Pili contribute to biofilm formation in vitro in Mycobacterium tuberculosis
Organized bacterial communities, or biofilms, provide an important reservoir for persistent cells that are inaccessible or tolerant to antibiotics. Curli pili are cell-surface structures produced by certain bacteria and have been implicated in biofilm formation in these species. In order to determin...
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description | Organized bacterial communities, or biofilms, provide an important reservoir for persistent cells that are inaccessible or tolerant to antibiotics. Curli pili are cell-surface structures produced by certain bacteria and have been implicated in biofilm formation in these species. In order to determine whether these structures, which were suggested to be encoded by the
Rv3312A
(
mtp
) gene, have a similar role in
Mycobacterium tuberculosis
, we generated a Δ
mtp
mutant and a
mtp
-complemented strain of a clinical isolate of
M. tuberculosis
and analyzed these strains for their ability to produce pili in comparison to the wild-type strain. Phenotypic analysis by transmission electron microscopy proved the essentiality of
mtp
for piliation in
M. tuberculosis
. We then compared biofilm formation of the derived strains in detergent-free Sauton’s media. Biofilm mass was quantified spectrophotometrically using crystal violet. Furthermore, we examined
mtp
gene expression by quantitative real-time PCR in wild-type cells grown under biofilm versus planktonic growth conditions. We found a 68.4 % reduction in biofilm mass in the mutant compared to the wild-type strain (
P
= 0.002). Complementation of the mutant resulted in a restoration of the wild-type biofilm phenotype (
P
= 0.022). We, however, found no significant difference between
mtp
expression in cells of the biofilm to those growing planktonically. Our findings highlight a crucial, but non-specific, role of pili in the biofilm lifestyle of
M. tuberculosis
and indicate that they may represent an important target for the development of therapeutics to attenuate biofilm formation, thereby potentially reducing persistence. |
doi_str_mv | 10.1007/s10482-013-9981-6 |
format | Article |
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Rv3312A
(
mtp
) gene, have a similar role in
Mycobacterium tuberculosis
, we generated a Δ
mtp
mutant and a
mtp
-complemented strain of a clinical isolate of
M. tuberculosis
and analyzed these strains for their ability to produce pili in comparison to the wild-type strain. Phenotypic analysis by transmission electron microscopy proved the essentiality of
mtp
for piliation in
M. tuberculosis
. We then compared biofilm formation of the derived strains in detergent-free Sauton’s media. Biofilm mass was quantified spectrophotometrically using crystal violet. Furthermore, we examined
mtp
gene expression by quantitative real-time PCR in wild-type cells grown under biofilm versus planktonic growth conditions. We found a 68.4 % reduction in biofilm mass in the mutant compared to the wild-type strain (
P
= 0.002). Complementation of the mutant resulted in a restoration of the wild-type biofilm phenotype (
P
= 0.022). We, however, found no significant difference between
mtp
expression in cells of the biofilm to those growing planktonically. Our findings highlight a crucial, but non-specific, role of pili in the biofilm lifestyle of
M. tuberculosis
and indicate that they may represent an important target for the development of therapeutics to attenuate biofilm formation, thereby potentially reducing persistence.</description><identifier>ISSN: 0003-6072</identifier><identifier>EISSN: 1572-9699</identifier><identifier>DOI: 10.1007/s10482-013-9981-6</identifier><identifier>PMID: 23907521</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Antibiotics ; Bacteria ; Bacterial Proteins - genetics ; Biofilms ; Biofilms - growth & development ; Biomedical and Life Sciences ; Fimbriae, Bacterial - genetics ; Fimbriae, Bacterial - physiology ; Fimbriae, Bacterial - ultrastructure ; Gene Deletion ; Gene Expression Profiling ; Genetic Complementation Test ; Gentian Violet - metabolism ; Growth conditions ; Life Sciences ; Medical Microbiology ; Microbiology ; Microscopy, Electron, Transmission ; Mycobacterium tuberculosis ; Mycobacterium tuberculosis - genetics ; Mycobacterium tuberculosis - physiology ; Mycobacterium tuberculosis - ultrastructure ; Original Paper ; Plant Sciences ; Real-Time Polymerase Chain Reaction ; Soil Science & Conservation ; Staining and Labeling ; Tuberculosis</subject><ispartof>Antonie