scieee Science in your language
[en] (orig)

Genome Sequences of Serratia Strains Revealed Common Genes in Both Serratomolides Gene Clusters

Abstract

This research was funded by FEDER funds through the program COMPETE - Programa Operacional Factores de Competitividade - and by national funds through Fundação para a Ciência e a Tecnologia (FCT), under the projects UID/EMS/00285/2020, PTWPTDC/AAG-REC/3839/2014; and by BIORECOVER Horizon2020 under grant agreement No 821096.

Read accessible full text

Genome Sequences of Serratia Strains Revealed Common Genes in Both Serratomolides Gene Clusters

Author: Marques-Pereira, Catarina,Proença, Diogo Neves,Morais, Paula V.
Publisher: MDPI
Year: 2020
DOI: 10.3390/biology9120482
Source: https://estudogeral.uc.pt/bitstream/10316/105812/1/Genome-sequences-of-serratia-strains-revealed-common-genes-in-both-serratomolides-gene-clustersBiology.pdf
biology
A icle
Genome Sequences o Se a ia S ains Re ealed
Common Genes in Bo h Se a omolides
Gene Clus e s
Ca a ina Ma ques-Pe ei a †, Diogo Ne es P oença * and Paula V. Mo ais
Depa men o Li e Sciences, Cen e o Mechanical Enginee ing, Ma e ials and P ocesses, Uni e si y o
Coimb a, Calçada Ma im de F ei as, 3000-456 Coimb a, Po ugal; [email p o ec ed] (C.M.-P.);
[email p o ec ed] (P.V.M.)
*Co espondence: [email p o ec ed]; Tel.: +351-239240798
†Cu en add ess: Cen e o Neu oscience and Cell Biology & Cen e o Inno a i e Biomedicine and
Bio echnology, Uni e si y o Coimb a, 3004-504 Coimb a, Po ugal.
Recei ed: 31 Oc obe 2020; Accep ed: 17 Decembe 2020; Published: 20 Decembe 2020


Simple Summa y:
Biosu ac an s a e amphiphilic molecules p oduced by mic oo ganisms wi h a
hyd ophilic and a hyd ophobic g oup, able o educe su ace ension. These molecules a e la gely
used in he en i onmen al, ood, pha maceu ical, medical, and cleaning indus ies, among o he s.
Se a ia s ains a e ubiqui ous mic oo ganisms wi h he abili y o p oduce biosu ac an s, such as
se awe ins. These ex acellula lipopep ides a e desc ibed as biocides agains many bac e ia and
ungi. This wo k used compa a i e genomics o de e mine he dis ibu ion and o ganiza ion o he
se awe ins W1 and W2 biosyn he ic gene clus e s in all he 84 publicly a ailable genomes o he
Se a ia genus. He e, he se awe in W1 gene clus e s’ o ganiza ion is epo ed o he i s ime.
The se awe in W1 biosyn he ic gene sw W and se awe in W2 biosyn he ic gene sw A we e p esen
in 17 and 11 Se a ia genomes, espec i ely. The same genes in he biosyn he ic clus e s ame he
sw W and sw A biosyn he ic genes. This wo k iden i ied ou genes common o all se awe in gene
clus e s, highligh ing hei key po en ial in he se awe ins biosyn he ic p ocess.
Abs ac : Se a ia s ains a e ubiqui ous mic oo ganisms wi h he abili y o p oduce se a omolides,
such as se awe ins. These ex acellula lipopep ides a e desc ibed as biocides agains many bac e ia
and ungi and may ha e a nema icidal ac i i y agains phy opa hogenic nema odes. Se awe ins
W1 and W2 om di e en s ains ha e di e en s uc u es ha migh be co ela ed wi h dis inc
genomic o ganiza ions. This wo k used compa a i e genomics o de e mine he dis ibu ion and he
o ganiza ion o he se awe ins biosyn he ic gene clus e s in all he 84 publicly a ailable genomes o
he Se a ia genus. The se awe in W1 and W2 gene clus e s’ o ganiza ion was es ablished using
an iSMASH so wa e and compa ed wi h single and sho da a p e iously desc ibed o YD25
T
Se a ia.
He e, he se awe in W1 gene clus e s’ o ganiza ion is epo ed o he i s ime. The se awe in
W1 biosyn he ic gene sw W was p esen in 17 Se a ia genomes. Eigh y di e en coding sequence
(CDS) we e assigned o he W1 gene clus e , 13 being common o all clus e s. The se awe in W2
sw A gene was p esen in 11 Se a ia genomes. The W2 gene clus e s included 68 CDS wi h 24 p esen
in all he clus e s. The genomic analysis showed he sw A gene cons i u es i e modules, ou wi h
h ee domains and one wi h ou domains, while he sw W gene cons i u es one module wi h ou
domains. This wo k iden i ied ou genes common o all se awe in gene clus e s, highligh ing hei
essen ial po en ial in he se awe ins biosyn he ic p ocess.
Keywo ds:
Se a ia; genome; se awe in; biosyn he ic gene clus e ; se a omolides; sw W gene;
sw A gene
Biology 2020,9, 482; doi:10.3390/biology9120482 www.mdpi.com/jou nal/biology
Biology 2020,9, 482 2 o 18
1. In oduc ion
Su ac an s a e amphiphilic molecules wi h a hyd ophilic and a hyd ophobic g oup, able o
educe su ace ension. These molecules a e la gely used in he en i onmen al, ood, pha maceu ical,
medical, and cleaning indus ies, among o he s [
1
–
3
]. Biosu ac an s a e seconda y me aboli es
p oduced by bac e ia, yeas , o ungi, capable o educing he su ace ension o ex acellula media [
4
].
They can ha e a a ie y o s uc u es, mainly di ided in o six majo g oups, namely, glycolipids,
lipopolysaccha ides, lipopep ides and phospholipids, and hyd oxyla ed and c oss-linked a y acids [
5
].
When compa ed wi h syn he ic su ac an s, biosu ac an s ha e highe biodeg adabili y, lowe oxici y,
and highe ac i i y a ex eme condi ions, such as high empe a u es, pH, and salini y [6].
Bac e ial species o he genus Se a ia belonging o he amily En e obac e iaceae a e G am-nega i e,
acul a i e anae obic, and od-shaped bac e ia [
7
,
8
]. They ha e been isola ed om di e en
en i onmen s, such as wa e , soil, plan s, insec s, and e eb a es [
9
]. Su aces in hese habi a s
ha e a a ie y o cha ac e is ics and can be hyd ophobic, hyd ophilic, ac al, smoo h, and axenic,
among o he s. To colonize hem, bac e ia om he genus Se a ia p oduce biosu ac an s (ex acellula
lipopep ides) as he se a omolides se awe in W1 [10], se awe in W2 [4], and se awe in W3 [11].
Mu an s o he se a omolides biosyn he ic genes ailed o o m colonies on nu i i e aga pla es and
hese lipopep ides we e sugges ed as p omo e s o a new ype o sp eading g ow h [4].
