Surveillance of antibiotic resistance in Neisseria gonorrhoeae in the WHO Western Pacific Region, 1998

This article published in Communicable Diseases Intelligence Volume 24, No 1, 20 January 2000 contains the annual report on Neisseria gonorrhoeae in the WHO Western Pacific Region, 1998.

Page last updated: 25 January 2000

A print friendly PDF version is available from this Communicable Diseases Intelligence issue's table of contents.


The WHO Western Pacific Gonococcal Antimicrobial Surveillance Programme1

Introduction | Methods | Results | Acknowledgements | References

Abstract

Effective treatment of gonorrhoea in the World Health Organization's Western Pacific Region is hampered by the emergence and spread of antibiotic resistant strains of Neisseria gonorrhoeae. A programme of surveillance of gonococcal susceptibility to antibiotics (GASP) continued in the region in 1998. A high proportion of isolates in many participating countries was resistant to quinolones and penicillins, continuing trends observed by this programme since 1992. Resistance to the later generation cephalosporins and to spectinomycin was absent or infrequent. Options for effective treatment of gonorrhoea in the region have been severely compromised by antibiotic resistance. Commun Dis Intell 2000;24:1-4.

Introduction

Even if considered simply in numeric terms, gonorrhoea remains a major global disease with an estimated 60 million cases of gonococcal disease occurring annually.1 About half of these cases occur in the World Health Organization's (WHO) Western Pacific (WP) and South East Asian (SEA) regions. Control of gonorrhoea (and other sexually transmitted diseases (STDs)), is a difficult and complex issue, but one essential component is the provision of effective antibiotic treatment. As well controlling the disease itself, appropriate therapy reduces morbidity associated with gonorrhoea such as pelvic inflammatory disease (PID) and neonatal ophthalmia. HIV transmission is also amplified in the presence of gonorrhoea, but this effect can be ameliorated if treatment is provided. In some settings this intervention substantially reduces HIV transmission.2 There are thus a number of important reasons why gonococcal disease should be properly treated.

One factor limiting the efficacy of antibiotics in gonococcal disease is the ability of the organism to develop resistance to them, and historically much of this resistance has appeared first in the WP and SEA regions. There is however, a strong correlation between likely outcome of antibiotic therapy and the in vitro susceptibility of gonococci. This means that if the susceptibility of prevalent gonococci to antibiotics is determined systematically using an epidemiological approach, a reliable guide to the choice of suitable standard treatment regimens can be provided in a country or region. There are a number of examples of country based systems of laboratory based surveillance in existence.3,4 The WHO WP Gonococcal Antimicrobial Surveillance Programme (WPR GASP) combines a number of these local networks and functions at a regional level. The WPR GASP has monitored the antibiotic susceptibility of gonococci isolated in the WPR since 1992.5 Results have been published annually in CDI since 1992.6-10

Top of page

Methods

A full description of the methods used by this programme has been published5 and includes details of sample sources, isolate selection, use of standardised testing methods, a programme specific external quality assurance component and the technical support and training provided under GASP auspices. These methods did not alter in 1998.

Top of page

Results and Discussion

Sixteen countries in the WPR contributed data on about 10,000 isolates in 1998.

As was expected from previous regional surveillance, resistance to the penicillins was widespread (Table 1). Both chromosomal (CMRNG) and plasmid mediated (PPNG) forms of resistance were common. The highest rates of penicillin resistance were reported from Korea (90%), the Philippines (82%), Vietnam (76%), Mongolia (70%), China - Hong Kong (69%), China (62%) and Singapore (59%). These percentages were the total of all forms of penicillin resistance. The proportion of PPNG has been declining in some centres, but CMRNG have become more prominent.

Table 1. Penicillin sensitivity of strains of Neisseria gonorrhoeae isolated in countries in the WHO WPR in 1998

Country
Number tested PPNG CMRNG All penicillin resistant
Number % Number % Number %
Australia
3,583
206
5.7
782
21.8
988
27.5
China
939
30
3.2
558
59.4
588
62.6
Fiji
836
33
4.0
40
4.8
73
8.8
Hong Kong (China)
2,255
59
2.6
1,497
66.4
1,556
69.0
Japan
190
1
0.5
15
7.9
16
8.4
Korea
134
99
74.0
21
15.6
120
89.6
Malaysia
na
-
-
-
-
-
-
Mongolia
27
7
26.0
12
44.0
19
70.0
New Caledonia
67
-
-
-
-
6
9.0
New Zealand
490
19
3.9
33
6.7
52
10.6
Papua New Guinea
197
50
25.0
23
12.0
62
37.0
Philippines
245
194
79.0
7
2.8
201
82.0
Singapore
768
439
57.2
12
1.6
451
58.8
Solomon Islands
34
0
 
0
 
0
 
Tonga
37
3
8.0
1
2.7
4
10.8
Vanuatu
89
-
-
-
-
32
35.9
Vietnam
158
99
62.7
22
13.9
121
76.6