van Leeuwenhoek, 2013-11, Vol.104 (5), p.725-735</ispartof><rights>Springer Science+Business Media Dordrecht 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c471t-302b09750fad6d35f6d7848af94b28c55471ef8388490b32d3c3eef40dc8e143</citedby><cites>FETCH-LOGICAL-c471t-302b09750fad6d35f6d7848af94b28c55471ef8388490b32d3c3eef40dc8e143</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10482-013-9981-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10482-013-9981-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27922,27923,41486,42555,51317</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23907521$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ramsugit, Saiyur</creatorcontrib><creatorcontrib>Guma, Sinenhlanhla</creatorcontrib><creatorcontrib>Pillay, Balakrishna</creatorcontrib><creatorcontrib>Jain, Paras</creatorcontrib><creatorcontrib>Larsen, Michelle H.</creatorcontrib><creatorcontrib>Danaviah, Siva</creatorcontrib><creatorcontrib>Pillay, Manormoney</creatorcontrib><title>Pili contribute to biofilm formation in vitro in Mycobacterium tuberculosis</title><title>Antonie van Leeuwenhoek</title><addtitle>Antonie van Leeuwenhoek</addtitle><addtitle>Antonie Van Leeuwenhoek</addtitle><description>Organized bacterial communities, or biofilms, provide an important reservoir for persistent cells that are inaccessible or tolerant to antibiotics. Curli pili are cell-surface structures produced by certain bacteria and have been implicated in biofilm formation in these species. In order to determine whether these structures, which were suggested to be encoded by the
Rv3312A
(
mtp
) gene, have a similar role in
Mycobacterium tuberculosis
, we generated a Δ
mtp
mutant and a
mtp
-complemented strain of a clinical isolate of
M. tuberculosis
and analyzed these strains for their ability to produce pili in comparison to the wild-type strain. Phenotypic analysis by transmission electron microscopy proved the essentiality of
mtp
for piliation in
M. tuberculosis
. We then compared biofilm formation of the derived strains in detergent-free Sauton’s media. Biofilm mass was quantified spectrophotometrically using crystal violet. Furthermore, we examined
mtp
gene expression by quantitative real-time PCR in wild-type cells grown under biofilm versus planktonic growth conditions. We found a 68.4 % reduction in biofilm mass in the mutant compared to the wild-type strain (
P
= 0.002). Complementation of the mutant resulted in a restoration of the wild-type biofilm phenotype (
P
= 0.022). We, however, found no significant difference between
mtp
expression in cells of the biofilm to those growing planktonically. Our findings highlight a crucial, but non-specific, role of pili in the biofilm lifestyle of
M. tuberculosis
and indicate that they may represent an important target for the development of therapeutics to attenuate biofilm formation, thereby potentially reducing persistence.</description><subject>Antibiotics</subject><subject>Bacteria</subject><subject>Bacterial Proteins - genetics</subject><subject>Biofilms</subject><subject>Biofilms - growth & development</subject><subject>Biomedical and Life Sciences</subject><subject>Fimbriae, Bacterial - genetics</subject><subject>Fimbriae, Bacterial - physiology</subject><subject>Fimbriae, Bacterial - ultrastructure</subject><subject>Gene Deletion</subject><subject>Gene Expression Profiling</subject><subject>Genetic Complementation Test</subject><subject>Gentian Violet - metabolism</subject><subject>Growth conditions</subject><subject>Life Sciences</subject><subject>Medical Microbiology</subject><subject>Microbiology</subject><subject>Microscopy, Electron, Transmission</subject><subject>Mycobacterium tuberculosis</subject><subject>Mycobacterium tuberculosis - genetics</subject><subject>Mycobacterium tuberculosis - physiology</subject><subject>Mycobacterium tuberculosis - ultrastructure</subject><subject>Original Paper</subject><subject>Plant Sciences</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>Soil Science & Conservation</subject><subject>Staining and Labeling</subject><subject>Tuberculosis</subject><issn>0003-6072</issn><issn>1572-9699</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkctKxTAQhoMoerw8gBspuHFTndyaZCniDRVdnH1o00QibaNJKpy3t-WoiCC4mgz58s-ED6FDDKcYQJwlDEySEjAtlZK4rDbQAnNBSlUptYkWAEDLCgTZQbspvUytqqTYRjuEKhCc4AW6e_KdL0wYcvTNmG2RQ9H44HzXFy7Evs4-DIUfinefY5gPDysTmtpkG_3YF3lsbDRjF5JP-2jL1V2yB591Dy2vLpcXN-X94_Xtxfl9aZjAuaRAGlCCg6vbqqXcVa2QTNZOsYZIw_lEWSeplExBQ0lLDbXWMWiNtJjRPXSyjn2N4W20KeveJ2O7rh5sGJPGrJJUKODVP1BGGaacqgk9_oW-hDEO0z9minBFKZ8pvKZMDClF6_Rr9H0dVxqDnp3otRM9OdGzEz0vcfSZPDa9bb9ffEmYALIG0nQ1PNv4Y_SfqR9e95XH</recordid><startdate>20131101</startdate><enddate>20131101</enddate><creator>Ramsugit, Saiyur</creator><creator>Guma, Sinenhlanhla</creator><creator>Pillay, Balakrishna</creator><creator>Jain, Paras</creator><creator>Larsen, Michelle H.