Bo h he se awe in W1 and W2 biosyn he ic genes (sw W and sw A genes) belong o a
Non-Ribosomal Pep ide Syn he ase (NRPS) gene clus e [
12
,
13
]. Condensa ion, adenyla ion, hiola ion,
and hioes e ase domains a e de ec able in bo h se awe in gene clus e s. Along wi h o he p o eins,
such as PPTase o acyl ca ie p o eins (ACP) [
12
,
14
], se awe in W1 and W2 biosyn he ic p o eins a e
able o syn hesize se awe in W1 and W2 lipopep ides. Se awe in W1 has a symme ic s uc u e
composed o wo se ine amino acids and wo a y acids (3-hyd oxydecanoic) [
4
] while se awe in W2
is a cyclic pep ide con aining i e amino acids. This lipopep ide p omo es lagellum sp eading g ow h,
con ibu ing speci ically o su ace bac e ial ansloca ion [
4
], and was able o demons a e an imic obial
ac i i y agains many bac e ia and ungi and an an i umo al ac i i y agains Hela cells [
13
]. The Se a ia
s ains p oducing se awe in W1 showed he highes b oad-spec um an imic obial ac i i y agains
clinical, ood, and en i onmen al bac e ial pa hogens compa ed wi h he Se a ia s ains p oducing
se awe in W2 [
15
]. A s ain o S. ma cescens showed he capaci y o inhibi an endophy ic ungus due
o i s p oduc ion o compounds, namely, se awe ins [16].
Due o he limi ed in o ma ion on his opic, in his s udy, we pe o med a compa a i e genomic
analysis o de e mine he dis ibu ion and he o ganiza ion o he se awe ins biosyn he ic gene
clus e s in all he 84 publicly a ailable genomes o he Se a ia genus. He e, we epo a deep analysis o
he se awe in W1 and W2 gene clus e s and es ablish hei o ganiza ion using an iSMASH so wa e.
In pa icula , o he i s ime, we show he se awe in W1 gene clus e s’ o ganiza ion. These analyses
showed he p esence o ou genes common o all he se awe in gene clus e s, highligh ing hei key
po en ial in he se awe ins biosyn he ic p ocess.
2. Ma e ials and Me hods
2.1. Bac e ial S ains, Da a Collec ion, and Genomes
Eigh y- ou Se a ia genomes a ailable on NCBI, ep esen ing all he publicly a ailable genomes,
we e included in his s udy (Table S1), ob ained om 49 di e en hos s and isola ed om 29
coun ies [13,17–49].
Se awe in W1 and W2 biosyn he ic gene clus e p edic ion was pe o med in all he 84
comple e and d a Se a ia genomes publicly a ailable, using he web pla o m an iSMASH 3.0 [
50
].
This inpu da ase includes s ains belonging o S. ma cescens,S. lique aciens,S. g imesii,S. nema odiphila,
S. plymu hica
, and S. u eily ica, as well as s ains no cha ac e ized o he species le el. An iSMASH
analysis ou pu was examined o iden i y he se awe ins biosyn he ic genes clus e s. The e o e,
o ind he sw W and sw A genes, BLAST analysis was pe o med o all p o ein sequences, codi ied by
Biology 2020,9, 482 3 o 18
each gene o he NRPS p edic ing me aboli e clus e s, using he NCBI [
51
] da abase. Clus e bounda ies
we e p edic ed wi h he CASSIS algo i hm speci ied o he NRPS domains [50].
2.2. Phylogene ic Analysis
The 16S RNA sequences o he 47 Se a ia s ains, which showed he p esence o se awe ins genes
in hei genomes (Table 1), we e selec ed o phylogene ic analysis. These sequences we e compa ed wi h
he sequences a ailable in he EMBL/GenBank da abase using he BLASTN ne wo k se ices [
51
], and
wi h sequences a ailable a he Ez axon-e se e (h p://ez axon-e.ezbiocloud.ne /) [
52
]. Sequences we e
aligned wi hin he SINA alignmen se ice [
53
]. Sequences we e included in he 16S RNA-based Li ing
T ee P ojec (LTP, elease 115) da abase (h p://www.a b-sil a.de/p ojec s/li ing- ee/) by pa simony
implemen ed in he ARB so wa e package e sion 5.5 [
54
]. Phylogene ic dend og ams o his s udy
s ains and closes e e ence sequences we e cons uc ed using he Neighbo -Joining and Randomized
Axele a ed Maximum Likelihood (RAxML) me hod wi h he GTRGAMMA model [
55
] included in he
ARB so wa e [54].
Table 1.
Se a ia s ains wi h he sw W and sw A genes iden i ied h ough an iSMASH so wa e.
An iSMASH so wa e was used in 84 Se a ia genomes (see Table S1). X ep esen s he p esence o
genes sw W and sw A in se en een and ele en genomes, espec i ely.
Bac e ial S ain Accession Numbe sw W sw A
Se a ia sp. AS12 CP002774.1 X
Se a ia sp. AS13 CP002775.1 X
Se a ia sp. FS14 CP005927.1 X
Se a ia sp. SCBI CP003424.1 X
Se a ia sp. YD25 CP016948.1 X
Se a ia sp. SSNIH1 CP026383.1 X
Se a ia sp. PWN146 LT575490.1 X
Se a ia ma cescens s ain UMH8 CP018927.1 X
Se a ia ma cescens s ain IOMTU 115 AB894481.1 X
Se a ia ma cescens subsp. ma cescens ATCC 13880 JMPQ01000033.1 X
Se a ia ma cescens s ain CDC_813-60 DP21 JOVM01000004.1 X
Se a ia nema odiphila DZ0503SBS1 s ain DSM 21420 JPUX00000000.1 X
Se a ia ma cescens VGH107 AORJ00000000.1 X
Se a ia ma cescens EGD-HP20 AVSR00000000.1 X
Se a ia ma cescens WW4 CP003959.1 X
Se a ia ma cescens BIDMC 81 JJMZ01000006.1 X
Se a ia s ain TEL NODE_13 LDEG01000018.1 X
Se a ia plymu hica NBRC 102599TBCTU00000000.1 X
Se a ia g imesii isola e BXF1 LT883155.1 X
Se a ia g imesii s ain A2 JGVP00000000.1 X
Se a ia plymu hica AS9 CP002773.1 X
Se a ia ma cescens SM39 AP013063.1 X
Se a ia ma cescens SmUNAM836 CP012685.1 X
Se a ia ma cescens BIDMC 44 JAPD01000005.1 X
Se a ia u eily ica L 5/4 LG59 JSFB01000001.1 X
Se a ia ma cescens RSC-14 CP012639.1 X
Se a ia ma cescens subsp. ma cescens AH0650_Sm1 AG2 LFJS01000014.1 X
Se a ia ma cescens subsp. ma cescens Db11 HG326223.1 X
2.3. Se awe ins Biosyn he ic Gene Clus e s Analysis
The NRPS gene clus e , whe e bo h he se awe in W1 and W2 biosyn he ic genes belong,
was analyzed he e by using an iSMASH so wa e [
50
]. The econs uc ion o he domains, modules,
and s uc u es o he se awe ins was pe o med by using Phy e2 idimensional p edic ion [
56
],
using he se awe in W1 biosyn he ic p o ein om Se a ia sp. AS13, and W2 om Se a ia sp. PWN146.