Resistance to the quinolone antibiotics (QRNG) continued to increase in a number of centres or else was maintained in a high proportion of isolates in 1998 (Table 2). Quinolone resistance in gonococci results only from different but additive chromosomal changes, and there is no plasmid-mediated transmission. Some of these alterations occur only in the presence of previous mutations. For example, parC changes are seen only after alterations in gyrA have appeared. This means that levels of resistance in QRNG (as determined by Minimal Inhibitory Concentrations - MICs) show a sequential change. Because of this incremental nature of quinolone resistance, it is relevant to monitor both low (MIC of ciprofloxacin 0.06 to 0.5 mg/L) and high level (MIC of ciprofloxacin ≥ 1 mg/L) resistance to quinolone antibiotics. Quinolone resistance was assessed in 13 countries in 1998 and QRNG were found in 11, the exceptions being Fiji and the Solomon Islands. In excess of 90% of isolates in China and China - Hong Kong were QRNG and about half in each setting possessed high level resistance. Both of these focal points had high proportions of QRNG in 1997 but the total QRNG percentages in 1998 were even higher and the proportion of high level QRNG also increased. The Philippines had a high proportion of high level QRNG (63%), also continuing a pattern observed for some time. Korea (62%) and Japan (52%) again reported a high percentage of QRNG, but most were in the category of lower level QRNG. Other centres such as Vietnam, Papua New Guinea and Singapore show a lower proportion of mixed low and high level QRNG. In other countries (Australia, New Zealand), QRNG are most often represented by imported strains but with some endemic transmission also occurring. Previous observations summarised the position with regard to QRNG in the WPR as a trend showing more countries recording the presence of QRNG, a higher proportion of QRNG being recorded in these countries each year, and higher MICs in those QRNG present. These observations remain pertinent for 1998.


Table 2. Quinolone resistance in strains of Neisseria gonorrhoeae isolated in countries in the WHO WPR in 1998

Country
Number tested Less susceptible Resistant
Number % Number %
Australia
3,583
70
2.0
116
3.2
China
912
332
36.4
509
54.2
Fiji
Not stated
0
0.0
0
0.0
Hong Kong (China)
2,255
993
44.0
1,100
48.8
Japan
190
95
50.0
5
2.6
Korea
134
69
51.5
15
11.2
Malaysia
na
na
na
na
na
New Caledonia
67
2
3.0
5
7.5
New Zealand
490
7
1.4
6
1.2
Papua New Guinea
187
1
0.5
6
3.2
Philippines
245
3
1.2
155
63.0
Singapore
768
34
4.4
55
7.2
Solomon Islands
34
0
0.0
0
0.0
Vietnam
160
15
9.4
13
8.1
Top of page

All isolates remained sensitive to the third generation cephalosporin ceftriaxone. These results would also apply to the oral equivalent cefixime, but not necessarily to earlier generation cephalosporins. Some increase in MICs to ceftriaxone was again noted in some centres. Although this decrease in susceptibility has yet to translate into clinical resistance, continued observation of this aspect of evolving gonococcal resistance is advisable.

Spectinomycin resistance is rarely encountered in the WPR and only in sporadic cases (Table 3). Only five strains from over 900 examined in China were spectinomycin resistant in 1998. This may reflect the low frequency of use of this injectable agent in the region. The aminoglycoside antibiotic gentamicin is sometimes used in the region for the treatment of gonorrhoea because of cost considerations. No data are available on patterns of resistance to this agent.

Table 3. Spectinomycin resistance in isolates of Neisseria gonorrhoeae in countries in the WHO WPR in 1998

Country
Number tested Number % Resistant
Australia
3,583
0.0
0.0
China
939
5.0
0.5
Japan
190
0.0
0.0
Korea
134
0.0
0.0
New Caledonia
67
0.0
0.0
Papua New Guinea
59
0.0
0.0
Philippines
245
0.0
0.0
Singapore
768
0.0
0.0
Solomon Islands
34
0.0
0.0
Vietnam
156
0.0
0.0


Tetracyclines are not a recommended treatment for gonorrhoea. However their ready availability and low cost means that they are often used in the informal health sector in a number of countries. A special form of high level resistance to tetracyclines exists and is disseminated by plasmid exchange. Strains with this form of resistance are known as TRNG. Trends in the spread of TRNG have been followed in the WPR as an exercise in the monitoring of emerging antibiotic resistance (Table 4). TRNG have been clustered in certain countries in the WPR, notably Singapore and Malaysia, for some time. Over 80% of isolates in Singapore were TRNG in 1998 and in the Solomon Islands 75% of strains were TRNG. The other centre with a high rate of TRNG was Vietnam (36%). Six other centres had TRNG rates of less than 10% and in Japan and Korea no TRNG were detected. The increase in TRNG rates in Singapore and the Solomon Islands was the only real change in TRNG distribution in the WPR in 1998.

