growth of the donor on the filter surface. However, this hypothesis is highly unlikely, as
conditions of anaerobiosis and acidic pH are strongly inhibitory to Ti
plasmid conjugation (39). Similarly, the low transfer frequencies at early times cannot reflect the need to overcome an
inhibitor present in the medium; conjugal transfer of the
accR and traM mutants of pTiC58 is not
inhibited by fresh medium, even at very low population densities (Fig.
4).
The induction of TraR to levels sufficient to activate tra gene expression is itself not simple. In the wild-type case, the activity of the transcription factor is inhibited by TraM, also coded for by the Ti plasmid (21). This antiactivator binds to TraR, thereby preventing activation of expression of the tra regulon (22, 26a). Thus, induction of traR expression is not sufficient to immediately activate the tra regulon, even when AAI is present in nonlimiting amounts. Rather, TraR first must accumulate to a level in excess of that of TraM. Finally, once TraR has been activated by AAI, the tra regulon must be expressed and the components of the transfer machinery must be assembled.
Actual expression of the tra regulon, as assessed by a
traA::lacZ reporter fusion, mirrored
the kinetics of development of conjugation competence in the donor
population (Fig. 3). Thus, transcription is dependent on induction by
the conjugal opines and also on the accumulation of the donors to a
critical density. This threshold population level can be lowered by
addition of the acyl-HSL signal (Fig. 3), indicating that quorum
sensing operates at the level of transcription. Addition of AAI at the
time of opine induction led to levels of traA expression
substantially higher than those finally obtained by cultures induced
with the opine only (Fig. 3). Yet, at comparable threshold population
levels between 106 and 107 CFU per
cm2, the two donor cultures transferred the Ti plasmid at
similar frequencies (Fig. 2 and data not shown). Thus, the
extraordinarily high level of traA expression observed in
the donor culture incubated with opines and AAI did not translate to
higher levels of conjugation. Similarly, increased levels of
tra gene expression from the octopine-type Ti plasmid pTiR10
do not result in higher frequencies of plasmid transfer
(14). Ti plasmid copy number is up-regulated five- to
sevenfold by TraR and AAI (25). We suggest that the very high levels of -galactosidase present in donors cultured with opines
and AAI are due to this increase in plasmid copy number rather than to
increased rates of transcription of the tra regulon itself.
The effect is cumulative; cells incubated with opines only do not
exhibit this high level of activity until late in the cycle because the
increase in Ti plasmid copy number is itself controlled by quorum
sensing and does not become a factor until after the threshold
population level is reached.
Remarkably, the quorum dependency of conjugal transfer is reliant upon supercontrol of TraR. Releasing TraR from the control of opines or of TraM results in donors that become competent for conjugal transfer at population densities several orders of magnitude lower than that required by the wild-type system (Fig. 4). While it could be argued that these donors still may show a density dependence for transfer, the threshold is well below that intended by the system. Transfer by these two mutant donor types still requires TraR and AAI. Thus, abolishing supercontrol separates autoinduction, which is dependent on the activator and its acyl-HSL signal, from quorum sensing. Given this differentiation, it is clear that autoinduction and quorum sensing are not synonymous. We propose that the former term be used as first defined by Nealson et al. (29): the self-induced expression of a gene system in response to a signal produced by the population of bacteria itself. On the other hand, the population density-dependent character of quorum sensing is an outcome of autoinduction and, depending on the system, may or may not require additional regulatory components.
Clearly, Ti plasmid transfer is regulated in a population-dependent manner. However, quorum sensing requires not only TraR and AAI but also control of traR expression by the opine regulon and TraR activity by TraM. From our results, we propose an integrated model in which, in the absence of the conjugal opines, expression of traR on pTiC58 is repressed by AccR (Fig. 6A). However, under such conditions, the arc operon is expressed at a basal level sufficiently high to produce enough TraR to activate the tra regulon. TraM serves to inactivate this small amount of TraR, thus preventing premature conjugation (Fig. 6A). When opines are present, AccR is inactivated, expression of the arc operon is derepressed, and TraR is produced in amounts sufficient to overcome the available TraM (Fig. 6B). At the same time, AAI is accumulating in the environment, and when the signal has reached its threshold level corresponding to some critical population size, TraR is activated and induces expression of the tra regulon. Following gene expression, the conjugal apparatus is assembled and the donors become competent to transfer the Ti plasmid.
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While the model is consistent with the available information, it is not at all clear why conjugation should be dependent upon the size of the donor population. Transfer of the Ti plasmids is important in two respects. First, such transfer provides a mechanism by which this virulence element can test new chromosomal backgrounds for greater fitness in a given environment (12). Second, Ti plasmids evolve in part by recombination with other, dissimilar Ti and opine-catabolism plasmids (31). We have proposed that the quorum-sensing system evolved in response to the need of the Ti plasmid to transfer from tumorigenic donors to such Agrobacterium recipients (12). Consistent with this hypothesis, nonpathogenic agrobacteria, some with large opine-catabolic plasmids, commonly are isolated from crown gall tumors and surrounding soils (3, 4, 27, 28). Thus, a large population of primed donors would maximize the probability that these recipients are efficiently mated. Our results showing that such recipients may not be fully competent to receive a Ti plasmid (Fig. 5) suggest that there exist genetic barriers to the transfer of these elements and provide an additional impetus for the induction of conjugation among all members of the donor population.
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ACKNOWLEDGMENTS |
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We thank Zhao-Qing Luo, Pei-Li Li, Philippe Oger, and Clay Fuqua for helpful discussions and David Cook and Pei-Li Li for excellent graphics assistance.
This work was supported in part by grant no. R01 GM52465 from the NIH to S.K.F.
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FOOTNOTES |
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* Corresponding author. Mailing address: Department of Crop Sciences, University of Illinois at Urbana-Champaign, 240 Edward R. Madigan Laboratory, 1201 West Gregory Dr., Urbana, IL 61801. Phone: (217) 333-1524. Fax: (217) 244-7830. E-mail: stephenf{at}uiuc.edu.
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REFERENCES |
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Top
Abstract
Introduction
Materials and Methods
Results
Discussion
References
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| ALL ASM JOURNALS |
) are expressed as
transconjugants per input donor and donor population densities (
)
are expressed as CFU per square centimeter. Each mating was quantified
in triplicate, and the experiment was repeated three times. The results
of a representative experiment are presented. (C) The results of the
two experiments in which transfer frequency is expressed as a function
of the donor population density. 