PubChem 2D was used o explo e he chemical in o ma ion o he se awe ins using he bac e ial
models men ioned abo e.
The conca ena ed amino acid sequences o each se awe in biosyn he ic gene clus e we e
o ganized by p o ein iden i ica ion in he same o de o allow a clus e alignmen wi h Clus alW
Biology 2020,9, 482 4 o 18
in MEGAX so wa e [
57
]. The se awe in W1 biosyn he ic p o eins om 17 Se a ia genomes
and se awe in W2 biosyn he ic p o eins om 11 Se a ia genomes we e sepa a ely aligned.
The e olu iona y ela ionship be ween he clus e s and be ween he se awe in biosyn he ic p o ein
sequences we e es ablished using he Neighbo -Joining me hod, Poisson model [
58
], in MEGAX
so wa e [
57
]. The aligned and o ganized clus e genes we e ep esen ed in an e olu iona y ee
acco ding o he size, di ec ion, and accession numbe s iden i ied wi h he NCBI BLAST da abase [
51
].
Func ions o he co e p o eins in all clus e s we e sea ched on UniP o [59].
3. Resul s
3.1. Bac e ial Phylogeny and Compa a i e Genomics o Se a ia spp.
All he 84 Se a ia s ains selec ed o his s udy had hei genome publicly a ailable a NCBI.
Acco ding o he Neighbo -Joining and Maximum-Likelihood phylogene ic ees based on 16S RNA
gene sequences, 14 s ains belong o S. ma cescens, wo s ains belong o S. plymu hica, wo s ains
belong o S. g imesii, one s ain belongs o S. lique aciens, one s ain belongs o S. nema odiphila, one s ain
belongs o S. u eily ica, and 63 s ains could no be assigned o species le el due o a simila i y lowe
han 97% (Figu e 1). Genomes o he Se a ia s ains ha e a size om 5.0 Mbp o 7.7 Mbp and he G +C
con en a ies om 45.9 o 60.1 mol%.
Biology 2020, 9, x 4 o 19
PubChem 2D was used o explo e he chemical in o ma ion o he se awe ins using he bac e ial
models men ioned abo e.
The conca ena ed amino acid sequences o each se awe in biosyn he ic gene clus e we e
o ganized by p o ein iden i ica ion in he same o de o allow a clus e alignmen wi h Clus alW in
MEGAX so wa e [57]. The se awe in W1 biosyn he ic p o eins om 17 Se a ia genomes and
se awe in W2 biosyn he ic p o eins om 11 Se a ia genomes we e sepa a ely aligned. The
e olu iona y ela ionship be ween he clus e s and be ween he se awe in biosyn he ic p o ein
sequences we e es ablished using he Neighbo -Joining me hod, Poisson model [58], in MEGAX
so wa e [57]. The aligned and o ganized clus e genes we e ep esen ed in an e olu iona y ee
acco ding o he size, di ec ion, and accession numbe s iden i ied wi h he NCBI BLAST da abase [51].
Func ions o he co e p o eins in all clus e s we e sea ched on UniP o [59].
3. Resul s
3.1. Bac e ial Phylogeny and Compa a i e Genomics o Se a ia spp.
All he 84 Se a ia s ains selec ed o his s udy had hei genome publicly a ailable a NCBI.
Acco ding o he Neighbo -Joining and Maximum-Likelihood phylogene ic ees based on 16S RNA
gene sequences, 14 s ains belong o S. ma cescens, wo s ains belong o S. plymu hica, wo s ains
belong o S. g imesii, one s ain belongs o S. lique aciens, one s ain belongs o S. nema odiphila, one
s ain belongs o S. u eily ica, and 63 s ains could no be assigned o species le el due o a simila i y
lowe han 97% (Figu e 1). Genomes o he Se a ia s ains ha e a size om 5.0 Mbp o 7.7 Mbp and
he G + C con en a ies om 45.9 o 60.1 mol%.
Figu e 1. A phylogene ic dend og am based on a compa ison o he 16S RNA gene sequence o he
Se a ia s ains used in his s udy and he ype o s ains. The ee was c ea ed using he Neighbo -
Joining me hod in ARB so wa e. The numbe s on he ee indica e he pe cen ages o boo s ap
sampling, de i ed om 1000 eplica ions; alues below 50% a e no shown. In blue a e shown he
Se a ia s ains ha showed he p esence o he se awe in W1 biosyn he ic gene clus e and in g een
a e shown he Se a ia s ains ha showed he p esence o he se awe in W2 biosyn he ic gene
clus e . The ype species Esche ichia coli DSM 30083T was used as he ou g oup. Scale ba , 1 in e ed
nucleo ide subs i u ion pe 100 nucleo ides.
Figu e 1.
A phylogene ic dend og am based on a compa ison o he 16S RNA gene sequence o he
Se a ia s ains used in his s udy and he ype o s ains. The ee was c ea ed using he Neighbo -Joining
me hod in ARB so wa e. The numbe s on he ee indica e he pe cen ages o boo s ap sampling,
de i ed om 1000 eplica ions; alues below 50% a e no shown. In blue a e shown he Se a ia
s ains ha showed he p esence o he se awe in W1 biosyn he ic gene clus e and in g een a e
shown he Se a ia s ains ha showed he p esence o he se awe in W2 biosyn he ic gene clus e .
The ype species Esche ichia coli DSM 30083
T
was used as he ou g oup. Scale ba , 1 in e ed nucleo ide
subs i u ion pe 100 nucleo ides.
Bioin o ma ic analysis h ough an iSMASH so wa e showed ha he se awe in W1 biosyn he ic
gene was p esen in 17 Se a ia genomes, s ains ATCC 13880, CDC_813-60 DP21, UMH8, IOMTU 115,
DSM 21420, VGH107, EGD-HP20, WW4, FS14, BIDMC81, TEL NODE_13, NBRC 102599
T
, BXF1, A2,
AS13, AS9, and AS12 (Table 1and Table S2). The se awe in W2 biosyn he ic gene was p esen in 11
Biology 2020,9, 482 5 o 18
Se a ia s ains, PWN146, SSNIH1, SM39, SmUNAM836, BIDMC 44, L 5/4 LG59, RSC-14, AH0650_Sm1
AG2, Db11, SCBI, and YD25T(Table 1and Table S3).
3.2. Se awe in W1 Biosyn he ic Gene Clus e s
All se awe in W1 biosyn he ic gene clus e s we e iden i ied as NRPS clus e s. Mo eo e ,
he bioin o ma ic analysis p edic ed an a chi ec u e including he domains condensa ion (C),
adenyla ion (A), hiola ion (T), and hioes e ase (TE) in all he se awe in W1 biosyn he ic genes
(Figu e 2).