Table 4. High level tetracycline resistance, TRNG, in strains of Neisseria gonorrhoeae isolated in countries in the WHO WPR in 1998

Country
Number tested Number % TRNG
Australia
3,583
24
6.7
China
828
24
2.9
Japan
190
0
0.0
Korea
134
0
0.0
Mongolia
27
0
0.0
New Zealand
490
25
5.1
Papua New Guinea
187
9
4.8
Philippines
245
17
6.9
Singapore
768
648
84.0
Solomon Islands
34
25
74.0
Vietnam
156
56
35.9


Other agents are sometimes used in the WPR mainly because of cost considerations. For example, chloramphenicol/thiamphenicol continues as a recommended treatment in some jurisdictions. Again only scanty data are available on the resistance patterns to these antibiotics. These data do, however, indicate that resistance is present in a significant number of strains tested.

The changes observed in the 1998 susceptibility patterns of gonococci found in the region were incremental. However, this increase was on top of an already high and worrying level of resistance. The observations confirmed the limited options for treatment in the WPR of a disease of high incidence. Those treatment options available are often in a cost bracket that makes their use difficult even when they are a 'recommended' treatment. However, substitution of cheaper but less efficacious agents is in the longer term more expensive and counter-productive.

Top of page

Acknowledgements

The following members of the WHO Western Pacific Gonococcal Antimicrobial Surveillance Programme supplied data in 1998 for the WPR GASP:

Members of the Australian Gonococcal Surveillance Programme throughout Australia; Ye Shunzhang and Su Xiaohong, Nanjing, China; M. Shah, Suva, Fiji; K. M. Kam, Hong Kong; Toshiro Kuroki, Yokohama and M. Tanaka, Fukuoka, Japan; K. Lee and Y. Chong, Seoul, Korea; Erdenechimeg, Ulaanbaatar, Mongolia; B. Garin, Noumea, New Caledonia; M. Brett, Wellington and M. Brokenshire, Auckland, New Zealand; Tony Lupiwa Papua New Guinea; C. C. Carlos, Manila, Philippines; A. E. Ling, Singapore; A. Darcy, Solomon Islands; Ane Tone Ika, Nuku'alofa, Tonga; H. Wamle Vanuatu; Le Thi Phuong, Hanoi, Vietnam.

Author affiliation

1. Address for correspondence: J. W. Tapsall, WHO Collaborating Centre for STD and HIV, Department of Microbiology, The Prince of Wales Hospital, Randwick, Sydney, New South Wales, Australia 2031; Fax + 61 2 9398 4275; E-mail j.tapsall@unsw.edu.au.

Top of page

References

1. Gerbase AC, Rowley JT, Heymann DHL, Berkley SFB, Piot P. Global prevalence and incidence estimates of selected curable STDs. Sex Transm Inf 1998;74(suppl 1):S12-S16.

2. Cohen MS. Sexually transmitted diseases enhance HIV transmission: no longer a hypothesis. Lancet 1998;351(suppl III):5-7.

3. Growitz RJ, Nakashima AK, Moran JS, Knapp JS. Sentinel surveillance for antimicrobial resistance in Neisseria gonorrhoeae - United States, 1988-1991 MMWR 1993;42(SS3):29-39.

4. Australian Gonococcal Surveillance Programme. Penicillin sensitivity testing of gonococci in Australia: development of Australian gonococcal surveillance programme. Br J Vener Dis 1984;60:226-230.

5. WHO Western Pacific Region Gonococcal Surveillance Programme. Surveillance of antibiotic susceptibility of Neisseria gonorrhoeae in the WHO Western Pacific Region 1992-4. Genitourin Med 1997;73:355-361.

6. The World Health Organization Western Pacific Region Gonococcal Surveillance Programme. 1992 Annual Report. Commun Dis Intell 1994,18:61-63.

7. The World Health Organization Western Pacific Region Gonococcal Surveillance Programme. 1993 annual report. Commun Dis Intell 1994;18:307-310.

8. The World Health Organization Western Pacific Region Gonococcal Surveillance Programme. 1994 annual report. Commun Dis Intell 1995;19:495-499.

9. The World Health Organization Western Pacific Gonococcal Antimicrobial Surveillance Programme. Antimicrobial resistance in gonococci, Western Pacific region, 1995. Commun Dis Intell 1996;20:425-428.

10. The World Health Organization Western Pacific Gonococcal Antimicrobial Surveillance Programme. Resistance in gonococci isolated in the WHO Western Pacific Region to various anticrobials used in the treatment of gonorrhoeae, 1997. Commun Dis Intell 1998;22:288-291.


This article was published in Communicable Diseases Intelligence Volume 24, No 1, 20 January 2000.

Communicable Diseases Intelligence subscriptions

Sign-up to email updates: Subscribe Now

This issue - Vol 24, No 1, 20 January 2000