Free Standard AU & NZ Shipping For All Book Orders Over $80!
Register      Login
Sexual Health Sexual Health Society
Publishing on sexual health from the widest perspective
RESEARCH ARTICLE

Prevalence of porA pseudogene deletion among Neisseria gonorrhoeae isolates referred to the UK’s Gonococcal Resistance to Antimicrobials Surveillance Program

Martina Toby A , Pamela Saunders B , Michelle Cole B , Vlad Grigorjev B , Sarah Alexander B C and Catherine Ison B
+ Author Affiliations
- Author Affiliations

A 56 Dean Street, Soho, London, W1D 6AQ, UK.

B Sexually Transmitted Bacteria Reference Unit, Public Health England, 61 Colindale Avenue, London, NW9 5EQ, UK.

C Corresponding author. Email: Sarah.Alexander@phe.gov.uk

Sexual Health 14(4) 392-393 https://doi.org/10.1071/SH16162
Submitted: 26 August 2016  Accepted: 22 February 2017   Published: 18 May 2017

Abstract

porA pseudogene-negative Neisseria gonorrhoeae isolates produce false-negative results when examined by polymerase chain reaction (PCR) with porA pseudogene targets. In the present study, 533 representative gonococcal isolates received in 2011 via the Gonococcal Resistance to Antimicrobials Surveillance Program were examined to determine the prevalence of porA-negative isolates. Less than 0.4% (2/533) of isolates were found to be reproducibly negative with the porA real-time PCR but were confirmed as N. gonorrhoeae with molecular, biochemical and immunological confirmatory tests. Sequencing revealed both isolates contained the Neisseria meningitidis porA gene. Low prevalence indicates that although these isolates do not present a major public health problem, microbiologists should remain vigilant.


References

[1]  Toby M, Saunders P, Ison CA. Survey of the laboratory diagnosis of gonorrhoea and chlamydial infection in the UK. Sex Transm Infect 2015; 91 299
Survey of the laboratory diagnosis of gonorrhoea and chlamydial infection in the UK.Crossref | GoogleScholarGoogle Scholar |

[2]  Golparian D, Johansson E, Unemo M. Clinical Neisseria gonorrhoeae isolate with a N. meningitidis porA gene and no prolyliminopeptidase activity, Sweden, 2011 – danger of false-negative genetic and culture diagnostic results. Euro Surveill 2012; 17 20102

[3]  Eastick K, Winter A, Jamdar S. Identification of Neisseria gonorrhoeae isolates with a recombinant porA gene in Scotland, United Kingdom, 2010 to 2011. Euro Surveill 2012; 17 20101

[4]  Whiley DM, Limnios A, Moon NJ, Gehrig N, Goire N, Hogan T, Lam A, Jacob K, Lambert SB, Nissen MD, Sloots TP. False-negative results using Neisseria gonorrhoeae porA pseudogene PCR – a clinical gonococcal isolate with an N. meningitidis porA sequence, Australia, March 2011. Euro Surveill 2011; 16 19874

[5]  Ison C, Golparian D, Saunders P, Chisholm S, Unemo M. Evolution of Neisseria gonorrhoeae is a continuing challenge for molecular detection of gonorrhoeae: false negative gonococcal porA mutants are spreading internationally. Sex Transm Infect 2013; 89 197–201.
Evolution of Neisseria gonorrhoeae is a continuing challenge for molecular detection of gonorrhoeae: false negative gonococcal porA mutants are spreading internationally.Crossref | GoogleScholarGoogle Scholar |

[6]  Health Protection Agency. GRASP 2011 Report: the gonococcal resistance to antimicrobials surveillance programme. 2012. Available online at: http://webarchive.nationalarchives.gov.uk/20140714084352/http://www.hpa.org.uk/webc/HPAwebFile/HPAweb_C/1317136030908 [verified 23 April 2017].

[7]  Whiley DM, Sloots TP. Comparison of three in-house multiplex PCR assays for the detection of Neisseria gonorrhoeae and Chlamydia trachomatis using real-time and conventional detection methodologies. Pathology 2005; 37 364–70.
Comparison of three in-house multiplex PCR assays for the detection of Neisseria gonorrhoeae and Chlamydia trachomatis using real-time and conventional detection methodologies.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXhtV2hu7vE&md5=4007bfbe61b9cd992d35fdc34c056690CAS |

[8]  Tabrizi SN, Chen S, Tapsall J, Garland SM. Evaluation of opa-based real-time PCR for detection of Neisseria gonorrhoeae. Sex Transm Dis 2005; 32 199–202.
Evaluation of opa-based real-time PCR for detection of Neisseria gonorrhoeae.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXhsF2ltrg%3D&md5=f7a9191b73008eeb3e58ef96e3f1ae13CAS |

[9]  Public Health England. Guidance for the detection of gonorrhoea in England 2014. 2014. Available online at: https://www.gov.uk/government/uploads/system/uploads/attachment_data/file/405293/170215_Gonorrhoea_testing_guidance_REVISED__2_.pdf [verified 23 April 2017].