Biology 2020, 9, x 5 o 19
Bioin o ma ic analysis h ough an iSMASH so wa e showed ha he se awe in W1
biosyn he ic gene was p esen in 17 Se a ia genomes, s ains ATCC 13880, CDC_813-60 DP21,
UMH8, IOMTU 115, DSM 21420, VGH107, EGD-HP20, WW4, FS14, BIDMC81, TEL NODE_13, NBRC
102599T, BXF1, A2, AS13, AS9, and AS12 (Tables 1 and S2). The se awe in W2 biosyn he ic gene was
p esen in 11 Se a ia s ains, PWN146, SSNIH1, SM39, SmUNAM836, BIDMC 44, L 5/4 LG59, RSC-
14, AH0650_Sm1 AG2, Db11, SCBI, and YD25T (Tables 1 and S3).
3.2. Se awe in W1 Biosyn he ic Gene Clus e s
All se awe in W1 biosyn he ic gene clus e s we e iden i ied as NRPS clus e s. Mo eo e , he
bioin o ma ic analysis p edic ed an a chi ec u e including he domains condensa ion (C),
adenyla ion (A), hiola ion (T), and hioes e ase (TE) in all he se awe in W1 biosyn he ic genes
(Figu e 2).
Figu e 2. Se awe in W1: om he biosyn he ic gene clus e o he s uc u e o se awe in W1.
Gene ic o ganiza ion o he genome o Se a ia s ain AS13 by an iSMASH analysis, Phy e2
idimensional p edic ion o se awe in W1 biosyn he ic p o ein, and PubChem 2D s uc u e o
se awe in W1. (a) Se awe in W1 biosyn he ic gene clus e wi h iden i ica ion o he s wW co e
gene; (b) sw W gene o ganiza ion: C, condensa ion domain; A, adenyla ion domain; T, hiola ion
domain; and TE, hioes e ase domain; (c) biosyn he ic p o ein wi h he condensa ion, adenyla ion,
hiola ion, and hioes e ase domains; (d) se awe in W1 2D s uc u e.
To con i m he iden i ica ion o he sw W gene e ealed by an iSMASH, each sw W was que ied
o NCBI BLASTP, in o de o ind he closes ela i e and de e mine he iden i y pe cen age (Tables
2 and S2). The p o ein om he se awe in W1 biosyn he ic gene (sw W) showed an iden i y
pe cen age ha anges om 77.79% o 100% as he closes iden i ica ion by using BLASTP (Table 2).
Figu e 2.
Se awe in W1: om he biosyn he ic gene clus e o he s uc u e o se awe in
W1. Gene ic o ganiza ion o he genome o Se a ia s ain AS13 by an iSMASH analysis, Phy e2
idimensional p edic ion o se awe in W1 biosyn he ic p o ein, and PubChem 2D s uc u e o
se awe in W1. (
a
) Se awe in W1 biosyn he ic gene clus e wi h iden i ica ion o he s wW co e gene;
(
b
)sw W gene o ganiza ion: C, condensa ion domain; A, adenyla ion domain; T, hiola ion domain;
and TE, hioes e ase domain; (
c
) biosyn he ic p o ein wi h he condensa ion, adenyla ion, hiola ion,
and hioes e ase domains; (d) se awe in W1 2D s uc u e.
To con i m he iden i ica ion o he sw W gene e ealed by an iSMASH, each sw W was que ied
o NCBI BLASTP, in o de o ind he closes ela i e and de e mine he iden i y pe cen age (Table 2
and Table S2). The p o ein om he se awe in W1 biosyn he ic gene (sw W) showed an iden i y
pe cen age ha anges om 77.79% o 100% as he closes iden i ica ion by using BLASTP (Table 2).

Biology 2020,9, 482 6 o 18
Table 2.
The se awe in W1 gene (sw W) o each s ain in his s udy and he accession numbe s and
iden i ica ion o he sw W gene’s closes ela i es using BLASTP.
Bac e ial S ain sw W Closes Rela i e
Genes Accession Numbe Iden i y Pe cen age
Se a ia ma cescens
EGD-HP20
non- ibosomal pep ide
syn he ase ERH70695.1 99.52
Se a ia ma cescens WW4 se awe in W1
syn he ase AGE20181.1 100
Se a ia sp. FS14 pu a i e se awe in W1
syn he ase AIA46701.1 100
Se a ia ma cescens
VGH107
amino acid adenyla ion
p o ein EMF04443.1 99.12
Se a ia nema odiphila
DZ0503SBS1 s ain DSM
21420
non- ibosomal pep ide
syn he ase KFF87803.1 99.31
Se a ia ma cescens s ain
IOMTU 115
pu a i e se awe in W1
syn he ase BAO21138.1 99.92
Se a ia ma cescens s ain
UMH8
non- ibosomal pep ide
syn he ase ASM18665.1 99.01
Se a ia ma cescens subsp.
ma cescens ATCC 13880
amino acid adenyla ion
domain-con aining
p o ein
KFD14984.1 98.57
Se a ia ma cescens s ain
CDC_813-60 DP21
non- ibosomal pep ide
syn he ase KFL05097.1 98.63
Se a ia ma cescens
BIDMC 81
non- ibosomal pep ide
syn he ase EZQ62923.1 95.12
Se a ia s ain TEL
NODE_13
non- ibosomal pep ide
syn he ase KLE36484.1 95.05
Se a ia plymu hica NBRC
102599T
non- ibosomal pep ide
syn he ase WP_063202307.1 81.71
Se a ia sp. AS13 non- ibosomal pep ide
syn he ase AEG30284.1 81.48
Se a ia plymu hica AS9 non- ibosomal pep ide
syn he ase AEF47625.1 81.48
Se a ia sp. AS12 non- ibosomal pep ide
syn he ase WP_013814722.1 81.48
Se a ia g imesii isola e
BXF1
amino acid adenyla ion
domain-con aining
p o ein
SMZ58711.1 77.79
Se a ia g imesii s ain A2
non- ibosomal pep ide
syn he ase KFB89923.1 78.17
Eigh y di e en genes om he se awe in W1 biosyn he ic gene clus e we e iden i ied. Fi een
genes a e common o all 17 gene clus e s (Figu e 3and Table S4), such as genes encoding o
mu ein hyd olase e ec o p o ein L gB and mu ein hyd olase egula o L gA, bo h wi h hyd olase
ac i i y; LysR egula o y p o ein wi h DNA-binding ansc ip ion ac o ac i i y; a sodium-hyd ogen
an ipo e and xan hine-u acil- i amin C pe mease, bo h wi h ansmemb ane anspo ac i i y;
glyoxalase–bleomycin esis ance p o ein and glu a hione S- ans e ase domain p o ein, bo h wi h a
dioxygenase ac i i y; 3-oxoacyl-(acyl-ca ie -p o ein) educ ase; single-s anded DNA-binding p o ein;
exonuclease ABC subuni A; mal ose O-ace yl ans e ase; and a oma ic amino acid amino ans e ase.
No conside ing s ain NRBC 102599
T
, an addi ional se en genes we e ound o be common o all
s ains in he se awe in W1 biosyn he ic gene clus e (Figu e 3). Mo eo e , 15 genes a e exclusi e o
he S. plymu hica NBRC 102599Tbiosyn he ic gene clus e (Figu e 3).