</creator><creator>Danaviah, Siva</creator><creator>Pillay, Manormoney</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QL</scope><scope>7T7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20131101</creationdate><title>Pili contribute to biofilm formation in vitro in Mycobacterium tuberculosis</title><author>Ramsugit, Saiyur ; Guma, Sinenhlanhla ; Pillay, Balakrishna ; Jain, Paras ; Larsen, Michelle H. ; Danaviah, Siva ; Pillay, Manormoney</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c471t-302b09750fad6d35f6d7848af94b28c55471ef8388490b32d3c3eef40dc8e143</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Antibiotics</topic><topic>Bacteria</topic><topic>Bacterial Proteins - 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Academic</collection><jtitle>Antonie van Leeuwenhoek</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ramsugit, Saiyur</au><au>Guma, Sinenhlanhla</au><au>Pillay, Balakrishna</au><au>Jain, Paras</au><au>Larsen, Michelle H.</au><au>Danaviah, Siva</au><au>Pillay, Manormoney</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pili contribute to biofilm formation in vitro in Mycobacterium tuberculosis</atitle><jtitle>Antonie van Leeuwenhoek</jtitle><stitle>Antonie van Leeuwenhoek</stitle><addtitle>Antonie Van Leeuwenhoek</addtitle><date>2013-11-01</date><risdate>2013</risdate><volume>104</volume><issue>5</issue><spage>725</spage><epage>735</epage><pages>725-735</pages><issn>0003-6072</issn><eissn>1572-9699</eissn><abstract>Organized bacterial communities, or biofilms, provide an important reservoir for persistent cells that are inaccessible or tolerant to antibiotics. Curli pili are cell-surface structures produced by certain bacteria and have been implicated in biofilm formation in these species. In order to determine whether these structures, which were suggested to be encoded by the
Rv3312A
(
mtp
) gene, have a similar role in
Mycobacterium tuberculosis
, we generated a Δ
mtp
mutant and a
mtp
-complemented strain of a clinical isolate of
M. tuberculosis
and analyzed these strains for their ability to produce pili in comparison to the wild-type strain. Phenotypic analysis by transmission electron microscopy proved the essentiality of
mtp
for piliation in
M. tuberculosis
. We then compared biofilm formation of the derived strains in detergent-free Sauton’s media. Biofilm mass was quantified spectrophotometrically using crystal violet. Furthermore, we examined
mtp
gene expression by quantitative real-time PCR in wild-type cells grown under biofilm versus planktonic growth conditions. We found a 68.4 % reduction in biofilm mass in the mutant compared to the wild-type strain (
P
= 0.002). Complementation of the mutant resulted in a restoration of the wild-type biofilm phenotype (
P
= 0.022). We, however, found no significant difference between
mtp
expression in cells of the biofilm to those growing planktonically. Our findings highlight a crucial, but non-specific, role of pili in the biofilm lifestyle of
M. tuberculosis
and indicate that they may represent an important target for the development of therapeutics to attenuate biofilm formation, thereby potentially reducing persistence.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>23907521</pmid><doi>10.1007/s10482-013-9981-6</doi><tpages>11</tpages></addata></record> |
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subjects | Antibiotics Bacteria Bacterial Proteins - genetics Biofilms Biofilms - growth & development Biomedical and Life Sciences Fimbriae, Bacterial - genetics Fimbriae, Bacterial - physiology Fimbriae, Bacterial - ultrastructure Gene Deletion Gene Expression Profiling Genetic Complementation Test Gentian Violet - metabolism Growth conditions Life Sciences Medical Microbiology Microbiology Microscopy, Electron, Transmission Mycobacterium tuberculosis Mycobacterium tuberculosis - genetics Mycobacterium tuberculosis - physiology Mycobacterium tuberculosis - ultrastructure Original Paper Plant Sciences Real-Time Polymerase Chain Reaction Soil Science & Conservation Staining and Labeling Tuberculosis |
title | Pili contribute to biofilm formation in vitro in Mycobacterium tuberculosis |
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