Streptococcus suis serotyping by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry

被引:16
作者
Chaiden, Chadaporn [1 ]
Jaresitthikunchai, Janthima [2 ]
Kerdsin, Anusak [3 ]
Meekhanon, Nattakan [4 ]
Roytrakul, Sittiruk [2 ]
Nuanualsuwan, Suphachai [1 ,5 ]
机构
[1] Chulalongkorn Univ, Dept Vet Publ Hlth, Fac Vet Sci, Bangkok, Thailand
[2] Natl Sci & Technol Dev Agcy, Natl Ctr Genet Engn & Biotechnol, Funct Ingredients & Food Innovat Res Grp, Funct Prote Technol Lab, Pathum Thani, Thailand
[3] Kasetsart Univ, Fac Publ Hlth, Chalermphrakiat Sakon Nakhon Prov Campus, Sakon Nakhon, Thailand
[4] Kasetsart Univ, Fac Vet Technol, Dept Vet Technol, Bangkok, Thailand
[5] Chulalongkorn Univ, Res Unit, Food Risk Hub, Bangkok, Thailand
关键词
DESORPTION IONIZATION-TIME; IDENTIFICATION; BACTERIA; PIGS;
D O I
10.1371/journal.pone.0249682
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Streptococcus suis, particularly S. suis serotype 2 (SS2), is an important zoonotic pathogen causing meningitis in humans worldwide. Although the proper classification of the causative and pathogenic serotype is salutary for the clinical diagnosis, cross-reactions leading to the indistinguishability of serotypes by the current serotyping methods are significant limitations. In the present study, matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) analysis of extracted peptides was developed to improve the classification of serotype of S. suis. The peptide mass fingerprint (PMFs) database of S. suis was generated from the whole-cell peptides of 32 reference strains of S. suis isolates obtained from pigs. Thirty-two human S. suis isolates from clinical cases in Thailand were used to validate this alternative serotyping method in direct comparison to the multiplex (m)PCR approach. All reference strains, representing 32 serotypes of S. suis, exhibited their individual PMFs patterns, thus allowing differentiation from one another. Highly pathogenic SS2 and SS14 were clearly differentiated from the otherwise serologically closely related SS1/2 and SS1, respectively. The developed MALDI-TOF-MS serotyping method correctly classified the serotype in 68.8% (22/32) of the same serotype isolates generated from the PMFs database; while the validity for the clinical human isolates was 62.5% (20/32). The agreement between the MALDI-TOF-MS and mPCR serotyping was moderate with a Kappa score of 0.522, considering that mPCR could correctly serotype up to 75%. The present study demonstrated that PMFs from the developed MALDI-TOF-MS-based method could successfully discriminate the previously indistinguishable highly pathogenic SS2 and SS14 from SS1/2 and SS1, respectively. Moreover, this serotyping method distinguished pathogenic SS6, and so is an alternative approach of choice to rapidly and reliably serotype clinically pathogenic S. suis isolates.
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页数:14
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