Biology 2020,9, 482 7 o 18
Biology 2020, 9, x 7 o 19
Figu e 3. Se awe in W1 gene clus e analysis. The phylogene ic ela ionship was es ablished wi h Mega X so wa e by he Neighbo -Joining me hod on aligned
se awe in W1 gene clus e s o Se a ia s ains ATCC 13880, CDC_813-60 DP21, UMH8, IOMTU 115, DSM 21420, VGH107, EGD-HP20, WW4, FS14, BIDMC81, TEL
NODE_13, NBRC 102599, BXF1, A2, AS13, AS9, and AS12. (a) Phylogene ic ee based on p o ein sequences o he se awe in W1 biosyn he ic gene clus e on an
es ablished gene ic o ganiza ion. (b) Se awe in W1 biosyn he ic gene clus e s based on na u al gene ic o ganiza ion. (c) Compa ison o he phylogene ic ee based
on p o ein sequences o he se awe in W1 biosyn he ic gene clus e s (le ) wi h he phylogene ic ee o he se awe in W1 biosyn hesis p o ein ( igh ). The scale
ba o 0.050 in e s he nucleo ide subs i u ions pe 100 nucleo ides.
Figu e 3.
Se awe in W1 gene clus e analysis. The phylogene ic ela ionship was es ablished wi h Mega X so wa e by he Neighbo -Joining me hod on aligned
se awe in W1 gene clus e s o Se a ia s ains ATCC 13880, CDC_813-60 DP21, UMH8, IOMTU 115, DSM 21420, VGH107, EGD-HP20, WW4, FS14, BIDMC81, TEL
NODE_13, NBRC 102599, BXF1, A2, AS13, AS9, and AS12. (
a
) Phylogene ic ee based on p o ein sequences o he se awe in W1 biosyn he ic gene clus e on an
es ablished gene ic o ganiza ion. (
b
) Se awe in W1 biosyn he ic gene clus e s based on na u al gene ic o ganiza ion. (
c
) Compa ison o he phylogene ic ee based
on p o ein sequences o he se awe in W1 biosyn he ic gene clus e s (le ) wi h he phylogene ic ee o he se awe in W1 biosyn hesis p o ein ( igh ). The scale ba
o 0.050 in e s he nucleo ide subs i u ions pe 100 nucleo ides.
Biology 2020,9, 482 8 o 18
The ela ionship be ween s ains es ablished based on he analysis o he conca ena ed genes
o he W1 biosyn he ic gene clus e de ined he same clus e s as he ela ionships de ined based on
he sw W gene analysis, excep o S. plymu hica NBRC 102599
T
, which is disco dan . The posi ion o
S. plymu hica
NBRC 102599
T
in W1 phylogene ic ee highligh s he di e en gene composi ion o he
W1 biosyn he ic clus e o he s ain. On he o he hand, in he sw W phylogene ic ee, S. plymu hica
NBRC 102599T o ms a sis e g oup wi h Se a ia s ains AS13, AS9, and AS12 (Figu e 3).
In he se awe in W1 biosyn he ic gene clus e , so wa e p edic ion iden i ied ou genes in ol ed
in PKS-NRPS (PolyKe ide Syn hases Non-Ribosomal Pep ide Syn he ases), encoding o enoyl educ ase
quinone oxido educ ase (only p esen in se en s ains), ke o educ ase 3-oxoacyl-(acyl-ca ie -p o ein)
educ ase (p esen in all s ains), enoyl educ ase dehyd ogenase (absen in wo s ains), and a oma ic
amino acid amino ans e ase (p esen in all s ains) (Table 3and Table S4, Figu e 3).
Table 3.
The PKS gene accession numbe s om he sw W biosyn he ic gene clus e s p edic ed by
an iSMASH so wa e.
Bac e ial S ain
Enoyl educ ase
Quinone
Oxido educ ase
Ke o educ ase
3-Oxoacyl-(Acyl-Ca ie -P o ein)
Reduc ase
Enoyl educ ase
Dehyd ogenase
A oma ic Amino
Acid
Amino ans e ase
Se a ia ma cescens EGD-HP20 ERH70706.1 ERH70710.1 ERH70714.1
Se a ia ma cescens WW4 AGE20192.1 AGE20197.1 AGE20201.1
Se a ia sp. FS14 AIA46690.1 AIA46685.1 AIA46681.1
Se a ia ma cescens VGH107 EMF04432.1 EMF04427.1 EMF04423.1
Se a ia nema odiphila
DZ0503SBS1 s ain DSM 21420
KFF87792.1 KFF87787.1 KFF87783.1
Se a ia ma cescens s ain
IOMTU 115 BAO21148.1 BAO21153.1 BAO21155.1
Se a ia ma cescens s ain
UMH8 ASM18675.1 ASM18680.1 ASM18684.1
Se a ia ma cescens subsp.
Ma cescens ATCC 13880 KFD14974.1 KFD14969.1 KFD14965.1
Se a ia ma cescens s ain
CDC_813-60 DP21 KFL04091.1 KFL03204.1 KFL04717.1
Se a ia ma cescens BIDMC 81 EZQ62938.1 EZQ62913.1 EZQ62903.1
Se a ia s ain TEL NODE_13 KLE36470.1 KLE36494.1 KLE36503.1
Se a ia plymu hica NBRC
102599TWP_063202297.1 WP_062868864.1 WP_006328339.1
Se a ia sp. AS13 AEG30270.1 AEG30294.1 AEG30297.1 AEG30301.1
Se a ia plymu hica AS9 AEF47611.1 AEF47635.1 AEF47638.1 AEF47642.1
Se a ia sp. AS12 WP_013814712.1 WP_013814732.1 WP_013814734.1 WP_013814736.1
Se a ia g imesii isola e BXF1 SMZ58698.1 SMZ58721.1 SMZ58727.1 SMZ58731.1
Se a ia g imesii s ain A2 KFB89936.1 KFB89913.1 KFB89904.1
3.3. Se awe in W2 Biosyn he ic Gene Clus e s
E e y se awe in W2 biosyn he ic gene (sw A) showed an a chi ec u e composed o i e modules,
each wi h a condensa ion (C1, C2, C3, C4, and C5), adenyla ion (A1, A2, A3, A4, and A5), and hiola ion
(T1, T2, T3, T4, and T5) domain. Module 5 has an addi ional hioes e ase (TE) domain. This o ganiza ion
is sha ed by all he se awe in W2 biosyn he ic genes (Figu e 4).
Biology 2020,9, 482 9 o 18
Biology 2020, 9, x 9 o 19
Figu e 4. Se awe in W2: om he biosyn he ic gene clus e o he s uc u e o se awe in W2.
Gene ic o ganiza ion o he genome o Se a ia s ain PWN146 by an iSMASH analysis, Phy e2
idimensional p edic ion o he se awe in W2 biosyn he ic p o ein, and PubChem 2D s uc u e o
se awe in W2. (a) Se awe in W2 biosyn he ic gene clus e wi h iden i ica ion o he sw A co e gene;
(b) sw A gene o ganiza ion: i e modules (M1–M5) wi h C, condensa ion domain; A, adenyla ion
domain; T, hiola ion domain; and TE, hioes e ase domain; (c) biosyn he ic p o ein wi h i e modules
(M1–M5), each composed o condensa ion, adenyla ion, and hiola ion domains, and in he las
module an addi ional hioes e ase domain.
To con i m he iden i ica ion o he sw A gene e ealed by an iSMASH, each sw A was, as
men ioned abo e, que ied o NCBI BLASTX, in o de o ind he closes ela i e and de e mine he
iden i y pe cen age (Tables 4 and S3). The p o ein coded by he biosyn he ic genes o se awe in W2
(sw A) showed an iden i y pe cen age ha anges om 76.38% o 99.4% as he closes iden i ica ion
by using BLASTX (Table 4).
Table 4. The se awe in W2 gene (sw A) o each s ain in his s udy and he accession numbe s and
iden i ica ion o he sw A gene’s closes ela i es using BLASTX.
Bac e ial S ain sw A Closes Rela i e Genes Accession Numbe Iden i y
Pe cen age
Se a ia ma cescens SM39 Se a ia ma cescens SM39 DNA, comple e
genome BAO35825.1 76.70
Se a ia ma cescens SmUNAM836 Se a ia ma cescens s ain SmUNAM836,
comple e genome ALE98111.1 76.70
Se a ia sp. SSNIH1 Se a ia sp. SSNIH1 ch omosome,
comple e genome AUY16873.1 76.70
Se a ia sp. PWN146
Se a ia ma cescens isola e
PWN146_assembly genome assembly,
ch omosome
SAY45247.1 77.02
Se a ia u eily ica L 5/4 LG59 Se a ia ma cescens s ain UMH7,
comple e genome KKO55915.1 76.38
Se a ia ma cescens RSC-14 Se a ia ma cescens s ain RSC-14,
comple e genome ALD45109.1 76.38
Se a ia ma cescens BIDMC 44 Se a ia ma cescens s ain 1274 genome ETX44761.1 77.35
Se a ia sp. YD25 Se a ia sp. YD25, comple e genome AOF02338.1 93.57
Se a ia sp. SCBI Se a ia sp. SCBI, comple e genome AIM23801.1 93.44
Se a ia ma cescens subsp. ma cescens
AH0650_Sm1 AG2
Se a ia ma cescens s ain BWH-23
ch omosome, comple e genome KMU50701.1 99.40
Se a ia ma cescens subsp. ma cescens Db11 Se a ia ma cescens subsp. ma cescens
Db11, comple e genome CDG14244.1 99.32
Figu e 4.
Se awe in W2: om he biosyn he ic gene clus e o he s uc u e o se awe in W2. Gene ic
o ganiza ion o he genome o Se a ia s ain PWN146 by an iSMASH analysis, Phy e2 idimensional
p edic ion o he se awe in W2 biosyn he ic p o ein, and PubChem 2D s uc u e o se awe in
W2. (
a
) Se awe in W2 biosyn he ic gene clus e wi h iden i ica ion o he sw A co e gene; (
b
)sw A
gene o ganiza ion: i e modules (M1–M5) wi h C, condensa ion domain; A, adenyla ion domain; T,
hiola ion domain; and TE, hioes e ase domain; (
c
) biosyn he ic p o ein wi h i e modules (M1–M5),
each composed o condensa ion, adenyla ion, and hiola ion domains, and in he las module an
addi ional hioes e ase domain.
To con i m he iden i ica ion o he sw A gene e ealed by an iSMASH, each sw A was, as men ioned
abo e, que ied o NCBI BLASTX, in o de o ind he closes ela i e and de e mine he iden i y
pe cen age (Table 4and Table S3). The p o ein coded by he biosyn he ic genes o se awe in W2
(sw A) showed an iden i y pe cen age ha anges om 76.38% o 99.4% as he closes iden i ica ion by
using BLASTX (Table 4).
Table 4.
The se awe in W2 gene (sw A) o each s ain in his s udy and he accession numbe s and
iden i ica ion o he sw A gene’s closes ela i es using BLASTX.
Bac e ial S ain sw A Closes Rela i e Genes Accession Numbe Iden i y Pe cen age
Se a ia ma cescens SM39 Se a ia ma cescens SM39 DNA,
comple e genome BAO35825.1 76.70
Se a ia ma cescens SmUNAM836 Se a ia ma cescens s ain SmUNAM836,
comple e genome ALE98111.1 76.70
Se a ia sp. SSNIH1 Se a ia sp. SSNIH1 ch omosome,
comple e genome AUY16873.1 76.70
Se a ia sp. PWN146
Se a ia ma cescens isola e
PWN146_assembly genome assembly,
ch omosome
SAY45247.1 77.02
Se a ia u eily ica L 5/4 LG59 Se a ia ma cescens s ain UMH7,
comple e genome KKO55915.1 76.38
Se a ia ma cescens RSC-14 Se a ia ma cescens s ain RSC-14,
comple e genome ALD45109.1 76.38
Se a ia ma cescens BIDMC 44 Se a ia ma cescens s ain 1274 genome ETX44761.1 77.35
Se a ia sp. YD25 Se a ia sp. YD25, comple e genome AOF02338.1 93.57
Se a ia sp. SCBI Se a ia sp. SCBI, comple e genome AIM23801.1 93.44
Se a ia ma cescens subsp. ma cescens
AH0650_Sm1 AG2
Se a ia ma cescens s ain BWH-23
ch omosome, comple e genome KMU50701.1 99.40
Se a ia ma cescens subsp. ma cescens Db11 Se a ia ma cescens subsp. ma cescens
Db11, comple e genome CDG14244.1 99.32
Six y-eigh genes we e iden i ied in he se awe in W2 biosyn he ic gene clus e s (Figu e 5and
Table S5). Twen y- ou genes we e p esen in all he s ains’ gene clus e s (Figu e 5), namely, he
Biology 2020,9, 482 16 o 18
26.
Abebe, E.; Abebe-Akele, F.; Mo ison, J.; Coope , V.; Thomas, W.K. An insec pa hogenic symbiosis be ween
aCaeno habdi is and Se a ia.Vi ulence 2011,2, 158–161. [C ossRe ] [PubMed]
27.
Lepho o, T.E.; Fea he s on, J.; G ay, V.M. D a Whole-genome sequence o Se a ia sp. s ain TEL,
associa ed wi h Oscheius sp. TEL-2014 (Nema oda: Rhabdi idae) isola ed om a g assland in Sou h A ica.
Genome Announc. 2015,3, e00747-15. [C ossRe ] [PubMed]
28.
Wan, Y.; Go ie, C.L.; Jenney, A.; Mi ce a, M.; Hol , K.E. D a genome sequence o a clinical isola e o Se a ia
ma cescens, s ain AH0650_Sm1. Genome Announc. 2015,3, e01007-15. [C ossRe ]
29.
Neupane, S.; Finlay, R.D.; Als öm, S.; Goodwin, L.; Ky pides, N.C.; Lucas, S.; Lapidus, A.; B uce, D.;
Pi luck, S.; Pe e s, L.; e al. Comple e genome sequence o Se a ia plymu hica s ain AS12. S and. Genom. Sci.
2012,6, 165–173. [C ossRe ]
30.
Neupane, S.; Finlay, R.D.; Ky pides, N.C.; Goodwin, L.; Als öm, S.; Lucas, S.; Land, M.; Han, J.; Lapidus, A.;
Cheng, J.-F.; e al. Comple e genome sequence o he plan -associa ed Se a ia plymu hica s ain AS13. S and.
Genom. Sci. 2012,7, 22–30. [C ossRe ]
31.
Neupane, S.; Högbe g, N.; Als öm, S.; Lucas, S.; Han, J.; Lapidus, A.; Cheng, J.F.; B uce, D.; Goodwin, L.;
Pi luck, S.; e al. Comple e genome sequence o he apese ed plan -g ow h p omo ing Se a ia plymu hica
s ain AS9. S and. Genom. Sci. 2012,6, 54–62. [C ossRe ]
32.
Neupane, S.; Goodwin, L.A.; Högbe g, N.; Ky pides, N.C.; Als öm, S.; B uce, D.; Quin ana, B.; Munk, C.;
Daligaul , H.; Teshima, H.; e al. Non-con iguous inished genome sequence o plan -g ow h p omo ing
Se a ia p o eamaculans S4. S and. Genom. Sci. 2013,8, 441–449. [C ossRe ]
33.
Bai, Y.; Mülle , D.B.; S ini as, G.; Ga ido-O e , R.; Po ho , E.; Ro , M.; Domb owski, N.; Münch, P.C.;
Spaepen, S.; Remus-Emse mann, M.; e al. Func ional o e lap o he A abidopsis lea and oo mic obio a.
Na u e 2015,528, 364–369. [C ossRe ] [PubMed]
34.
Chung, W.C.; Chen, L.L.; Lo, W.S.; Kuo, P.A.; Tu, J.; Kuo, C.H. Comple e genome sequence o Se a ia
ma cescens WW4. Genome Announc. 2013,1, 5–6. [C ossRe ] [PubMed]
35.
Siozios, S.; Ces a o, A.; Kau , R.; Pe o , I.; Ro a-S abelli, O.; An o a, G. D a genome sequence o he
Wolbachia endosymbion o D osophila suzukii.Genome Announc. 2013,1, e00032-13. [C ossRe ] [PubMed]
36.
Fine an, P.C.; Cans, C.I.; Ramsay, J.P.; Wil , N.M.; Cossyleon, D.; Mcneil, M.B.; Williamson, N.R.; Monson, R.E.;
Beche , S.A.; S an on, J.L.; e al. D a genome sequence o Se a ia sp. s ain ATCC 39006, a model
bac e ium o analysis o he biosyn hesis and egula ion o p odigiosin, a ca bapenem, and gas esicles.
Genome Announc. 2013,1, e01039-13. [C ossRe ] [PubMed]
37.
Alabed, D.; Huo, N.; Gu, Y.; McCue, K.F.; Thomson, J.G. D a genome sequence o Se a ia sp. 1D1416.
Mic obiol. Resou . Announc. 2019,8, e01354-18. [C ossRe ] [PubMed]
38.
Kopac, S.; Bea y, H.; Gialopsos, P.; Hun emann, M.; Clum, A.; Spunde, A.; Pillay, M.; Palaniappan, K.;
Va ghese, N.; Mikhailo a, N.; e al. High-quali y d a genome sequences o eigh bac e ia isola ed om
ungus ga dens g own by T achymy mex sep en ionalis An s. Mic obiol. Resou . Announc.
2018
,7, e00871-18.
[C ossRe ]
39.
Li, P.; Kwok, A.H.Y.; Jiang, J.; Ran, T.; Xu, D.; Wang, W.; Leung, F.C. Compa a i e genome analyses o Se a ia
ma cescens FS14 e eals i s high an agonis ic po en ial. PLoS ONE 2015,10, e0123061. [C ossRe ]
40.
Roach, D.J.; Bu on, J.N.; Lee, C.; S ackhouse, B.; Bu le -Wu, S.M.; Cookson, B.T.; Shendu e, J.; Salipan e, S.J.
A yea o in ec ion in he in ensi e ca e uni : P ospec i e whole genome sequencing o bac e ial clinical
isola es e eals c yp ic ansmissions and no el mic obio a. PLoS Gene . 2015,11, e1005413. [C ossRe ]
41.
Daligaul , H.E.; Da enpo , K.W.; Minogue, T.D.; B oomall, S.M.; B uce, D.C.; Chain, P.S.; Coyne, S.R.;
Gibbons, H.S.; Jaissle, J.; Rosenzweig, C.N.; e al. Genome assembly o Se a ia ma cescens ype s ain ATCC
13880. Genome Announc. 2014,2. [C ossRe ]
42.
Da is, E.W., II; Weisbe g, A.J.; Tabima, J.F.; G unwald, N.J.; Chang, J.H. Gall-ID: Tools o geno yping
gall-causing phy opa hogenic bac e ia. Pee J 2016,4, e2222. [C ossRe ]
43.
Weinga en, R.A.; Johnson, R.C.; Conlan, S.; Ramsbu g, A.M.; Dekke , J.P.; Lau, A.F.; Khil, P.; Odom, R.T.;
Deming, C.; Pa k, M.; e al. Genomic analysis o hospi al plumbing e eals di e se ese oi o bac e ial
plasmids con e ing ca bapenem esis ance. MBio 2018,9, e02011-17. [C ossRe ] [PubMed]
44.
Kwak, Y.; Khan, A.R.; Shin, J.H. Genome sequence o Se a ia nema odiphila DSM 21420T, a symbio ic
bac e ium om en omopa hogenic nema ode. J. Bio echnol. 2015,193, 1–2. [C ossRe ] [PubMed]

Biology 2020,9, 482 17 o 18
45.
Pei, D.; Hill-Clemons, C.; Ca issimo, G.; Yu, W.; Ve nick, K.D.; Xu, J. D a genome sequences o wo s ains
o Se a ia spp. om he midgu o he mala ia mosqui o Anopheles gambiae.Genome Announc.
2016
,3,
e00090-15. [C ossRe ] [PubMed]
46.
Poehlein, A.; F eese, H.M.; Daniel, R.; Simeono a, D.D. D a genome sequence o Se a ia sp. s ain DD3,
isola ed om he gu s o Daphnia magna.Genome Announc. 2014,2, e00903-14. [C ossRe ] [PubMed]
47.
Chen, X.; Hi chings, M.D.; Mendoza, J.E.; Balanza, V.; Facey, P.D.; Dyson, P.J.; Bielza, P.; Del Sol, R.
Compa a i e genomics o acul a i e bac e ial symbion s isola ed om Eu opean o ius species e eals an
ances al symbio ic associa ion. F on . Mic obiol. 2017,8, 1969. [C ossRe ] [PubMed]
48.
Nicholson, W.L.; Leona d, M.T.; Faja do-Ca azos, P.; Panayo o a, N.; Fa me ie, W.G.; T iple , E.W.;
Schue ge , A.C. Comple e genome sequence o Se a ia lique aciens s ain ATCC 27592. Genome Announc.
2013,1, e00548-13. [C ossRe ] [PubMed]
49.
Iguchi, A.; Nagaya, Y.; P adel, E.; Ooka, T.; Ogu a, Y.; Ka su a, K.; Ku okawa, K.; Oshima, K.; Ha o i, M.;
Pa khill, J.; e al. Genome e olu ion and plas ici y o Se a ia ma cescens, an impo an mul id ug- esis an
nosocomial pa hogen. Genome Biol. E ol. 2014,6, 2096–2110. [C ossRe ]
50.
Webe , T.; Blin, K.; Duddela, S.; K ug, D.; Kim, H.U.; B uccole i, R.; Lee, S.Y.; Fischbach, M.A.; Mülle , R.;
Wohlleben, W.; e al. an iSMASH 3.0—a comp ehensi e esou ce o he genome mining o biosyn he ic gene
clus e s. Nucleic Acids Res. 2015,43, W237–W243. [C ossRe ]
51.
Al schul, S.F.; Madden, T.L.; Schä e , A.A.; Zhang, J.; Zhang, Z.; Mille , W.; Lipman, D.J. Gapped BLAST and
PSI-BLAST: A new gene a ion o p o ein da abase sea ch p og ams. Nucleic Acids Res.
1997
,25, 3389–3402.
[C ossRe ]
52.
Kim, O.-S.; Cho, Y.-J.; Lee, K.; Yoon, S.-H.; Kim, M.; Na, H.; Pa k, S.-C.; Jeon, Y.S.; Lee, J.-H.; Yi, H.; e al.
In oducing EzTaxon-e: A p oka yo ic 16S RNA gene sequence da abase wi h phylo ypes ha ep esen
uncul u ed species. In . J. Sys . E ol. Mic obiol. 2012,62, 716–721. [C ossRe ]
53.
P uesse, E.; Peplies, J.; Glöckne , F.O. SINA: Accu a e high- h oughpu mul iple sequence alignmen o
ibosomal RNA genes. Bioin o ma ics 2012,28, 1823–1829. [C ossRe ]
54.
Ludwig, W.; S unk, O.; Wes am, R.; Rich e , L.; Meie , H.; Yadhukuma ; Buchne , A.; Lai, T.; S eppi, S.;
Jobb, G.; e al. ARB: A so wa e en i onmen o sequence da a. Nucleic Acids Res.
2004
,32, 1363–1371.
[C ossRe ] [PubMed]
55.
S ama akis, A. RAxML-VI-HPC: Maximum likelihood-based phylogene ic analyses wi h housands o axa
and mixed models. Bioin o ma ics 2006,22, 2688–2690. [C ossRe ] [PubMed]
56.
Kelley, L.A.; Mezulis, S.; Ya es, C.M.; Wass, M.N.; S e nbe g, M.J.E. The Phy e2 web po al o p o ein
modeling, p edic ion and analysis. Na . P o oc. 2015,10, 845–858. [C ossRe ]
57.
Kuma , S.; S eche , G.; Li, M.; Knyaz, C.; Tamu a, K. MEGA X: Molecula e olu iona y gene ics analysis
ac oss compu ing pla o ms. Mol. Biol. E ol. 2018,35, 1547–1549. [C ossRe ] [PubMed]
58.
Sai ou, N.; Nei, M. The neighbo -joining me hod: A new me hod o econs uc ing phylogene ic ees.
Mol. Biol. E ol. 1987,4, 406–425. [PubMed]
59.
UniP o : A wo ldwide hub o p o ein knowledge. Nucleic Acids Res.
2019
,47, D506–D515. [C ossRe ]
[PubMed]
60.
Ande son, M.T.; Mi chell, L.A.; Zhao, L.; Mobleya, H.L.T. Capsule p oduc ion and glucose me abolism
dic a e i ness du ing Se a ia ma cescens bac e emia. MBio 2017,8, e00740-17. [C ossRe ]
61.
Nascimen o, F.X.; Espada, M.; Ba bosa, P.; Rossi, M.J.; Vicen e, C.S.L.; Mo a, M. Non-speci ic ansien
mu ualism be ween he plan pa asi ic nema ode, Bu saphelenchus xylophilus, and he oppo unis ic
bac e ium Se a ia quini o ans BXF1, a plan -g ow h p omo ing pine endophy e wi h an agonis ic e ec s.
En i on. Mic obiol. 2016,18, 5265–5276. [C ossRe ]
62.
Yang, Y.; Jin, H.; Chen, Y.; Lin, W.; Wang, C.; Chen, Z.; Han, N.; Bian, H.; Zhu, M.; Wang, J. A chlo oplas
en elope memb ane p o ein con aining a pu a i e L gB domain ela ed o he con ol o bac e ial dea h and
lysis is equi ed o chlo oplas de elopmen in A abidopsis haliana.New Phy ol.
2012
,193, 81–95. [C ossRe ]
63.
Cha bonnie , T.; Le Coq, D.; McGo e n, S.; Calab e, M.; Delumeau, O.; Ayme ich, S.; Jules, M. Molecula and
physiological logics o he py u a e-induced esponse o a no el anspo e in Bacillus sub ilis.MBio
2017
,8,
e00976-17. [C ossRe ] [PubMed]
64.
Wang, I.-N.; Smi h, D.L.; Young, R. Holins: The p o ein clocks o bac e iophage in ec ions. Annu. Re .
Mic obiol. 2000,54, 799–825. [C ossRe ]
Biology 2020,9, 482 18 o 18
65.
Ahn, S.-J.; Rice, K.C.; Oleas, J.; Bayles, K.W.; Bu ne, R.A. The S ep ococcus mu ans Cid and L g sys ems
modula e i ulence ai s in esponse o mul iple en i onmen al signals. Mic obiology
2010
,156, 3136–3147.
[C ossRe ] [PubMed]
66.
an den Eske , M.H.; Ko
á
cs,
Á
.T.; Kuipe s, O.P. F om cell dea h o me abolism: Holin-an iholin homologues
wi h new unc ions. MBio 2017,8, e01963-17. [C ossRe ] [PubMed]
67.
Pao, S.S.; Paulsen, I.T.; Saie , M.H. Majo acili a o supe amily. Mic obiol. Mol. Biol. Re .
1998
,62, 1–34.
[C ossRe ]
68.
D’A genio, D.A.; Mille , S.I. Cyclic di-GMP as a bac e ial second messenge . Mic obiology
2004
,150, 2497–2502.
[C ossRe ] [PubMed]
Publishe ’s No e:
MDPI s ays neu al wi h ega d o ju isdic ional claims in published maps and ins i u ional
a ilia ions.
©
2020 by he au ho s. Licensee MDPI, Basel, Swi ze land. This a icle is an open access
a icle dis ibu ed unde he e ms and condi ions o he C ea i e Commons A ibu ion
(CC BY) license (h p://c ea i ecommons.o g/licenses/by/4.0/).